35 PROCESSING/MANUFACTURING/UTILITIES jobs

The incumbent will be responsible to set up and operate a variety of machines used for preparation to complete Electron Beam Welded components. They will be responsible for their work area to ensure the safe and efficient operation of their area.  They will set up and monitor the production of product through their area and actively participate in the continuous improvement process for safety, production and quality.  Flexibility in performing other duties to support the manufacturing and timely delivery of our customer's products will be required. Some experience with Fusion Welding/Electron Beam Welding and knowledge of metallurgy would be an asset.

Shift Work Required Knowledge of CNC Lathes and Fanuc controls Experience with blue print reading, cutting tool selection and set ups an asset,  willing to train the right individual Trouble shooting abilities for work with a wide variety of material Knowledge with the use of precision measuring instruments  

F & P Mfg. Inc., offers an exciting and rewarding career opportunity in a fast paced, highly automated, state-of-the-art automotive parts manufacturing facility located in Tottenham, located 40 minutes north of the Toronto airport. F & P Mfg. Inc., is a tier one automotive parts supplier producing suspension components and pedal assemblies for Honda. We are a complete manufacturing facility and have been stamping, welding, painting and assembling parts for 30 years. We have 900 associates working at our 2 on site manufacturing plants. Position Summary : Work with Asst. Manager and other New Model members to develop and review process plans and equipment installation for new model launches. Hours of work: 7:30 am-4:00 pm Position Responsibilities : Develop Process Plans for welding and assembly processes for New Model launches. Coordinate and schedule procurement of equipment. Control project investment. Coordinate with outside vendors and customers. Prepare documents and present to upper management. Communicate with all internal departments and outside vendors. Install equipment, review and apply best manufacturing processes. Other duties and responsibilities as required. Qualifications: Engineering diploma in related field. Experience in manufacturing processes highly preferred. Excellent organizational, communication and coordination skills. Able to travel and work flexible hours. We offer a competitive wage and benefit package including incentive bonus, paid overtime, complete medical, dental, prescription drug programs, and a company paid pension plan worth 5% of base salary. If you are interested in this challenging opportunity, please submit your resume and diploma/transcript. As part of our commitment to ensuring our employment practices are fair, accessible and inclusive of persons with disabilities, please note that accommodations are available, upon request, throughout the recruitment, selection and assessment process for any applicants with disabilities.

Project Administrator (Quality Assurance – New Model) F & P Mfg., Inc., offers an exciting and rewarding career opportunity in a fast paced, highly automated, state-of-the-art automotive parts manufacturing facility located in Tottenham, located 40 minutes north of the Toronto airport. F & P Mfg., Inc., is a tier one automotive parts supplier producing suspension components and pedal assemblies for Honda. We are a complete manufacturing facility and have been stamping, welding, painting and assembling parts for 30 years. We have 900 associates working at our 2 on site manufacturing plants. Position Summary :  Administer New Model Projects Position Responsibilities: Main customer contact for ew model projects Administer new model quotation process Administer new model drawing control process Facilitate project management team meetings Facilitate project phase gate evaluations Coordinate trial events Control new model trial event part inventory Qualifications: Post-secondary education in a related field Experience with project administration , from conception to completion Ability to prepare and interpret flow charts, schedules and step-by-step action plans Solid organizational skills, including multitasking and time-management Strong communication and teamwork skills Familiarity with risk management Familiarity with metal forming and welding processes and how they interact Understanding of IATF16949 and APQP would be an asset Computer knowledge and experience with Microsoft Project, Excel, Work and Power Point would be an asset.  

Quality Technical Support- Metalforming F & P Mfg., Inc., offers an exciting and rewarding career opportunity in a fast paced, highly automated, state-of-the-art automotive parts manufacturing facility located in Tottenham, located 40 minutes north of the Toronto airport. F & P Mfg., Inc., is a tier one automotive parts supplier producing suspension components and pedal assemblies for Honda. We are a complete manufacturing facility and have been stamping, welding, painting and assembling parts for 30 years. We have 900 associates working at our 2 on site manufacturing plants. Position Summary :   Support quality related activities for the Metalforming department (Stamping, Hydroforming, Die Maintenance, Milling) to meet internal and customer requirements. Hours of work: 7:30am-4:00pm Monday- Friday Position Responsibilities : Ensure processes are performed according to Control Plans and QMS standards. Investigate incidents of outflow and implement required containment and sorting. Apply suitable techniques to determine root cause, temporary and permanent countermeasures. Review similar processes to prevent repeat occurrences. Monitor and disposition parts on QA hold. Report status to QA management. Perform internal QMS audits as scheduled. Participate in Quality Committee meetings. Participate in die trials and weld fit up reviews. Participate in New Model core teams as applicable and help develop related documentation for the new projects. Participate in QA drawing review meetings. Generate monthly Cost of Poor Performance reports highlighting quality cost reduction activities and countermeasures to high PPM. Liaison with employees and management members on quality related matters Qualifications: Post-secondary education in a related field 1-2 years’ experience in manufacturing/quality. Understanding of ISO/TS16949, SPC, quality problem solving tools and APQP. Experience in automotive manufacturing. Working knowledge of all metal forming processes. Thoroughly versed in use of array of measuring & testing equipment. Organizational skills. Leadership and communication skills. Able to work independently. Computer knowledge.

F & P Mfg., Inc., offers an exciting and rewarding career opportunity in a fast paced, highly automated, state-of-the-art automotive parts manufacturing facility located in Tottenham, located 40 minutes north of the Toronto airport. F & P Mfg., Inc., is a tier one automotive parts supplier producing suspension components and pedal assemblies for Honda. We are a complete manufacturing facility and have been stamping, welding, painting and assembling parts for 30 years. We have 900 associates working at our 2 on site manufacturing plants. Position Summary : Support Logistics/ Supply Chain operation and facilitate continuous improvements Hours of work: 7:30 am-4:00 pm Position Responsibilities : Determine the number of loads required & make shipping schedules. Coordinate the optimisation of the supply chain. Coordinate with freight carriers improvements to transit visibility. Develop plans and implement improvements to inventory accuracy. Develop plans and implement improvements to material flow. Coordinate schedule between inter-corporate companies &/or carriers. Ensures all loads meet their intended destination on time. Follow up on loads, in and outbound on transit. Track transportation costs and KPI’s. Providing support for Customs documentation and statuary requirements Qualifications: Minimum of 5 years working experience with inventory control/supply chain/ materials management High level of mathematical and analytical skills Strong understanding of production processes Project management experience and skills Experience with MRP/ERP Systems In-depth knowledge of warehouse management systems Excellent customer service, negotiation, organization and communication skills Experience in the automotive parts manufacturing industry strongly preferred We offer a competitive wage and benefit package including incentive bonus, paid overtime, complete medical, dental, prescription and drug programs, and a company paid pension plan worth 5% of base salary. If you are interested in this challenging opportunity, please submit your resume and diploma or official transcript via email.

F & P Mfg., Inc., offers an exciting and rewarding career opportunity in a fast paced, highly automated, state-of-the-art automotive parts manufacturing facility located in Tottenham, located 40 minutes north of the Toronto airport. F & P Mfg., Inc., is a tier one automotive parts supplier producing suspension components and pedal assemblies for several automotive makers, in both Canada and in the U.S. We are a complete manufacturing facility and have been stamping, welding, painting and assembling parts for 30 years. We have 900 associates working at our 2 on site manufacturing plants. F&P's welding department consists of a number of automated production lines that uses mainly GMAW robotic processes as well as some Resistance welding technology. This equipment includes a wide variety of Robots such as, Panasonic Tawers, Fanuc material handlers, OTC welding systems as well as Yaskawa Motoman. All equipment is PLC controlled using either Omron or Allen Bradley PLC's. Welding also includes a variety of highly automated equipment such as vision systems and the use of laser technology, 350 welding robotic systems and over 400 total robots. Together these areas offer maintenance staff the opportunity to work on a wide range of highly automated equipment in a continuous improvement work environment. Hours of work: Biweekly rotation of days (7:00am-3:00pm) and afternoons (3:00pm-11:00pm) Position Responsibilities : Perform highly diversified duties to repair and maintain automated production equipment Diagnose problems, replace or repair parts, detect and replace defective parts, test and make adjustments to automated production equipment Perform regular preventative maintenance on machines and equipment Use of programmable logic control systems (PLC’s) to program and troubleshoot automated equipment Use of robotic systems to program and troubleshoot Other duties as assigned to ensure up-time of automated production equipment, etc Qualifications: Post-secondary education in Electrical, Mechanical, Robotics or related field Minimum of 2 years’ experience in a manufacturing environment Experience in trouble shooting and equipment maintenance of electrical, mechanical, pneumatic, hydraulic and robotics problems on automated equipment Ability to read and understand Operations Standards, blue prints, maintenance and equipment manuals, etc. PLC programming experience highly desirable Wage range for this position is $24.50 - $27.30 per hour, plus $0.60 shift premium for afternoons and $0.80 shift premium for midnights. Benefit package includes an incentive bonus program worth 7.5% of base pay, paid overtime, complete medical, dental, vision care, prescription drug programs, and a company paid pension plan worth 5% of base pay. For more information about F & P, please got to www.fandpmfg.com . If you are interested in this challenging opportunity, please submit your resume and diploma/official transcript to recruiting@fandpmfg.com.

F&P's Assembly Department consists of Assembly lines and Bushing insertion presses. This equipment includes, PLC controlled Conveyor systems, which use Fanuc Robot's for material handling, Vision detecting systems, D/C fastening systems, LVDT positioning units, HMI interface, and Overhead off load lift systems. Bushing insertion systems, are PLC controlled using Load cells, LVDT's, Hydraulic CVL's and Vision systems. Together these areas offer maintenance staff the opportunity to work on a wide range of highly automated equipment in a continuous improvement work environment. Hours of work: Biweekly rotation of days (6:30am-3:00pm) and afternoons (3:00pm-11:30pm) Position Responsibilities : Perform highly diversified duties to repair and maintain automated production equipment Diagnose problems, replace or repair parts, detect and replace defective parts, test and make adjustments to automated production equipment Use of PLC's to program and troubleshoot automated equipment Use of robotic systems to program and troubleshoot Other duties as assigned to ensure up-time of automated production equipment, etc. Perform regular preventative maintenance on machines and equipment Qualifications: Post-secondary education in Electrical, Mechanical, Robotics or related field Minimum of 2 years’ experience in a manufacturing environment Experience in trouble shooting and equipment maintenance of electrical, mechanical, pneumatic, hydraulic and robotics problems on automated equipment Able to replace and repair equipment when required (under 24V) Must be able to demonstrate the ability to replace and repair equipment when required PLC programming experience highly desirable   Wage range for this position is $24.50 - $27.30 per hour. Benefit package includes an incentive bonus program worth 7.5% of base pay, paid overtime, complete medical, dental, vision care, prescription drug programs, and a company paid pension plan worth 5% of base pay. For more information about F & P, please got to www.fandpmfg.com. If you are interested in this challenging opportunity, please submit your resume and diploma or official transcript.

Responsibilities: Delivery and pick-up of parts to and from customers and sub-contractors within the greater Toronto area, and our locations in Orillia Accurate completion of related paperwork and documentation Vehicle cleanliness and maintenance Able to manage changes in work load and scheduling Hours are 7:00am - 3:00pm Monday - Friday (this may require some flexibility depending on customer requirements)  

High pressure waterblasting of paint booth grating & car carriers on 3rd shift. 

People Store Staffing is now hiring for Quality Controller/Verifier for our client that manufactures automotive safety equipment in Collingwood. Job Description: Inspect partially finished and finished products, operate basic machinery, document defects, organize product, assembles, packages and labels rolls or cut pieces for shipping, hand eye coordination, work well in a team, attention to detail and ability to prioritize. Company Perks: Full Time Pay Increases OT over 40 hours Benefits Position Starts at $16.50 plus shift premiums of .50 and $1 OT over 40 hours If you feel that you would be a good fit for any of these positions you can apply by emailing your resume to Katelynn Eddy at barrie@peoplestore.ca If these positions are not exactly what you are looking for please feel free to call to discuss other opportunities at (705) 728-6167, as not all positions are advertised.

Manufacturing Technician Positions Available People Store Staffing has partnered with a very loyal company in Collingwood and together we are hiring for Manufacturing Associates! Pay Rate: Starting at $15/Hr - $20/Hr - depending on position Description: Quality inspections, assembly, loading/unloading, heavy lifting, cutting/trimming, operating machinery and packaging. What the client offers: Full time, ongoing work Will to Train Pay increase after 6 months and 1 year Friendly and positive environment Advancements for those who work hard Bonuses available OT available Shift Rotation: Days/Afternoons/Nights

Wednesday Nov 21st 2018 12:30 pm to 3 pm Tracks Employment - 50 Hume Street, Collingwood We are now Hiring for the following: Full Time Forklift Operators/Material Handlers $16-$18/Hr Quality Control $16.50-$18/Hr Weavers $16.50-$18/Hr Manufacturing Technicians $15-$19/Hr

People Store Staffing is now hiring for Material Handlers Job Description: Required to have one or more years’ experience in a material handler role, knowledge of automotive lifting devices, work well with others and have the ability to lift 50lbs repetitively. Company Perks: Full Time Pay Increases OT over 40 hours Benefits Position Starts at $15.50 plus shift premiums of .50 and $1 OT over 40 hours If you feel that you would be a good fit for any of these positions you can apply by emailing your resume to Katelynn Eddy at barrie@peoplestore.ca If these positions are not exactly what you are looking for please feel free to call to discuss other opportunities at (705) 728-6167, as not all positions are advertised.

Tasks vary depending what needs to be completed each day Fork Lift Licence would be an asset but not required Must have good work Ethic - with a small team good attendance is mandatory  

Senior Microbiologist - 18000GAS Description About Baxter  Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook. Summary The Senior Microbiologist Support activities in the Sterility Assurance department to ensure timely completion of tasks and compliance with applicable requirements.   Acts as the delegate to the Sterility Assurance Supervisor in all matters as required and in their absence. Perform daily tasks in the respective areas as required and provides back up to other areas of the Sterility Assurance Department when needed. General Expectations The top two priorities for all Baxter Alliston employees are Safety and Quality: Safety:   Support our goal to achieve a “Zero Harm Environment”, by ensuring the safety of yourself and your co-workers through: Following all safety procedures Understanding potential hazards in your area Wearing appropriate PPE Reporting all incidents / near-misses / concerns Embracing 6s Quality : Ensure the quality of our products to ensure patient safety and achieve our mission of “Saving and Sustaining Lives”.  This can be achieved through: Following Good Manufacturing Practices (GMP) Adhering to all quality procedures Completing training on-time Doing it Right the First Time Reporting any quality concerns immediately. As part of the plant’s Enterprise Management System (EMS), all employees must embrace a culture of Continuous Improvement by: Participating in improvement activities Identifying and implementing continuous improvement ideas Participating in Tier meetings Recognizing your peers, and Embracing 6s. Identifying and implementing VIP’s (Value Improvement Project) Embrace continuous learning Utilize Leader Standard Work Utilize Root Cause Analysis tools to identify and prevent problems from recurring and drive measurable results. Essential Duties and Responsibilities: Review daily results and paperwork from Environmental, Particulate Matter and Pyrogen labs. Support review of paperwork from Sterilizer Quals as needed.  Read and document results of appropriately incubated samples. Address all out of limits and positive test results by completing trending analysis (OOL investigation), retest procedures, gram staining, thermal death testing, microscopic analysis etc. Review and sign off completed paperwork prior to being sent to the Documentation Centre.  Compile data required for monthly, quarterly and annual trending. Coordinate required testing and compile/review resulting data for CWRs and validations.  Conduct sterility testing for stability and import samples, initial and fractional qualification studies and requalification’s by open and closed method filtration and/or drop tests and macerations, in accordance with SOP requirements, completing all required documentation.  Collect and organize production samples and check for discrepancies against sterilized sample record. Maintain equipment and area for testing to ensure endotoxin free product and perform bacterial endotoxin testing per specification.  Compile data required for monthly, quarterly and annual trending.  Perform required testing and complete documentation required for critical work request and protocols by prioritizing daily and weekly testing schedules to allow time for required tests.  Assist in completion of OOL and CAPA investigations, and resolution of audit observations. Participate in and support plant projects and validations as required.  Drive continuous improvement of environmental controls by performing real time risk assessments in classified areas. Work on improvement projects and validations as assigned.  Maintain 6S within the lab areas assigned. Provide back-up coverage to the Sterility Assurance Department when needed.  Maintain equipment inventories and order laboratory supplies as needed. Ensure equipment calibrations are performed in a timely manner. Prepare and sterilize laboratory equipment to ensure its availability for use, dispose of biohazard materials appropriately, and perform monthly preventive maintenance. Monitor incubator and refrigerator charts and thermometers daily.    Qualifications   Education: University Degree, B.Sc designation, or equivalent academic qualifications and work experience required.   Major Subjects / Specialties Microbiology Quality Assurance   Type of Experience Required: Experience in a manufacturing environment Proficiency in Word & Excel Previous experience working in a Quality function Knowledge of Aseptic Technique and Microbiological Methods Environmental monitoring Working experience in a regulated microbiology lab and understanding of industry best laboratory practices, techniques.   Preferred: Previous experience with Laboratory Information Management System (LIMS) Validation experience within Life Sciences manufacturing environment - Writing and executing validation protocols. CAPA investigation QA experience in a pharma manufacturing environment Microbiological testing lab experience in the pharmaceutical industry Knowledge of GMP, ISO standards, and regulatory/corporate requirements   Years of Experience Required:  4-5 years   Preferred: 5+ of successful progressively responsible experience.   Additional Skills / Special Training / Technical Skills Required: Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. Time management / prioritization. Strong analytical and problem solving skills and critical thinking abilities Strong process and project management capabilities. Excellent oral and written communication skills that have been demonstrated through presentations/seminars, oversight of projects, etc. Strong technical writing skills. Must be required to work a schedule outside business hours and/or flexible shifts. Intermediate level of proficiency with MS Office and Laboratory information management system(LIMS) Experience with continuous improvement methodologies, LEAN, 6S, Kaizen, Six Sigma Strong communication skills, ability to work with all levels of the organization. Strong ability to balance multiple priorities with excellent time management skills. Detail oriented with the ability to work under pressure. Uncompromising dedication to quality. Must comply with Good Laboratory Practices Understanding of Sterility Assurance principles relating to moist heat terminal sterilization.   Preferred: Understanding of EMS through the application of LEAN tools in a laboratory environment.   A Career That Matters Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.   Thank you for your interest and application to Baxter. All applications will be reviewed and those candidates selected for consideration will be contacted directly.   Baxter is committed to creating and maintaining a barrier-free environment for all employees and customers. We believe in integration and equal opportunity and we are committed to treating all people with dignity and respect. Should you need assistance at any point during the recruitment process please contact Human Resources at 705-440-2704.

Chemistry Laboratory Supervisor - 18000IWN Description About Baxter  Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook.   Chemistry Lab Supervisor Supervise chemistry staff to complete receiving and inspection activities and initial chemistry, stability and raw material testing in a timely manner, ensuring equipment and procedures are in place and optimizing the efficiency of required process(es) in the Chemistry Lab.  Responsible for recruiting, training, and coaching all direct reports and support of indirect reports.   General Expectations The top two priorities for all Baxter Alliston employees are Safety and Quality:   Safety:   Support our goal to achieve a “Zero Harm Environment”, by: Following all safety procedures, Understanding potential hazards in your area. Wearing appropriate PPE. Reporting all incidents / near-misses / concerns. Embracing 6s.   Quality : Ensure the quality of our products to ensure patient safety and achieve our mission of “Saving and Sustaining Lives”.  This can be achieved through: Following Good Manufacturing Practices (GMP). Adhering to all quality procedures. Completing training on-time. Doing it Right the First Time Reporting any quality concerns immediately.   As part of the plant’s Enterprise Management System (EMS), all employees must embrace a culture of Continuous Improvement by: Participating in improvement activities. Identifying and implementing continuous improvement ideas. Participating in Tier meetings. Recognizing your peers. Embracing 6s. Identifying and implementing VIP’s (Value Improvement Project). Embracing continuous learning. Utilizing leader Standard Work, Utilizing Root Cause Analysis tools to identify and prevent problems from recurring and driving measurable results. Supervise, co-ordinate and monitor the activities of QM chemistry staff on three shifts to ensure complete receiving and inspection activities and initial chemistry, stability and raw material  testing is executed in an efficient and timely manner in accordance with all local, Corporate, Regulatory and USP requirements. Manage out of limit and/or nonconformance investigations, including mentoring chemists on the investigation process. Manage or support management of change control in the laboratory. Support plant testing goals by organizing chemist work schedules, identifying and communicating testing priorities, approving all appropriate test data, and interacting with the plant Documentation centre (where necessary) to meet plant targets. Implement quality and process improvement opportunities to maximize laboratory efficiency and capacity by troubleshooting equipment issues, scheduling monthly preventative maintenance schedules, adopting test method improvements and implementing appropriate corrective and preventative measures to avoid exceptions. Co-ordinate recruitment of new chemists and train new staff in order to conduct all necessary receipt and testing. Conduct monthly check-ins with all direct reports. Provide feedback on indirect reports to the other Chemistry Supervisor. Develop and implement equipment and testing procedures by writing and executing appropriate validation protocols in the QM lab. Ensure integrity, compliance and quality of all data generated by the QM lab. Qualifications   Education Level Required : B.Sc. (Chemistry or other appropriate Science)   Preferred: M.Sc. or Ph.D. Degree (Chemistry)   Major Subjects / Specialties Required: Analytical Chemistry, Biochemistry, other Chemistry-Related Disciplines.   Type of Experience Required: Previous experience in a GMP environment Experience with USP and other compendial test methods Successful record of people management, including demonstrated ability to motivate and mentor. In-depth knowledge of GMP, ISO, Regulatory and other applicable standards   Preferred: Knowledge of Corporate Quality requirements Practical experience using Lean tools (6S, Kaizen, Value Stream Mapping) Six Sigma Black or Green Belt designation Previous experience with Terminal sterilization validation   Years of Experience Required: 3 - 5 years progressive experience in a chemistry lab environment   Preferred: 5+ years of successful supervisory experience over a chemistry lab in a pharmaceutical environment.   Additional Skills / Special Training / Technical Skills Required: Strong understanding of Health Canada GMP and Medical Device Regulations. Thorough knowledge of applicable procedures, specifications, regulations and standards. Strong process and project management capabilities. Strong written and oral communication skills, negotiation skills, ability to work with all levels of the organization. Previous experience writing protocols Ability to build strong relationships with internal and external customers. Strong ability to balance multiple priorities. Intermediate level MS Office (Excel, Word, PowerPoint). Experience with a Laboratory Information Management System (LIMS). Analytical chemical testing lab experience in the pharmaceutical industry and knowledge of GMP, ISO standards, and regulatory/corporate requirements.   Preferred: Validation experience within a life sciences manufacturing environment. Experience implementing 6S;  EMS in a manufacturing environment, with practical experience using Lean tools. Understanding of FDA Drug GMP Regulations. Proficiency in Trackwise System   A Career That Matters Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.   Thank you for your interest and application to Baxter.  All applications will be reviewed and those candidates selected for consideration will be contacted directly. Baxter is committed to creating and maintaining a barrier-free environment for all employees and customers. We believe in integration and equal opportunity and we are committed to treating all people with dignity and respect.

Quality Technician- Contract 1 year- Afternoon - 18000IF2 Description About Baxter  Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook. Summary Perform final physical testing to ensure product and packing operations conforms to specifications, standard operating procedures and product structures. Responsible for transport, issue and reconciliation of labels to the production lines (PPB, Powders, Concentrates, Viaflex Packing). Responsible for issuance and reconciliation of hot stamps to the production lines (Viaflex Filling, Altair).   Perform review of subassembly QA records to ensure GDP. Support QA Operators in the Viaflex Filling Department with Particulate Matter inspection during short production runs, where required. General Expectations The top two priorities for all Baxter Alliston employees are Safety and Quality: Safety: Support our goal to achieve a “Zero Harm Environment”, by ensuring the safety of yourself and your co-workers through: Following all safety procedures Understanding potential hazards in your area Reporting all incidents / near-misses / concerns Embracing 6s   Quality: Ensure the quality of our products to ensure patient safety and achieve our mission of “Saving and Sustaining Lives”. This can be achieved through: Following Good Manufacturing Practices (GMP) Adhering to all quality procedures Completing training on-time Doing it Right the First Time, and Reporting any quality concerns immediately.   As part of the plant’s Enterprise Management System (EMS), all employees must embrace a culture of Continuous Improvement by: Participating in improvement activities Identifying and implementing continuous improvement ideas Participating in Tier meetings Recognizing your peers Embracing 6s. Essential Duties and Responsibilities Inspect random final physical samples for various defects as per specifications. Complete EBR work orders. Conduct any retesting i.e. level inspections and warehouse counts if necessary. Perform line clearances and QA inspections and document on final retention paperwork for finished goods re-inspections (as required) Pull finished good reserves samples Coordinate and deliver labels to the appropriate filling/packing lines. Coordinate and issue hot stamps to the appropriate filling lines. Coordinate and deliver direction inserts to the packing lines.  Maintain Label Control Room inventory of supplies, forms, QA stamps, etc & initiate computerized requisitions as required. Maintain hot stamp inventory and reconcile stamps, deliver new stamps, destroy/ deface obsolete stamps. Remove and prepare all expired batch records for shredding, co-ordinate pick-ups with company to perform shredding. Support QA Operators in the Viaflex Filling Department with Particulate Matter inspection during short production runs, where required. Qualifications   Education Level   Required:  Successful completion of High School or GED, Mathematics, English and computers Preferred : Post-secondary education in Quality Assurance   Type of Experience   Required: Previous record keeping, QA or QM Checker experience and proven ability/strength in Good Documentation Practices. Previous manufacturing experiences within a GMP environment   Preferred: Knowledge of GMP, ISO Standards, GLP Practical experience using Lean tools   Years of Experience   Required: 1 year Preferred: 3+ years manufacturing experience with exposure to various areas of the plant.   Additional Skills / Special Training / Technical Skills Required: Strong communication skills, ability to work with all levels of the organization. Ability to build strong relationships with internal and external customers. Strong ability to balance multiple priorities with excellent time management skills. Detail oriented with the ability to work under pressure. Ability to work in a team environment as well as the ability to be self-motivated and be able to work with minimum supervision. Strong analytical and problem solving skills and critical thinking abilities. Intermediate proficiency in Word, Excel & Powerpoint. Intermediate proficiency in Word, Excel & Powerpoint.   Preferred: Experience in a wide variety of positions within the plant (internal candidates) Previous experience with JDE GME & EBR   A Career That Matters Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.   Thank you for your interest and application to Baxter.  All applications will be reviewed and those candidates selected for consideration will be contacted directly.   Baxter is committed to creating and maintaining a barrier-free environment for all employees and customers. We believe in integration and equal opportunity and we are committed to treating all people with dignity and respect.

Production Operator- Night Shift - 18000HM1 Description About Baxter  Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook. Summary We are currently looking for energetic, hard-working Filling Operators at our Alliston facility. Starting wage is $18.00 plus applicable shift premium.  The Filling Operator is responsible for performing the following duties on a rotating basis on the line: Visual Inspection of IV bag assembly, Filling IV solution in various bag sizes, placing bags into protective overwrap, loading bags onto sterilizer trays. These are temporary full-time contracts with the possibility of extension or permanent status in the future.   Due to the nature of our business, Baxter follows Good Manufacturing Practices (GMP) which requires our employees to focus on cleanliness and contamination control. Other aspects of GMP that must be observed are no makeup or jewelry in the production areas.   Qualifications Completion of High School or GED Required (Proof will be requested) Previous experience working in a fast paced environment (experience working in an assembly line setting is preferred) Excellent  pinch grip and hand grip strength is required to be successful Flexibility to work afternoons, midnights and weekends when required Positive attitude, and an ability to work in a team setting with a focus on quality assurance and attention to detail.   A Career That Matters Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.   Baxter is committed to creating and maintaining a barrier-free environment for all employees and customers. We believe in integration and equal opportunity and we are committed to treating all people with dignity and respect.   Thank you for your interest and application to Baxter.  All applications will be reviewed and those candidates selected for consideration will be contacted directly.

Equipment Operator - Midnight - 18000JJ6 Description About Baxter  Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook. Summary We have the following exciting opportunity at our Manufacturing facility located in beautiful Alliston, just 1 hour North of Toronto’s Center. Full-time Weekend Shift plus 2- steady 8 hour shifts during the week 11pm-11am Saturday and Sunday – 24 hours/week $19.00/hour ($2.00 Weekend Shift Premium) Total 40 hours weekly   Essential Duties and Responsibilities  This position is responsible for IV bag assembly where you will operate our plastic cutting, grinding and blending equipment. The Equipment Operator, Plastics is also responsible for troubleshooting and making minor equipment adjustments in order to produce a quality product in an efficient manner. This role is 40 hours per week and there is an opportunity to take part in a Production Technician training course with Georgian College for those that meet the performance requirements.   Qualifications   Completion of High School or GED Required (Proof will be requested) Ability to work weekend shifts (12 hour nights Fridays and Saturdays) Previous experience working in a fast-paced environment (experience working in an assembly line setting is preferred) Experience in troubleshooting mechanical problems Demonstrated problem solving skills Proven ability to show initiative, a positive attitude, and an ability to work in a team setting with a focus on quality assurance and attention to detail. Must be available to train during the week at full time hours for an approximate 6 week period.   A Career That Matters Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.   Thank you for your interest and application to Baxter. All applications will be reviewed and those candidates selected for consideration will be contacted directly.   Baxter is committed to creating and maintaining a barrier-free environment for all employees and customers. We believe in integration and equal opportunity and we are committed to treating all people with dignity and respect. Should you need assistance at any point during the recruitment process please contact Human Resources at 705-440-2704.

Chemist - Contract - 18000IRW Description About Baxter  Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook. Summary Our commitment to our mission means we are there when patients and healthcare professionals need us, during the critical moments that matter most. We have the following opportunity at our Manufacturing facility in Alliston, located 1 hour North of Toronto. Essential Duties and Responsibilities: Perform chemical analysis to ensure product acceptability. Ensure that final products meet required standards before release by analyzing them using instrumental and wet chemical techniques according to the specifications.  Analyze in-process samples using a variety of assays and procedures, taking appropriate action if the result is out of the specified limits.  Maintain chemistry lab in good order Perform analytical chemical analysis to ensure products meet required standards using instrumental and wet chemical techniques according to specifications. Compile analysis reports by entering results into the Laboratory Information Management System (LIMS) approving them and forwarding to the Document center Ensure that production lines make products within specification limits by analyzing in-process samples using variety of assays and procedures, taking appropriate action if the result is out of specified limits Support departmental 6s efforts by maintaining all work areas in a clean and orderly state, disposing of waste, cleaning glass ware and removing expired chemicals / reagents. Maintain chemistry lab in good order by housecleaning, disposing waste, cleaning glassware and removing expired chemicals/ reagents Perform required preventative maintenance on equipment's in QM lab. to ensure proper functioning and delivery of consistent and reliable results. Contact manufacturers of equipment and arrange for service in event of malfunction of equipment Qualifications University Degree, Bachelor of Science Majoring in Analytical Chemistry or Biochemistry 1-2 years of analytical chemical testing lab experience. Over 2 years of chemical lab experience in a pharmaceutical industry is preferred Familiarity with laboratory equipment in a Quality Management Laboratory Proficiency in MS Office and laboratory computerized systems Must have strong organizational and time management skills Highly effective analytical and problem solving skills and critical thinking abilities Highly effective communication and interpersonal skills Experience performing analytical testing in compliance with specification requirements Instrumental techniques such as HPLC, ICP-MS, GC Atomic Absorption, UV-VIS spectroscopy, Flame Photometry and IR spectroscopy Knowledge of GMP, ISO and regulatory requirements Familiarity with LIMS is an asset Technical writing experience is an asset A Career That Matters Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.   Thank you for your interest and application to Baxter. All applications will be reviewed and those candidates selected for consideration will be contacted directly.   Baxter is committed to creating and maintaining a barrier-free environment for all employees and customers. We believe in integration and equal opportunity and we are committed to treating all people with dignity and respect. Should you need assistance at any point during the recruitment process please contact Human Resources at 705-440-2704.   Due to the nature of our business, Baxter follows Good Manufacturing Practices (GMP) which requires our employees to focus on cleanliness and contamination control. Other aspects of GMP that must be observed are no makeup or jewelry in the production areas.

Chemist - 18000IRQ Description About Baxter  Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook. Summary Our commitment to our mission means we are there when patients and healthcare professionals need us, during the critical moments that matter most. We have the following opportunity at our Manufacturing facility in Alliston, located 1 hour North of Toronto. Essential Duties and Responsibilities:   Perform chemical analysis to ensure product acceptability. Ensure that final products meet required standards before release by analyzing them using instrumental and wet chemical techniques according to the specifications.  Analyze in-process samples using a variety of assays and procedures, taking appropriate action if the result is out of the specified limits.  Maintain chemistry lab in good order Perform analytical chemical analysis to ensure products meet required standards using instrumental and wet chemical techniques according to specifications. Compile analysis reports by entering results into the Laboratory Information Management System (LIMS) approving them and forwarding to the Document center Ensure that production lines make products within specification limits by analyzing in-process samples using variety of assays and procedures, taking appropriate action if the result is out of specified limits Support departmental 6s efforts by maintaining all work areas in a clean and orderly state, disposing of waste, cleaning glass ware and removing expired chemicals / reagents. Maintain chemistry lab in good order by housecleaning, disposing waste, cleaning glassware and removing expired chemicals/ reagents Perform required preventative maintenance on equipment's in QM lab. to ensure proper functioning and delivery of consistent and reliable results. Contact manufacturers of equipment   Qualifications   University Degree, Bachelor of Science Majoring in Analytical Chemistry or Biochemistry 1-2 years of analytical chemical testing lab experience. Over 2 years of chemical lab experience in a pharmaceutical industry is preferred Familiarity with laboratory equipment in a Quality Management Laboratory Proficiency in MS Office and laboratory computerized systems Must have strong organizational and time management skills Highly effective analytical and problem solving skills and critical thinking abilities Highly effective communication and interpersonal skills Experience performing analytical testing in compliance with specification requirements Instrumental techniques such as HPLC, ICP-MS, GC Atomic Absorption, UV-VIS spectroscopy, Flame Photometry and IR spectroscopy Knowledge of GMP, ISO and regulatory requirements Familiarity with LIMS is an asset Technical writing experience is an asset   A Career That Matters Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.   Thank you for your interest and application to Baxter. All applications will be reviewed and those candidates selected for consideration will be contacted directly.   Baxter is committed to creating and maintaining a barrier-free environment for all employees and customers. We believe in integration and equal opportunity and we are committed to treating all people with dignity and respect. Should you need assistance at any point during the recruitment process please contact Human Resources at 705-440-2704.   Due to the nature of our business, Baxter follows Good Manufacturing Practices (GMP) which requires our employees to focus on cleanliness and contamination control. Other aspects of GMP that must be observed are no makeup or jewelry in the production areas.

Production Supervisor - Midnight - 18000JFB About Baxter  Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical care, nutrition, renal, hospital and surgical products. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. With products, technologies and therapies available in more than 100 countries, Baxter’s employees worldwide are now building upon the company’s rich heritage of medical breakthroughs to advance the next generation of transformative healthcare innovations. To learn more, visit www.baxter.com and follow us on Twitter, LinkedIn and Facebook. Summary The Filling Supervisor coordinates the filling of high volume IV codes using highly sophisticated automated equipment.  They monitor the activities of team members and machinery to fill the required amount of product at the least cost, consistent with quality standards and specifications. The position is responsible for the cleaning and sanitization of the equipment and facility in this area. Utilize Baxter’s Shared Commitment’s as a framework to lead their team and help drive a high performing culture.   The top two priorities for all Baxter Alliston employees are Safety and Quality: Safety:  Support our goal to achieve a “Zero Harm Environment”, by ensuring the safety of yourself and your co-workers through: Following all safety procedures. Understanding potential hazards in your area. Wearing appropriate ppe reporting all incidents / near-misses / concerns Embracing 6s   Quality: Ensure the quality of our products to ensure patient safety and achieve our mission of “Saving and Sustaining Lives”.  This can be achieved through: Following Good Manufacturing Practices (GMP) Adhering to all quality procedures Completing training on-time Doing it Right the First Time, and reporting any quality concerns immediately.   As part of the plant’s Enterprise Management System (EMS), all employees must embrace a culture of Continuous Improvement by: Participating in improvement activities. Identifying and implementing continuous improvement ideas. Participating in Tier meetings. Recognizing your peers, and embracing 6s. Identifying and implementing VIP’s (Value Improvement Project) embrace continuous learning. Utilize Leader Standard Work. Utilize Root Cause Analysis tools to identify and prevent problems from recurring and drive measurable results.   Major Responsibilities / Activities Meet financial commitments by ensuring that the budgeted labour standards are met throughout the year, as well as assisting in establishing budget, production standards and manufacturing expenses for the department for the next year. Set-up, adjusts, trouble-shoots and repairs the automated equipment on the line(s). Supply technical support to employees to resolve quality and equipment issues. Improve the effectiveness of all team members by providing documented training, coaching employees during feedback reviews, and daily activities to improve skills, providing recognition for good performance.  Also ensures company policies are applied consistently and fairly and takes appropriate action to correct unacceptable behaviors. Identify and implement Value Improvement Projects to reduce product cost or improve quality by monitoring scrap and efficiencies, reviewing results with employees and implementing IDEAs to improve processes. Ensure all activities and products are in compliance with specifications and GMP’s by reviewing all batch records, taking appropriate actions to respond to out of tolerance produce and identifying corrective actions to prevent non-conformances. Maintain the facility and equipment to meet all GMP and 6S requirements.   Qualifications Education Level Required:  Post Secondary education Major Subjects Required English, Math, Communications Mechanical and or Electrical aptitude Type of Experience Required: Experience within a manufacturing operation Strong mechanical aptitude and equipment trouble-shooting ability. Practical experience using Lean tools (6S, LSW, VM, DA, Kaizen, Value Stream Mapping) 3 – 5 years of manufacturing experience. Preferred: Knowledge of GMP, ISO standards, and regulatory/corporate requirements. Previous supervisory experience within the pharmaceutical manufacturing industry Additional Skills / Special Training / Technical Skills Required: People Management Experience – people management, coaching and team development skills. Strong communication skills, ability to work with all levels of the organization. Strong ability to balance multiple priorities in a fast paced, high pressure environment. Self-motivated with the ability to take a leading role in the continuous improvement cycle to reduce and improve product quality in the department. Strong analytical and problem solving skills and critical thinking abilities. Intermediate proficiency in Word, Excel & PowerPoint, EBR, JDE GME and AS400\Kronos. Good working knowledge of SOP’s/specs, blueprints, PCS’s and BOM’s A Career That Matters Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.   Thank you for your interest and application to Baxter. All applications will be reviewed and those candidates selected for consideration will be contacted directly.   Baxter is committed to creating and maintaining a barrier-free environment for all employees and customers. We believe in integration and equal opportunity and we are committed to treating all people with dignity and respect. Should you need assistance at any point during the recruitment process please contact Human Resources at 705-440-2704.   Due to the nature of our business, Baxter follows Good Manufacturing Practices (GMP) which requires our employees to focus on cleanliness and contamination control. Other aspects of GMP that must be observed are no makeup or jewelry in the production areas.

Picking up scrap metals/ car parts from  dealerships  - Must be able lift 50 IBS 

Recycling cardboard, plastics, garbages. Baling cardboard and plastic utilizing a baler. Picking up water using a ride along autoscrubber. Sorting recycled materials. Cleaning bathrooms, mopping, sweeping, dusting, vacuuming. Being able to strip and wax floors. Self starter.

NOW HIRING!!!!!! WE ARE GROWING! SPS IS LOOKING FOR ASSOCIATES LIKE YOU TO JOIN OUR FLOURISHING TEAM! WE ARE OFFERING FULL TIME PERMANENT POSITIONS (WITH BENEFITS) APPLY TODAY IN PERSON AT 6795 INDUSTRIAL PARKWAY, ALLISTON ONTARIO OR SEND IN YOUR RESUME TO RECRUITING@SIMCOEPARTS.COM VISIT OUR WEBSITE FOR MORE INFORMATION AT WWW.SIMCOEPARTS.COM

Arranging freight, getting quotes, filling out customs forms, filling out weigh bills, recording incoming and outgoing materials, filling out all courier forms, UPS etc. shop orders, packaging, forklift experience, experience with hand tools, saws, nail guns, must be able to lift up to 50 pounds, good hand writing, self-starter, work with little supervision  

General Labour position located within Bolton, Ontario . Client is a lumber company  Monday – Thursday 6:30am – 4:30pm Friday 6:30am – 12pm  

Candidate to perform light, industrial assembly processes for automotive windows with a maximum individual lifting weight of 15lbs./6 kg, while standing on anti-fatigue matting for an 8-hour shift, with two 10 minute breaks and 30 minute lunch break. All associates are assigned a different job process in their rotation every two (2) hours. Associates are first trained to perform four different assembly processes and gradually learn various additional job processes. Associates to utilize hand tools/jigs to apply rubber edging and moldings, apply primer, clips, holders, etc. on various models and types of automotive windows. Assembly job processes provide work within shoulder to waist range in front of body, work on height-adjustable tables, some processes are along a belt-style assembly line, with processes laid out to limit walking/moving (max. 5 ft. radius). Lift assists are utilized for loading rear windows and front windshields to assembly process areas, while loading rear windows to “shipping carts” is done with two associates, and loading front windshields to “shipping carts” is done by lift assist.  Associates are working with front windshields, rear windows, front and rear door windows, and small door quarter windows.  Shift work with premiums available and pay increases after 3 months. 

WALK IN FOR YOUR ON THE SPOT INTERVIEW WITH IS2 AND  START THE NEXT DAY! WORK FOR ONE OF  CANADA'S TOP EMPLOYER. IS2 has immediate openings. We are now hiring  Production Workers ,  General Labourers  and  Machine Operators  in Bradford! Days: 6:00am-2:00pm Afternoons: 2:15pm-10:15pm Nights: 10:15pm-6:00am THIS IS NOT SHIFT WORK. CHOOSE A SHIFT THAT WORKS AROUND YOUR SCHEDULE! Why you'll want this position: Stable work with full-time hours and potential for overtime. Clean, friendly and adaptable working environment. Opportunity to excel in the automotive industry. Work for one of Canada's Top 50 Employers. What you'll need to do on a daily basis: Light automotive assembly General assembly of metal products on production line Lifting up to 30 lbs

KTH Shelburne is looking to grow our team! We are actively recruiting for Full Time Production Associates – join our innovative team of production associates today!   Our Production Associates are responsible for the safe and efficient operation of our equipment while ensuring we produce high quality parts. A Routine Day: Handling parts and baskets in a safe manner Maintain line speed and quality of products Complete all quality checks as outlined in operation standards Ensure all documentation is accurately completed The Perks: Competitive wages with scheduled increased Company paid uniforms Company provided PPE Annual work boot and safety glasses allowance Attendance Bonuses (bi-weekly & quarterly) Annual performance Bonus Successful Characteristics: Ability to support overtime and weekend production as needed Capability to work in a challenging but rewarding environment Strong attention to detail Ability to work a two-shift rotation (days and afternoons) Both a team player and independent worker At KTH Shelburne, we have built a team environment where all of our associates contribute each day to our success.       In accordance with the OHRC and the AODA, KTH is committed to providing accommodation in its recruitment processes to applicants with disabilities, upon request. If you require accommodation at any time during the recruitment process or in order to successfully submit an application, please reach out to a member of the KTH Human Resources department

KTH Shelburne is looking to grow our team! We are actively recruiting for Full Time Production Associates – join our innovative team of production associates today!   Our Production Associates are responsible for the safe and efficient operation of our equipment while ensuring we produce high quality parts. A Routine Day: Handling parts and baskets in a safe manner Maintain line speed and quality of products Complete all quality checks as outlined in operation standards Ensure all documentation is accurately completed The Perks: Competitive wages with scheduled increased Company paid uniforms Company provided PPE Annual work boot and safety glasses allowance Attendance Bonuses (bi-weekly & quarterly) Annual performance Bonus Successful Characteristics: Ability to support overtime and weekend production as needed Capability to work in a challenging but rewarding environment Strong attention to detail Ability to work a two-shift rotation (days and afternoons) Both a team player and independent worker At KTH Shelburne, we have built a team environment where all of our associates contribute each day to our success.       In accordance with the OHRC and the AODA, KTH is committed to providing accommodation in its recruitment processes to applicants with disabilities, upon request. If you require accommodation at any time during the recruitment process or in order to successfully submit an application, please reach out to a member of the KTH Human Resources department

KTH Shelburne is a leader in automotive frame components. We have built a team environment where all of our associates contribute to our overall success. KTH Shelburne is now accepting applications for an Industrial Electrician . The Job: Troubleshoot equipment problems (Electrically, Mechanically) Daily check for any Safety issues and countermeasure Complete assigned Safety work orders Responsible for equipment in their assigned areas and other areas as directed Fill out Trouble Reports for extended downtime Accurately fill out daily reports Inspect your areas for problems and equipment item Evaluating problems, provide and implement countermeasures Completion of Work orders and Preventative Maintenance tasks Implement improvements and countermeasures What we look for: Licensed Electrician Position requires professionalism and service orientation Electrical background is essential with prior experience using PLC’s along with programming and teaching robots Experience working in an automotive or equivalent industry Strong mechanical skills Ability to diagnose problems and effectively implement countermeasures The Perks: Competitive wages and an attractive vacation package Pension Plan Group benefits – vision, medical and dental Work boot and safety glasses allowance Attendance incentives and annual performance bonus Tuition reimbursement In accordance with the OHRC and the AODA, KTH is committed to providing accommodation in its recruitment processes to applicants with disabilities, upon request. If you require accommodation at any time during the recruitment process or in order to successfully submit an application, please reach out to a member of the KTH Human Resources department.

KTH Shelburne Mfg.,Inc - Shelburne, ON KTH is a World Class Supplier of automotive frame components. KTH Shelburne is now accepting applications for a Full-Time Quality Assurance Associate . Successful candidate for this position must be a team player and able to work in a fast paced manufacturing environment. Some of the duties of our associates include: Support the overall quality level of stamped and welded automotive assemblies Root cause analysis Attend line calls for issues related to the accuracy of parts and equipment Daily reporting to Management on process of projects Data trend analysis Other duties as assigned Experience: One to two years’ experience working in a fast-paced manufacturing environment Mechanical Engineering Technology Diploma or related discipline Key Assets: Hand tool experience Willing and able to support overtime and weekends as required Exhibit the ability to work in a challenging environment Willing and able to be a self-starter Steel toe CSA approved boots that cover the ankle are required We offer our Associates: Competitive wages Company paid uniforms We provide all personal protective equipment Work boot and safety glasses allowance Attendance incentives and annual performance bonus In accordance with the OHRC and the AODA, KTH is committed to providing accommodation in its recruitment processes to applicants with disabilities, upon request. If you require accommodation at any time during the recruitment process or in order to successfully submit an application, please reach out to a member of the KTH Human Resources department.