Job Title: Analyst, Product Surveillance II
Location (On-site, Remote, or Hybrid?): Burlington, MA (onsite)
Contract Duration: Contract until 04/16/2027
Working hours: 8:00 AM - 5:00 PM
Total hours: 40
PURPOSE OF THE ROLE
Analyst, Product Surveillance II-(Sr Quality Specialist)Main Purpose of the Role:Conduct quality-related activities to deliver consistent, high-quality documents, services, products and processes. Ensurecompliance with worldwide regulatory expectations/requirements.TOP SKILLS/EXPERIENCE
Experience with complaint handling, medical writing and cross functional communicationRegulatory knowledge and compliance expertiseData analysis skills with ability to use tools such as excel and Power BIMAIN RESPONSIBILITIES
Responsible for carrying out tasks related to core job responsibilities with little management oversight.May lead goals with cross-functional or broader scope.Provide solutions to a wide range of difficult problems.Solutions are compliant, innovative, thorough, practical and consistent with organizational objectives.Responsible for demonstration of core competencies and may be measured against some selected leadership competencies inconjunction with growth and development plan.Identify and elevate areas for continuous improvement.May perform other duties as assigned.May provide oversight to one or more QA professionals and/or contractors.Scope limited to one specific QA function but has general knowledge of other related disciplines.Interacts with employees, manager, and cross-functional peers.May represent team on cross-functional project teams with other functional leaders.Implements tactical activities related to assignment.Able to contribute functional skills and expertise broadly.Directly influences project direction and scope.May lead projects within function.Decisions may have short- and long-term impact.EDUCATION
Education Level Major/Field of Study or EquivalentBachelor’s Degree (± 5+ years) In life sciences or engineering.or An equivalent combination of education and work experienceEXPERIENCE DETAILS
Minimum 4 years In Quality or related field.Preferred Healthcare industry and experience in quality function.Utilize understanding of how their function supports the business and of technical/businesscompetencies to drive continuous improvement results.Demonstrates proven track record utilizing core & technical competenciesCompany DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: Assembler I
Location: Pomona, CA (onsite)
Contract Duration: 1 year
Work Hours: 6:00AM - 2:30PM
Primary Function:
This role will be responsible for a variety of assembly and non-assembly functions in support of manufacturing goals.
Job Duties:
Operates equipment used to manufacture products.Assembles, checks, and inspects products against departmental procedures.Responsible for recognizing product or equipment problems that arise during the mfg. process and escalating to Line Lead or Supervisor.May be required to assist with the set-up and the clean-up of mfg. equipment.Active participation in Lean Initiatives.Works on assignments that are routine in nature, requiring limited judgment.Responsible for exhibiting professional behavior with both internal/ external business associates that reflects positively on the company and is consistent with the company’s policies and practices.Understands and is aware of the quality consequences which may occur from the improper performance of their specific job.Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing, and testing activities.Carries out duties in compliance with established business policies.Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.Perform other duties and projects, as assigned.Physical Requirements:
Must be physically able to stand for prolonged periods, as this position is not done sitting down.Candidate may conduct repetitive movements including push/pull moving of product as needed from assembly area.No heavy lifting is required. Area does require occasional bending, stooping, and movement of completed product from one area to another, and ability to clean up the mfg equipment used for the area. Will be standing on feet for entire shift so comfortable closed toe shoes are required.Required skills:
2-5 yrs Assembling, filling and packaging reagents experience.No blueprints experience needed.Someone for pharma would be ideal but not required.As long as they have some packaging experience and can read work orders.Food environment experience also acceptableSoftware skills- minimal excel, basic computer skills Most documentation is printed out and written (not digital)Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: Operator I - 2nd Shift
Location: Irvine, CA (onsite)
Contract Duration: Contract until 02/17/2027
Working hours: 3p - 11:30p
Total hours: 40
Description:
For Irvine 2nd shift Hiring Blitz Thursday July 23rd 2:30p - 5:30p.
Operator I Job Description
This is a non-exempt position. This position is responsible for the production of high quality medical devices within a cleanroom environment.
a. Manual Assembling of medical devices.
b. Assemble and use tools under the microscope for long periods of time.
c. Hand soldering.
d. Cleanroom environment.
e. Maintain written and electronic documentation.
This position is responsible for the production of high quality medical devices within a manufacturing cell.Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.Required dress code for tour during interview and on-the job:
Clothing must be non-shedding and free of frayed hems or loose threads.Tassels, fringes, glitter, sequins (sewn or glued on), and any other items that could become dislodged are not allowed on clothing.To verify a fabric can be worn:
pull at the fabric tightly with fingers, if fibers are dislodged, the garment may not be worn in the production area.Sweaters, sweater vests, loose fiber garments, loose knit, or fleece may not be worn.All clothing must be clean and free of visible contamination (sand, mud, dirt, lint, etc.).All clothing, from the waist up, must fit under the lab coat/gown.Turtle necks or high-necked clothing shall not stick out above the neck of the lab coat/gown.Sleeves shall not stick out beyond the cuff of the lab coat/gown.Caps, hats, scarves or bandanas shall not be worn under the bouffant.
Head wraps/scarves worn to accommodate customs:
Must be covered with the bouffant and the tail end of the scarf must be fully covered by the lab coat/gown.Must be of tightly woven fabric, be clean, and laundered.Loose fitting clothing shall not be worn around machinery or soldering/brazing torches.Shoes must be worn at all times in the production area.Stockings or socks are required.The heel of a shoe must not be pointed or higher than 2 inches.Sandals, clogs, slippers, open toe, or open heel shoes are not allowed.Shoes with straps or weave where toes can be seen are not allowed.Changing shoes in the production area, other than a gowning room, is not allowed.Torsos, upper arms, and legs must be covered. Pants (above the ankle), skirts (above the ankle), skirts with slits, short shirts (above the navel), and sleeveless tops are not allowed.Skirts at the ankle are allowed, but full-length stockings, leggings, or pants must be worn under them.Nail polish, acrylic, artificial nails, or similar nail coatings are not allowed.Jewelry or body piercings that can pierce gloves or cannot be covered under gowning materials will not be allowed in the production area.Makeup shall not be worn.Lip balm in stick form is acceptable, when applied outside of production areas and prior to hand washing.Scented personal use products shall not be worn, except deodorant.Lotions shall not be applied after hand washing.Cover any open or bleeding wound with a bandage.Dont wear anything that could be offensive.Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: Analyst, Product Surveillance
Location: St. Paul, MN (onsite)
Contract Duration: Contract until 01/29/2027
Work Hours: 8am - 4pm
Description:
This position will analyze and submit complaints and/or investigate returned products from the field (some biohazard as they are used in surgery).
Under the direction of management, the Product Performance Analyst may perform two different functions. The first consists of managing product experience investigations and all activities pertaining to product experiences. This includes, but is not limited to: receiving and investigating reports of worldwide product experiences/events on a variety of products, entering information into the complaint database, participating in cross-functional projects, facilitating investigation findings of product issues, assist with internal and external audits, and providing comprehensive reports, analysis, and insights on product experiences, and may extract data from the complaint database to various teams (e.g. Regulatory, Quality Engineering).
The other role of the Product Performance Analyst I is to perform evaluations of returned products, coordinating product testing/analysis with other departments and external consultants, preparing technical reports of findings, operating and maintaining the Product Performance Laboratory and equipment, and collecting and evaluating analysis data and entering it into the complaint database.
The Product Performance Analyst I may assist in the trending of complaint data as requested by management, including preparation of trending charts utilizing the complaint database and other programs, in support of the department.
Main Responsibilities:
Initiates and manages the product experience file.Maintains accurate entry of product experiences in the database.Triages new product experience report files from time to time.Investigates events in a timely manner.Uses procedures, judgment, and experience to determine appropriate testing of returned products with occasional support; can ascertain when additional support is needed from other teams based on product analysis findings (e.g. potential manufacturing-related issues).Maintains accurate entry of product experiences in database.Records condition of returned products including observations and photographs.Interprets technical product specifications, Device History Records, or measurements obtained; and always utilizes safe biohazard and chemical handling practices.Communicates verbally and in writing both internally and externally regarding information needed specific to product experiences (e.g. physicians, hospital personnel, sales representatives, international offices).Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.Independently assesses the product experience to determine if a medical device report needs to be filed with various global regulatory agencies (e.g., FDA, European Competent Authorities).Independently assesses the complaint to determine if an escalation is required.Ensures accurate department procedures and work instructions are maintained.Supports inspections by regulatory agencies (e.g. FDA, TUV, BSI, etc.) as requested.Provide support to Legal Department regarding product complaints.Works collaboratively with cross-functional groups (e.g. QEs, R&D, medical affairs, medical education, etc.).May coordinate product testing/analysis with other departments and external consultants.May track returned products within the database, as appropriate.Supports the Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.Performs other related duties and responsibilities, on occasion, as assigned.Work environment varies from well lighted office/cubicle, low to moderate noise level, to a variety of conditions caused by travel requirements such as customer offices, research labs, hospitals, hotels, use of automobiles, commercial travel, weather, etc.Activities require a significant amount of sitting in front of a computer monitor, with some standing and walking.Significant use of hands and arms, plus finger dexterity to reach, point, write, type, operate a computer and other office equipment.Performs tasks that regularly require good correctable vision and hand/eye coordination.Activities also require significant use of voice and hearing for discussions with other employees.Performs tasks that regularly require good correctable vision and hand/eye coordination.Activities also require significant use of voice and hearing for discussions with other employees.Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: Machine Operator
Location: Mansfield, MA (Onsite)
Schedule: Full-time, 40 hours/week
Shift & Pay
1st Shift: 6:00 AM – 2:30 PM — $23.50/hour2nd Shift: 2:30 PM – 11:00 PM — $25.38/hourJob Summary
We are looking for a Machine Operator to operate computer-controlled machining equipment and help produce high-quality medical device components. This role involves machine operation, inspections, documentation, and following safety and quality standards in a manufacturing environment.
Responsibilities
Operate CNC and other computer-controlled machining equipment.Perform visual and dimensional inspections of parts.Complete first article inspections and quality checks.Follow Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).Record production and inspection data accurately in manufacturing systems.Maintain a clean, safe, and organized work area.Follow all ISO, FDA, environmental, and safety regulations.Complete all required training.Qualifications
High school diploma or GED required.0–3 years of manufacturing, production, machine operation, or related experience.Experience operating CNC or other automated equipment is a plus.Precision machining or medical device manufacturing experience preferred.Experience in a GMP or regulated manufacturing environment preferred.Basic mechanical and computer skills.Able to work independently and as part of a team.Basic troubleshooting skills for manufacturing equipment are a plus.Experience using measuring tools such as calipers, micrometers, dial indicators, and gauges is preferred.Must be able to read, write, and speak English.Basic math skills.Physical Requirements
Stand and/or walk for most of the shift (80%+).Lift up to 25 pounds.Work in a manufacturing/machine shop environment.Ability to stand, sit, and perform repetitive tasks for extended periods.Why Apply?
Competitive pay with shift differential.Full-time, consistent schedule.Opportunity to gain experience in the medical device industry.Clean, safety-focused manufacturing environment.Great opportunity for career growth.Apply today to start your career as a Machine Operator!
Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.1st shift - 6-2:30
2nd shift - 2:30 - 11
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
DESIRED MINIMUM QUALIFICATIONS:
A minimum of a High School diploma, G.E.D. is required.A minimum of 0-3 years of experience in Production, Operations, Manufacturing, and/or related discipline is required.Working knowledge in working with Citizen Lathes, Haas Grinders, Sunnen Hone, Centerless Grinders, and Fanuc Robotics is preferred.Knowledge and experience working with computer-controlled equipment is preferred.Precision machining experience is preferred.Experience working with the inspection and functional testing of manufactured components is preferred.Experience working in medical products.Manufacturing / machining is preferred.Experience working in a Good Manufacturing Practice (GMP) or another regulated environment is preferred.Basic mechanical and computer skills are required.The ability to work independently and in a team environment.The ability to operate and perform basic troubleshooting on various types of machine equipment is preferred.The ability to perform and record measurements using dial indicators, depth micrometers, verniers, shadowgraph, and gauges is preferred.The ability to communicate effectively (read, write and speak) in English is required. Basic math skills, with the ability to add, subtract, multiply, divide, compute percentages and work with decimals is required.The ability to stand and/or walk more than 80% of the time is required.The ability to lift to 25 pounds and to stand and sit for extended periods of time.The ability to work in a manufacturing/machine shop environment.The employee may be required to periodically lift and/or move up to 25 pounds frequently.Job Title: Embedded Software Engineer - Direct Hire
Location: Marshalltown, IA
Contract Duration: PERM
Note: Relocation Assistance is available for the right candidate.
Job Description:
In This Role, Your Responsibilities Will Be:
Uphold Safety as our #1 Value in all that we doDesign, develop, test, and debug firmware in C and C++ for microcontroller-based embedded systems, including low-level hardware interactionCollaborate with hardware, mechanical, and manufacturing, and engineering teamsDevelop solutions and requirements that satisfy customer needs for high reliability industrial applications while staying within challenging constraints such as low powerPerform code reviews and support software quality initiativesTroubleshoot and resolve firmware and embedded system issuesSupport product validation, verification, and production readiness activitiesResearch and evaluate emerging embedded technologies and industry trendsParticipate in project planning, estimation, and continuous improvement initiativesSupport the long-term development of Emerson's electric actuation portfolioWho You Are:
You identify and seize new opportunities and consistently look for ways to improve processes and outcomes. You are innovative and bring strong attention to detail when solving complex technical challenges. You collaborate effectively across teams, openly ask questions, and communicate clearly to ensure successful completion of projects. You adapt to changing priorities and take ownership in delivering high-quality results.For This Role, You Will Need:
Bachelor’s degree in Computer Engineering, Electrical Engineering, Computer Science, or related technical disciplineProfessional experience developing embedded software or firmware for microcontroller-based systemsStrong programming skills in C and C++Experience working with embedded systems and microcontroller-based productsAbility to read schematics and component datasheetsStrong problem-solving and debugging skillsExcellent written and verbal communication skillsLegal authorization to work in the United States without sponsorship now or in the futurePreferred Qualifications That Set You Apart:5+ years of firmware or embedded software development experienceExperience with real-time operating systems (RTOS)Experience debugging embedded hardware and software systemsFamiliarity with source control, defect tracking, and software development lifecycle processesKnowledge of industrial communication protocols such as Modbus and HARTExperience with object-oriented design methodologies and UMLExperience with C#Experience supporting products from concept through production releaseCompany DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Location: Piedmont, SC (Onsite)
Pay: $26.00/hour
Schedule: Monday–Friday | 6:00 AM – 2:00 PM
Contract Duration: Through November 7, 2026
Position Summary:
We are seeking a dependable Forklift Operator to support operations at a manufacturing facility in Piedmont, SC. This role involves operating a forklift to safely move materials throughout the facility. Experience operating a Yard Dog (Terminal Tractor/Yard Jockey) to move trailers or tank wagons is highly preferred.
Responsibilities:
Safely operate a forklift to transport materials and finished productsOperate a Yard Dog/Terminal Tractor to move trailers or tank wagons around the facility (if qualified)Load, unload, stage, and organize materialsPerform pre-shift equipment inspectionsFollow all safety procedures and company policiesSupport shipping, receiving, and logistics operationsMaintain a clean and organized work areaReport equipment issues to supervisionQualifications:
At least 1 year of forklift operating experienceYard Dog/Terminal Tractor experience preferredManufacturing, warehouse, or logistics experience preferredValid driver's license with an acceptable driving recordAbility to work safely in an industrial environmentStrong communication and teamwork skillsRequirements:
Background check requiredDrug screening requiredMotor Vehicle Record (MVR) review requiredARK2 physical examination requiredAbility to meet vision and hearing requirements for operating powered industrial equipmentJoin a team that values safety, reliability, and operational excellence.
Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: Operator I / Medical Device Assembler - 2nd Shift
Location: Irvine, CA (onsite)
Contract Duration: Contract until 02/17/2027
Working hours: 3p - 11:30p
Total hours: 40
Description:
For Irvine 2nd shift Hiring Blitz Thursday July 23rd 2:30p - 5:30p.
Operator I Job Description
This is a non-exempt position. This position is responsible for the production of high quality medical devices within a cleanroom environment.
a. Manual Assembling of medical devices.
b. Assemble and use tools under the microscope for long periods of time.
c. Hand soldering.
d. Cleanroom environment.
e. Maintain written and electronic documentation.
This position is responsible for the production of high quality medical devices within a manufacturing cell.Working under close supervision, may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.Required dress code for tour during interview and on-the job:
Clothing must be non-shedding and free of frayed hems or loose threads.Tassels, fringes, glitter, sequins (sewn or glued on), and any other items that could become dislodged are not allowed on clothing.To verify a fabric can be worn:
pull at the fabric tightly with fingers, if fibers are dislodged, the garment may not be worn in the production area.Sweaters, sweater vests, loose fiber garments, loose knit, or fleece may not be worn.All clothing must be clean and free of visible contamination (sand, mud, dirt, lint, etc.).All clothing, from the waist up, must fit under the lab coat/gown.Turtle necks or high-necked clothing shall not stick out above the neck of the lab coat/gown.Sleeves shall not stick out beyond the cuff of the lab coat/gown.Caps, hats, scarves or bandanas shall not be worn under the bouffant.
Head wraps/scarves worn to accommodate customs:
Must be covered with the bouffant and the tail end of the scarf must be fully covered by the lab coat/gown.Must be of tightly woven fabric, be clean, and laundered.Loose fitting clothing shall not be worn around machinery or soldering/brazing torches.Shoes must be worn at all times in the production area.Stockings or socks are required.The heel of a shoe must not be pointed or higher than 2 inches.Sandals, clogs, slippers, open toe, or open heel shoes are not allowed.Shoes with straps or weave where toes can be seen are not allowed.Changing shoes in the production area, other than a gowning room, is not allowed.Torsos, upper arms, and legs must be covered. Pants (above the ankle), skirts (above the ankle), skirts with slits, short shirts (above the navel), and sleeveless tops are not allowed.Skirts at the ankle are allowed, but full-length stockings, leggings, or pants must be worn under them.Nail polish, acrylic, artificial nails, or similar nail coatings are not allowed.Jewelry or body piercings that can pierce gloves or cannot be covered under gowning materials will not be allowed in the production area.Makeup shall not be worn.Lip balm in stick form is acceptable, when applied outside of production areas and prior to hand washing.Scented personal use products shall not be worn, except deodorant.Lotions shall not be applied after hand washing.Cover any open or bleeding wound with a bandage.Dont wear anything that could be offensive.Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: Assembler I
Location: Pomona, CA, 91767 (Onsite)
Contract Duration: 10-month contract to start, with the possibility of extension
Pay rate: $18 - $20/hr
Schedule: 1st Shift 6AM - 2:30PM
Client: Abbott Laboratories
Client job ID: ABOJP00047200
We offer medical, dental, vision, and 401(k) benefits.
Filling Operator / Packaging Reagent Description:
Very detailed work.Will use masterflex- set it up and give volume to fill. Have a guideline to reference.Lots of paperwork- basic knowledge of GMP, filling and packaging reagentsBasic mathLifting no more than 15 lbsOn feet all day- Rotating through tasks throughout the day.The position of Assembler I is within our CMI business unit located in California. Under general supervision, the scope of this position is responsible for setting up and performing adjustments to equipment used in support of manufacturing. Ability to diagnose and perform routine technical troubleshooting is required.
Assembler Primary Function:
This role will be responsible for a variety of assembly and non-assembly functions in support of manufacturing goals.
Job Duties:
Operates equipment used to manufacture products.Assembles, checks, and inspects products against departmental procedures.Responsible for recognizing product or equipment problems that arise during the mfg. process and escalating to Line Lead or Supervisor.May be required to assist with the set-up and the clean-up of mfg. equipment.Active participation in Lean Initiatives.Works on assignments that are routine in nature, requiring limited judgment.Responsible for exhibiting professional behavior with both internal/ external business associates that reflects positively on the company and is consistent with the company’s policies and practices.Understands and is aware of the quality consequences which may occur from the improper performance of their specific job.Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing, and testing activities.Carries out duties in compliance with established business policies.Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.Perform other duties and projects, as assigned.Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.
