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Quality Tech - Calibration

Job in Walker, Kent County, Michigan, USA
Listing for: West Pharmaceutical Services
Full Time position
Listed on 2026-03-05
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager, Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Working at West means having an opportunity to work by the side of our patients and customers, our global team members and the communities in which we operate – which all help contribute to a Healthier World.

At West, we are by the side of patients. The work we do impacts patients’ lives each and every day – our products are a critical part of healthcare delivery and we are proud of the role we play to improve patient health. We work by the side of our team members. We come together as one global team to deliver for our customers and help them address their challenges.

We are a diverse, close-knit community of professionals, where everyone has a voice and opportunity to learn and grow through mutual trust and respect. With a 95 year plus history, we have a track record for success, which includes reported sales of $2.14B in 2020. We serve by the side of our community. Giving back is in our DNA—our team members across more than 50 sites globally are involved with hundreds of charities that have special meaning to them through our West Without Borders team member-led giving program.

Job Summary:

In this role, you will maintain the calibration program by performing calibration, maintaining documentation, and investigating problems. Participate in new equipment/process validations where calibration support is necessary.

Essential Duties and Responsibilities:

  • Maintain calibration program in accordance with prescribed procedure assuring that calibrations are completed to schedule.
  • Calibrate all existing equipment within the program and assure new equipment is appropriately included in the calibration system.
  • Develop and maintain accurate record systems to assure easy retrieval and proper documentation of information.
  • Review and initiate changes to existing documentation in accordance with applicable procedures. Develop new methods and procedures to support new equipment additions to the system.
  • Participate in plant validation activities as needed.
  • Develop an understanding of Good Manufacturing Practice (GMP) and ISO requirements.
  • Maintain equipment in good working order. Assure work area is neat and orderly.
  • Inform Q.

    A. Supervisor and Q.A. Manager of discrepancies or potential problems that could negatively impact quality systems, product efficacy or safety conditions.
  • Performs other duties as assigned based on business needs.
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Basic Qualifications:

  • Education: High School or equivalent.
  • Experience: 0-3 years of experience.
  • Proficiency with PC and Microsoft Office;
    Knowledge of QMS Master Control, Measure Link and other Quality systems is preferred.
  • Must be able to prioritize and perform position responsibilities accurately and meet required deadlines.
  • Strong attention to detail;
    Strong problem identification/analysis and solving skills with hands-on approach.
  • Excellent verbal and written communication skills;
    Maintain an organized and clean quality Lab.
  • Ability to multi-task and prioritize in a fast-paced environment;
    Ability to interface with all personnel levels.
  • Motivated self-starter with ability to work independently on multiple assignments in a team environment.
  • Preferred

    Knowledge, Skills and Abilities:

  • Quality, Engineering or related degree
  • Knowledge and experience with FDA and ISO Quality Systems to include SPC and calibrations systems.
  • Travel Requirements:

  • Minimal travel may be required.
  • Physical and Mental Requirements:

  • While performing the duties of this job, the associate frequently is required to sit, walk, stand, balance, stoop, kneel, or crouch to support production needs. The associate may lift and/or move up to 25 pounds and occasionally lift and/or move more than 55 pounds.
  • West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply .

    Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.

    About the company

    West Pharmaceutical Services, Inc. is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products.

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