Technician, Quality Control 3
Millipore Corporation

Job Info

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Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Technician, Quality Control 3 is primarily responsible for testing by wet chemistry and sampling. Testing may include visual appearance, IR, Karl Fischer (KF) analysis, automatic and manual titration, and other compendial testing or instrumentation techniques. Additional responsibilities and support may include reagent inventory management, routine bulk sampling of incoming raw materials and primary/secondary packaging components for use in the manufacture of intermediates and final products, glassware cleaning, pipette verifications, environmental monitoring testing, bulk sampling, ordering supplies, cleaning verification swabbing, general lab audit readiness, peer review of documentation, report/deviation/OOS writing, support of documentation/organization (scanning/filing/copying) activities for QC or other departments, writing or revising standard operating procedures or other documentation, and participation in process improvement initiatives. The Technician, Quality Control 3 position, like all positions at MilliporeSigma, will require a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.

• Sample and analytically test raw materials or other analyses as assigned. Testing may involve visual appearance, IR, KF, GC, automatic titration, and other tests and instruments.
• Perform data entry activities in appropriate document control, inventory control software, etc.
• Write and revise SOPs including raw material specifications.
• Work in accordance with current GMP practices demonstrating proper safety and housekeeping practices.
• Maintain accurate and concise records, as well as assist with peer review of documentation for accuracy.
• May provide or request documents via email or phone transactions to customers or vendors.
• Perform annual retain or reagent inventory audits.

• Work on problems of moderate scope and exercise judgment within defined procedures and practices to determine appropriate action and obtain assistance from supervisor or more experienced staff when needed.
• Work cooperatively within the QC department and with other departments to achieve project goals.
• Work in compliance with effective procedures and regulatory requirements outlined in ICH Q7 and 21 CFR Parts 11, 210 and 211 as applicable. Work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines.

• Participate in OOS or deviation investigations via testing and good documentation/writing.
• Maintains laboratory in an audit-ready state which may include ordering reagents or supplies, cleaning glassware, waste management, dusting, vacuuming, and mopping laboratory areas.
• Miscellaneous duties and tasks as assigned.

ADDITIONAL LOCAL NEEDS

Environmental conditions: Work near moving mechanical parts. Frequently required to wear appropriate protective gear (hard hats, lab coats, safety glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protective equipment "PPE" to protect from toxic or corrosive chemicals in the forms of liquids, solids, vapors, or airborne particles. Must be willing to work with highly potent/hazardous materials requiring the use of proper PPE, which could include half/full face respirators, Saranex and/or Tyvek suits with powered respiration.

Physical requirements: Regularly required to sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch, or crawl for extended periods of time. Must occasionally lift and/or move up to 30 pounds unassisted and be capable of pushing and pulling heavy materials to complete assignments. May be required to lift more poundage with assistance. Must be able to speak, hear, taste, and smell. Specific vision requirements include close vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus. Regularly use phones, computers, computer monitors, and all office/laboratory equipment. Required to type at a computer keyboard and have the ability to read CRTs/computer monitors.

Who you are:

Minimum Qualifications

• High School Diploma or GED.
• 2+ years of quality control testing experience in a cGMP environment.

Preferred Qualifications

• Associate Degree with some chemistry or related biological sciences courses.
• Excellent written and verbal communication skills, as well as excellent documentation practices.
• Ability to work in a team environment.
• Ability to work in analytical testing labs with hazardous and toxic chemicals.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html

This job has expired.