About this opportunity
Work Your Magic with us! Start your next chapter and join MilliporeSigma.
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:
As the Quality Assurance Specialist 2, you will support our Contract Testing Services by ensuring compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and applicable regulatory requirements. This role performs routine to moderately complex quality tasks under supervision and is responsible for executing quality systems activities, including document review, investigations, and audit support. You will work collaboratively with various teams including QA and Operations to support compliance and maintain quality standards while developing proficiency in quality systems and regulatory requirements.
Shift - Tuesday - Saturday ; 10am - 6:30 pm
Review and approve controlled quality documents, including SOPs, laboratory and batch records, and other quality records.
Review and approve events/deviations, out-of-specification investigations, CAPAs, and change controls under appropriate oversight.
Participate in root cause analysis using approved problem-solving tools and methodologies.
Review study-related documents (e.g., protocols, technical specifications, data, certificates of analysis).
Support customer audits by coordinating laboratory tours and facilitating document reviews.
Support continuous improvement initiatives to enhance quality and compliance.
Conduct internal audits and systems inspections in accordance with applicable cGMP/GLP requirements.
Review and approve audit responses and applicable follow-up actions or CAPAs within assigned authority and under appropriate oversight.
Support maintenance of SOPs and adherence to global regulatory (e.g., FDA, EMA) and internal requirements.
Ensure accuracy, completeness, and compliance of documentation.
Who You Are:
Minimum Qualifications:
Bachelor’s Degree in any discipline with 2+ years' experience in Quality Assurance in a science field or a GxP environment.
OR
Associate’s Degree in any discipline with 4+ years in a Quality Assurance in a science field or GxP environment
OR
High school diploma or GED with 6+ years in a Quality Assurance in a science field or GxP environment
Preferred Qualifications:
Practical knowledge of 21 CFR 11, 58, 210 & 211, EU GMP, MHRA GLP & GMP, OECD GLP, ICH Q7, ISO 9001, and other applicable regulations, standards, and guidelines.
Familiarity with International regulations (EMA, MHRA).
Proficient knowledge and application of FDA and EU regulations (cGMP, GLP, Data Integrity).
Strong communication and interpersonal skills.
Acts ethically and ensures quality of own work and that of others.
Open-minded, flexibility and works with agility.
Ensures deadlines are met by taking initiative.
Works with cross-functional teams and builds networks within QA and Operations departments.
Collaborates with various teams to identify and implement improvements.
Pay Range for this position - $28/hr – 43/hr
Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1502 comparable Quality roles across 147 biopharma companies.
Salary context
261 of 1502 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1502 comparable roles
+ 48 more countries
Seniority mix
731 of 1502 peers have a known seniority level
Therapeutic area mix
3 of 1502 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
Or follow a whole field: get every new Quality job in the United States, and choose locations and companies.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.