Senior Quality Assurance Associate - 2nd Shift
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:
The Quality Assurance Operations representative is a driver of a mature quality culture, particularly through the implementation of quality assurance within operations. Quality assurance operations (QA Ops) function is present or easily accessible to operations in a Manufacturing facility to support data integrity, root cause analysis, data and batch review, document control and auditing.
Shift is 12pm-10:30pm Monday-Thursday
Preparation of documentation for production execution including batch records, supplemental logs, packaging and shipping and other documents in support of cGMP operations.
Presence in Production/QC and warehouse areas to review documentation whether paper or electronic, perform line clearances and perform QA checks.
Review batch records in a timely manner to meet committed release dates and ensure documentation, whether paper or electronic, is attributable, legible, traceable, permanent, contemporaneously recorded, original and accurate.
Prepare certificates of analysis and batch release documentation for accuracy and completion prior to final release of product.
Product release through the review of batch documentation.
Conduct self-inspection for the Madison/Verona site.
Who You Are
Minimum Qualifications:
Bachelor’s degree in any discipline.
3+ years of quality assurance experience.
OR
Associate’s degree in any discipline.
3+ years of GMP experience.
3+ years of quality assurance experience.
Preferred Qualifications:
Detailed knowledge of data integrity, data review, root cause analysis and auditing.
Highly developed interpersonal, written and verbal skills with attention to detail.
Strong team player – ability to collaborate across all departments within the organization to deliver on quality and regulatory commitments.
Ability to work autonomously, effectively manage time, and deliver results on time.
Pay Range for this position: $25-$39 per hour.
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here .
RSREMD
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 178 comparable Senior Quality roles across 58 biopharma companies.
Salary context
53 of 178 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 178 comparable roles
+ 22 more countries
Seniority mix
178 of 178 peers have a known seniority level
Therapeutic area mix
0 of 178 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
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.
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.