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:
In this role you will be part of the quality system, and ensure that components, in process products, and finished product meet their designated quality standards, and that the facility follows proper GMPs.
Responsibilities include but are not limited to:
Ensure that all retain samples are logged in and stored according to standard operating procedures, as well as ensuring the annual review of Finished Packaged Product Retain Samples occurs on a quarterly basis, providing a written report of results to quality management each quarter.
Coordinate inspection of Finished Packaged Product Retain Samples for customer complaints and provide written report of results as needed.
Inspects incoming components for adherence to quality standards and documents results.
Assist in inspection and labeling of raw materials. Work closely with Receiving and Production to ensure status is appropriate and up to date, both on the materials and in SAP.
Performs document revisions, deviation reviews, and processes change controls in existing Quality Systems.
Physical Attributes:
Lift and/or move up to 25 pounds.
Wear appropriate Personal Protective Equipment.
Who You Are:
Minimum Qualifications:
Bachelor’s Degree in Biology, Chemistry, or other Life Science discipline and 1+ years of GMP pharmaceutical industry experience.
OR
High School Diploma or GED and 3+ years of GMP pharmaceutical industry experience.
Preferred Qualifications:
Experience with computer software applications including Microsoft Excel, Word, and Access.
Experience with Quality Management computer systems and SAP.
Excellent interpersonal and team skills; work independently and carry out QA decisions based on GMPs and appropriate procedures.
Experience reading and interpreting documents such as quality standards, safety rules, operating and maintenance instructions, and procedure manuals.
Pay Range for this position: $29 - $44 / 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 757 comparable Quality roles across 94 biopharma companies.
Salary context
144 of 757 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 757 comparable roles
+ 42 more countries
Seniority mix
350 of 757 peers have a known seniority level
Therapeutic area mix
1 of 757 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.
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.