About this opportunity
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.
Your role
Develop and manage the Raw Material Support Program for the global Cell Culture Media sites to include:
Development of risk profiles of chemicals and materials used in the manufacture of cell culture media and related products, for example trace elements or trace impurity profiles.
Providing guidance to customers and internal teams on raw material changes including vendor, sourcing, and manufacturing process changes affecting raw materials.
Working closely with internal R&D, Quality, and Supplier Management Teams to determine potential impact of raw material changes to customer end use
Development and communication of risk mitigation strategies for materials deemed high risk for use in manufacture or for customer end use.
Coordinate the execution of testing of raw materials to support requests for data on high risk materials. This includes liaising with internal testing laboratories and external vendors for sample analysis.
Generate reports and communicate results to internal and external customer stakeholders. Reports may support customer process / product qualification endeavors, risk assessments, and investigations of non-conformances.
Generate or acquire data on raw materials used in the Cell Culture supply chain to develop qualification and / or release testing specifications.
Involvement with industry forums and groups in order to stay informed on market and industry needs regarding the Cell Culture Media supply chain.
Liaise with internal Manufacturing and Quality teams on batch troubleshooting as needed
Provide technical expertise to site Quality and Manufacturing teams during customer audits and investigations as needed.
Who you are
5-7 years Quality Control, R&D, and/or analytical experience. Cell culture manufacture, testing, and/or research desirable
3-5 years demonstrated experience leading projects or 5+ years as a key team member on projects cross functionally focused
3-5 years of risk management, assessment and mitigation experience
Fluent in English
Experienced in external customer facing communications and support.
Demonstrated proficiency writing technical reports, presentations, professional letters and memos
Demonstrated understanding of manufacturing and Quality systems in a GMP or regulated environment
Understanding of industrial large molecule drug production desirable but not required
Equivalent combination of education and experience
Able to analyze data sets and make technical recommendations based on data and knowledge of scientific and / or manufacturing principles
Understanding of sterile liquid and dry powder manufacturing, packaging, and testing for release to the regulated pharmaceutical and life sciences market
*내부 전보 확정 시 법인 이동이 필요한 경우, 퇴직급여 정산 또는 이전절차 및 각종 사내대출상환 절차가 필요할 수 있습니다. 내부 지원 시 해당 사항을 숙지하고 지원한 것으로 간주합니다.
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!
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 2526 comparable Manufacturing & CMC roles across 157 biopharma companies.
Salary context
639 of 2526 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 2526 comparable roles
+ 55 more countries
Seniority mix
1056 of 2526 peers have a known seniority level
Therapeutic area mix
5 of 2526 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.
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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.