Scientist II
Abbvie INC · 🌍 Singapore, SG
Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal — ask the recruiter.
- No government sponsor record hereNo government sponsor record covers this employer in this country.
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- Can’t check pay against the visa rulesNo salary stated. Singapore Employment Pass needs at least SGD 67,200 a year. Source: https://www.mom.gov.sg/passes-and-permits/employment-pass/eligibility, rules effective 2025-01-01.
- Confirmed live todayWhen a source last listed this job as open.
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No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
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Sponsor Radar — Abbvie INC
No government sponsor record covers this employer in this country.
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About the role
Purpose: Technical expert who independently investigates, identifies, develops, and optimizes new methods/techniques for critical project needs, to support both laboratory and commercial manufacturing processes. Apply scientific/engineering principles and statistical process design/analysis to develop robust antibody manufacturing processes. Act as lead scientist, critically evaluate scientific/regulatory advances, and integrate into R&D programs. Support manufacturing, process validation, regulatory submission, and continuous improvement for late-stage and commercial manufacturing of ADCs. Requires in-depth knowledge of late-phase process transfer, process validation, process improvements. Strong cross-functional communication needed. Major Responsibilities: 1. Resolve key project hurdles using technical expertise; support late-stage/commercial biologics manufacturing, tech transfer, process validation, investigations, troubleshooting, scale-up, continuous improvement 2. Work in dynamic/diverse team to support & troubleshoot current commercial manufacturing 3. Support/lead new product introduction at AbbVie sites or third-party manufacturers; ensure successful tech transfer, scale-up, validation 4. Support CMC life-cycle management and post-approval continued process validation for commercial antibody processes 5. Collaborate with process development on late-stage tech transfers, scale-up, and validation during transition to commercial manufacturing 6. Support product investigations/non-conformances; identify root causes; make scientific/quality recommendations 7. Author/review CMC sections of submissions; support agency inspections, inquiries, audits 8. Represent MSAT antibody group in CMC program teams; maintain strong internal/external relationships 9. Adhere to corporate standards (code of conduct, safety, GxP, controlled substances, animal care where applicable) • B.Sc. + 7+ years, OR M.Sc. + 5+ years relevant experience • Field: Biology, Biochemistry, Chemical or Biochemical Engineering, or related fields • Effective writer/communicator of research or regulatory materials AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html