Scientist II

Posted Yesterday
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Singapore, SGP
Hybrid
Senior level
Healthtech • Pharmaceutical
The Role
Leads scientific investigations, process development, scale-up, technology transfer, process validation, troubleshooting, and continuous improvement for late-stage and commercial antibody and ADC manufacturing. Supports new product introduction, CMC lifecycle management, product investigations, regulatory submissions, agency inspections, and manufacturing at internal or third-party sites. Collaborates cross-functionally with process development, manufacturing, quality, and regulatory teams while applying scientific, engineering, and statistical principles.
Summary Generated by Built In
Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

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)

Qualifications

• 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

Additional Information

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

Skills Required

  • Bachelor of Science in Biology, Biochemistry, Chemical Engineering, Biochemical Engineering, or a related field
  • At least 7 years of relevant experience with a B.Sc.
  • Master of Science in Biology, Biochemistry, Chemical Engineering, Biochemical Engineering, or a related field
  • At least 5 years of relevant experience with an M.Sc.
  • Effective written and verbal communication of research or regulatory materials
  • Experience with late-stage process transfer, process validation, process improvements, biologics manufacturing, and CMC activities

AbbVie Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AbbVie and has not been reviewed or approved by AbbVie.

  • Retirement Support — Retirement programs are portrayed as a standout, with a dollar‑for‑dollar 401(k) match up to 6% and an additional annual company contribution based on age and service. Feedback suggests this materially boosts perceived total compensation for many U.S. employees.
  • Parental & Family Support — Paid parental and caregiver leave are emphasized, including up to 12 weeks of fully paid parental leave for all parents and 4 weeks of paid caregiver leave in the U.S. Feedback suggests these policies are a meaningful differentiator for employees balancing family needs.
  • Leave & Time Off Breadth — Time off is described as extensive, with tiered vacation that scales with tenure, 17 company holidays, and two paid volunteer days in the U.S. Feedback suggests the breadth of leave contributes notably to overall benefits satisfaction.

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The Company
HQ: North Chicago, IL
56,000 Employees
Year Founded: 2013

What We Do

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.

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