Regional EM Engineering Lead
GSK
9 days ago
Remote friendly (King of Prussia, PA)
United States
Operations
Position Summary
- Ensure External Manufacturing delivers products to patients through strong engineering performance at CMO sites. Report to the External Manufacturing Engineering Lead and support new product introduction and supply continuity via engineering inputs (site assessments, capital management, troubleshooting, and multi-site engineering programs). Focus on Large Molecule Drug Substance engineering.
Responsibilities
- Be accountable for a portion of the External Manufacturing network (Large Molecule Drug Substance/Drug Product; Medicine Small Molecule API/secondary, including Antibody Drug Conjugates and Oligonucleotides) and support internal Large Molecule Drug Substance sites.
- Provide engineering performance accountability (equipment uptime, engineering safety, and quality compliance) via site visits/audits and virtual engagement.
- Oversee key capital project delivery to enable launches and supply continuity.
- Act as Large Molecule Drug Substance Engineering SME.
- Drive strategic objectives (safety improvements, waste elimination, product cycle time reduction).
- Deliver improvement programs (e.g., Extractables & Leachables, PFAS, obsolescence management).
- Provide engineering input into GSC strategy recommendations; possible ownership of External Manufacturing capital plan.
- Build engineering capability across the External Manufacturing team and external sites; collaborate with Smart Manufacturing and Tech teams.
Basic Qualification
- HND/associate degree in an engineering discipline (Chemical/Mechanical/Electrical/Automation).
- 10+ years’ relevant experience focused on Large Molecule Drug Substance.
- Experience delivering large capital projects.
- Experience with GSC Engineering Policies, Standards, and Project Management Framework.
Preferred Qualification
- Bachelor’s/Master’s in engineering.
- Drug Product Engineering; conjugation project/operations experience.
- Small molecule (primary/secondary) and high-toxicity API manufacture experience.
- Large Molecule Drug Substance/Drug Product capital delivery; GSC EHS Standards.
- Utilities/compliance/facilities engineering; external manufacturing site experience; relationship management.
Work Arrangements
- Hybrid model; ~25% domestic/international travel.
How to Apply
- Apply with CV and a short note describing how experience matches the role (include questions if any).
- Ensure External Manufacturing delivers products to patients through strong engineering performance at CMO sites. Report to the External Manufacturing Engineering Lead and support new product introduction and supply continuity via engineering inputs (site assessments, capital management, troubleshooting, and multi-site engineering programs). Focus on Large Molecule Drug Substance engineering.
Responsibilities
- Be accountable for a portion of the External Manufacturing network (Large Molecule Drug Substance/Drug Product; Medicine Small Molecule API/secondary, including Antibody Drug Conjugates and Oligonucleotides) and support internal Large Molecule Drug Substance sites.
- Provide engineering performance accountability (equipment uptime, engineering safety, and quality compliance) via site visits/audits and virtual engagement.
- Oversee key capital project delivery to enable launches and supply continuity.
- Act as Large Molecule Drug Substance Engineering SME.
- Drive strategic objectives (safety improvements, waste elimination, product cycle time reduction).
- Deliver improvement programs (e.g., Extractables & Leachables, PFAS, obsolescence management).
- Provide engineering input into GSC strategy recommendations; possible ownership of External Manufacturing capital plan.
- Build engineering capability across the External Manufacturing team and external sites; collaborate with Smart Manufacturing and Tech teams.
Basic Qualification
- HND/associate degree in an engineering discipline (Chemical/Mechanical/Electrical/Automation).
- 10+ years’ relevant experience focused on Large Molecule Drug Substance.
- Experience delivering large capital projects.
- Experience with GSC Engineering Policies, Standards, and Project Management Framework.
Preferred Qualification
- Bachelor’s/Master’s in engineering.
- Drug Product Engineering; conjugation project/operations experience.
- Small molecule (primary/secondary) and high-toxicity API manufacture experience.
- Large Molecule Drug Substance/Drug Product capital delivery; GSC EHS Standards.
- Utilities/compliance/facilities engineering; external manufacturing site experience; relationship management.
Work Arrangements
- Hybrid model; ~25% domestic/international travel.
How to Apply
- Apply with CV and a short note describing how experience matches the role (include questions if any).