Scientist IV, Product Support
Pfizer
August 29, 2026
Remote friendly (Andover, MA)
United States
Operations
What You Will Achieve
- Author and review GMP documents and reports
- Oversee qualifications; assess period of use; manage extension of reference materials
- Support change control, reagent studies, and instrument validation; fulfill commitments
- Author periodic method validation reviews and annual product reviews
- Manage method improvement, new technology implementation, and lifecycle activities
- Facilitate and perform method qualifications/validations/verifications, method transfers, and comparability studies
- Provide audit support for Board of Health inspections and regulatory responses
- Ensure timelines/deliverables to support product manufacturing
- Identify continued improvement (CI) opportunities; resolve technical issues; monitor product methods
- Participate in investigations/root cause analysis and resolve analytical issues
- Collaborate across functions and other Pfizer Biotech Network sites
Here Is What You Need (Minimum Requirements)
- BA/BS + 6 years; or MBA/MS + 4 years; or PhD/JD (any years)
- Proficiency with MS Office
- Excellent written/verbal communication; strong interpersonal skills
- Solid understanding of US/EU/ROW cGMP & GLP and auditing procedures
- In-depth understanding of protein characterization and production processes
- Prior method improvement experience; designing robustness studies
- Knowledge of protein analysis: HPLC/UPLC, peptide mapping, CE/gel, carbohydrate analysis, ICE, UV
- ELISA and bioassay experience (advantageous)
Bonus Points (Preferred Requirements)
- ICH/industry validation and lifecycle management guidelines; validation experience
- Laboratory automation; project management tools; stakeholder management
- Problem-solving, teamwork, organizational/time management
- Leadership/mentoring experience; regulatory/quality standards knowledge
- Experience with AI tools (e.g., ChatGPT/Microsoft Copilot) and responsible AI practices
Work Details
- Hybrid
- First shift Mon–Fri; some off-hours support may be required
Benefits (as stated)
- Global Performance Plan bonus target: 10% of base salary; 401(k) matching; retirement contribution; paid vacation/holidays/personal days; caregiver/parental and medical leave; medical/dental/vision
Application/Eligibility Instructions
- Candidates must be authorized to work in the U.S.; U.S. work visa sponsorship not available for this role now or in the future.
- Author and review GMP documents and reports
- Oversee qualifications; assess period of use; manage extension of reference materials
- Support change control, reagent studies, and instrument validation; fulfill commitments
- Author periodic method validation reviews and annual product reviews
- Manage method improvement, new technology implementation, and lifecycle activities
- Facilitate and perform method qualifications/validations/verifications, method transfers, and comparability studies
- Provide audit support for Board of Health inspections and regulatory responses
- Ensure timelines/deliverables to support product manufacturing
- Identify continued improvement (CI) opportunities; resolve technical issues; monitor product methods
- Participate in investigations/root cause analysis and resolve analytical issues
- Collaborate across functions and other Pfizer Biotech Network sites
Here Is What You Need (Minimum Requirements)
- BA/BS + 6 years; or MBA/MS + 4 years; or PhD/JD (any years)
- Proficiency with MS Office
- Excellent written/verbal communication; strong interpersonal skills
- Solid understanding of US/EU/ROW cGMP & GLP and auditing procedures
- In-depth understanding of protein characterization and production processes
- Prior method improvement experience; designing robustness studies
- Knowledge of protein analysis: HPLC/UPLC, peptide mapping, CE/gel, carbohydrate analysis, ICE, UV
- ELISA and bioassay experience (advantageous)
Bonus Points (Preferred Requirements)
- ICH/industry validation and lifecycle management guidelines; validation experience
- Laboratory automation; project management tools; stakeholder management
- Problem-solving, teamwork, organizational/time management
- Leadership/mentoring experience; regulatory/quality standards knowledge
- Experience with AI tools (e.g., ChatGPT/Microsoft Copilot) and responsible AI practices
Work Details
- Hybrid
- First shift Mon–Fri; some off-hours support may be required
Benefits (as stated)
- Global Performance Plan bonus target: 10% of base salary; 401(k) matching; retirement contribution; paid vacation/holidays/personal days; caregiver/parental and medical leave; medical/dental/vision
Application/Eligibility Instructions
- Candidates must be authorized to work in the U.S.; U.S. work visa sponsorship not available for this role now or in the future.