Scientist III

Position Overview

Support new and existing analytical method development and validation in a cGMP quality control analytical laboratory. Activities include method development, validation, qualification, and compendial verifications for clinical and commercial drug substance production. Support PAT method validation in production suites and contribute to Network Lab Strategy across Pfizer sites.

• Develop and validate analytical test methods, author test method documents, support specifications and list of test methods, and ensure effective method transfer from the technical support group to the release laboratory by training analysts.
• Draft and execute analytical method validation protocols for new material qualification.
• Provide technical support for new analytical methods, troubleshoot methods, conduct investigations, and implement method improvements.
• Collaborate with site functional areas such as Global Procurement, Quality Assurance, Site Technical Services, and Manufacturing Operations to support the site plan of record.
• Support sustainability of Integrated Manufacturing Excellence (IMEx) elements within the group.
• Identify technical issues, method performance issues, instrument malfunctions, and methodology problems and participate in investigations to mitigate.
• Maintain all related data and records in compliance with cGMPs and quality procedures.
• Write and review various technical documents in support of new material validations/verifications, investigations, and technical memos.
• Meet all timelines and deliverables in support of the Andover plan of record and instrument qualifications (IQ/OQ/PQ).
• Execute method validations for PAT test methods within manufacturing operations.

• Bachelor’s degree with 6+ years of experience or master’s degree with 4+ years of experience.
• Knowledge and practical application of relevant basic spectroscopic and chromatographic techniques.
• Ability to efficiently manage personal project timelines.
• Working understanding of cGMPs and regulatory guidance.
• Experience with GC and HPLC.
• Strong problem‑solving skills.
• Demonstrated planning and prioritization skills with focus on team success in meeting defined timelines; proactive team player.
• Proficiency with computer systems (Microsoft Office, LIMS, etc.).
• Excellent oral and written communication skills.

• Experience with Raman spectroscopy.
• Experience in method troubleshooting and laboratory investigations.
• Working understanding of IMEx principles.
• Knowledge of Empower Software.

• Normal lifting, sitting, standing and walking requirements to facilitate support of staff in the office and on the floor (laboratory, suites, etc.). Position is first shift Monday through Friday. Some off‑hour (night/weekend/holiday) support may be required.

The annual base salary ranges from $82,700.00 to $ and the position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. Comprehensive benefits include 401(k) with matching contributions, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, medical, prescription drug, dental and vision coverage. Benefits vary by location.

On Premise.

Pfizer is committed to equal opportunity in terms and conditions of employment for all employees and job applicants. This position requires permanent work authorization in the United States and the employer is an E‑Verify employer.