Scientist IV, Product Support

In this role, you will:

• Authoring and reviewing GMP documents and reports

• Overseeing qualifications, assessing period of use and managing extension of reference materials

• Supporting change control, reagent study and instrument validation, as well as fulfilling commitments

• Authoring periodic review of method validations and annual product reviews.

• Managing method improvement, new technology implementation and lifecycle activities

• Facilitating and performing method qualifications / validations / verifications, method transfers, and comparability studies

• Providing audit support for Board of Health inspections and regulatory responses

• Ensuring adherence to timelines and deliverables to support product manufacturing

• Identifying continued improvement (CI) opportunities, resolving technical issues and monitoring the methods of products

• Participating in investigations / root cause analysis and resolution regarding analytical issues

• Collaborating across functional areas and other Pfizer Biotech Network sites

(Minimum Requirements)

• BA/BS with at least 6 years of experience or MBA/MS with at least 4 years of experience or PhD/JD with any years of experience

• Proficiency in handling current MS Office Applications

• Excellent written and verbal communication skills

• Strong interpersonal abilities

• Solid understanding of US, EU, and ROW cGMP & GLP and auditing procedures

• Possesses an in-depth understanding of protein characterization and production processes.

• Has prior experience in method improvement, including designing studies to enhance method robustness

• Displays extensive knowledge in protein analysis techniques, including HPLC/UPLC, peptide mapping, CE/gel, carbo analysis, ICE, and UV.

• Experience with ELISA and bioassay methodologies is considered advantageous.

(Preferred Requirements)

• Knowledge of industry standards and ICH, and applicable guidelines in validation and life cycle management

• Validation experience

• Experience in laboratory automation

• Experience with project management tools, including stakeholder management

• Strong problem-solving skills

• Ability to work collaboratively in a team environment

• Excellent organizational and time management skills

• Experience in a leadership role within a laboratory setting

• Knowledge of regulatory requirements and quality standards

• Ability to mentor and develop junior team members

• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

• Work Location Assignment: Hybrid


The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.



 Relocation assistance may be available based on business needs and/or eligibility. 
 Candidates must be authorized to be employed in the U.S. by any employer. U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.