• Contribute to achievement of goals and influences at the work group/project team level.
• Assist in the establishment of analytical procedures and interpret results/technical data.
• Communicate progress, plans, requirements and risks to the senior analyst, manager, stakeholders in partner groups and higher management informally and, if required, formally through written reports and presentations.
• Actively participate and report progress into cross-functional project teams to meet customer expectations, project milestones and Good Manufacturing Practices {also c GMP} standards.
• Prepare and review technical documents, including validation protocols and reports, analytical test procedures, investigation reports, and change controls.
• Develop analytical methodologies and strategies needed to progress biotherapeutic products in the pipeline.
• Support development, qualification, validation, and transfer of cell-based and immunoassays in support of diverse portfolio in varying stages of clinical development.
• Analyze and communicate experimental results both orally and in written reports to colleagues and management.
• Provide the necessary documentation for regulatory submissions as required and writes deficiency responses.

• Bachelor's Degree with 3 to 6 years of experience OR Masters degree with 0 to 4 years of experience
• Experience with a variety of chromatographic instrumentation.
• Experience with collecting and analyzing mass spectral data.
• Experience with interdisciplinary drug development teams and industrial experience developing analytical strategies and methods in support of product and process development and to assess the quality and characteristics of biotherapeutics
• Experience working in a regulated environment, such as Good Laboratory Practices {part of Gx P}
• Demonstrated technical expertise in functional verification of design
• Working knowledge of applicable industry test standards, relevant regulatory guidance, Design Controls and Product Development Process
• Able to interact effectively with peers and leaders as part of a multi-disciplinary team
• Effective verbal and written communication skills

• Exceptional interpersonal skills preferred and a proven track record of teamwork, adaptability, innovation, leadership and initiative

• Work Location Assignment: On Premise

The annual base salary for this position ranges from $64,600.00 to $107,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% 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. Research and Development #LI-PFE