Why Patients Need You 

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.  Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients. 

What You Will Achieve 

You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients. 

Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R&D. 

As a Senior Associate scientist, your significant experience of applying knowledge of principles, concepts, and practices of the discipline will make you a critical member of the team. Your skill and knowledge will help in making decisions that require choosing among limited options. Your being proactive in team discussions will help in creating an environment of collaboration. 

It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. 

How You Will Achieve It 

• Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team. 

• Analyze and interpret results, makes decisions regarding the accuracy, completeness and compliance. 

• Serve on cross functional teams to represent Quality Control and facilitate communications and activities/projects between Quality Control and site departments and/or Network. 

• Assist Lab leadership in determining scheduling priorities and workload distribution to ensure customer needs are met. 

• Perform tasks associated with maintaining current Good Manufacturing Practices compliant Quality Control and Stability laboratories. 

• Record and maintain all related data and records in compliance with cGMP and quality procedures. 

• Train junior colleagues and develop training plans and oversee training activities for groups. 

• Responsible for contributing to laboratory investigations. 

• Perform testing including, but not limited to clinical and/or commercial product, raw materials and validation samples. 

• Perform laboratory support functions and maintain work area in a neat and orderly manner. 

• Participate in continuous improvement culture within laboratories utilizing continuous improvement tools. 

• Perform work consistent with Pfizer Values of Courage, Excellence, Equity, and Joy. 

Qualifications 

Must-Have 

• Applicant must have a High School Diploma (or Equivalent) and 6 years of relevant experience OR an associates degree with 4 years of experience OR a bachelors degree with 0+years of experience.

• Experience within the biopharmaceutical industry, including knowledge and experience relevant