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 AchieveYou 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 an Associate scientist, your strong foundation in general scientific practice and in the principles and concepts of the discipline will help us achieve our goals. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge.
It is your dedication and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve ItPerform tasks associated with maintaining Good Manufacturing Practices (also cGMP) compliant Quality Control and Stability laboratories.Support environmental monitoring and water collection in the QC (Quality Control) Microbiology laboratory.Act safely and follow Environment, Health and Safety requirements for site and QC laboratories.Apply existing techniques and procedures, with recommendations, and implement modifications for improved efficiency.Write cleaning validation protocol and reports and perform complex mathematical problems and data analysis.Support product transfers/new product development, regulatory queries, cost improvement projects or Drug Product plant support for Cleaning Validation.Operate within established HR policies and basic colleague relations guidelines.Write Standard Operating Procedures (SOPs), technical reports, project plans etc. independently.Contribute to the completion of team objectives and assigned project milestones.Exercise and build basic team effectiveness skills, such as commitment, feedback and consensus management, within the work group.QualificationsMust-HaveBachelor's DegreeDemonstrated experience in manufacturing, quality or engineering experience in the biotech or pharmaceutical industryFundamental understanding of laboratory instrumentation function and analytical method troubleshootingAptitude for good decision making based on procedures, guidance, and experienceExcellent oral, written and interpersonal communication skillsKnowledge of Microsoft Office applications, specifically Word and ExcelNice-to-HaveExperience with and in depth understanding of Microbiology testingExperience defending laboratory practices in regulatory auditsIn-depth knowledge of viable and non-viable environmental monitoring during pharmaceutical manufacturing and an understanding of aseptic techniquesEEO (Equal Employment Opportunity) & Employment EligibilityPfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.
About UsPfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We're looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.
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