Senior Associate Scientist page is loaded Senior Associate Scientist Bewerben locations United States - Massachusetts - Andover time type Vollzeit posted on Gestern ausgeschrieben job requisition id 4930049 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 At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. Your contributions will be pivotal in translating advanced science and technologies into impactful therapies and vaccines, ultimately improving patient outcomes globally. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, you will leverage cutting-edge design and process development capabilities to accelerate and deliver top-tier medicines to patients worldwide. How You Will Achieve It In this role, you will: Contribute to immediate work group goals and collaborate with team members to achieve project objectives Develop analytical methods for characterizing and supporting the manufacturing of therapeutic proteins and vaccines Implement technology and continuous process development to ensure success in drug discovery programs Serve as the primary Technical Expert for manufacturing methods, conducting scientific studies and recommending improvements for reliability, cost, safety, compliance, and environmental performance Support lab-scale processes and scaled-up processes for internal pilot production facilities Troubleshoot and improve established analytical test methods, ensuring accuracy and efficiency Represent Analytical Technology Research and Development in cross-functional project teams and participate in technical writing, review of analytical documentation, and regulatory submissions Maintain laboratory areas and equipment in a clean, safe, and functional order, complying with safety and regulatory requirements Independently plan and perform work assignments, interpret and present data, and provide analytical support for product transfers, new product development, and cost improvement projects Develop methods for Large Molecules Drug Products, while prioritizing work to meet project deadlines and solving moderately complex problems under moderate supervision Qualifications Must-Have Applicant must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience. Strong working knowledge of analytical chemistry principles Ability to perform complex data analysis Proficiency in troubleshooting technical issues Experience in planning and carrying out experiments independently Competence with complex instrumentation and software Excellent oral and written communication skills Nice-to-Have Strong knowledge and experience with international CMC regulatory requirements Familiarity with Current Good Manufacturing Practices (part of GxP) Technical capability in several major areas of analytical sciences Ability to work effectively in a team environment Strong organizational and time management skills
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