About This Opportunity
The details below reproduce the recorded source information. They have not been independently confirmed with the employer. Missing fields are not inferred from the role title. Check pfizer.wd1.myworkdayjobs.com for the current requirements and availability.
Full source description
- Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients
- Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance
- Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care
- By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy
- What You Will Achieve In this role, you will: Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records
- Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories
- Support media preparation, Bio ball culture handling, and conduct microbiology-related investigations
- Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data
- Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues
- Here Is What You Need (Minimum Requirements) M.Sc
- Microbiology or related masters with 8+ years of industry experience Strong technical skills in method validation and testing NPI MLT, BET, Sterility, Assay
- Bio-Assay expertise Method development for new products Experience in microbiological sterility testing Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations Detail-oriented with robust knowledge of Reagents management Familiarity with pharmacopeia methods and developments Effective written and verbal communication, as well as interpersonal skills Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical experience Strong understanding of computer system hardware, infrastructure, and networks Experience with Laboratory Information Management Systems (LIMS) Proficiency in data analysis and interpretation Knowledge of regulatory requirements and guidelines Strong problem-solving abilities Effective time management and organizational skills Ability to mentor and train junior colleagues 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: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates
- To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers
- Quality Assurance and Control
Application preparation
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Candidate Guidance
Preparation actions based on the recorded description. Suggestions below do not add to or replace the employer requirements.
- Technical preparation suggestion: choose one relevant implementation you actually built. Be ready to demonstrate a normal input, an invalid input, how you tested both, and one limitation. This is preparation advice, not an additional employer requirement.
- The source text does not provide clearly labelled eligibility or selection details. Read its full wording and ask the employer about missing mandatory conditions before investing time in an application.
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