Job Summary
Pfizer is seeking a highly motivated and detail-oriented Manufacturing Supervisor to oversee daily operations within our state-of-the-art biopharmaceutical production facility. This role is responsible for ensuring efficient, compliant, and high-quality manufacturing processes in alignment with Good Manufacturing Practices (GMP) and regulatory standards. The ideal candidate will lead cross-functional teams, drive continuous improvement initiatives, and ensure timely delivery of life-saving pharmaceutical products.
Key Responsibilities
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Supervise and coordinate daily manufacturing activities in the biopharmaceutical production unit.
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Ensure adherence to GMP, safety regulations, and company quality standards.
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Lead, coach, and develop a team of operators and technicians to achieve production targets.
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Monitor production processes, identify deviations, and implement corrective and preventive actions (CAPA).
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Collaborate with Quality Assurance, Quality Control, Engineering, and Supply Chain teams.
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Maintain accurate batch records, documentation, and compliance reports.
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Drive process optimization and continuous improvement initiatives (Lean, Six Sigma).
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Ensure proper utilization and maintenance of manufacturing equipment.
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Participate in audits and inspections, ensuring readiness and compliance at all times.
Required Skills and Qualifications
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Bachelor’s or Master’s degree in Biotechnology, Pharmaceutical Sciences, Chemical Engineering, or a related field.
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Strong understanding of GMP, regulatory requirements, and biopharmaceutical manufacturing processes.
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Proven leadership and team management skills.
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Excellent problem-solving and decision-making abilities.
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Strong communication and interpersonal skills.
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Proficiency in manufacturing systems, ERP tools, and documentation practices.
Experience
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Minimum of 5–8 years of experience in pharmaceutical or biopharmaceutical manufacturing.
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At least 2–3 years of supervisory or team leadership experience in a regulated environment.
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Hands-on experience in aseptic processing, upstream/downstream processing, or fill-finish operations is highly desirable.
Working Hours
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Full-time, onsite role at the manufacturing facility.
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Rotational shifts may be required, including weekends and holidays, depending on production schedules.
Knowledge, Skills, and Abilities
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In-depth knowledge of bioprocessing techniques and cleanroom operations.
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Ability to manage multiple priorities in a fast-paced environment.
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Strong analytical skills with attention to detail.
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Capability to lead under pressure and handle critical production issues effectively.
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Familiarity with health, safety, and environmental compliance standards.
Benefits
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Competitive salary and performance-based incentives.
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Comprehensive health, dental, and vision insurance.
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Retirement savings plans and employee stock options.
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Paid time off, holidays, and wellness programs.
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Learning and development opportunities with global exposure.
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Employee assistance programs and work-life balance initiatives.
Why Join Pfizer
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Be part of a global leader in biopharmaceutical innovation and healthcare advancement.
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Contribute to the production of life-saving medicines that impact millions worldwide.
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Work in a collaborative, inclusive, and growth-oriented environment.
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Access cutting-edge technology and continuous professional development opportunities.
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Join a company committed to integrity, excellence, and patient-centric values.
How to Apply
Interested candidates can apply through Pfizer’s official careers portal by submitting an updated resume and a cover letter detailing relevant experience. Shortlisted candidates will be contacted for further assessment and interviews.