Associate Manufacturing Compliance
Year Visakhapatnam, Andhra Pradesh, India
Job Description
- Bachelor\'s/Master\'s Degree in a scientific discipline with 2-5 years working experience in the Biotech/Pharmaceutical industry.
- Should have Knowledge of change management, CAPA Management and Quality risk Management.
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change control initiation for implementing Corrective and Preventative Actions (CAPA\xe2\x80\x99s) and process improvements in support of manufacturing operations -
Coordinate and prepare change control documentation that assesses and defines the scope, impact, risk, and regulatory impact associated with the change -
Review, edit, and revise controlled documentation in accordance with cGMP standards -
Coordinate and/or lead cross-functional meetings with multiple departments to drive change control implementation -
Provide advice and mentorship to cross-functional teams to enable successful and GMP compliant change controls.
Qualifications
Must-Have
- Bachelor\'s/Master\'s Degree
- Demonstrated working knowledge and understanding of sterile Manufacturing procedures.
- Knowledge of Good Manufacturing Practices {also cGMP}, validation principles, audit techniques, and working knowledge of change management.
- Effective communication skills, both verbal and written.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control
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Job Detail
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Job IdJD3151930
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IndustryNot mentioned
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Total Positions1
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Job Type:Full Time
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationVisakhapatnam, Andhra Pradesh, India
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EducationNot mentioned
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ExperienceYear