Require Quality Investigation Associate Manager at Pfizer - M.Pharm, B.Pharm, MSc Apply

Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.

Post : Quality Investigation Associate Manager

Job Description
• Investigate quality issues within manufacturing and quality laboratories
• Examine deviations, out-of-specification results, and atypical investigations
• Identify root causes and suggest effective corrective action plans
• Ensure all reports comply with regulatory requirements and company policies
• Contribute to moderately complex projects, managing your own time to meet targets
• Develop plans for short-term work activities within a collaborative team environment
• Apply skills and discipline knowledge to contribute to work within the Work Team
• Make decisions to resolve moderately complex problems in standard situations
• Work under general supervision, following established procedures and general instructions
• Periodically review work, and may review the work of other colleagues in a mentor role

Candidate Profile
• B.Pharm/M.Pharm/M.S(Pharmacy)/ M.Sc.(Chemistry/Microbiology)
• Experience with investigations, including conducting and writing investigations using methodology
• Familiarity with regulatory requirements and quality standards
• Strong analytical and critical thinking skills
• Ability to manage multiple projects simultaneously
• Experience with root cause analysis and corrective action plans
• Excellent organizational skills
• Ability to mentor and guide junior colleagues
• Strong interpersonal skills and the ability to foster a collaborative team environment

• Preferably 6- 8 years' experience in Quality Assurance function of sterile manufacturing facility.
• Proven record of problem-solving and decision-making skills
• Experience in the pharmaceutical sterile industry
• Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems
• Ability to work both independently and collaboratively
• Effective communication skills, both written and verbal
• Computer literate with superior skills in managing Excel spreadsheets

Additional Information
Experience : 6- 8 years
Qualification : M.Pharm, B.Pharm, M.Sc
Location : Vizag
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 20th October 2025