Immediate Opening: Quality Investigation Associate Manager at Pfizer (Vizag) for Sterile Manufacturing

Pfizer, a leading global biopharmaceutical company dedicated to developing, manufacturing, and delivering quality, safe, and effective prescription medicines, is inviting applications for an experienced professional to join its Quality Assurance team.

This is a critical position within the manufacturing and quality laboratories at their Vizag facility.

Position Details and Requirements

Post Title: Quality Investigation Associate Manager
Location: Vizag
Preferred Experience: 6–8 years (preferably in the Quality Assurance function of a sterile manufacturing facility).
Qualifications Required: B.Pharm, M.Pharm, M.S (Pharmacy), M.Sc. (Chemistry/Microbiology).
Industry Type: Pharma/Healthcare/Clinical research
Application End Date: 20th October 2025

Job Description: Core Responsibilities

The Quality Investigation Associate Manager will play a vital role in maintaining the highest quality and compliance standards within the facility. Key responsibilities include:

Investigation Management: Leading the investigation of various quality issues, including manufacturing deviations, out-of-specification (OOS) results, and atypical laboratory investigations.
Root Cause Analysis (RCA) & CAPA: Identifying definitive root causes for quality issues and proposing effective Corrective Action and Preventive Action (CAPA) plans.
Compliance & Reporting: Ensuring that all investigative reports are thoroughly documented and comply with stringent regulatory requirements and internal company policies.
Project and Time Management: Contributing to moderately complex projects, effectively managing personal time, and developing plans for short-term activities within a collaborative team environment.
Mentorship: Working under general supervision and established procedures while having the opportunity to review the work of and mentor junior colleagues.

Candidate Profile: Essential Skills and Knowledge

Pfizer is seeking candidates with a strong background and proven record in the sterile pharmaceutical industry.

Technical Expertise: Proven experience with investigations, including conducting and writing reports using robust methodology. Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems.
Regulatory Knowledge: Deep familiarity with global regulatory requirements and quality standards.
Analytical Skills: Strong analytical, critical thinking, problem-solving, and decision-making skills. Experience with Root Cause Analysis and CAPA is essential.
Soft Skills: Excellent organizational and interpersonal skills. The ability to work both independently and collaboratively, and to mentor and guide junior colleagues is highly valued.
Computer Literacy: Superior skills in managing databases and Excel spreadsheets, in addition to general computer literacy.

This role requires a dedicated professional with a proven record of making effective decisions to resolve complex quality problems in a fast-paced, regulated environment.