Associate Manager

3 weeks ago

Vizag, India Pfizer Full time

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Use Your Power for PurposeEvery day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients.What You Will AchieveIn this role, you will:Investigate quality issues within manufacturing and quality laboratoriesExamine deviations, out-of-specification results, and atypical investigationsIdentify root causes and suggest effective corrective action plansEnsure all reports comply with regulatory requirements and company policiesContribute to moderately complex projects, managing your own time to meet targetsDevelop plans for short-term work activities within a collaborative team environmentApply skills and discipline knowledge to contribute to work within the Work TeamMake decisions to resolve moderately complex problems in standard situationsWork under general supervision, following established procedures and general instructionsPeriodically review work, and may review the work of other colleagues in a mentor roleHere Is What You Need (Minimum Requirements)Candidate should possess a B. Pharm degree with a minimum of 8 years of experience, an M. Pharm degree with at least 6 years of experience, or an associated degree with a minimum of 10 years of experience.Proven record of problem-solving and decision-making.Experience in the Injectable pharmaceutical industry.Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems.Ability to work independently and collaboratively.Effective communication skills (written and verbal).Advanced skills in managing MS-Office, SIPOC, DMAIC methodology, Continuous Improvement (CI) tools.Bonus Points If You Have (Preferred Requirements)Experience with investigations, including conducting and writing investigations using structured methodologies.Familiarity with regulatory requirements and quality standards in pharmaceutical industry.Strong analytical and critical thinking abilities for problem-solving and process improvement.Ability to manage multiple projects simultaneously.Experience with root cause analysis and implementing action plans.Excellent organizational and time-management capabilities.Ability to mentor and guide junior colleagues.Strong collaboration and team building skills to create a positive work environment.Work Location Assignment: On PremisePfizer 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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