Every 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 Achieve
In this role, you will:
- 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
Here 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 Premise
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
Top Skills
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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Pfizer Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.







