Posted:1 month ago|
Platform:
Work from Office
Full Time
Use Your Power for Purpose
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.
Quality Assurance and Control
Pfizer
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