Job Description

Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve
You will help us in investigation of our quality issues in manufacturing and quality laboratories. You will investigate deviations and out-of-specification results and atypical result investigations. Your problem solving skills will help to identify root cause and suggest appropriate corrective action plan. Your attention to detail will help us ensure that the reports are aligned to regulatory requirements and company policies.
As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams.
It is your hard work and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It

• Contribute to the completion of complex projects and manage own time to meet agreed targets.
• Develop plans for work activities on own projects within a team.
• Perform, lead and review deviation investigation reports, change control and validation/qualification.
• Provide direct input or coaching support for other functional groups in investigations.
• Manage investigations and apply relevant and necessary actions/ systems to ensure appropriate levels of compliance.

Qualifications
Must-Have

• Bachelor or Master Degree in Pharmaceutical Sciences
• 7+ years' experience in Chemical Laboratory or chemical laboratory Quality Assurance, specifically in sterile Injectable manufacturing facility
• At least 3+ years of experience in conducting/reviewing and approving the laboratory investigations
• Technical experience in laboratory testing and validation processes. Must have handled the HPLC, GC and UV spectrophotometer etc.
• Proven record of problem solving, decision-making skills and application of process improvement tools
• Strong background and knowledge in manufacturing, compliance and technology investigations, processes and systems
• Must be comfortable working both independently and collaboratively
• Effective communication skills are required, both written and verbal
• Computer literate, with superior skills in managing Excel spreadsheets

Nice-to-Have

• Green Belt/Black Belt certification
• Experience in eQMS/Trackwise, SAP, gLIMS and EAMS

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
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