QC Analyst

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 flexible innovative and customer-oriented. Whether you are engaged in development maintenance compliance or analysis through research programs your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the needs of those we serve.

What You Will Achieve

In this role you will:

• Take responsibility for individual contributions to achieve team deliverables represent the work group within department teams and foster a positive team environment.
• Manage personal time and professional development prioritize own workflow and assist in prioritizing the workflow of less-experienced colleagues.
• Complete various assignments based on established procedures identify delivery and process improvements troubleshoot issues and provide direction and training to team members.
• Share knowledge within and across multiple work groups.
• Proactively identify and resolve non-routine problems making decisions between multiple options in a structured environment.
• Work under general supervision independently complete recurring assignments and refer new or unusual problems to the supervisor.
• Ensure non-standard work is reviewed for sound technical judgment and hold oneself accountable to Pfizer standards guidelines and values potentially training others.
• Perform routine analytical testing for stability samples evaluate results and keep the supervisor informed of all results and project statuses daily.
• Participate in required job training provide Certificates of Analysis (COAs) within the 3-day time limit and investigate manufacturing issues to implement corrective and preventative actions.
• Notify responsible persons of deviations or needed change control to ensure compliance and meticulously follow all Standard Operating Procedures (SOP) and written test procedures.

Here Is What You Need (Minimum Requirements)

• A Bachelors Degree
• 6 months years experience
• Strong understanding of Good Manufacturing Practices (GMP)
• Excellent problem-solving skills and attention to detail
• Proficiency in software relevant to the role e.g. Microsoft Excel LIMS PDOCS Empower
• High-level technical writing and verbal communication skills
• Strong organizational and time management skills
• Positive attitude and ability to work effectively in a team environment

Bonus Points If You Have (Preferred Requirements)

• Experience in Chemistry Analytical Techniques e.g. ACC pH UV HPLC KF CGE SDS-Page electrophoresis
• Ability to adapt to changing priorities and manage multiple tasks simultaneously
• Ability to make decisions in a structured environment
• Experience working with lean lab techniques i.e. 5S CI Standard work TPM
• Excellent interpersonal skills and ability to work collaboratively with cross-functional teams
• Demonstrated ability to train and mentor less-experienced colleagues