QC Lab Analyst

Pfizer

72d • $66,500 - $110,900

About The Position

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.

Requirements

• Bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience.
• Demonstrated technical skills in method validation and testing.
• Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations.
• Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
• Strong written and verbal communication skills.
• Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation.
• High productivity and organizational skills.
• Ability to multi-task coupled with a low error rate and attention to detail.
• Demonstrate flexibility/agility and engagement in a changing environment.

Nice To Haves

• Experience with laboratory work (Western blot, microbiology/aseptic technique, plate reader/spectrophotometer, HPLC).
• cGMP documentation experience.
• Proven track record in leading continuous improvement projects.
• Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis.
• Strong problem-solving skills and attention to detail.
• Ability to manage multiple priorities and meet deadlines.
• Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels.

Responsibilities

• Perform routine quality control testing of a biologic drug substance, its intermediates, and related materials in accordance with site policies, departmental procedures, compendial methods, and cGMP regulations.
• Complete training activities and maintain records, equipment, basic lab supplies, and reagents in accordance with cGMP requirements.
• Work effectively in a team laboratory environment.
• Recognize atypical data, inform supervision of relevant problems, and offer possible solutions.
• Comprehend and perform both routine and non-routine analyses from compendial and internal sources.
• Contribute to the completion of specific team objectives and assigned project milestones.

Benefits

• 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution.
• Paid vacation, holiday and personal days.
• Paid caregiver/parental and medical leave.
• Health benefits to include medical, prescription drug, dental and vision coverage.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Bachelor's degree
• Number of Employees: 5,001-10,000 employees