API In-Plant Laboratory Analyst V

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 flexible innovative and customer-oriented quality culture is rooted in science and risk-based compliance. 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 highest standards making a meaningful difference in the lives of those we serve. Join us in our mission to improve patient outcomes through excellence in every aspect of our work.

What You Will Achieve

• Serve as a key resource and lead other team members within your area of expertise.

• Manage personal time and professional development taking accountability for your results and prioritizing workflow.

• Contribute to project and departmental tasks providing direction and training to team members and will act as a lead worker.

• Be recognized as a LEAD or Subject Matter Expert in your field.

• Proactively identify and resolve basic complexity problems considering wider implications.

• Promote an environment conducive to inclusion accountability and joy.

• Participate appropriately in the IMEx PCT.

• Complete assignments independently selecting appropriate methods and ensuring team assignments are completed.

• Review non-standard work for technical soundness and review others work.

• Adhere to Pfizer standards guidelines and values influencing teams and contributing to the development of departmental standards and guidelines.

• Provide input for performance assessments ensure timely and compliant documentation and develop processes to enhance cGMP standards.

• Maintain high standards of safety and housekeeping participate in Continuous Improvement projects and ensure adherence to all policies and procedures while providing training and conducting peer reviews.

Here Is What You Need (Minimum Requirements)

• High School Diploma or GED

• 6 years of experience

• Certifications in the relevant areas if applicable

• Ability to write clear technical documents

• Good organizational and time management skills

• Proficiency in Microsoft Office

• Experience with laboratory equipment and procedures

• Knowledge of Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP)

Bonus Points If You Have (Preferred Requirements)

• Bachelors Degree

• Pharmaceutical quality control and stability experience

• Effective problem-solving skills

• Strong analytical skills

• Strong attention to detail

• Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity

PHYSICAL/MENTAL REQUIREMENTS

Laboratory and office work requiring walking standing and sitting throughout a shift. Lifting of items less than 25 kg.

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

This position requires colleagues to work weekends and/or holidays to meet business or customer needs. All Laboratory colleagues adhere to safe work practices such as wearing appropriate personal protective equipment including lab coat safety glasses and gloves. There is no routine travel associated with this position.

12 hour shift (7p-7:30a)

Work Location Assignment:On Premise

OTHER JOB DETAILS

Last Date to Apply for Job: May 19th 2026

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN O-1 H-1B etc.) is not available for this role now or in the future.