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 highest standards making a real 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
In this role you will:
Provides strategic and scientific oversight to the Bioassay Laboratory
Ensures testing plans methods and equipment are in place to assure reliability of product in conjunction with product design and specifications.
Tests and inspects products to determine compliance with specifications.
Performs laboratory tests on finished products raw materials and in-process material in support of the companys quality control program.
Provides support to operations and other line functions in day-to-day operations
Supports Quality in the development of Short-range and long-range operating objectives staffing requirements and succession plans
Work is achieved by individual or through project teams utilizing technical or subject matter expertise to achieve results.
Requires relevant scientific education skills and knowledge.
Here Is What You Need (Minimum Requirements)
Applicant must have a bachelors degree with at least 4 years of
experience; OR a masters degree with at least 2 years of experience; OR a PhD with 0 years of experience; OR as associates degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience
Experience in QC/laboratory management
Previous experience leading people is preferred
Experience with analytical laboratory techniques/technologies
Knowledge of GMP guidelines
Knowledge and experience with Quality Systems
Strategic and Innovative Thinking
Expertise with bioassay techniques such as: ELISA Slot Blot SDS-PAGE etc.
Problem Solving and Critical Thinking Skills
Bonus Points If You Have (Preferred Requirements)
Knowledge in the application of statistical tools root cause analysis and/or six sigma methodologies
Experience with environmental testing utility monitoring analytical testing microbial identification and sterility testing
Expertise in Quality Control (QC) instruments and accuracy specifications
Ability to manage projects and ongoing work activities of moderate complexity
Excellent verbal and written communication skills
Ability to foster teamwork and colleague development
Experience using common AI tools including generative technologies such as ChatGPT or Microsoft Copilot to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices includingrisk management and ethical use
PHYSICAL/MENTAL REQUIREMENTS
Ability to stand for 2 or more hours at a time.
Ability to lift 40 lbs.
Ability to work in front of a computer for 2 or more hours at a time.
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
May be required to support activities after working hours.
May be required to support weekend activities from time to time.
OTHER JOB DETAILS
Last Date to Apply for Job: April 6 2026.
Referral Bonus Eligibility: YES
Eligible for Relocation Package: NO
Work Location Assignment:On Premise
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.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status. Pfizer also complies with all applicable national state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing please email. This is to be used solely for accommodation requests with respect to the accessibility of our website online application process and/or interviewing. Requests for any other reason will not be returned.
Required Experience:
Manager
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