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Supervisor - Investigations, Environmental Control

Rocky Mount, North Carolina, US
Closing date
Sep 27, 2023

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Academic / Research
Conservation science
Salary Type
Employment Type
Full time
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 be a member of Pfizer's dedicated and highly effective quality assurance and control team. You will be responsible for reviewing and approving environmental monitoring investigations to support our quality program. Your contribution to aseptic compliance will help Pfizer provide safe drugs to patients.

Your understanding of will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R&D.

As a Team lead, you will be involved in leading work teams within your division, including the technical and financial resources of the team. Thanks to your technical skills, you will coach your direct reports on day to day activities. You will be relied on to solve complex problems within your area of expertise.

It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It
  • Manage multiple projects and schedule work activities within a work team and ensure agreed upon timelines are met.
  • Review and approve environmental monitoring investigations.
  • Review laboratory data to ensure compliance with approved methodologies.
  • Build capabilities of the Process-Centric Team according to skills needs assessments.
  • Engage with business partner to identify areas of improvement across the site.
  • Manage review and approval of Good Manufacturing Practices {also cGMP} documentation, such as procedures, data and reports.


  • Bachelor's Degree
  • 6+ years' experience
  • Supervisory experience
  • Knowledge of Good Manufacturing Practices {also cGMP} compliance requirements for Quality Control Laboratories
  • Experience with leading colleagues and/or projects
  • Strong people management experience
  • Demonstrated skills in collaboration, attention to detail, and communication skills
  • Ability to handle complex and detailed situations with a focus on quality
  • Experience conducting investigations

  • Relevant pharmaceutical experience.
  • Experience with microbiological risk assessments
  • Knowledge of Laboratory Information Management Systems
  • Working knowledge and understanding of environmental monitoring requirements as it relates to method qualification and testing of components and finished products


Ability to aseptically gown


Overtime required as necessary

Work Location Assignment: On Premise

Last day to apply: October , 2023

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

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 provider's 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.

Quality Assurance and Control

This employer is a corporate member of myGwork - LGBTQ+ professionals, the business community for LGBTQ+ professionals, students, inclusive employers & anyone who believes in workplace equality.

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