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 designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients.  

What You Will Achieve

In this role, you will:

Investigate quality issues within manufacturing and quality laboratories

Examine deviations, out-of-specification results, and atypical investigations

Identify root causes and suggest effective corrective action plans

Ensure all reports comply with regulatory requirements and company policies

Contribute to moderately complex projects, managing your own time to meet targets

Develop plans for short-term work activities within a collaborative team environment

Apply skills and discipline knowledge to contribute to work within the Work Team

Make decisions to resolve moderately complex problems in standard situations

Work under general supervision, following established procedures and general instructions

Periodically review work, and may review the work of other colleagues in a mentor role

Here Is What You Need (Minimum Requirements)

BA/BS with at least 2 years of experience or MBA/MS with any years of experience or associate's degree with at least 6 years of experience or high school diploma (or equivalent) with at least 8 years of relevant experience

Proven record of problem-solving and decision-making skills

Experience in the pharmaceutical industry

Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems

Ability to work both independently and collaboratively

Effective communication skills, both written and verbal

Computer literate with superior skills in managing Excel spreadsheets

Bonus Points If You Have (Preferred Requirements)

Master's degree

Experience with investigations, including conducting and writing investigations using methodology

Familiarity with regulatory requirements and quality standards

Strong analytical and critical thinking skills

Ability to manage multiple projects simultaneously

Experience with root cause analysis and corrective action plans

Excellent organizational skills

Ability to mentor and guide junior colleagues

Strong interpersonal skills and the ability to foster a collaborative team environment

  
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Quality Assurance and Control

#LI-PFE