About this opportunity
Use Your Power for Purpose
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. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.
What You Will Achieve
In this role, you will:
Review and approve master batch records and completed batch records for the manufacture, packaging, and labelling of intermediates and active pharmaceutical ingredients (APIs), ensuring compliance with Pfizer quality standards and registered regulatory specifications.
Perform disposition of intermediates and active pharmaceutical ingredients (APIs).
Review and approve cleaning instructions and records, ensuring compliance with Pfizer Global and Local Document Standards and ICH guidelines.
Review and approve GMP documents, including SOPs, protocols, reports, and change controls, for compliance with Pfizer Global and Local Document Standards.
Ensure compliance with quality procedures, regulatory requirements, and current Good Manufacturing Practices (cGMP).
Review and approve deviations in accordance with site procedures, including investigation reports, root cause analyses, corrective and preventive actions, and quality, validation, stability, and regulatory impact assessments conducted with subject matter experts.
Maintain quality tracking systems and metrics to proactively identify trends and atypical observations.
Support preparation of Annual Product Records, evaluate trends and atypical observations, and recommend improvement actions.
Maintain inspection readiness and support regulatory and customer inspections. Participate actively in GMP walkdowns to keep site operations and facilities inspection-ready.
Support maintenance of the validated state of GMP systems and processes.
Support regulatory submissions and respond to regulatory queries promptly.
Uphold Pfizer's code of conduct and values, demonstrate Pfizer actionable attributes.
Contribute actively within the assigned Value Stream Team (VST) by reporting performance against metrics, identifying and resolving issues, and escalating concerns appropriately.
Support continuous improvement of Quality Assurance systems, as needed.
Participate actively in safety initiatives and conduct Environment, Health and Safety (EHS) investigations as required.
Here Is What You Need (Minimum Requirements)
Diploma with at least 4 years of relevant experience or BA/BS with at least 1 year of relevant experience
Experience in the pharmaceutical industry and Quality administered systems
Sound knowledge of current Good Manufacturing Practices (part of GxP)
Ability to work effectively in a team environment, both within one's own team and interdepartmental teams
Effective written and oral communication skills
Bonus Points If You Have (Preferred Requirements)
Experience at a manufacturing site.
Managing and writing deviations
Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control management
Strong problem-solving skills
Ability to work independently and as part of a team
Excellent time management and multitasking abilities
Experience using common AI tools, including generative technologies such as Microsoft Copilot to support problem solving and enhance
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.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1065 comparable Quality roles across 134 biopharma companies.
Salary context
211 of 1065 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1065 comparable roles
+ 43 more countries
Seniority mix
524 of 1065 peers have a known seniority level
Therapeutic area mix
2 of 1065 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.