Senior Validation Engineer

This job is with Pfizer, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

Use Your Power for Purpose
At Pfizer, we believe that every role contributes to our mission of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, you'll play a pivotal role in accelerating the delivery of medicines to the world.
What You Will Achieve
In this role, you will:
Lead the completion of assigned complex projects, meet agreed targets and develop plans for work activities on projects within a team.

Provide high level data analysis support for Quality Investigations or troubleshooting.

Comprehensive understanding of {Current} Good Manufacturing Practices {part of GxP} guidelines outlined in Code of Federal Regulations.

Ensure compliance with latest Pfizer Standards for validation and qualification activities.

Point contact SME for routine Quality systems, such as Change Control, Quality Agreement, Documentation, Submission authoring and Investigations.

Author or approve protocols and final reports, perform on floor executions of validations.

Coordinate and communicate all testing with affected functional groups and evaluate test results.

Maintain Site Validation Master Plan. Support regulatory audits through the preparation and interaction with auditors in areas related to sterility assurance equipment, capex qualifications, computerized systems, process or cleaning validations as assigned.

Provide expertise for troubleshooting and resolution of issues related to sterility assurance equipment, capex qualifications, computerized systems, process or cleaning validations as assigned.

Assess potential impact of changes to qualified systems Identify and implement validation best practices to continuously improve the site validation program.

Lead and Support product transfers/new product development, regulatory queries, cost improvement projects or Drug Product plant support for Validation.

Ensure integration of validation schedule in production schedule for implementation of validation activities and conduct validation deviations, participate in deviation investigations to identify root causes and define corrective and/or preventative actions. Support the unit where needed to assure due dates and customer needs are met.

Here Is What You Need   (Minimum Requirements)
Applicant must have a bachelor's degree with at least 2 years of   experience; OR a master's degree with more than 0+ years of experience   OR an associate's degree with 6 years of experience; OR a high school   diploma (or equivalent) and 8 years of     relevant     experience.

Strong understanding of cGMPs, ISPE, Data Integrity, 21 CFR Part 11, industry good practices for IQ/OQ/PQ and Standard Operating Procedures.

Ability to work independently with limited managerial oversight

Strong verbal and written communication skills

Bonus Points If You Have   (Preferred Requirements)
5+ years of direct validation experience in minimum one of the field of validations:
Equipment qualifications, CSV, Aseptic validations, process or cleaning validations.

Strong technical knowledge and experience with  validation/qualification  of pharmaceutical processes, equipment, utilities, facilities and/or computer systems as related to sterile products and medical devices

Exposure to multiple validation work streams

PHYSICAL/MENTAL REQUIREMENTS
Requires routine sitting, standing, walking, listening and talking

Acute mental and visual attention at all times

Handle multiple projects while managing frequent interruptions

Requires moderate lifting or moving up to 25 pounds (lbs)

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Requires regular onsite attendance

Must have the ability to work effectively under strict deadlines

Must be able and willing to work beyond office hours which may include weekends and holidays

Must be capable of supporting up to 10% travel (domestic and international)

Other Job Details:
Relocation support available
Work Location Assignment:
On Premise
Last day to apply: 11/21

The annual base salary for this position ranges from $80 300,00 to $. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 10,0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage.

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