Process Engineer II, Technical Compliance

Technical Compliance Support Team Member

Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer's mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.

As a member of the Technical Compliance Support team, you will work cross-functionally to implement changes within Operations, ensure compliance of the manufacturing suites, support audits / inspections, support risk assessments, and CAL OOTs. You will coordinate and perform compliance walkthroughs of the manufacturing areas. You will support and own low risk change controls as well as participating in other change controls by performing impact assessments ensuring that the change will not negatively impact operations.

You will own multiple projects at a time and will be responsible for delivering to the milestones on time. You will also be responsible for owning activities such as CAPAs, change actions, revising SOPs. The Technical Compliance Support team supports all the manufacturing suites in Andover which will enable you to work with multiple teams within and outside Operations Support.

Here is what you need (minimum requirements):

• BA/BS degree with any years of experience, or Associate's degree with 4+ years of experience, or high school diploma (or equivalent) with 6+ years of relevant experience.
• Knowledge of process equipment and manufacturing operations.
• Ability to follow standard operating procedures and regulatory guidelines.
• Basic understanding of Current Good Manufacturing Practices.
• Strong organizational skills to manage project tasks and meet deadlines.
• Technical documentation skills for production and process approvals.

Bonus points if you have (preferred requirements):

• Experience with in the pharmaceutical industry
• Experience with writing Change Controls
• Experience in deviations as responsible person
• Familiarity with programs such as Veeva Vault, EAMS, PDOCs
• Experience with Six Sigma or other operational excellence programs

Physical/mental requirements:

• Daily routine may require standing for long periods of time and/or walking throughout the suite including up and down stairs.
• Must be able to don cleanroom gowns.
• The incumbent needs to take the necessary safety precautions when working within the manufacturing suites.
• The incumbent must be able to express ideas into SOPs, assessments, and be able to use a multitude of programs including Excel, Word, Power Point, etc.

Non-standard work schedule, travel or environment requirements:

This is a first shift, Monday to Friday role; however, this group supports the manufacturing suites which operate outside those hours. Occasionally, support will be required outside of the normal first shift hours. This is an on-site role with occasional work from home available.

Other job details:

• Last day to apply:
  July 3rd, 2026.