Sr. Associate TechOps CSV

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 

Pfizer Sanford provides Drug Substance and Drug products to facilities around the globe. This position works as part of a cross-functional team to perform technical tasks as they relate to support for different validation program efforts, including equipment validation, computer system validation, process validation cleaning validation.  These validation efforts will help ensure that our equipment, systems, and processes are reproducibly functioning as intended to support our efforts to manufacture medicines for patients. As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate explaining difficult issues and establishing consensus between teams. 

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 

• Authoring of technical reports (periodic reviews, validation protocols) or assessments (materials or components). 

• Facilitating reviews/seeking feedback from multiple internal or external stakeholders. 

• Ability to manage multiple activities simultaneously. 

• Liaise with site functions such as Manufacturing, Planning, QA, QC, Operations, and Regulatory Affairs 

• Participating in right-first-time and continuous improvement relative to supported validation programs (processes or procedures). 

• Will be responsible for increasingly more complex projects and responsibilities. 

• Planning of timelines with intermediate milestones to meet deadlines. 

• The position requires execution of multiple projects at the same time and good communication skills to keep, peers, and area management up to date with progress of all projects in order to ensure validations are completed in a timely manner and on schedule. 

Qualifications 

Must-Have 

• Applicant must have High School Diploma (or Equivalent) with six years of relevant experience; OR an Associate's degree with four years of experience; OR a Bachelor's degree with 2-4 years of experience.  Relevant experience/degree must be in engineering or science (for example, biology, chemistry, biochemistry, materials or computer science). 

• Demonstrated experience with computer system validation - life cycle management. 

• Skilled in Microsoft Word and Excel. 

• Ability to work in a team environment and complete tasks independently.