7 days old

Validation Associate

Pfizer
Mulgrave
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**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**



As a Validation Associate you will execute revalidation activities for site Facilities, Equipment and Services. The role is responsible for ensuring existing equipment and facilities are requalified in a timely and compliant manner and ensures the site maintains its critical regulatory compliance commitments. Your problem-solving ability will help us troubleshoot validation problems for equipment and performance processes and conduct analysis of testing results and process anomalies. Your documentation skills will guide the writing, review and approval of for validation process documents and technical reports related to equipment, products and processes.



As an associate, your focus on the job will contribute in achieving scheduled tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues. It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.



**How You Will Achieve It**



+ Completion of the HEPA testing tasks incorporating the planning, scheduling, coordinating, conducting, reporting, issue resolution and completion of qualification activities with relevant key stakeholders (as appropriate)

+ Perform and manage facility, equipment and services qualification activities identified as part of routine scheduled or reactionary compliance activities, remediation or project/business requirements in accordance with company policies and procedures

+ Execute work in accordance with agreed business objectives and assigned time frames

+ Integrate qualification outcomes into Pfizer quality management systems

+ Prepare documentation which may include but not limited to qualification documents and master supporting documents.

+ Communicate issues/work progress to and manage expectations of team/key stakeholders

+ Provide support to site/project qualification activities

+ Participate in and provide information for OOS and deviation incidents and events



**Qualifications**



**Must-Have**



+ HEPA filter testing proficiency

+ Degree level qualification preferably in Engineering/ Science

+ Proficiency in Word/ Excel / Outlook / Project (or equivalent)

+ Excellent English both written and oral.

+ Mechanical aptitude

+ Strong analytical and problem solving skills.

+ Quality and detail focus

+ Good communication skills, proactive, good initiative and ability to work under pressure.



**Nice-to-Have**



+ Validation experience in a similar field: 2-5 years

+ Technical writing experience

+ Pharmaceutical Industry validation experience

+ Working knowledge of equipment qualification



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
Posted: 2021-06-07 Expires: 2021-07-08
Sponsored by:
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Validation Associate

Pfizer
Mulgrave

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