9 days old

Validation Junior Supervisor

Pfizer
Francofonte, Sicilia 96015
Pfizer is recruiting an expert and enthusiastic Validation Junior Supervisor for the manufacturing site in Catania.



**Mission**



The Validation Junior Supervisor will be responsible for equipment validation within manufacturing facility located in Catania, Italy.

S/he will help to demonstrate systems are running according to necessary specifications and operate within regulations to ensure data integrity and the production of quality products. Knowledge of GMP and management of quality through quality systems.

Reports to the Validation Senior Supervisor.



**Main Responsibilities**



+ Plan and coordinates periodic equipment validation activities as per Standard Operating Procedures (SOPs), protocols and regulatory guidelines;

+ Lead the equipment validation team;

+ Execute Annual Product Review (APRR);

+ Coordinate and communicates all testing with affected functional groups and evaluates test results;

+ Supervise validation activities to include Change Control initiation, protocol preparation, scheduling, protocol execution, data review and final report generation;

+ Participate and presents data in Regulatory Agency, Customer, Corporate and Internal audits when necessary;

+ Participate in development/ improvements to the validation program as needed to remain current with cGMPs and industry standards;

+ Participate in deviation investigations to identify root causes and define corrective and/or preventative actions (CA/PA);

+ Provide support for additional focus area if needed;

+ Manage minor projects which include all operational and financial aspects. Drive quality, safety and continuous improvement related activities;

+ Deliver training and support to ensure efficient use and deployment of equipment.



**Qualifications**



+ Bachelor or Masters degree in Chemistry, CTF, Engineering;

+ At least 3 years of pharmaceutical industry experience required for consideration, in the role of People Manager;

+ Knowledge of GMP and management of quality through quality systems;

+ Knowledge and experience with equipment, as related to sterile products;

+ Understanding of process parameters, and knowledge management with experience of trouble shooting manufacturing and equipment/facility processes;

+ English knowledge;

+ Planning and organizational skills to project;

+ Good interpersonal, organizational and communication skills (both oral and written) and demonstrated skills in team working;

+ Proven ability to deliver technical reports and presentations.



**Other Info**



+ Personal Protective Equipment such as gloves, a full Tyvek suit and breathable air or filtering face piece may be required.

+ The incumbent must be able to work multiple shifts as needed to meet deadlines



**Deadline to apply: Oct. 21/2020**

**\#LI-PFE**



Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.



Engineering

Categories

Posted: 2020-10-13 Expires: 2020-11-12

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Validation Junior Supervisor

Pfizer
Francofonte, Sicilia 96015

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