Computer System Validation Officer

7 days left

Location
Hertfordshire
Salary
Experience Dependent
Posted
02 Aug 2019
Closes
30 Aug 2019
Ref
J5631975
Contact
Rhys Evans
Contract Type
Permanent
Hours
Full Time
An exciting opportunity has just opened for a Computer Systems Validation Officer to join a leading pharmaceutical company based in the Hertfordshire area. As the Computer Systems Validation Officer, you will be responsible for all validation activities on controlled laboratory systems and ensuring their compliance to regulatory requirements.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Computer Systems Validation Officer will be varied. However, the key duties and responsibilities are as follows:

1. You will partner with several groups and functions including Operations, Information Technology and Quality to ensure the regulatory requirements for equipment control systems and laboratory information management systems (LIMS) validation, are implemented and improved upon on a regular basis.

2. As the Computer Systems Validation Officer, you will coordinate the validation and life cycle maintenance, leading and specialising in computer and controlled systems validation, as appropriate.

3. You will author, review and approve Validation Documentation for the site to ensure validation activities are built into project plans to give compliance with company and regulatory validation standards.

4. As the Computer Systems Validation Officer, you will maintain the Computer System Validation Master Plan and document matrices; run and support the roll out of standard validation processes, ensuring their adherence.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Computer Systems Validation Officer, we are looking to identify the following on your profile and history:

1. Relevant Life Sciences degree.

2. Proven industry experience in delivery of Computer Systems Validation within a highly regulated environment.

3. A working knowledge and practical experience of working in a GMP environment with LIMS and other document / enterprise management systems.

Key Words: CSV | Computer Systems Validation | Validation | VMP | Validation Master Plan | LIMS | Laboratory Information Management Systems | CDS | Chromatography Data Systems | eDMS | Electronic Document Management Systems | CDMS | Controlled Document Management Systems | SAP | Systems , Applications , Products | ERP | Enterprise Resource Planning | Pharmaceutical | Life Science | Biopharmaceutical | Biotechnology

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

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