Validation Specialist

Location
Cambridgeshire
Salary
£20 to £33 per hour
Posted
13 Jun 2017
Closes
11 Jul 2017
Ref
J3995
Contact
Georgia St John-Smith
Contract Type
Contract
Hours
Full Time
We are currently looking for a Validation Specialist to join a leading Pharmaceutical company based in the Cambridgeshire area. As the Validation Specialist you will bring your experience with Process and Cleaning Validation within the Pharmaceutical Industry to various Validation Projects.

You will be responsible for supporting the introduction and validation of new equipment, processes and pharmaceutical products.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Validation Specialist will be varied however the key duties and responsibilities are as follows:

1. To ensure products are manufactured using equipment, processes and procedures that comply with the GxP requirements specified by both the Regulatory Authorities and Company Policy.

2. Provide input into validation projects in accordance with GxP and departmental SOP's. As well as supporting the introduction and validation of new equipment, processes and products.

3. Maintain the system for on-going review of validation projects including filing, storage and retrieval of validation related documentation to ensure compliance with Regulatory and corporate requirements.

4. Participate in the testing phase of a project, acting either as a Tester or a QA witness to verify test performance and outcome, and where necessary producing technical reports to agreed standards.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Validation Specialist we are looking to identify the following on your profile and past history:

1. Relevant degree in a Scientific Discipline

2. Proven industry experience in the Pharmaceutical Industry with hands on experience with Process Validation and Cleaning Validation.

3. A working knowledge and practical experience with Equipment Validation, Facility and Utility Validation, Risk Assessments, Change Control, Calibration, Auditing, and Statistical Process Control is desirable.

Key Words: Validation / Pharmaceutical / GMP / Equipment Validation / Process Validation / Validation Engineer / Validation Officer / Documentation / GXP / Cleaning Validation / Tester / Testing / QA / Quality Assurance / Facility Validation / Utility Validation / Process Control / Auditing / Audit / FDA / MHRA / Risk Assessment

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant 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 processionals and scientists. We look forward to helping you with your next career moves.

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