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QC Equipment Technical Specialist

Job Posted: 2 days ago

Salary: £ Competitive
Job Type: Permanent
Location: Hatfield

Expire in: a month

Job Description

Talentmark are recruiting for a QC Equipment Technical Specialist, to join a long-established global pharma company, based in Hertfordshire on a 12-month Fixed Term Contract. 

 The Role:
 The Equipment Technical Specialist will be responsible for supporting all QC equipment and associated electronic systems through the equipment’s life cycle used within the Quality Control Laboratory. This includes supporting all technical developments within manufacturing laboratory as well as third party contracting activities to ensure operation in accordance with the requirements of the departmental Standard Operating Procedures and cGMP. 

 Responsibilities:

Ensure Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and Eisai Corporate expectations.  
Support and deliver the required qualification and validation of lab QC equipment, processes and systems to ensure performance in line with lab procedures, GMP and GAMP guidelines for process, equipment and electronic systems.
Support the procurement of new equipment and providing forecast for new/replacement lab equipment/software.
Lead the maintenance of lab procedures supporting Qualification and Validation ensuring they are current with updated requirements for Qualification and Validation and cGMP, cGxP expectations.
Coordinate and lead equipment service and repair activities.
Support QC team members with training and education on use of specialist QC equipment as required.
Ensure user access to systems is maintained in line with procedures and support is provided to facilitate the set up and change management of system data to ensure continuous system availability and functionality.Your Skills:

Strong knowledge of pharmaceutical Quality Control equipment and electronic system qualification, and validation.
Ability to understand and analyse user requirements to facilitate changes and system improvements.
Working knowledge of electronic systems, CSV and GAMP requirements.
Good understanding of the requirements of data integrity and application to system management.
Working knowledge of Quality Control Systems and analytical software and electronic Quality Systems. 
Thorough understanding of GMP Guidelines and Regulations.Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence

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