Description
Are you a QA/Change Control Specialist interested in working for one of Irelands leading names in High-Tech Pharmaceutical Engineering?
Are you looking for something new?!
Then stop what you are doing and read on!
Title: QA/Change Control Specialist
Rate: Negotiable
Location: Cork, Ireland
Positions Available: 1 Engineer
Type: Contract (18 Months Rolling)
A Fantastic new role has just opened up at one of our leading Irish based clients offering the successful candidate the opportunity to join a hard-working team working on exciting projects in the pharmaceutical sector.
The proposed start date is Mid/Late June - We need YOU
Responsibilities include:
- Position will involve progressing and reviewing change control documentation from all areas on site.
- Act as a technical expert in area of responsibility for change control management and the change control process, and work with minimum supervision.
- When a change is proposed, in area of change control responsibility, participate in defining change control strategies and project timelines, for the most efficient way of progressing proposed change with minimum disruption to the site.
- Review change control documentation received for clarity, ensuring relevant supportive data has/will be generated.
- Confirm categorisation of site change control
- Establish productive working relationships with colleagues within project teams at site and other regulatory/change control subsidiaries.
- Link in with site Change Owners in terms of what change control would need to be reviewed by CMC regulatory personnel to determine impact to Clinical/commercial licenses for proposed changes.
- Provide Change control support as required during HA inspections
- Provide change control training to the site for change originators and reviewers of proposed changes
- Leverage off the network in terms of change control guidance and support for biologics and vaccines when required.
- Provide guidance and support to the site in terms of client change control business processes and systems
- Support the application and management of site licenses and GMP certificates.
- Update manufacturing authorization to ensure that site documentation is in line with approved registrations.
- Carry out annual product reviews from Change Control Perspective
- Project management skills
Requirements:
- Degree in Biological Sciences, Biochemical engineering or related discipline. Advanced degree preferred
If you are interested please do not hesitate to email or call me!
(see below)