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Technical Operations Specialist (Process Validation), Cork
Client:
Life Science Recruitment
Location:
Cork, Ireland
Job Category:
Other
EU work permit required:
Yes
Job Reference:
aaedb289d4fe
Job Views:
78
Posted:
21.01.2025
Expiry Date:
07.03.2025
Job Description:
We’re currently recruiting for an exciting opportunity with an award-winning Biopharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties
1. Develop Technical Operations documentation as required (e.g. strategies, plans, protocols, procedures, reports).
2. Review and approve documents prepared by other Technical Operations colleagues.
3. Execute Technical Operations protocols as required.
4. Liaise with Manufacturing to provide support where required with routine operations / project based work.
5. Prepare reports for executed protocols for review and approval.
6. Initiate and implement change control activities in accordance with site procedures.
7. Track and resolve exceptions/events/deviations during Technical Operations activities.
8. Co-ordinate Technical Operations document review and approval.
9. Collate and organize Technical Operations files for turnover to QADC.
10. Attend identified training, required to fulfil the role of a Technical Operations Specialist.
Education & Experience
1. Bachelors Degree in a scientific/technical discipline required.
2. Experience in Projects, New product introduction (e.g. Supporting: Process Improvement Projects / Process Validation campaigns).
3. Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. Ability to apply cGMP regulations and guidelines to all aspects of Technical Operations activities.
If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or emailprotected for further information.
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