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Details
Commercial Attribute Science Snr Associate
| Reference: | AS35041 | Location: |
Dublin |
| Qualification: | Degree | Experience: | See description |
| Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
May be suitable for:
Analytical Chemist, Nurse Associate
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. 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.
This role will be responsible for Forensics & Defects activities involving forensic identification of Drug Product defects and maintain and produce extensive defect panels used to support automated and manual visual inspection of vial (liquid / lyophilised) and syringe packaged drug products.
Duties:
- Leads / assists forensic investigation and identification of defects arising from drug product manufacture at ADL and write up of these investigations to cGMP standards.
- Be accountable for the maintenance, distribution and upkeep of extensive defect panels used for the set-up, training and characterization of automated / semi-automated / manual finished drug product visual inspection equipment at ADL.
- Act as support for the Attribute Sciences function on cross functional teams/programs
- Timely documentation of Analytical data in the electronic notebook system.
- Understanding of data flow in laboratory systems and data integrity.
- Participate in the peer review of analytical data.
- Compliance with Standard Operating Procedures for the Attribute Sciences Laboratory.
- Ensure the laboratory is operated in a safe and environmentally friendly manner.
- Ensure ongoing compliance with phase appropriate GMP, including compliance within the LMS training system.
- Ensure high levels of Laboratory housekeeping are maintained including inventory control of samples and consumables.
- Ensure timely completion of Laboratory Investigations, Deviations , PMAFs
- Participate in internal/external audits/inspections as required.
- Plan and implement procedures and systems to maximise operating efficiency.
- Manage and contribute to the achievements of department productivity and goals.
- Engage with the Continuous Improvement Process and MyGreenLab® philosophy.
- 3-6 years of experience in the Pharmaceutical Industry with a third level qualification (Degree) in Analytical Chemistry/ Biochemistry or related discipline.
- Experience with Regulatory inspections and interaction with inspectors is preferable.
- Experience with developing, validating, troubleshooting, analytical methods.
- Understanding of the Change Control and Variation Management Process.
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
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