LSC have a great contract opportunity for a Sr QA Compliance Specialist to join a Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.
If you have 3+ years experience in Quality Assurance in a biotech manufacturing setting and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Preparation, review and approval of Material Qualification Documentation.
- QA disposition of raw materials, level 1 & level 2 consumables.
- Authoring, review and approval of QA-related procedures.
- QA review, assessment and approval activities for Biologics Manufacture, as applicable, for: Change controls, Deviations/Investigations, Supplier Investigations, CAPAs, Supplier Change Notifications (SCN), Other associated documentation
- Be a core team member of the QA Compliance Materials Management team engaging in other support activities as required.
ARE YOUR SKILLS A MATCH?
- BSc in Science or related discipline with a minimum of 3 years' QA or related experience in a Biologics or Pharmaceutical environment
- A clear understanding of cGMP requirements for manufacturing and/or systems and compliance
- Knowledge of material qualification & SAP would be a distinct advantage
- Required to work on his/her own initiative in addition to working as part of a team. Must be able to work across a team matrix to meet accelerated timelines.
Please apply directly to this advert or contact Kathy Gillen on 021 4718212 for more details.
To apply for our contract roles you must hold a Stamp 1G or Stamp 4 work visa. LSC cannot provide visa/work permit sponsorship.
