LSC have a great contract opportunity for an Automation Compliance Specialist to join an innovative and rapidly growing Biopharmaceutical company in Limerick.
If you have 5 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Manage Deviations, CAPA, Change Control, Audits, and Quality risk management.
- Reviewing and maintain procedures, polices and other instructional documents with a focus on continuous improvement.
- Maintaining electronic systems used for change control and deviation management.
- Responsible for the approval of deviation notification, driving deviation investigation and tracking implementation through to closure of associated corrective action.
- Coordinate Compliance activities with and seek team support from QA, Validation Engineering and Manufacturing.
- Responsible for generating and maintaining Life cycle document across automation platforms.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Primary degree in Science /Engineering discipline
- 5 years' experience working with validated Automation systems in the pharmaceutical manufacturing environment.
- Direct experience and in-depth knowledge of automation platform desirable.
- Ability to work on own initiative, without direct supervision from management.
- Team player with an ability to work well across various departments on site as well as business partners.
- Excellent written, presentation, communication and investigation skills.
- Deadline focused individual.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Gráinne Hodnett at LSC on 021 4777329 if you have any more questions about this role!
