LSC have a great contract opportunity for a Technical Specialist to join a leading biotech company based in Dublin.
If you have 2 years of experience and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Risk lead of the contamination control and downstream QRA.
- Responsible for Downstream Quality Risk Assessments (QRA's), including contamination control QRA's Responsibility for the timely, accurate and efficient management of documents including access and revision control.
- Manage and implement on the floor documentation control system.
- Drive the Documentation Life Cycle System to ensure documents are approved in as per Scheduling requirements.
- Work with various Subject Matter Experts to ensure technical documentation updates are approved.
- Creation and revision of Standard operating Procedures (SOPs) Work Instructions (WI's) as required
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Degree in a relevant Qualification and Biopharmaceutical experience
- Self-motivated with excellent organizational skills
- Experience Working in a Pharmaceutical GMP regulated industry.
- Excellent verbal and written communication skills
- Ability to work independently and as part of a team in a cross functional collaborative environment.
- High level of attention to detail
- Experience working with GMP Documentation Management Systems
For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available currently.
Apply via this advert or contact Grainne Hodnett on 021 4777 329 if you have any more questions about this opportunity!
