LSC have a great contract opportunity for a QC Analyst to join a Cork based Biopharmaceutical company.
If you have 4+ years of experience within a GMP environment and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Perform primary review of QC raw data and trend results.
- Prepare protocols, summaries, and reports, including documents submitted directly to pharmaceutical regulatory agencies.
- Draft and update QC Standard Operating Procedures (SOPs).
- Act as a technical subject matter expert (SME) and provide training and support to other analysts in areas of expertise.
- Evaluate analytical and microbiological results against defined acceptance criteria.
- Conduct and document laboratory investigations through to completion.
- Maintain the laboratory in a constant state of audit and inspection readiness.
- Interact directly with regulatory agency inspectors during audits and inspections.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- BSc in a scientific or engineering discipline with 5+ years of relevant cGMP laboratory experience.
- MSc with 3+ years of relevant cGMP laboratory experience.
- Excellent written and verbal communication skills.
- Strong customer focus, with personal accountability for speed, quality, and accuracy of delivery.
- Self motivated, with the ability to work under pressure in a fast paced environment.
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please understand that we are unable to provide visa sponsorship. Thank you for your understanding.
Apply via this advert or contact Jenny Murphy at LSC on 021-4777329 if you have any more questions about this opportunity!
