Elusav Recruitment have an excellent opportunity with a leading global Pharma and Biopharma company who is seeking a QC Chemistry Analyst to bring value to their state-of-the-art facility in Waterford.
This is an excellent opportunity to work with a global and progressive leader, with modern labs, with a lot of change and growth in their Waterford site.
This role allows opportunity to become highly skilled within the team and gain experience in all areas essential to the running of a chemistry department.
Responsibilities: Provide analytical chemistry services and support to Site.
Effective interaction with other departments on mattersrelated to raw materials, intermediates and finished batchreleases.
In particular, close contact maintained with QualityAssurance Production, Engineering and Planners.
Maintain, update and issue chemical methods, specificationsand SOPs in compliance to pharmacopeial and regulatoryrequirements.
Assist with training of the analysts in areas of expertise andknowledge and in new methods, SOPs and updates.
Trend such results, record on COAs where required andcomplete OOSs investigations on a timely basis.
Update the QC Team Leader on potential problems andhighlight improvements where possible by use of the normalcommunication means.
Ensure all quality documentation and records are completeand currentEnsure QC laboratories meet current Good LaboratoryPractice (cGLP) requirements.
Ensure relevant procedures are correctly defined andfollowed.
Ensure that critical chemical testing and related equipmentmeets current validation requirements (IQ, OQ, PQ) whererequired.
Audit and review chemistry test results on a daily basis andensure compliance with cGLP.
Checking/auditing laboratory notebooks and analyticalreports.
Ensure compliance to cGMP at all times.
Requirements: Degree in Science ( Chemistry or Biochemistry preferred).
Postgraduate studies as appropriate to augment primary degree.
2+ years experience working in a manufacturing environment preferred.
Skills: HPLC Chemistry UPLC