A great opportunity to join a large and growing pharmaceutical company in County Waterford! This role is on day shift Monday-Friday.
Details on the role below, if you are interested apply today!
Description:
Provide analytical chemistry services and support to Site.
• Effective interaction with other departments on matters
related to raw materials, intermediates and finished batch
releases. In particular, close contact maintained with Quality
Assurance Production, Engineering and Planners.
• Maintain, update and issue chemical methods, specifications
and SOP’s in compliance to pharmacopoeial and regulatory
requirements.
• Assist with training of the analysts in areas of expertise and
knowledge and in new methods, SOP’s and updates.
• Trend such results, record on COA’s where required and
complete OOS’s investigations on a timely basis.
• Update the QC Team Leader on potential problems and
highlight improvements where possible by use of the normal
communication means.
• Ensure all quality documentation and records are complete
and current
Ensure QC laboratories meet current Good Laboratory
Practice (cGLP) requirements.
• Ensure relevant procedures are correctly defined and
followed
• Ensure that critical chemical testing and related equipment
meets current validation requirements (IQ, OQ, PQ) where
required.
• Audit and review chemistry test results on a daily basis and
ensure compliance with cGLP.
• Checking/auditing laboratory notebooks and analytical
reports
• Ensure compliance to cGMP at all times
Degree in Science ( Chemistry or Biochemistry preferred). Postgraduate studies as appropriate to augment primary degree.
2-3 years experience working in a manufacturing environment preferred