QC Analyst

Role overview

SGS is a global leader in testing, inspection, and certification, supporting a broad mix of industries across Ireland. This role sits within the Scientific In-sourcing team, where on-site technical and QC support is provided to meet client staffing needs under the direction of ISL technical and operational teams. The organisation is committed to strict technical and GMP compliance and to protecting the quality and safety of medicines used by patients.

Because of team growth, an experienced QC Analyst is now required to join the expanding Scientific In-sourcing function.

What you will do

You will test pharmaceutical materials, including raw materials and drug substances, in a GMP-controlled laboratory environment, following client procedures and quality systems. The work will centre mainly on GC and HPLC analysis, with additional analytical methods used as needed.

• Complete training from SGS and the client, gain qualification in relevant analytical methods, keep your training fully up to date, and support the training of other analysts when qualified.
• Perform testing in line with approved procedures and applicable regulatory expectations.
• Keep laboratory equipment in proper working order and ensure calibrations are completed at the required intervals.
• Track and manage the stock and status of materials needed for analysis.
• Where qualified, check and verify results produced by other analysts against requirements.
• Enter data accurately into the LIMS system.
• Review laboratory test outcomes and complete batch analysis close-out activities.
• Meet target timelines, update visibility tools, and share testing progress during meetings.
• Keep laboratories clean, orderly, and maintained to a high housekeeping standard.
• Produce and maintain accurate lab records, delivering work right first time and on schedule.
• Prepare and update required documentation such as SOPs, methods, and reports.
• Collaborate effectively with the team to meet and exceed customer expectations and support client and SGS KPIs relating to investigations, training, productivity, and on-time testing.
• Escalate and document any atypical or aberrant results, including related investigations, to the relevant contact.
• Take the lead on laboratory investigations and deviations when needed.
• Help maintain a safe workplace that remains audit ready at all times.
• Identify and help implement improvements in safety, environmental performance, quality, and service.
• Work with your manager on personal development and career progression.

Requirements

• Degree-level science education in Chemistry or an equivalent science qualification at Level 7.
• At least 2 years of experience working in a GMP laboratory; this is a mandatory requirement.
• Hands-on experience with current Good Manufacturing Practices, data integrity, and analytical techniques such as HPLC, GC, KF, IR, PSD, X-ray, and wet chemistry.
• Strong organisational ability and clear written and verbal communication skills.
• A collaborative, adaptable approach with a strong customer-service mindset.
• High standards for quality and laboratory safety.
• Comfort using laboratory computer systems, including LIMS and Trackwise.

Additional information

This is a site-based position in Wicklow, County Wicklow, Ireland. Applicants must be immediately eligible to work in Ireland. SGS also looks for the following behaviours: integrity, flexibility, initiative, strong analytical thinking, problem solving, results focus, good time management, attention to detail, professionalism with clients, contractors and colleagues, and compliance with SGS and client policies and procedures. The company is an equal opportunity employer and values diversity.

To apply, submit your CV.