QC Analyst

About SGS

SGS is the global leader in testing, inspection, and certification services, operating across numerous industry sectors worldwide. With over 140 years of experience, SGS is dedicated to ensuring safety and quality in products through rigorous standards and innovative testing solutions.

Role Overview

We are currently seeking an experienced QC Analyst to join our expanding Scientific In-sourcing team. This role involves performing testing on pharmaceutical substances such as raw materials and drug substances within a GMP-compliant environment, primarily focusing on gas chromatography (GC) and high-performance liquid chromatography (HPLC), alongside other analytical methods as necessary.

Key Responsibilities

• Complete comprehensive training provided by SGS and clients to become proficient in relevant analytical techniques, actively maintaining up-to-date qualifications and training colleagues where qualified.
• Execute testing in strict accordance with established procedures and regulatory standards.
• Ensure laboratory equipment is properly maintained and calibrated at the prescribed intervals.
• Manage inventory and track the status of analytical materials.
• Verify and review test results from other analysts when authorized, ensuring compliance.
• Accurately enter data into Laboratory Information Management Systems (LIMS).
• Evaluate test outcomes, closing out batch analyses appropriately.
• Meet all testing deadlines, update progress tracking tools, and communicate testing status in meetings.
• Maintain an organized and clean laboratory environment adhering to high housekeeping standards.
• Produce precise lab records guaranteeing work is completed accurately and timely.
• Develop and maintain essential documentation including SOPs, methods, and reports.
• Collaborate as an effective team member to meet and surpass client and company key performance indicators related to investigations, training, productivity, and punctual testing.
• Report and document any atypical or irregular results, conducting investigations as necessary.
• Lead laboratory investigations and manage deviations where required.
• Maintain a safe workplace environment in readiness for audits.
• Identify and implement improvements in safety, environmental practices, quality, and service.
• Engage in continuous self-development and career progression in consultation with leadership.

Qualifications and Experience

• Degree in Chemistry or equivalent scientific qualification (Level 7).
• Minimum of 2 years post-qualification experience in a GMP laboratory; GMP experience is essential.
• Strong understanding and demonstrated experience with Good Manufacturing Practices, data integrity, and analytical technologies such as HPLC, GC, Karl Fischer titration, IR spectroscopy, particle size distribution (PSD), X-ray techniques, and wet chemistry.
• Excellent organizational skills coupled with effective verbal and written communication.
• Team-oriented, adaptable to evolving requirements, with a strong customer service focus.
• Commitment to high standards of quality and safety.
• Proficiency with laboratory computer systems including LIMS and Trackwise.

Additional Information

• Expected behavioral qualities include integrity, flexibility, the ability to work independently, analytical problem-solving capabilities, results-driven mindset, time management skills, attention to detail, and professionalism in interactions with clients, contractors, and colleagues.
• Compliance with SGS and client policies and procedures is mandatory.
• Candidates must have immediate eligibility to work in Ireland. This is an on-site position based at Loughbeg, County Cork.
• SGS is an equal opportunity employer embracing workplace diversity.