QC Analyst

Main Purpose of Role

Testing of pharmaceutical substances e.g. raw materials and drug substances in a GMP environment in accordance with clients' procedures and quality systems. The main focus will be GC and HPLC analysis, along with a range of other analytical techniques as required.

Key Accountabilities

- Receive training from SGS and client and get trained in relevant analytical techniques.
- Train other analysts where appropriately qualified
- Carry out testing in accordance to the valid testing procedures and regulatory requirements
- Ensure that laboratory equipment is well maintained, and calibrations are carried out at the designated frequencies
- Manage inventory and status of materials required for analysis
- When qualified to do so, verify and review results generated by other analysts for compliance with requirements
- Ensure correct data entry to LIMS
- Assessment of testing results generated in the laboratory and close out of batch analysis
- Ensure that all target dates are met. Update visibility tools and communicate status of testing at meetings
- Maintain laboratories to a high housekeeping standard
- Ensure high standard of lab records, with work completed Right First Time and on time
- Write and maintain necessary documentation (SOPs, methods, reports etc)
- Work as part of the team ensuring customer expectations are met and exceeded. Support achievement of client and SGS Key Performance Indicators, such as around investigations, training, productivity and on-time testing
- Notify appropriate contact and document results and investigations for any atypical or aberrant results
- Lead Laboratory investigations and deviations if required
- Maintenance of a safe working environment, in a state of audit readiness
- Identification and implementation of safety, environmental, quality and service improvements
- Work with their leader to ensure self-development and progression
- At all times, adopt a safe behaviour by exercising due regard for the health and safety of yourself, colleagues, and clients, in line with the Company’s policies and procedures
- Ensure full compliance with the Company’s Code of Integrity, and act in accordance with SGS Ireland’s Equality & Diversity Policy

- Science Degree in Chemistry or equivelent (Level 7 minimum)
- 2 years experience in a GMP laboratory.
- Data Integrity and sound knowledge of analytical technologies (HPLC, GC, KF, IR, PSD, Xray, Wet chemistry)
- Team player, flexible to evolving needs with a strong customer service mentality
- Excellent quality and safety standards
- Aptitude in lab computer systems, including LIMS and Trackwise

We offer you:

An opportunity to develop and international career in a friendly, supportive, approachable working environment with a down-to-earth culture. Continuous learning with the chance to expand and enrich your career with our dedicated training team to support your career development opportunities across SGS.

- An attractive compensation and benefits package including
- Bonus
- Healthcare
- Pension
- Enhanced annual leave

To apply please submit your CV.

SGS is the world's leading Inspection, Verification, Testing and Certification company. We are recognised as the global benchmark for quality and integrity. With more than 98,000 employees, we operate a network of more than 2,650 offices and laboratories around the world. We deliver global service with local expertise, to market leading clients across 10 different industries worldwide.

Our client services include providing SGS QC analysts and technical support staff on-site to fulfill staffing requirements (Scientific In-sourcing), all under the supervision and guidance of ISL technical and operational teams. Like all SGS personnel, they are committed to upholding stringent technical and GMP standards, ensuring the safety of medications for the multitude of patients relying on the products we test.

Due to growth, we have an exciting opportunity for an experienced QC Analyst to join our growing Scientific In-sourcing team.