Company Description

SGS are the world’s leading testing, inspection and certification company SGS Group. We deliver solutions to a wide range of industry sectors in Ireland. Enjoy a truly rewarding career in a global, multicultural organisation with a proud heritage that has been making the world a better, safer place for over 140 years.

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.

Job Description

Testing of pharmaceutical substances e.g. raw materials and drug substances in a GMP environment in accordance with clients' procedures and quality systems. 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 qualified in relevant analytical techniques. Maintain own training 100% current. 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

Qualifications

Qualifications

Education and training:

Science Graduate in Chemistry or equivalent science education (Level 7)
Necessary job experience: At least 2 years' (PQE) experience in a GMP laboratory. GMP experience is a minimum requirement for this position.
Professional requirements: Demonstrated Experience with current Good Manufacturing Practices, Data Integrity and sound knowledge of analytical technologies (HPLC, GC, KF, IR, PSD, Xray, Wet chemistry)
Good organizational skills and strong communication – written and verbal
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

Additional Information

Additional information

Expected Behaviors:

Integrity, flexibility, working under own initiative
Strong analytical ability and associated problem solving
Results and performance driven
Good time management & attention to detail
Professionalism; with the client, contractors and colleagues at all times
Compliance with SGS and client policies and procedures

To apply please submit your CV.

Candidates must be immediately eligible to work in Ireland, this is a site based role.

We are an equal opportunity employer and value diversity at our company.