QC Analyst

SGS; Cork; On-site; EUR 40,000 - 60,000; Full time

Benefits offered by this job

Friendly working environment

Training programs

Career development opportunities

Job summary

SGS Ireland is seeking an experienced QC Analyst to join the Scientific In-sourcing team. The role focuses on testing pharmaceutical substances in a GMP environment, with primary emphasis on GC and HPLC analyses and related techniques.

Key responsibilities include training, performing analyses, maintaining instruments, ensuring data integrity, and contributing to investigations and deviations as needed. A Science degree in Chemistry and GMP PQE are required.

Qualifications

• 2 years GMP laboratory PQE.
• Data integrity and knowledge of analytical technologies (HPLC, GC, KF, IR, PSD, X-ray, Wet chemistry).
• Aptitude with lab computer systems including LIMS and TrackWise.
• Team player with flexible attitude and customer service mindset.
• Excellent quality and safety standards.

Responsibilities

• Receive training from SGS and client in relevant analytical techniques.
• Train other analysts where qualified.
• Carry out testing according to procedures and regulatory requirements.
• Maintain laboratory equipment and calibration schedules.
• Manage inventory and status of materials for analysis.
• Verify and review results for compliance when qualified to do so.
• Ensure accurate data entry to LIMS and proper documentation.

Skills

GMP experience

Data integrity

Team player

Quality & safety focus

Lab data entry

Education

Science degree in Chemistry (Level 7+)

Tools

LIMS

TrackWise

HPLC

GC

KF

Job 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

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

Qualifications

• Science Degree in Chemistry or equivelent (Level 7 minimum)
• 2 years experience in a GMP laboratory PQE.
• 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

Additional Information

• Integrity
• Strong analytical ability and associated problem solving
• Excellent communication skills both verbal & written
• Good time management & attention to detail
• Results and performance driven
• Compliance with SGS policies and procedures
• Compliance with SGS and client policies and procedures

Benefits

SGS offer a friendly, supportive, approachable working environment with a down-to-earth culture

• 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
• Career development opportunities across SGS

SGS is an equal opportunities employer.