QC Lab Analyst — 12-Month Contract (Rotating Day/Night Shift)

SmartRecruiters, Inc.; Sligo; On-site; EUR 32,000 - 42,000; Full time

Job summary

AbbVie in Sligo is seeking a QC Analyst for a 12-month fixed-term contract on a 12-hour rotating days and nights schedule. The role requires hands-on HPLC or GC experience and strict data integrity within a pharmaceutical lab.

The position involves working under cGMP and GLP, maintaining accurate records, and ensuring testing of raw materials is completed on time. Training of new analysts and support for product transfers are part of the role.

Qualifications

• 6 months of experience in HPLC or GC.
• Experience operating to cGMP standards utilizing laboratory equipment.
• Pharmaceutical manufacturing experience desirable but not essential.

Responsibilities

• Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements.
• Understand Regulations and business processes required to maintain Laboratory Data Integrity.
• Be responsible for housekeeping duties in the lab.
• Be responsible for the timely completion of chemical testing of raw material.
• Ensure that all test equipment is used and maintained correctly.
• Be responsible for raising change requests and data verification as assigned.
• Ensure all in-process sampling and testing are completed in a timely manner.
• Maintain up-to-date, complete, and precise records of all tests performed.
• Adhere to cGMP and GLP requirements.
• Assist in the resolution of quality problems as required.
• Develop and change in-house laboratory procedures as appropriate.
• Aid in training of new analyst.
• Support the transfer of new products.
• Adhere to and support all EHS & E standards, procedures and policies.

Skills

HPLC

GC

cGMP

Data integrity

Job description

AbbVie in Sligo is seeking a QC Analyst for a 12-month fixed-term contract on a 12-hour rotating days and nights schedule. The role requires hands-on HPLC or GC experience and strict data integrity within a pharmaceutical lab.

The position involves working under cGMP and GLP, maintaining accurate records, and ensuring testing of raw materials is completed on time. Training of new analysts and support for product transfers are part of the role.