QC Lab Analyst - 12-Month Contract, Rotating Day/Night

AbbVie Inc.; Ireland; On-site; EUR 34,000 - 48,000; Full time

Job summary

Qualifications

• 3rd level qualification in a relevant Science discipline.
• A minimum of 6 months of experience in HPLC or GC.
• Experience operating to cGMP standards utilizing laboratory equipment.
• Previous experience in a pharmaceutical manufacturing environment is 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

Lab techniques

Regulatory compliance

Documentation

Education

Bachelors degree in a relevant Science discipline

Tools

HPLC

GC

Job description