Title: QC Stability Analyst
Location: Meath
Contract Type: Fixed Term 

We are recruiting a QC Stability Analyst for a Biopharmaceutical Manufacturer in Co. Meath. This is a fantastic opportunity to join a leading pharma company. This is initially a 6-month contract. This role will be responsible for Quality Control Stability and associated laboratory activities. 

What you will do:

• Support activities including general lab readiness, audit readiness in compliance with GMP requirements.

• Be part of a motivated and high performing team. 

• Contribute to a continuous improvement environment and bring problem solving and troubleshooting capabilities.

• Demonstrate a commitment to learning and personal development.

• Consistently deliver on specific area Key Performance Indicators.

• Operate to the highest standards of Safety, Quality and Compliance.

• Author, Review and Approve Stability Protocols and Stability Reports

• Develop and enroll Stability Programs on LIMS

• Perform stability pulls as per Stability schedule

• Aliquot stability pulls in a timely manner and deliver to the relevant testing Laboratory

• Collate stability data in relevant stability reports

• Perform trending in a timely manner

• Assist in laboratory investigations as appropriate

What skills you will need:

• Degree qualification in Science

• 2 years experience in the biotechnology or pharmaceutical industry.

• Preferably Lean Six Sigma experience.

• Ability to think logically and be proactive under pressure.

• Ability to work as part of a team and on own initiative in a constructive manner.

• Flexible and self-motivated.