We are seeking a skilled professional to fill an exciting opportunity in the pharmaceutical industry. This position is ideal for individuals who thrive in laboratory settings and are passionate about analytical technology.
### Job Description
The selected candidate will be responsible for ensuring high levels of competency in laboratory methods and procedures. Key duties include:
• Reviewing and approving laboratory test results, ensuring they meet relevant guidelines such as ICH, USP, and EP standards.
• Performing analytical testing activities related to method validation and technical transfer, guaranteeing all methods comply with regulatory requirements.
• Executing validation, operation, maintenance, calibration, and troubleshooting of equipment and associated software to ensure seamless functionality and data accuracy.
• Preparing and reviewing reports on quality control processes and protocols to verify that all relevant equipment is qualified for cGMP use.
• Ensuring timely completion, review, and approval of testing tasks, adhering to agreed-upon turnaround times.
• Overseeing quality control activities, guaranteeing compliance with product license commitments, cGMP regulations, and company quality standards.
• Collaborating with other QC analysts to train them on laboratory methods and procedures as required.
### Required Skills and Qualifications
To succeed in this role, applicants must possess:
* A BSc (Honors) degree in a scientific or technical discipline.
* At least 2 years' experience in a QC laboratory-testing environment within the biological and/or pharmaceutical industry.
* Proficiency in HPLC, Capillary Electrophoresis, UPLC/ Mass Spec techniques.
### Benefits
This opportunity offers a dynamic work environment where you can develop your skills and knowledge in analytical technology while contributing to the success of our organization.
### How to Apply
For more information, please contact us at +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie