JO-2505-552214
NEW ROLE : QC Analyst - pharmaceutical/chemical manufacturing facility Co Laois.
Midlands – Co Laois, commutable from Offaly, Kildare, North Tipperary and surrounds
CPL are working with our client partner to hire an QC Analyst for their GMP certified chemical production facility in Laois. The plant has been purpose built to support their client portfolio who are primarily in the Bio- Pharma, General Pharma and API manufacturing industries.
Role
- Conduct routine and non-routine analyses of raw materials, in-process samples, final products, and stability samples, following established procedures accurately and efficiently.
- Utilise a range of analytical techniques, including Gas Chromatography (GC), UV-visible spectroscopy, titrations, and other relevant methods for product analysis.
- Ensure all laboratory equipment and instruments are properly calibrated, maintained, and operated in line with Standard Operating Procedures (SOPs).
- Accurately document all analytical procedures, results, and observations, maintaining detailed records in compliance with regulatory requirements.
- Assist in developing and revising departmental procedures, work instructions, test methods, and SOPs to improve efficiency and effectiveness.
- Collaborate with team members to investigate and troubleshoot any analytical issues, providing solutions and corrective actions as needed.
- Maintain a clean, organised, and safe laboratory environment in compliance with current Good Manufacturing Practices (cGMP).
- Participate in company-provided safety and training programs to ensure adherence to safety protocols and overall laboratory standards.
- Build effective working relationships within and across departments, fostering a cooperative work environment.
Requirements:
- A bachelor’s degree in chemistry, biochemistry, or a related field, with a solid understanding of analytical chemistry.
- Experience in an analytical laboratory setting, with knowledge of GC and UV-Vis spectroscopy. Familiarity with other analytical techniques is a plus.
- Understanding of Good Manufacturing Practices (GMPs) and regulatory guidelines relevant to laboratory operations.
- Strong focus on accuracy and detail, with the ability to meticulously document processes and adhere to protocols.
- Excellent troubleshooting abilities, with a proactive approach to identifying and resolving issues effectively.
- Clear and concise verbal and written communication skills for efficient collaboration and reporting.
- Ability to work both independently and as part of a team, with a proactive and reliable approach to tasks
Reach out to [email protected]
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