Description
CLS is currently experiencing significant growth and is looking for dedicated, solutions-driven professionals with a flexible approach to join our team. Founded in 1994, Complete Laboratory Solutions (CLS) is Ireland’s most highly accredited contract laboratory, providing industry-leading sampling, analysis, and skilled micro and analytical analysts on contract to clients across the food, environmental, medical device, biopharmaceutical, and pharmaceutical sectors. We deliver customised managed service solutions, allowing clients to have our expert team on-site at their own facilities or outsource those services to us here at CLS.
Job title: QC Chemist II Location: Cork
Duties & Responsibilities
1. Implement and adhere to company Quality Management Systems on a daily basis, ensuring all documentation is in compliance with cGMP standards.
2. Perform daily calibrations on laboratory equipment.
3. Adhere to and enforce company Health and Safety procedures including laboratory waste management.
4. Tests and raw materials, intermediates and finished product samples according to written procedures.
5. Reviews data and results of testing to ensure compliance to appropriate specifications and protocols. Conducts procedure updates in QC lab and GMP reviews of logbooks.
6. Assists in the training of QC staff as needed.
7. Provide support with audit/inspection requirements to ensure company compliance/readiness.
8. Contribute to the continuous improvement of company internal processes and QMS including root cause analysis of any system or equipment issues applying scientific problem-solving skills.
9. Actively promote compliance with regulatory requirements and execute cGMP in the performance of all daily activities and all applicable job functions, including maintenance of accurate record.
The Ideal Candidate Will Have
1. 2+ years of relevant experience and a BS degree in Chemistry or equivalent.
2. Relevant experience in a pharmaceutical operations environment.
Key Skills
1. Working knowledge of GMPs, pharmacopeial and regulatory requirements for testing and validation.
2. Advanced knowledge of current Good Manufacturing Practices (GMPs).
3. Ability to work effectively with a team to accomplish organisational goals.
4. Knowledge of HPLC and UPLC Systems.
5. Detail oriented with strong organizational and problem-solving skills.
6. Strong verbal, written, and interpersonal communication skills are required.
7. Self-motivating with the ability to multi-task and work on own initiative.
8. Proficiency in Microsoft Office.
What We Offer
1. A dynamic and collaborative work environment.
2. Opportunities for professional development and career progression.
3. Exposure to regulatory audits and compliance strategies.
4. Competitive salary and benefits package.
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