QC Chemist

Berkley Group; Cork; On-site; EUR 45,000 - 60,000; Full time

Job summary

Our client in Cork is seeking an experienced QC Chemist to perform analytical testing and support QA and manufacturing collaborations. The role requires a strong background in HPLC/UPLC/GC within a GMP-regulated environment and a focus on compliance with cGMP, SOPs, and regulatory standards.

Candidates should hold a Bachelor’s or Master’s degree in Chemistry or related fields, with at least 3 years of QC laboratory experience in the pharma/biopharma sector and proven proficiency with Empower or

Qualifications

• 3 years' experience in a QC pharmaceutical laboratory.
• Experience with HPLC, UPLC, and GC instrumentation.
• Knowledge of GMP and regulatory standards (FDA, EMA, ICH).
• Excellent attention to detail and documentation.
• Strong communication and teamwork skills.

Responsibilities

• Perform analytical testing on raw materials, intermediates, and finished products using HPLC, UPLC, and GC in a GMP-regulated environment.
• Prepare, review, and approve laboratory documentation including test methods, protocols, and reports.
• Ensure all testing is conducted in line with cGMP, SOPs, and regulatory requirements.
• Participate in OOS/OOT investigations, deviation reports, and CAPAs as needed.
• Support method development, validation, and equipment qualification activities where required.
• Maintain laboratory equipment and ensure calibration and preventive maintenance schedules are adhered to.
• Collaborate with cross-functional teams including QA, manufacturing, and validation.

Skills

Attention to detail

Documentation

Organizational skills

Communication

Teamwork

Education

Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related discipline

Tools

HPLC

UPLC

GC

Empower

Job description

QC Chemist

Our client in Cork is seeking an experienced

• Perform analytical testing on raw materials, intermediates, and finished products using HPLC, UPLC, and GC in a GMP-regulated environment.
• Prepare, review, and approve laboratory documentation including test methods, protocols, and reports.
• Ensure all testing is conducted in line with cGMP, SOPs, and regulatory requirements.
• Participate in OOS/OOT investigations, deviation reports, and CAPAs as needed.
• Support method development, validation, and equipment qualification activities where required.
• Maintain laboratory equipment and ensure calibration and preventive maintenance schedules are adhered to.
• Collaborate with cross-functional teams including QA, manufacturing, and validation.

Requirements:

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related discipline
• Minimum of 3 years' experience in a QC laboratory environment in the pharmaceutical or biopharmaceutical industry
• Proven experience using HPLC, UPLC, and GC instrumentation and associated software (e.g., Empower)
• Strong knowledge of GMP and regulatory standards (FDA, EMA, ICH)
• Excellent attention to detail, documentation, and organizational skills
• Strong communication and teamwork skills