QC Supervisor

Cpl Healthcare; Connacht; On-site; EUR 55,000 - 75,000; Full time

Job summary

A leading biotech company in Sligo is seeking a QC Laboratory Supervisor to manage the operations of the quality control lab. This role requires overseeing lab activities, ensuring compliance with EU GMP regulations, and maintaining high-quality standards while leading a team of technicians. The successful candidate will have a strong background in regulatory compliance, data analysis, and significant experience in quality control and supervisory roles.

Qualifications

• Minimum of 5 years of quality control lab experience.
• At least 2 years in a supervisory or management role.

Responsibilities

• Supervise daily operations of the QC lab to ensure compliance.
• Train and mentor laboratory technicians.
• Develop and implement SOPs to maintain quality standards.

Skills

Regulatory standards understanding

Data analysis

Education

Bachelor’s degree in Pharmaceutical Science, Biology, Chemistry

Master’s degree (preferred)

Job description

JO-2506-553469

NEW ROLE : QC Laboratory Supervisor

Sligo

Permanent

Why you should consider this role?

Our client is an expanding biotech site and is going from strength to strength. The senior leadership team are very inclusive and feedback from placed candidates working there is that the variety and type of work they are undertaking is very interesting.

Role

• Supervise daily operations of the QC lab, ensuring all activities align with company protocols and regulatory requirements.

• Train, mentor, and evaluate the performance of a team of laboratory technicians

• Develop and implement standard operating procedures (SOPs) to maintain high-quality standards.

• Coordinate with other departments to ensure seamless workflow and communication.

• Review and approve test results before batch release of product.

• Identify and address any deviations from SOPs or regulatory standards.

• Implement corrective actions to resolve any issues and prevent recurrence.

• Ensure compliance with all relevant EU GMP regulations.

• Oversee the validation and verification of new testing procedures and technologies.

• Troubleshoot technical issues and provide solutions.

• Maintain accurate and detailed records of all QC activities.

• Generate and analyze data reports to monitor lab performance.

• Present findings to senior management and make recommendations for improvements as identified.

Requirements

• Strong understanding of regulatory standards and compliance.

• Ability to analyze and interpret complex data.

• Bachelor’s degree in Pharmaceutical Science, , Biology, Chemistry, or a related science field. A Master’s degree is preferred.

• Minimum of 5 years of quality control lab experience.

• Experience in a supervisory or management role- ideally 2 years.