Quality Assurance Specialist: cGMP, Audits & Training

Adecco; Waterford; On-site; EUR 42,000 - 64,000; Full time

Job summary

Genzyme is seeking a Quality Assurance professional to join our on-site team, ensuring products are manufactured, stored and packaged in accordance with cGMP standards and internal quality procedures.

The role involves developing GMP training packages, delivering training, preparing and reviewing procedures and batch records, and conducting audits across all departments to uphold the quality system and drive continuous improvement.

Qualifications

• Degree in science or related discipline (third level).
• Minimum 2 years' experience in a similar role.
• Experience in a GMP environment is required.
• Very good knowledge of cGMP in a regulated environment.
• Excellent accuracy and attention to detail.
• Excellent interpersonal skills.
• Good presentation skills.
• Working knowledge of computer packages.
• Flexible approach - comfortable with on-going change.

Responsibilities

• Work as part of the Quality Assurance team on site ensuring products are manufactured, stored and packaged in accordance with cGMP.
• Support the development of GMP training packages and delivery of training.
• Participate in the preparation and review of procedures and batch documentation.
• Perform audits of all departments to agreed schedule.
• Ensure the quality system is effectively implemented and maintained.
• Ensure practices meet cGMP requirements.
• Actively contribute to continuous improvement initiatives.
• Participate in internal supplier and regulatory audits and key quality initiatives.

Skills

Attention to detail

Interpersonal skills

Presentation skills

Flexibility

Teamwork

Self-starter

Computer skills

Education

Degree in science or related discipline

Tools

Computer packages

Job description

Genzyme is seeking a Quality Assurance professional to join our on-site team, ensuring products are manufactured, stored and packaged in accordance with cGMP standards and internal quality procedures.

The role involves developing GMP training packages, delivering training, preparing and reviewing procedures and batch records, and conducting audits across all departments to uphold the quality system and drive continuous improvement.