Quality Assurance Specialist

QA Resources Ltd; Cork; Hybrid; EUR 46,000 - 65,000; Full time

Job summary

QA Resources Ltd in Cork is currently recruiting for a QA / Quality Specialist on behalf of a leading pharmaceutical company. This is an initial 3-month contract role focused on batch release documentation review.

You will assess Master Batch Records and electronic batch records, ensuring compliance with cGMPs and internal procedures. The ideal candidate has a degree in science or quality and strong documentation experience.

Qualifications

• Degree in Science, Quality, or a related Technical field.
• Experience in GMP Manufacturing or Quality Assurance environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing operations.
• Strong experience with documentation review.
• Strong written and verbal communication skills.

Responsibilities

• Review/approval of new and updated Master Batch Records / Electronic Batch Records.
• Review and approve production documentation such as executed electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures.

Skills

Documentation review

Communication skills

Education

Degree in Science or Quality field

Job description

QA Resources is currently recruiting for a QA / Quality Specialist on behalf of a leading pharmaceutical company based in Cork. This is an initial 3-month project specific contract role.

Job Summary:

The QA / Quality Specialist will be part of a project team responsible for reviewing batch release documentation.

Responsibilities:

• Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records
• Review and approve production documentation such as executed electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures

Education and Experience:

• Degree in Science, Quality, or a related Technical field.
• Experience in GMP Manufacturing or Quality Assurance environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing operations.
• Strong experience with documentation review
• Strong written and verbal communication skills

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***