Aseptic QA Specialist - Sterile Manufacturing

Grifols Worldwide Operations Limited; Dublin; On-site; EUR 80,000 - 100,000; Full time

Job summary

A pharmaceutical manufacturing company located in Dublin seeks a QA Manufacturing Specialist to ensure aseptic compliance and uphold GMP standards in their new facility. The ideal candidate will have experience in a GMP-regulated setup, proficient in QMS processes, and possess a relevant degree. The role offers competitive salary, career development opportunities, and wellness activities. Interested candidates are encouraged to apply regardless of doubts about qualifications.

Benefits

Highly competitive salary

Group pension scheme

Private Medical Insurance

Career development opportunities

Education allowance

Wellness activities

Qualifications

• Minimum 3 years' experience in a pharmaceutical manufacturing environment with EU GMP regulation.
• Minimum 5 years' experience in aseptic manufacturing preferred.

Responsibilities

• Ensure compliance with cGxP requirements.
• Perform facility walkthrough audits and maintain GMP compliance.
• Support manufacturing and quality activities.

Skills

Experience in a Sterile Pharmaceutical GMP-regulated facility

Experience in GMP cleanrooms using RABS technology

Familiarity with QMS processes

Understanding of GMP regulation and guidance

Proficient in MS Office

Education

Bachelor's or Master's degree in Pharmaceutical Sciences or Administration

Tools

Batch Records

LIMS

Veeva Vault

Trackwise

Job description

A pharmaceutical manufacturing company located in Dublin seeks a QA Manufacturing Specialist to ensure aseptic compliance and uphold GMP standards in their new facility. The ideal candidate will have experience in a GMP-regulated setup, proficient in QMS processes, and possess a relevant degree. The role offers competitive salary, career development opportunities, and wellness activities. Interested candidates are encouraged to apply regardless of doubts about qualifications.