QA Manufacturing Analyst (Environmental Monitoring)
- Recruiter
- Grifols
- Location
- Dublin, Dublin South
- Salary
- Negotiable
- Posted
- 09 Feb 2023
- Closes
- 16 Feb 2023
- Ref
- 08
- Contact
- Elidyah Muabana
- Sector
- Manufacturing
- Job Type
- Permanent
- Hours
- Full-time
QA Manufacturing Analyst (Environmental Monitoring)
We are looking for a QA Manufacturing Analyst is required for a new purification and aseptic filling plant for the blood protein albumin at Grifols Worldwide Operations (GWWO).
Reporting directly to the Quality Assurance Monitoring Supervisor of Grifols Worldwide Operations (GWWO).
This role offers a chance to work in a state-of-the-art facility, in an innovative Biotechnology company with excellent career development opportunities and a clear and committed patient focus.
Day to day responsibilities:
- Act as a delegate for the quality environmental supervisor when required.
- Liaise with Validation, Quality Control, Quality Manufacturing Assurance, Maintenance and the Operations team on execution of monitoring protocols.
- Provide quality performance information as required
- Ensure regular Quality interaction with other Departments
- Reviewing and support sampling plans for water systems.
- Routine sampling of Purified Water and Water for Injection.
- Assist and participate in qualification of clean rooms and sterilisation processes, aseptic gowning and
Skills and Experience:
- To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
- The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions)Excellent communication skills
- Excellent communication skills
- Self-motivated
- Good organizational skills
- Flexibility
- Cleanroom performing Environmental Monitoring within the aseptic pharmaceutical/medical devices industry.
- Deep knowledge and understanding of the aseptic regulatory requirements
- Minimum of BSc. Degree or equivalent third level education and at least 2 years' experience working in an aseptic pharmaceutical/ medical devices industry.
- Grade C/D environmental monitoring experience.
- Possibility of Grade A/B environmental monitoring experience.
- Benefits Package
- Contract of Employment: Permanent position
- Shift Work
If interested, please apply for immediate consideration.