Cleaning Validation Engineer
- Cork
- Contract
- Commissioning, Qualification and Validation
We have a great opportunity for Cleaning Validation Engineer to join our client, a research-based biopharmaceutical company, on their journey of discovering, developing, and commercialising innovative medicines and researching and developing antiviral drugs used in the treatment of HIV/AIDS, hepatitis B, hepatitis C, influenza, and COVID-19.
Responsibilities:
- Performing cleaning verification calculations and plans for detergent, API and Micro on our clinical manufacturing process train.
- Taking cleaning samples, delivering to QC and then compiling results and releasing equipment
- Performing cleaning assessments of new equipment
- Day to day support of commercial PV/CV (routine monitoring program, cleaning deviations, process transfers)
Requirements:
- 3-5 years’ experience as a validation specialist in a pharmaceutical or a highly regulated environment and a B.Sc.
- Degree or other qualification in Chemical Engineering, Biochemistry, Microbiology, Chemistry or a related field.
If this role is of interest to you, please apply now!
#LI-AB2
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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Andre
I manage this role.