QC Microbiologist
- Randstad
- 2500.00 - 3200.00
- 32-40 uren
- Project vanaf een jaar
- MBO
Opdrachtgever
Our client is a leading Project Management and Engineering company serving the pharmaceuticals industry around the world.
Opdrachtgever
Our client is a leading Project Management and Engineering company serving the pharmaceuticals industry around the world. Their reputation is based on forming successful partnerships with clients, providing them with innovative designs and cost effective solutions in the context of sound judgment, strong management and technical excellence.
functie Vereisten
- Minimal MBO diploma in a relevant area.
- 1 to 2 years experience with GMP.
- QC lab experience in pharma industry is a plus; implies knowledge of equipment.
- Equipment used: any common lab equipment such as sterility and toxin testing..
- Experience with coordinating calibration activities.
Wat krijg je?
- Pension entitlement (15.9% employer contribution, 7.5% employee contribution)
- Collective WGA / WIA insurance
- NBBU collective labour agreement through equal remuneration
- 25 holidays days
- 8% holiday allowance
- 100% payment in case of illness in the first year
- Travel allowance per kilometer or through public transport
Werkzaamheden
- Management of the whole life cycle of all QC systems.
- Ensure calibration and maintenance are executed in a timely manner without impacting the release testing.
- Ensuring instrument availability on the lab, including new equipment introduction and acting as main point of contact for the maintenance team to minimize equipment downtime.
- Keep overview of new systems and ensure implementation timelines are available.
- Act as an advisor and technical resource to quality control department.
- Monitor the GMP systems currently in place to ensure compliance with documented policies and safety regulations.
- Actively represent QC with support from TL in projects regarding QC Systems.
- Lead investigations and supporting continuous improvement initiatives
- Write, review and/or implement deviations, change controls and CAPAs.
- User management of QC systems and review of this according to procedures.
- Perform audit trail and parameters review of QC systems in a timely manner.
- Interact with other departments and within QC in a professional manner and join in applicable meetings.
- Support other groups within QC to reach the departmental goals.
TAGCLOUD
qualitycontrol#GMP
#pharma
#laboratory
#calibration
