Functietitel: Assistant Scientist cGMP

Functieomschrijving:

For one of our partners in the Netherlands (South Holland), we are currently looking for an Assistant Scientist cGMP. You’ll take part on all activities related to Release and Stability testing of cGMP TOX and clinical batches of Biopharmaceutical products (Vaccines).

• Ensure that a high level of Quality is maintained in the department
• Perform assays like: VP-QPCR, QPA, RP-HPLC, DCS, Sub-Visible Particle, W, pH, Osmolality, HC DNA, HCP-ELISA and ID-PCR with a ‘first time right attitude’
• Work precisely, meticulously and on time data delivery with expected quality (perform assay, assay review and training)
• Accurate completion of documentation such as assay run sheets (ARS), lab note books and logbooks
• Actively participate in setting up documentation to ensure compliance
• Participate in continuous improvement projects that progresses the department in quality, EHS and efficiency gain
• Write and, or review quality incidents (Invalid assay records, events, deviations, CAPA’s) records and help reduce the lead times

Company:

Pauwels Consulting is a fast-growing technical consultancy firm with a large portfolio of international corporate clients in Engineering, Pharma and IT. We deliver consultancy and turnkey projects to leading companies in Belgium and beyond.

At Pauwels Consulting we value your talent and ambitions. That is why we invest heavily in the continuous education, personal coaching and individual development of all our consultants. At Pauwels Consulting, you will find a challenging and inspiring work environment every single day.

Are you interested in working for top companies in your industry and do you like to improve your skills and expertise every day? Then we should definitely meet! We look forward to hearing from you via phone (+32 9 324 70 80) or e-mail (jobs (at) pauwelsconsulting.com).

• A position with responsability within a leading international company
• Personal development through learning on the job and additional external trainings
• A market oriented compensation, including a range of fringe benefits

• MLO or Bachelor (HLO) level
• 2-5 years of experience in the Pharmaceutical industry
• Experience with cGMP is a must
• Experience with quality incidents (events, deviations, CAPA’s) is a plus
• Fluent in English is mandatory, in Dutch is a plus

Werkgever Naam: Pauwels Consulting

Werkgever adres: Pauwels Consulting, , 9000 GENT, BELGIE

Vorm van contact: Céline Van Puymbrouck

Job korte beschrijving: Elektronica-ingenieurs

Land: Nederland

Regio: NEDERLAND

Contractduur: Vast

Contract type: Voltijds

Ervaring: Tussen 2 en 5 jaar

Bron van jobaanbieding:
VDAB, Openbare diensten voor arbeidsvoorziening, België

Hoe toe te passen: Bel WERKGEVER