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R&D Technical Leader
Eingestellt von Harvey Nash IT Recruitment Belgium
Gesuchte Skills: Engineer, Marketing
Projektbeschreibung
One of our clients, a contract research organisation in analytical sciences currently requires an R&D Technical Leader with experience in Virology
Start: ASAP
Length: long term
Location: Mons Area
The company provides the pharmaceutical industry with all theanalytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products.
Job description:
Working in a team involved in in-house analytical development projects,as a Technical Leader, you will manage R do the technical follow-up of analyses (troubleshooting);write and/or verify reports; communicate internally and give training;
manage documentation related to the analyses done; assist the Team Manager in the preparation of practical work and the writing of protocols (development, qualification, validation and transfer);
validate experimental results and ensure protocols are respected.
The analytical techniques used are Q-PCR, immunoassays, bioassays, microscopy, classical and molecular virology and sequencing.
Depending on your skills and ambitions, progression in the job is possible.
Education:
PhD or Master/Engineer, specialisation Biology/Virology.
Skills:
Technical skills:
Thorough theoretical knowledge and practical experience of amplification of cell lines, cell based assays (microscopy, UV/plate,fluorescence), FACS and Real Time PCR.
Good theoretical knowledge and practical experience of viral production, viral titration, analysis of cytopathic, haemadsorption, haemagglutination effects, molecular virology and viral safety.
Pluses:
Knowledge and practical experience of assays by microplate spectrophotometer (ELISA), Gel electrophoresis, Western blot and sequencing.
General skills:
Good knowledge of the pharmaceutical sector.
Pluses:
Notions of biological medicinal products (mAbs, ADCs, proteins, recombinant peptides) and regulations associated (EMA and FDA).
Notions of GMP and GLP/GCLP quality norms.
Language skills:
In addition to proficiency in French, good command of English.
Experience:
At least 2 years' practical experience in pharmaceutical sector in development, validation and application of analytical methods in aforementioned techniques in pharmaceutical sector.
Experience in Projects Management.
Pluses:
Experience in Team Management
Tags: QC, R&D, Viral production, virology, Q-PCR, immunoassays,EMA, FDA
Start: ASAP
Length: long term
Location: Mons Area
The company provides the pharmaceutical industry with all theanalytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products.
Job description:
Working in a team involved in in-house analytical development projects,as a Technical Leader, you will manage R do the technical follow-up of analyses (troubleshooting);write and/or verify reports; communicate internally and give training;
manage documentation related to the analyses done; assist the Team Manager in the preparation of practical work and the writing of protocols (development, qualification, validation and transfer);
validate experimental results and ensure protocols are respected.
The analytical techniques used are Q-PCR, immunoassays, bioassays, microscopy, classical and molecular virology and sequencing.
Depending on your skills and ambitions, progression in the job is possible.
Education:
PhD or Master/Engineer, specialisation Biology/Virology.
Skills:
Technical skills:
Thorough theoretical knowledge and practical experience of amplification of cell lines, cell based assays (microscopy, UV/plate,fluorescence), FACS and Real Time PCR.
Good theoretical knowledge and practical experience of viral production, viral titration, analysis of cytopathic, haemadsorption, haemagglutination effects, molecular virology and viral safety.
Pluses:
Knowledge and practical experience of assays by microplate spectrophotometer (ELISA), Gel electrophoresis, Western blot and sequencing.
General skills:
Good knowledge of the pharmaceutical sector.
Pluses:
Notions of biological medicinal products (mAbs, ADCs, proteins, recombinant peptides) and regulations associated (EMA and FDA).
Notions of GMP and GLP/GCLP quality norms.
Language skills:
In addition to proficiency in French, good command of English.
Experience:
At least 2 years' practical experience in pharmaceutical sector in development, validation and application of analytical methods in aforementioned techniques in pharmaceutical sector.
Experience in Projects Management.
Pluses:
Experience in Team Management
Tags: QC, R&D, Viral production, virology, Q-PCR, immunoassays,EMA, FDA
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Marketing/Vertrieb, Ingenieurwesen/Technik