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Productieverantwoordelijke in Waals-Brabant:
7
jobs
Equipment & Data Integrity Associate
- Jefferson Wells
- Braine-l'Alleud
- Onbepaalde duur, Zelfstandige
- Participate as a data integrity expert in projects and validation of stand-alone computerized...
- In the context of new laboratory equipment installation projects:
R&D automation Engineer
- Jefferson Wells
- Louvain-la-Neuve
- Onbepaalde duur, Zelfstandige
- Together with the experts of the team you will contribute to the analysis of automation...
- You will be in charge of developing software by analyzing, programming, testing and putting into...
QC specialist
- Jefferson Wells
- Braine-l'Alleud
- Onbepaalde duur, Zelfstandige
- Change control creation and follow up
- Actions follow up
Technicien QA des opérations de production - CDI - PolyPeptide
- Start People
- Braine-l'Alleud
- Onbepaalde duur
- Vous êtes passionné par l'Assurance Qualité pharmaceutique
- Vous êtes extrêmement précis et avez la volonté de participer à l'élaboration de produits...
Préparateur.trice de commande alimentaire
- Actief Interim Nivelles
- Braine-l'Alleud
Pour notre partenaire privilégié, leader dans le secteur des épices, nous sommes à la recherche de plusieurs préparateurs.trices de commande...
JD_INDUSTRIE23 Responsable de production
- FloWell International SA
- Waals-Brabant
- Onbepaalde duur
Gérer l'équipe de production- Gérer le planning de production- Gérer la gestion documentaires de l'atelier- Gérer les compétences au sein de...
Head of Division Laboratories & Certification
- ANPI
- Louvain-la-Neuve
- Onbepaalde duur
- U bent verantwoordelijk voor het dagelijks beheer van de divisies, valideert processen en zorgt...
- U zorgt ervoor dat het projectmanagement van de divisies wordt gecoördineerd en geoptimaliseerd en...
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QC specialist
Brabant Wallon – contracting
QC specialist
Functieomschrijving
Support GMP activities in the laboratory such as
- Change control creation and follow up
- Actions follow up
- Training matrix review and documentation
- Protocol, study execution and report for compendial feasibility
- Update/review of laboratory documentation: analytical methods; analytical instructions; coaching’s modules,…
- Ensure follow-up and compliance of procedures and instructions, and update if needed.
- Ensure follow-up of corrective actions and preventive actions.
- Support product launches and prepare documentation requested by authorities
- Update of batches documentation according to specifications
- Support documentation linked to in process analyses
Profiel
- Master’s degree required in analytical chemistry ,biochemistry (HPLC, GC, IR, UV, Empower, etc) or equivalent
- Expertise in the pharmaceutical analysis for min. 5 years
- Experience in GMP
- Strong organization skills with proven records
- Proven project leadership skills including planning, monitoring, compendial verification with protocol and reports, decision making and reporting;
- Proven experience in documentation creation, update to support QC activity
- Ensure required corrective actions are taken and put in place and lead the implementation in collaboration with the QA, team leaders and technicians
- Understanding of all analytical disciplines related to CMC for late stage development and commercial products (analytical development, stability testing and quality control of drug substance, drug product, raw material and intermediate).
Aanbod
- Bedrijfswagen
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.
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