QA / Validation Project Engineer / Project Manager (f/m)
NNE Pharmaplan - Belgique
QA / Validation Project Engineer / Project Manager (f/m) – full time (100%) Introduction NNE Pharmaplan is a rapidly growing company... future. Currently we are opening a new office in Belgium. Therefore, NNE Pharmaplan is looking for a QA / Validation Project Engineer or Project...
Futurestep - Maastricht, Limburg - Maaseik, Limbourg
, an international biotech company, leader in advanced cell therapy, we are currently looking for QA/QP Manager The new manufacturing facility of our client... main accountabilities for this role are: All site QA activities, operation and maintenance of GMP Quality Management System Release of tissue material for GMP...
Senior QA consultant - 6 months - Region of Antwerp
Real Pharma is urgently looking for an experienced QA consultant for the general QMS, involving documentation management, releases, hold..., recall, CAPA, audit and general admin tasks. Profile: - Approximately 5 years experience in Quality Assurance - Knowledge in Medical Devices...
QA / Validation Project Engineer / Project Manager (f/m)
NNE Pharmaplan - Belgique
, engineering and user). QA / Validation Project Engineer / Project Manager (f/m) – full time (100%) Introduction NNE Pharmaplan is a rapidly growing... in the future. Currently we are opening a new office in Belgium. Therefore, NNE Pharmaplan is looking for a QA / Validation Project Engineer...
Mosaic Regulatory Solutions - Louvain, Brabant Flamand
Our client are a global pharmaceutical company who are market leaders in distribution services across medical devices, consumable... and pharmaceuticals. They are offering an excellent opportunity as a Head QA/QP. GCP QA Manager - Reading Company: Location: Reading Salary: On Application...
Barrington James Europe - Belgique
My client is a leading Medical Device company who are expanding within their chosen therapy area. This is an excellent opportunity for the... successful candidate to progress their career within Class III implantable products. Head of QA Company: Location: Belgium Salary: 100,000+ Closing Date: 19...
Quality & Risk Manager, Global Medical Affairs
INC Research - Bruxelles
job ID: RES8226 Position Title: Quality & Risk Manager, Global Medical Affairs Working Location: Belgium Employment Status: Full-Time... responsibilities listed hereafter. Core Responsibilities: 1. Provide support for Global Medical Affairs (GMA) Risk Management • Support the business...
Quality Assurance officer development & validation
Innogenetics - Zwijnaarde, Flandre-Orientale
a reproducible & consistent way in accordance to compliance & business requirements Develop, implement and manage QA methodologies in order to ensure... & regulatory requirements The job – accountabilities Develop and/or oversee validation strategies & its implementation: The QA officer development...
Senior Regulatory Affairs / Quality Specialist
Volt Europe - Brabant Flamand
basis as well as in the Benelux region.Working from their Benelux head office the role of Senior QA/RA specialist will support regulatory... European Quality department in the UK. •Pharmacovigilance and quality complaint handling. •Support of product and medical information teams...
Johnson & Johnson Family of Companies - Beerse, Anvers
The Johnson & Johnson Consumer portfolio consists of registered medicines, medical devices and cosmetics. The Quality Assurance Manager... includes the QA responsibility for Belgium as well as Luxemburg and the Netherlands. You will lead a team of 2 QA professionals in Benelux...
Senior Regulatory Affairs / Quality Specialist
Volt Europe Limited - Hoeilaart, Brabant Flamand
basis as well as in the Benelux region. Working from their Benelux head office the role of Senior QA/RA specialist will support regulatory... European Quality department in the UK. - Pharmacovigilance and quality complaint handling. - Support of product and medical information teams...
UCB - Bruxelles
and maintaining compliance with local regulations; Collaborate with other Drug Safety teams, Clinical Development, Medical Affairs, QA, RA, Non-Clinical... respecting and maintaining compliance with local regulations; Collaborate with other Drug Safety teams, Clinical Development, Medical Affairs, QA, RA...
Quality Assurance Specialist - GMP
KELLY SCIENTIFIC RESOURCES - Brabant Flamand
. You will be located at the Headquarters in Belgium (Leuven) and will report to the Deputy Head of QA. • Reviewing and management of GMP related documents in... • Masters degree in biotechnology, biology, pharmacy, biochemistry, bio-medical or medical sciences or bio-engineering; • Extra degree...
Michael Page - Hasselt, Limbourg
Our client is major producer of medical devices and pharmaceuticals with their European Distribution Centre in Belgium... FAGG licensing • You will assure only approved products are distributed within EMEA • You will manage the QA system of the site...
Instituut voor Tropische Geneeskunde - Anvers
and methodological information between activities, QA pharmacists and partners to improve their technical quality. You foster the development of in-house... and strengthening our work with the actors involved in the program. Your profile: - You hold a master degree in medical or biomedical science, economics...
Manager, Biomarkers Operations
Janssen Pharmaceutica - Beerse, Anvers
with CT representatives from other functional areas, such as Global Clinical Operations (GCO), clinical group, medical writers, biostatistics... leads, Regulatory, Legal, Medical Writing, Data Management. Trains and mentors new personnel in department procedures and project specific...
Quality Affairs Specialist (Qualified Person)
Person) à Brussels: A key QA position with a $BN Biopharmaceutical and Medical Device company. Our client is a global medical device...
Sr. Manager - Immunotherapeutics BU (Late Oncology Clinical Development Manager)
GlaxoSmithKline Biologicals - Rixensart, Brabant Wallon
Employment Status: Full-Time Regular Required Experience: 8 years Required Education: Medical Doctor Travel Required: 0... (internally/externally) - Represents GCRD on global/regional Project teams. Liaises internally with Regulatory, R&D, manufacturing, QA&QC...
Covance - Bruxelles
a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) In...), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory...
Manager, Biomarkers Operations
Johnson & Johnson Family of Companies - Beerse, Anvers
closely with CT representatives from other functional areas, such as Global Clinical Operations (GCO), clinical group, medical writers..., Biomarker leads, Regulatory, Legal, Medical Writing, Data Management. Trains and mentors new personnel in department procedures and project specific...