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Synergie Medical zoekt: in-vivo research technician
* Observing and treating mice under study. * Performing behavioural studies, such as Morris Water Maze or Object Recognition test. *Histological or biomedical analyses, such as Elisa, Western analises. *Analising data and documenting findings. * Suggesting improvements in the methods an analyses. * Working ...
DATA ANALYST BIOTECH
For a bio-tech company located in Gent, we are looking for a Data Analyst. With the hiring of a data analyst, te company wants to complete its team of biometricians that is responsible for experimental design and data analysis in the field of agricultural crops. The data originate from laboratory, greenhouse ...
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Product Manager Alzheimer Disease
Contrat : full time, permanent
with opinion leaders. • Bachelor or master education (scientific background such as biotechnology, biology
The job – Baseline The diagnostic testing for Alzheimer’s disease is a new and growing market and the challenge for the PM AD will be to ensure that the products are designed and launched as an integrated solution for the routine lab. A good understanding of the needs of a routine In Vitro Diagnostic ...
Process Validation Consultant
Contrat : Temporary / Contract
engineer, agronomy engineer, chemical engineer, biotechnology )Expertise in Secondary operations
The Company The Harvey Nash Group was founded in the UK in 1988, and now has offices throughout Europe, America and Asia. The Harvey Nash Group is known for the thousands of successful assignments completed throughout the world. From more than 39 offices, and with 5000 staff and associates, we offer ...
Process Robustness Validation Engineer
Contrat : Employee
, biotechnology, …) · Expertise in Secondary operations (formulation, Filling and freeze-drying) · 2 to 5 years
PROCESS ROBUSTNESS VALIDATION ENGINEER Regio n Walloon-Brabant Job description Participate in the Process Validation (PV) and Process Robustness activities mainly on secondary manufacturing processes (i.e. immunostimulants, adsorption, formulation, filling and freeze-drying), for both under-development ...
Finance Assistant - Brussels
Contrat : Employee
and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. We are currently seeking a Finance Assistant for our office ...
Technical Service Scientist
Contrat : full time
- and Biotechnology, Animal Health, Chemistry or veterinary - Minimum 3 to 5 years of working experience - Experience
To become part of the PP MQAH Innovation Team for the regions Europe, Africa & Asia, based in Drongen, who will be a key member of our team by: Managing and executing European clinical and field tests to confirm product efficiency and support product sales and marking Develop and present product and ...
TRAINING CONSULTANT
Contrat : Employee
· Set up a matrix to keep track of training Profile · Master in Chemistry, Bio-Chemistry, Bio-Technology
TRAINING CONSULTANT Kempen Job description The Training Consultant coordinates and designs training material for the operations group according to the guidelines set up by operations. Tasks · Organize, coordinate and provide training of operations procedures for operators · Organize, coordinate and ...
Quality Assurance officer development & validation
Contrat : full time, permanent
, biotechnology or medical device industry • Minimum 5 years of experience with validation in a pharmaceutical
The job – Purpose & Baseline Develop, organise & manage the validation activities within Innogenetics to ensure that in vitro diagnostic products are manufactured in a reproducible & consistent way in accordance to compliance & business requirements Develop, implement and manage QA methodologies in ...
MANUFACTURING MANAGER
Contrat : full time, permanent
Supervisory level, preferably within a biotechnological recombinant protein manufacturing environment
Plans and coordinates daily operations to meet production schedules, product standards and operational costs within all relevant cGMP requirements. Prepares production, personnel and financial reports to achieve production goals. Establishes operating policies and procedures to achieve production schedules, ...
QA COMPLIANCE VALIDATION CONSULTANT
Contrat : Employee
with supervision / coaching Profile · University degree (Biotechnology, Agronomy, Chemistry or Pharmacy) · Good
QA COMPLIANCE VALIDATION CONSULTANT Brabant- Wallon Job description The QA COMPLIANCE VALIDATION CONSULTANT will provide QA support to validation activities. · Review / Approve IQ / OQ / PQ Protocols · Review / Approve IQ / OQ / PQ Reports · Ensure the compliance in all validation activities · Review ...
QA Compliance validation & project supervisor
Contrat : Temporary / Contract
in autonomy with supervision/coaching PREREQUISITES Education - University degree (Biotechnology, Agronomy
HARVEY NASH is currently looking for a QA compliance validation & project supervisor for one of its customer. FUNCTION DESCRIPTION - Provide QA support to validation activitiesKEY RESPONSIBILITIES - Review/Approve IQ/OQ/PQ Protocols - Review/Approve IQ/OQ/PQ Reports - Ensure the compliance in all validation ...
Product Manager Alzheimer Disease
The job – Baseline The diagnostic testing for Alzheimer’s disease is a new and growing market and the challenge for the PM AD will be to ensure that the products are designed and launched as an integrated solution for the routine lab. A good understanding of the needs of a routine In Vitro Diagnostic ...
Head of Medical Affairs – exciting biotech company!
If you are looking for a unique position that will give you the chance to set up an entire division for an exciting biotech company I am offering you just such a chance. I am currently working with an innovative company who are preparing to launch a first in class compound to focus on a niche disease. ...
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