REQUIREMENTS University degree in Chemistry, Pharmacy or other life science degree Significant experience in Quality Management for Pharmaceutical and Medical Device products Excellent knowledge on GMP guidelines, ideally from production Significant leadership experience Travelling around
SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...
ROLE DESCRIPTION For a very interesting bluechip company in the food industry I am in search for a passionate Sr. Quality Assurance Manager. Strong technical and communication skills are essential in this role. There are multiple plants you will be responsible for and you have to be
the internal & external audits - The company has serveral laboratories both in and outside of Europe - In general: set up a quality plan REQUIREMENTS - PhD or MSc with a relevant background - Atleast 5 years of hands-on Quality Assurance experience (focus on GCP, GLP
to development quality system - Identify training gaps and areas for improving - Support regulatory compliance to GCP/GVP REQUIREMENTS - University degree in Life Sciences or related field - At least 5 yeas of experience in highly regulated pharma environment - Experience dealing
this role you will be responsible for managing 10+ manufacturing sites in Europe from a quality perspective. RESPONSIBILITIES - Making sure that Plants are in compliance according to relevant guidelines such as cGMP - Representing European plants on Quality matters - End
will be responsible for all GCP/GVP actitivies. RESPONSIBILITIES - GCP/GVP auditing and inspections - Clinical Quality management - Contract management of service providers - Line Management of auditing team globally REQUIREMENTS - Strong
risks, through audit activities and data analysis, and elevate to immediate manager for immediate and long-term resolution - Provide GCP compliance interpretation, consultation, training, and other supportive services necessary to maintain and improve the quality of research for timely product
onderdeel in hun groei en succes. ROLE DESCRIPTION In deze positie zul je verantwoordelijk zijn voor 5 plants, waarvan 2 in Nederland en 3 in Europa. 75% strategisch en 25% operationeel bezig zijn. Ongeveer 30% reizen. Iedere plant heeft een quality
will be build the coming next months and you will have 2 or 3 direct reports. You report directly to the management team. RESPONSIBILITIES - Supplier quality management: Ensure that the plastics, resins the company buys meet the quality and food safety standards
120-145k gross a year (!) Salary package includes a car, etc. It is a new position. Looking for a experienced talented EHS Director EMEA. The first mission will be to design the system and make it alive and happening on the Gemba. The goal is to create a safety culture with 0 accidents, quality accidents
superiority. - Food safety: Ensure compliance of Co-Man on hygiene prerequisite and best practices, food safety index, control plans, surveillance plans. - Quality: Ensure the finished product quality is in line with our specifications and control the level of those specifications to keep quality consumer at
to the Quality Director. RESPONSIBILITIES - Manage the Quality Department. - Meet and exceed the laboratories' KPI's. - Decreasing defects and performing continuous improvement in product release. - Troubleshooting. - Develop a lab strategy in line with the company's
The Corporate Quality Assurance Manager is responsible for food safety and quality for the company's 3 production sites. This position combines both strategic and operational responsibilities. As the Corporate QA Manager, you will manage the Quality Department (6 fte) and report to the Operations
Regulatory Affairs Regional Director will play a strategic role in the process of launching new products on the European market by regulatory affairs support including drug master file submissions, drug product dossier registrations and regulatory intelligence research. He or she will closely
meetings, business trips, corporate events, ... guest reception and service cooperation with public institutions and counterparties coordination of efficient information flow and a cooperation with departments verifying transaltions realisation of on-going tasks assigned by a Director settling business Requirements: higher education in a concerned field (in silicate production is an advantage) minimum ...