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 ...
the same time this position is far from easy. Our client is looking for a senior really talented Quality Manager. RESPONSIBILITIES - Bringing alignment and synergy through all 4 plants worldwide regarding quality for the total value stream. - Get the Quality up
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
FDA 21CFR820 and the EU In Vitro Diagnostics Directive (98/79/EC) - Further develop and implement the quality management system culture within the company - Ensure that all customer complaints are responded to within appropriate time frames and escalated appropriately through the vigilance process
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
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
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
reports directly to the Managing Director. RESPONSIBILITIES - Manage the Quality Department (2 direct reports). - Ensure product quality compliant with quality systems and legislation. - Participate in continuous improvement projects. - Conduct internal audits, support
customer and internal organization. It is your challenge to lead a cross functional project team to meet Quality, Cost and Delivery targets of the project. You will report directly to the Director of Project Management. Senior Project Manager (automotive) Miejsce pracy: Września Nr referencyjny: What do we expect from you? You have a (technical) degree on a MsC level. Senior professional with (international ...