DESCRIPTION GMP Auditor (m/w) in unbefristeter Festanstellung RESPONSIBILITIES • Eigenständige Planung und Durchführung von GMP-Audits bei Lieferanten • Erstellung von Auditberichten • Nachverfolgung von Maßnahmen • Sicherstellung der Behebung von
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 ...
- Our client is looking for support in their auditing team. - This role is focused on quality audits for GCP, GLP, RA and PV. RESPONSIBILITIES - Responsible for the quality audits in R&D clinical (GCP), non-clinical (GLP), Regulatory Affairs (RA) and/or
Clinical Quality QMS REQUIREMENTS - University degree in a Scientific Discipline or related - 5+ years of experience, with experience in GCP / GVP Auditing - Excellent English Skills Are you interested and do want to apply for this role, please
suppliers) and based on engineering principles; analyze results, make recommendations, and develop reports - Identify and ensure the optimization of complex Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process
action management - Providing training and support to colleagues throughout the company in all scenarios regarding quality management, GCP and GVP. - Leading and participating in projects to continuously improve the quality of GVP and GCP. - Preparing regulatory authority assessments and audits ...
auditing for Quality with a focus on GvP RESPONSIBILITIES - Auditing focussed on GCP and GvP (Pharmacovigilance) - Audit reporting - Improve processes in Pharmacovigilance and Clinical Research - Support local affiliates - Improve the Clinical Quality QMS
engineering degree, preferably in biomedical engineering, or similar education level • Minimum of 5 years work experience in medical device or pharmaceutical industry or equivalent, minimum 3 in quality-related functions • In-depth understanding on quality systems and regulated processes, esp. according
ROLE DESCRIPTION You will apply knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and systems/procedures to optimize internal and external device manufacturing and device distribution. Other important activity is to develop and
ROLE DESCRIPTION Zeer dynamische job waarin je in een team van 15 Lead Auditors zelfstandig zal opereren en je analytisch vermogen inzetten. Auditor werkt vanaf huis 2 tot 3 dagen bij klanten, wordt volledig gefacilliteerd in alle zaken door medewerkers. Deze audits zullen
improvement projects to maximise efficiency, quality and safety - evaluate trial productions - stay informed on technological market trends and developments - realize innovations - co-work with different departments such as Production, R&D and Quality REQUIREMENTS - BSc
control: conformity against technological documentation, internal process and documentation supervision, processes correction, improvement opportunities identification.• Process improvements & efficiency improvements, technical and technological improvements (improvement projects), processes optimization ...
Process Engineering. You will develop and introduce manufacturing processes. Next to that, you will work on process and machine specifications, risk analysis and FMEA transfers. RESPONSIBILITIES - Design manufacturing processes - Design process and machine
Process Engineer Slatina, Jud. Olt (Romania) NR REF.: 1084849 Your new companyPrysmian Group, the world’s leading designer and manufacturer of energy and communications cables. We make life better for people living in communities the world over, through the delivery of cutting-edge power
for product optimalization of plastic bottles with medical food liquids. You are responsible for two of the major process assembly lines. You will be in contact with different operators, mechanics and the teamleader. Together you will discuss points that need optimalization after which you will be
THE COMPANY Our client is a professional Pharmaceutical organization, based in Noord-Holland Netherlands. They are a rapidly growing and innovative organization that combines research and the production of high-quality medicines. They strive
Supervision over quality systems - IATF16949 Team Management Creating policy and standards into the overall quality management process, defining quality procedures Undertaking internal quality audits Representing company in front of major customers and suppliers Requirements: Minimum 3 years of