RESPONSIBILITIES - Leading the quality management (quality assurance) for the whole site - R&D product licensing - Clinical & non-clinical studies - SOPs - Planning and Execution of Audits - Participation in R&D projects REQUIREMENTS - Degree in
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
- 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
on problems in quality and supplier service. In this position you report to the corporate assurance manager. REQUIREMENTS Master degree food related. Professional experience of minimum 5 years in a QA Position in food You have passed a registered management lead
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
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
will be functioning as a process engineer to optimise the overall plant performance and production operation. You will be responsible for the continuous collection of information and updates in process engineering to deliver high quality innovative solutions. You will for example be involved in the
an execution of technical assistance to chemical production - Responsible for the improvement of safety, cos reduction, environment and quality of the production process - Applying the different proven methodologies you will optimise different technical processes - Leading the continues improvement
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 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
accordance with accepted internal standards. - Monitor implementation of audit recommendations. - Participate in the process of planning audits. - Create and update mapping of risk areas that help to identify existing risks within the company. - Evaluate controls and risk management procedures in terms of Profile description - University degree in economics, finance or banking. - Minimum 4 years of experience in ...
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