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
instructions) to enable the seamless knowledge transfer of project and manufacturing processes - Lead Auditor regarding quality compliance audit of 3PLs as well as suppliers and Distributors and monitor status and progress of Supplier Corrective Actions REQUIREMENTS ...
results and client feedback. - Coach employees and raise awareness for quality issues. REQUIREMENTS - Bachelor's or Master's Degree in Bio-Engineering, Industrial Engineering Chemistry, Biochemistry, or similar. - At least 5 years of experience as QA Managers in the
make sure their employees harmonize with their collaborative organizational culture. ROLE DESCRIPTION You will be reviewing the steps of production to make sure they are in line with the company’s Quality Management System. You will be
- Maintain the quality system. - Conduct internal and external audits. - Follow up on internal and external complaints. - Giving trainings to staff members. - Review and improve production processes. - Advise the Board on QA issues. REQUIREMENTS - Bachelor's
south of Baden-Wurttemberg and is to be filled immediately on a permanent basis. ROLE DESCRIPTION As a Senior Quality Manager you will be responsible for assigned quality systems. There you will be responsible for proposing quality metrics for
instructions. - Organise the audit plan and support/carry out audits. - Liaise with external parties, such as clients, suppliers and authorities. - Handle client questions and complaints. - Participate in continuous improvement projects. REQUIREMENTS - Bachelor's or
implement quality systems for all activities linked to warehousing and Distribution at an EMEA level. RESPONSIBILITIES · Investigate complex manufacturing product quality and compliance issues for all production processes prior to final product release based
a Quality representative to improve awareness, visibility, and communication on quality initiatives supporting departmental, functional, site, divisional and corporate quality goals and priorities. You will act as the key interface with site operations as it pertains to Supplier Quality Issues. Demonstrate
reports, afther each audit What we offer? - 400 PLN per day (inspection in Poland) / 760 PLN (inspection abroad) - Daily allowance and mileage - Notebook - Possibility to continue working in the company, afther the trial period
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
chemistry) or related field (e.g. veterinary); (or equivalent experience) - +5 years of clinical/industry/health authority experience in regulated industry; - +5 years Quality Assurance auditing experience - Technical knowledge in Pharmacovigilance, preclinical and/or clinical drug development - Knowledge
Host client audits and regulatory inspections and manage the audit report responses. - Effectively interact with other Quality managers, Operations managers and stakeholders to maintain quality and help introduce new quality objectives. - Liaise with clients on all GMP or QP related matters ...
critical subcontractors and customers - Audit finished product suppliers and critical subcontractors - Maintain existing regulatory filings/ licenses, managing updates and related change control processes - Provide input for the resolution of complaints and non-conformities - Release finished products ...
Capgemini’s in-house agency, EDGE Creative, has over 40 copywriters, marketers, designers and developers from a wide variety of backgrounds and nationalities. We are looking for a Content Marketer to join us and fuel our continued growth. Based in Krakow, Poland, the Content Marketer will work in a global team with the industry's sharpest and most experienced marketers, consultants and sales teams. He ...
instructions. - Updating the quality system where necessary. REQUIREMENTS - Bachelor's Degree in Biosciences, Master's Degree in Bio-Engineering, or similar. - At least 5 years of experience with Quality Assurance in the food industry. - Experience with FSSC 22000 or ISO
Reporting directly to the Plant Director and having 5 quality specialist reporting to you. RESPONSIBILITIES - Translate the requirements, knowledge and experience regarding safety and quality. - Monitoring government aims to ensure the safety and quality. - Translate