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Quality assurance lead Jobs in Dallgow-Döberitz
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Quality assurance lead • dallgow doberitz
Quality Manager (m / f / d)
HEC Pharm GmbHKleinmachnow, Brandenburg, DEVerkaufsberater in Teilzeit Berlin B5 Calvin Klein Outlet (m / w / d)
PVHWustermark, GermanyNCR Cell Quality Technician (w / m / d)
AlstomHennigsdorf, BB, DE- Gesponsert
Team Lead Digital Enabling (m / w / d)
operational services GmbH & Co. KGKleinmachnow- Gesponsert
Head of Product (m / w / d) - Data & KI Weiterbildungspr
DSI Education GmbHHennigsdorf, Germany- Gesponsert
Quality & Regulatory Affairs Manager (m / w / d)
CLR - Chemisches Laboratorium Dr. Kurt Richter GmbHKleinmachnowMitarbeiter Quality- Gate (m / w / d)
AlphaConsult KGFalkensee, DeutschlandCategory Manager Raw Materials
DSJ GlobalBrandenburg- Gesponsert
Engineering Manager (m / f / d)
softgarden e-recruiting gmbhKleinmachnowSozialpädagog •in (w / m / d)
TÜV RheinlandNauenQualitätsplaner / Quality Engineer
J&S GmbH Automotive TechnologyWustermark, DEStaff Fullstack Engineer (d / f / m)
0333 eBay Group Services GmbHKleinmachnow- Gesponsert
Quality Officer (m / w / d)
Lindera GmbHFalkensee, Germany- Gesponsert
Personalized Internet Ads Assesor (DE) Remote
TELUS InternationalReinickendorf, Reinickendorf- Gesponsert
Medizinische Fachangestellte (MFA) als Assistenz in der Arbeitsmedizin (w / m / d)
TÜV Rheinland Service GmbHKleinmachnow- Gesponsert
Remote Search Analyst Germany m,f,d
TELUS DigitalFalkensee, Germany- Gesponsert
Test Automation Engineer (m / w / d)
aconso AGFalkensee, GermanyQuality Manager (m / f / d)
HEC Pharm GmbHKleinmachnow, Brandenburg, DEAbout us HEC Pharm GmbH is a major supplier of generic medicinal products to the German pharmaceutical market. HEC Pharm GmbH is a subsidiary of Sunshine Lake Pharma Co., L.T.D, China and has been active in Germany for 14 years. Both companies are organizationally part of the HEC Pharm Group, a multi-billion-dollar company with 20,000 employees operating in China, USA, Germany, UK, Japan, and Korea. Homepage : https : / / hecpharm.de / To strengthen our Regulatory Affairs and Quality Department, we are seeking a quality manager to work closely with the department head. This role includes both technical and administrative tasks and offers insights into pharmaceutical regulatory processes in a dynamic and international environment. Your responsibilities : Provide administrative and operational support to the department head, including meeting coordination, documentation follow-up, and communication support; Establishment and maintenance of GDP (Good Distribution Practice) system; Maintain documents, records, and meta-information in our document management system; Read and follow regulations, directives, German laws, guidelines, and internal SOPs; Preparation for and participation in audits and inspections; Prepare documents for serialization of products, products tracking, mockups, management of products release and pharmacovigilance in the EU; Collect technical information for regulated processes and implement CAPAs. Your qualifications : At least a bachelor degree from a university (preferably listed in the top 500 of Times Higher Education ranking) in a relevant scientific field (Please send a copy of your diploma with courses and grades); Additional qualifications, such as graduate university degree, regulatory and quality trainings, and experience in the pharma industry are of advantage; Familiarity with EU GMP / GDP guidelines and document management systems; Good reading and writing skills, in particular for regulatory and technical texts; High degree of analytical thinking, interest in regulatory affairs and quality, and attention to details; Good communication skills and willingness to put your team above your own personal interests; High level of proficiency in English language, good German (at least B2 level), additional knowledge of Chinese is a plus. We offer A responsible position in an international pharmaceutical company with offices in Germany and UK; Start-up atmosphere with flat hierarchies and short decision-making paths; Flexible working hours and the option to work from home; A dynamic mix of technical and administrative tasks in the field of Regulatory Affairs and Quality; A supportive, diverse, and collaborative team culture; Opportunities for individual development and insights into European regulatory processes. Contact Ms. Susie Lue [email protected]