Associate Director, Regulatory Cmc

**Snr Director Regulatory - Contract**: In collaboration with a well funded fast paced BioTech, BioTalent are looking to connect a seasoned Regulatory Industry professional to fulfil EU and UK requirements in alignment with the Global Team. This role will offer you - 3-6 month rolling contract - Ability to work part time - Hourly pay rate - Remote...

**Position**: Associate Director, International Commercial Training **Reports to**:Head of Insights, Analytics and Distribution **Location**:Zug Switzerland **Position Summary**: Apellis is seeking an experienced and engaged commercial professional for the role of Associate Director, Commercial Training, International Region. It is an outstanding...

Job Description Writes, edits, and reviews Essential Documents, including informed consent forms, patient information, and other project-specific clinical documentation Writes, edits, reviews, finalizes, and tracks clinical study report (CSR) patient safety narratives Collects and tracks documents for CSR appendices, in support of the Quality Control...

Proclinical are recruiting a Regulatory Project Manager for a pharmaceutical organisation. This role is on a contract basis and is located in Zug. *** **Responsibilities**: - Handle regulatory duties affiliated with the development, assistance, and deployment of the company's non-medical and medical device software products. - Supervise and examine both...

**Site Name**: USA - Pennsylvania - Philadelphia, Switzerland - Zug, UK - London **Posted Date**: Feb 7 2024 The Director, Publications will lead the establishment of a Strategic Publication Plan in alignment with Global Medical Plans, medical/scientific communication strategy and objectives. In addition, the Global Publications Director will ensure that...

**Summary**: The Talent Acquisition Lead - International Region (Associate Director) is responsible for end-to-end sourcing and recruiting strategies as well as on-boarding for the International Region (Europe and Australia/NZ). You are responsible for developing and executing the Talent Acquisition strategy in partnership with the Head International HR, HR...

**Summary**: The Talent Acquisition Lead - International Region (Associate Director) is responsible for end-to-end sourcing and recruiting strategies as well as on-boarding for the International Region (Europe and Australia/NZ). You are responsible for developing and executing the Talent Acquisition strategy in partnership with the Head International HR, HR...

Job Description Resource Management and Training: Participation in QM resource allocation Resource allocation of QA auditors Facilitation of professional development and career advancement of Quality Management staff Administrative supervision of Quality Management staff, jointly with Senior Director Quality Management Participation in...

Position Summary: The Director, Regional Clinical Trial Operations is a critical role responsible for leading the Regional Clinical Trial Operations (RCTO) team in trial execution of all trials within a molecule or therapeutic area and in helping build the strategic vision of the European team. This position will take a primary role in providing leadership...

Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. You will: Conduct and report all types of onsite monitoring visits Be involved in study startup and feasibility research ...

Was ist meine Funktion? Koordination des PLCM (Product Life Cycle Management) und Änderungen der GCC (Global Change Control) und Artwork für kommerzielle Produkte. Überwachung von Änderungen an Wirkstoff (DS) und Arzneimittelprodukt (DP) im globalen Änderungsmanagement, die sich auf Fertigwaren (FG) einer Marke in der Wachstumsphase auswirken. ...

Job Description Key Responsibilities: - In cooperation with International QA team, establish and maintain corporate quality objectives, actively promote an effective quality management system (QMS) in CEE region. - Ensure documented system is in place to support GMP/GDP compliance management both internally and externally, with all manufacturers and third...

**Site Name**: UK - London - Brentford, Baar Onyx, Switzerland - Zug, USA - Pennsylvania - Upper Providence **Posted Date**: Apr 4 2024 **Medical Director, Global Medical Affairs - Hematology**: The Global Medical Director role is a unique opportunity for an experienced, innovative, and proactive medical professional to facilitate the understanding of the...

Was ist meine Funktion? Koordination des PLCM (Product Life Cycle Management) und Änderungen der GCC (Global Change Control) und Artwork für kommerzielle Produkte. Überwachung von Änderungen an Wirkstoff (DS) und Arzneimittelprodukt (DP) im globalen Änderungsmanagement, die sich auf Fertigwaren (FG) einer Marke in der Wachstumsphase auswirken. ...

**Job Overview** The position of the Director global Quality of SHL Medical AG holds overall responsibility for compliance to all applicable regulations pertaining to all operations functioning on the assigned site as well as corporate compliance to all applicable regulations including cGMP pertaining to all the markets currently being served by the...

What is my function? Coordination of PLCM (Product Life Cycle Management) and changes to GCC (Global Change Control) and Artwork for commercial products. Monitoring changes to Drug Substance (DS) and Drug Product (DP) in global change management affecting Finished Goods (FG) of a brand in the growth phase. Ensuring alignment of Artwork with technical...

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What is my function? Coordination of PLCM (Product Life Cycle Management) and changes to GCC (Global Change Control) and Artwork for commercial products. Monitoring changes to Drug Substance (DS) and Drug Product (DP) in global change management affecting Finished Goods (FG) of a brand in the growth phase. Ensuring alignment of Artwork with technical...

Title**:Medical Affairs Coordinator** Location(s): Zug, Switzerland Level of position: Senior Specialist Position type: office-based, in alignment with BlueFlex model* Reporting Line: The position reports to the Associate Director, International Medical Affairs **How will your role help us transform hope into reality?** This position reports into the...

In a global team of trade compliance specialists spanning different countries and cultures, the role involves ensuring compliant trade at our Swiss site in Buchs, in line with all relevant trade compliance regulations. Responsibilities include overseeing transactional processes related to regulated product orders, conducting internal and external audits,...