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CMC Project Coordinator

Glenmark Pharmaceuticals S.A.

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Glenmark Pharmaceuticals (www.glenmarkpharma.com) is a research-led, global, fully integrated pharmaceutical company. The group is present in more than 40 countries including the USA and Europe. Our Swiss operation encompasses the Company’s Biological Research and Development Centre located in the Canton of Neuchâtel and focuses on the discovery and development of novel biological entities comprising monoclonal antibodies and proprietary bispecific format. We provide an attractive, international and multicultural research environment with career opportunities for scientists engaged in applied biomedical sciences. Located in a beautiful area of Switzerland, we are a rapidly growing company with an attractive and competitive early research and development portfolio in the areas of immuno-oncology, respiratory and dermatology research.


 

CMC Project Coordinator

Glenmark Pharmaceuticals www.glenmarkpharma.com is a research-led global fully integrated pharmaceutical company. The group is present in more than 40 countries including the USA and Europe. Our Swiss operation encompasses the Company's Biological Research and Development Centre located in the Canton of Neuchâtel and focuses on the discovery and development of novel biological entities comprising monoclonal antibodies and proprietary bispecific format. We provide an attractive international and multicultural research environment with career opportunities for scientists engaged in applied biomedical sciences. Located in a beautiful area of Switzerland we are a rapidly growing company with an attractive and competitive early research and development portfolio in the areas of immuno-oncology respiratory and dermatology research.
CMC Project Coordinator OVERVIEW
In this role you will support the CMC Chemistry Manufacturing and Control project leads and manage all aspects of coordination linked to CMC project management.
RESPONSIBILITIES

Coordinate activities between Glenmark's departments Manufacturing R D Process Development Quality and different vendor service and manufacturing sites in the US and Europe with the support of project leads. The incumbent will be responsible for the following tasks

Manage project task timelines for each allocated project or sub-project
Manage drafting review and finalization of all relevant documentation reports gantt charts ..
Centralize project documentation and manage shared documentation Sharepoint
Assist in the organization of regular meetings and drafting of minutes
Manage action tracker and ensure timely follow up of actions
Facilitate coordination with consultants and/or technical experts

Organize and manage shipment of samples and product

Preparation of shipments and related documentation
Track delivery of samples and product to vendor service or manufacturing sites
Ensure conformity of shipment and delivery

Perform other relevant responsibilities as required.

REQUIREMENTS

Bachelor's degree in scientific subject biotechnology cell biology chemical engineering or related discipline highly desired but will consider a combination of education and experience
At least 2-3 years of work experience in pharmaceutical industry
Demonstrated skills in planning and organisation
Knowledge of project management tools Microsoft Project
Strong interpersonal and communication skills
Ability to work both independently as well as part of a team
Proactive methodical and customer-oriented
Basic knowledge of GMP and related guidelines
Some industrial experience in monoclonal antibodies manufacturing is a plus
Fluency in both French and English both written and verbal

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