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Centre for Cellular and Molecular Platforms (C-CAMP), is a Dept. of Biotechnology (Govt. of India) initiative and a not for profit organization based in Bangalore. We act as an enabler of Bioscience Research, Innovation and Entrepreneurship by providing Research, Development, Training and Services in State Of The Art Technology Platforms. As a part C-CAMP's mandate of promoting entrepreneurship and innovation, C-CAMP has created and fostered an entrepreneur-friendly culture in and around academic/research environment through its involvement in seed funding schemes for Startups, Entrepreneur Mentorship program and Bio-incubation facility.
Check the space below for vacancies.

To bolster our team we are seeking highly motivated, self-driven team players for following positions - 

Job Title: QMS (Quality Management System) Executive
Job summary:
CCAMP’s NBM MedTech µFab with its ‘Design to Manufacture’ approach offers its design and technological expertise for rapid conversion of an idea into the product. It is envisioned to pioneer path-breaking innovation and quick to market acceleration of microfluidic chips.
Candidate will be leading Quality Management System development and implementation. We are scouting for an expert in ISO 13485 QMS. This position will have responsibility for a variety of Quality Management (QMS) Processes: especially systems Equipment Preventive Maintenance, Corrective and Preventive Action (CAPA), internal and external audit, and various quality continuous improvement activities.
Responsibilities and Duties:
Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
Ensure that all in-house systems and procedures are updated, revised, and modified on a continuing basis to meet the needs of external certification bodies.
Leads audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
Prepares reports and/or necessary documentation (ex, Corrective and Preventative Actions) and provides to applicable stakeholders, both internal and external.
Ensures the quality assurance programs and policies are maintained to satisfy all customer requirements and audits.
Produce written reports and make presentations.
Undertake continuous training and development.
Work within a GMP regulated manufacturing area to provide and assist in the implementation of quality-related continuous improvement opportunities.
Comply with health, safety and environmental policies.
Experience: Minimum 2 Years of experience in ISO 13485 QMS implementation
Qualification and skills:
-Candidate should be an engineering graduate or postgraduate with relevant experience. He/she must have excellent interpersonal skill and ability to manage a variety of cross-functional team members. 
-Candidate should have excellent presentation, report preparation, and project planning skills.
-Desirable:  Strong knowledge of medical device rapid prototyping, manufacturing techniques 
Job Location: Centre for Cellular and Molecular Platform, Bellary Road, Bangalore – 560065
Please fill in the application form at (Apply Now) and send your resumé and a brief message to get in touch with us, mentioning name of the position applying for, to     
Please refer to this position in the subject line of your e-mail. Candidates whose profile matches our requirement will be contacted directly. Please note that application will be considered only if  the form is filled in and  email hr attaching the CV.
This is a contractual position,  and compensation is based on qualification and experience. 
Last date of receipt of  application, as given above, is  5th February 2022.