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Sr.Executive Officer (Regulatory Affairs) @ Hindustan Syringes

Home > Quality (QA-QC)

 Sr.Executive Officer (Regulatory Affairs)

Job Description

He needs to be dynamic with excellent leadership qualities and having sound theoretical & practical knowledge sense of applications, Exposure in QMS & implementation, Calibration/Validation and QA regulations (National and International). Persons having knowledge in medical devices will be preferred. Candidate must be from medical devices or pharmaceutical industry.

  The Regulatory role will be responsible for ensuring that process controls in place meet all corporate standards and for preventing the outflow of defects from the process. The candidate must have proven track record for developing and executing standardization. The Executive/Officer must have the exposure of regulatory affairs & Audits both Domestic & International  Regulations . He/ she will have a broad knowledge of the QMS/ testing and quality landscape. The successful candidate must possess outstanding teamwork, interpersonal and communication skills.

Employement Category:

Employement Type: Full time
Industry: Medical / Healthcare
Role Category: Quality (QA-QC)
Functional Area: Not Applicable
Role/Responsibilies: Sr.Executive Officer (Regulatory Affairs)

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Keyskills:   qms regulations pharmaceutical industry regulatory compliance regulatory qa regulatory affairs regulatory examinations domestic medical devices international national audits both

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Hindustan Syringes

HMD, the leader in Medical Devices; Dispovan Syringes and Needles, Surgical Blades, Blood Collection Tubes, Cannulas, AD Syringes (KOJAK) etc. is a CE ISO 9001 and ISO 13485 certified company Growing at a compound rate of 35% to 40% annually, it is poised to cross the 800 crores rupees mark