46 Job openings found

Job OverviewThe Regulatory affairs team supports all the departments within the organization towards all regulatory requirements including approvals, reports, information sought etc. Such regulatory offices include DGCA, Various Ministries, AAI etc. The official under the role will engage with o fficials from the key regulators and maintain records and submission docs.

Position:          Engineering Head Location:         Bhopal Experience:     12 - 15 Years Industries:      Pharma - Formulation Responsibilities: Leadership and Management Lead and manage a team of engineers, technicians, and contractors. Develop and implement engineering strategies and goals. Mentor and develop team members' skills and expertise. Technical Oversight Ensure compliance with regulatory requirements, industry ...

We are having an urgent opening for the position of Assistant Manager/Manager Legal for a reputed company at the Andheri location. Roles & Responsibilities: To handle contracts independently and deal with Legal compliances- Contract drafting, vetting of agreements. Experience in handling a wide range of contracts – vendors, customers, and service providers. Handling of ...

KEY RESPONSIBILITIES Responsible for leading the design, implementation, and maintenance of comprehensive security measures across all stages of medical device development, ensuring compliance with relevant regulations and standards while protecting patient data and device integrity Lead the design and implementation of secure architectures for new medical devices, considering connectivity, data protection, access ...

Interacting with clients located PAN India Manage the entire sales cycle, from prospecting to meeting and closing Perform market research Be a key player and contributor to the direction of this growing sales team Crush sales targets on a weekly, monthly and quarterly basis Knowledge of Digital Marketing will be an added advantage Knowledge of Business ...

The job description is as below: Candidate having experience of Dossier Compilation, Liasioning with Regulatory consultant. Collect and compiled documents from each and every department and submit to client. Regulatory assistance to client. Preferable experience in ROW, Middle East and Latin America Market. Office time: 9:00 AM to 5:30 PM Job location -Mehsana for further details call ...

Purpose of the Job identify existing deviations, take corrective actions and prevent recurrence. Take pro-active actions to Quality Assurance aspects. Drive improvement projects. Requirements: Education - Degree in Engineering or Software (e.g. mechanical engineering, electrical engineering, industrial engineering) Work Experience: Minimum 5 years of professional experience, preferably in the Medical Device industry Experience in Quality Assurance, Regulatory Affairs, ...

Dossier preparation as per the ACTD & CTD (Module I, II, III, IV and V) guideline. Technical documents like Raw Material and finished products specification, manufacturing process, Product development report, stability reports, process validations preparation & review. Analytical method validation review as per the ICH guideline. Drug Master File review Technical query response to the ...

Position:        QA Manager Location:        Ankleshwar Experience:     15 - 18 Years Industries:     Pharma - API   Responsibilities: Day to Day planning and execution of various activities in QA Execution/review/Approval & monitoring of process validation activities. Preparation, review, Approval of process validation Protocol/Report. Preparation, review and Approval of Annual Product Reviews Handling of Change Controls ...

The job description is as below: Keep in touch with international legislation, guidelines and customer practices  Keep up to the date with a company’s product range Ensure that a company’s products comply with the current regulations. Coordinate, prepare and review all appropriate documents, for example, dossier and submit them to regulatory authorities within a ...