if a vacancy occurs due to resignation of an employee in any place in the future, the candidate on the waiting list will be given appointment orders without conducting a fresh recruitment process
Proficient in routine laboratory techniques like sterile handling, instrument calibration, validation, and documentation. Must demonstrate good written and communication skills.
Capable to handle analytical method development, Implementation, Validation as per requirement. Should have experience of Analytical method transfer to QC.
Regulatory Affairs Specialist is responsible for ensuring that medical devices comply with all applicable regulations in India and international markets
First Class M.Pharm, MS (Pharm) Masters in Pharmacognosy or Bachelor of Ayurvedic Medicine and Surgery. PhD in Natural Product Chemistry, Life Sciences, Pharmaceutical Sciences or related disciplines.
ECHS invites applications to engage following Medical, Para Medical & Non-Medical staff on contractual basis in 05 ECHS Polyclinics at Kolhapur, Sangli, Satara, Karad and Chiplun
First Class Masters Degree in Pharmacology, Life-Sciences from a recognized university. Experience in the Research field and scientific writing. Candidates with proficiency in computer application will be preferred.
knowledge of various sophisticated instrumental methods for qualitative and quantitative analysis of tissue engineered constructs and regenerative technology development for clinical translation.
The ECHS Central Organisation is located at Delhi and functions under the Chief of Staff Committee (COSC) through AG and DGDC&W in Army HQ. The Central organisation is headed by Managing Director, ECHS, a serving Major General. There are 28 Regional Centres ECHS and 426 ECHS Polyclinics. ECHS is also an attached office of Dept of Ex-Servivemen Welfare (DoESW), Ministry of Defence (MoD) as are Directorate General Resettlement(DGR) and Kendriya Sainik Board (KSB).
Clinical batch data review, method validation, and stability study evaluations as per cGMP & regulatory norms. Routine analysis of clinical samples and stability samples.
Confirms that site staff have completed and documented the required trainings appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.
Maintain effective relationship with the end stakeholders medical scientific community within the allocated Global Business Unit and product – with an end objective to develop education and communication content as per requirement
Support Cross-functional team like Analytical Development, Formulation Development during product development and align documentation as per HC guidelines and Extend support for any other Regulatory related Function.
Ensure team members are trained and competent in all delivery areas. Assist the team during high work volumes by completing LTO accountabilities. Apply scientific knowledge to create compelling medical content and communications.