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 Through Manpower Outsourcing Services Providing Agency, applications are being accepted for the following open positions at Indian Pharmacopoeia Commission (IPC), an autonomous institution under the Ministry of Health & Family Welfare, Ghaziabad, which are available only on a contract basis. Vacancy circular for the post of Sr. Pharmacovigilance Associate. Interested candidates should submit their application online through Google Form with the following link: https://lnkd.in/d-MyKTny Period of engagement: The tenure of contract will be for period of one year. However, in case the work and conduct of the staff is not found to be satisfactory during the contract tenure, the services may be terminated at any time without assigning any reason thereof. General Instructions: 1.The competent authority reserves the right to increase or decrease the number of vacancies and reject/select/cancel the applications received without assigning any reason. 2. Interview will be conducted at IPC, G

 We are a multinational biopharmaceutical firm that is improving the lives of people in more than 120 countries by developing novel, cost-effective treatments for autoimmune disorders, cancer, and diabetes.        Pharmaceutical Engaging with one of the most cutting-edge biopharmaceutical businesses in the world offers a fantastic chance to make a long-lasting difference in the health of the globe. This is an opportunity to collaborate with some of the most talented individuals in the fields of research, healthcare, biotechnology, and pharmaceuticals. The opportunities are unlimited when a bright and varied group of people collaborate to achieve the shared objective of lowering the cost of healthcare and increasing its accessibility for all. Biocon Hiring Freshers Bsc, M.sc, B.Pharm, M.Pharm Apply Now Post : Research associate Research Trainee Scientist Qualification : B.Pharm, M.Pharm, B.Sc., or M.Sc What degree is required for positions of research trainee, research associate, and

  Apply now for a Regulatory Affairs position at Sun Pharma. Sun Pharma has expanded to rank first in India and fourth globally in terms of generic medication sales. We have developed over 2000 goods that are distributed in over 100 countries worldwide because to our enthusiasm for research. Over 40 manufacturing facilities on six continents and numerous R&D centres across the world support our global presence. At Sun, innovation lies at its core. Regulatory Affairs Position Available ■ Place of work: Baroda ■ Experience: 2–6 years reviewing all data and paperwork relevant to product registrations for various health agencies; grade: Executive / Sr. Executive. Work Duties:  ■ Assemble registration dossiers for submission to the US Food and Drug Administration, Health Canada, Europe, Australia/New Zealand, Japan, and Israel, among other health agencies. • Get ready to reply to letters of deficiency that you get from different organisations. • Keep track of post-approval and life-cycl

 Opening at Mangalam Drugs and Organics Limited Vapi Department: Production Executive with 7 to 10 Years of Documentation Experience in AI Only -To review and sign the completed BMR/BPR/ECR etc & other quality documents and ensure before submitting to QA, To implement new products/technologies as part of cross-functional team with R&D and Process Engineering. To work closely with chemists, officers and shift in charge. -To co-ordinate QMS related activities like process validation, cleaning validation, deviation and change control, To perform self-inspection. Department:CQA Executive with 7 to 10 Years of Experience in API Only -To co-ordinate & monitor the COA related activity. -To prepare & review the validation protocols and reports along with the compilation of data coordination with concern department, To Review APQR as and when required, To support QMS activity, To prepare & review of SMF/VMP/OM etc. -To prepare & review the MFC/BMR/BPR/ECR/BRPR/SRR for it

tcs hiring Clinical Research Coordinator // tcs hiring  any graduate 2023  The Clinical Data Manager I (CDM) leads and coordinates Data Management (DM) deliverables from database design set-up, through cleaning and reporting to database locking, ensuring that the completeness, accuracy and consistency of clinical data meets the quality standards and regulatory requirements for analysis and reporting.  The CDM II is a member of the Data Management staff. Serve as primary contact for DM with all relevant parties both internally (e.g. Project Management, Clinical Monitoring, Biostatistics and other functional groups) and externally (e.g. sponsors, external vendors, investigational sites) Plan and project the resources required including management of tasks, timelines, risk and quality Keep track on budget, forecasts and manage changes of scope requests Participate in the review of study documents (e.g. protocol, (electronic) case report forms (eCRFs), safety plans/manuals and statistical

patients through building partnerships with biotech and pharmaceutical companies around the world. Our mission is to continuously make it sure, secure, faster, and cheaper for therapeutic pharmaceutical companies to develop novel solutions. Premas Biotech was founded in 2005 with the vision of transforming drug development. We have acquired in-depth expertise and built state-of-the-art technology platforms to provide quality products that are second to none. Premas biotech hiring Executive/Senior Executive - Downstream Process //  Premas employs a world-class team of more than 150 dedicated scientists and managers, who have successfully developed over 650 molecules. By fostering an innovative and inclusive culture, we have created an ecosystem for establishing productive, long-term partnerships with our clients. We aim to be problem-solvers for our customers, by actively listening and being accessible 24/7 wherever we are needed. We innovate based on our customers’ needs. Our organizat