58 Job openings found

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices  Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical Device Regulation ...

Internal Job Description Contribution in management and control of both site project/transfer as well as donor Documentation, such as Product transfer protocols, product transfer checklist, associated BMRs, Master Documents, etc. • Preparing & review of the Product Transfer Documents, i.e. Product Transfer checklist Product transfer protocol and Report • Preparation and Review of ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information abou t the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like ...

1. Summary of the roleThe Role will assist Healthcare business growth by developing Biopharmaceutical and Biotechnology business development activities. A techno-Commercial role with good understanding of bio-pharma market and ability to establish the Bio-Pharma products Range. 2. Education and Experience: B. Pharmacy/BiotechExperience: 3 to 5 Years in B2B Pharma/Bio-Pharma SegmentsNotice Period ...

Manage day-to-day transportation and logistics services for multinational account base. Start operations by inserting data into CNC control units. Set up and operate equipment to produce food contact grade PVC plastic film. Operate and tend machines to prepare and make PVC or consumer products for storage or shipment. Perform root cause and corrective action ...

    Regulatory Affairs Officer (RA) Qualification: B.Pharm/ M.Pharm Experience: Minimum 3 years in regulatory affairs for the ROW (Rest of the World) market, with a total of 3 to 5 years of experience. Job Description: Preparing dossiers as per country-specific guidelines. Compiling and reviewing documents. Coordinating with QA for documentation. Addressing queries raised by respective countries' FDA. Bond: 18-month ...

Preparation of Certificate of Pharmaceutical Product. Expertise in liaising, coordinating inspections with regulatory agencies (FDA ISO    9000) Knowledge of Microsoft Office, Microsoft Excel, ERP etc. Goal Oriented and Results Driven Team Leader. Expertise in writing, reviewing & approving lab procedures / documentations, Out off   Specification                     reports, batch records, protocols, etc. Review of QC related ...

Description: Job Description: Candidate should have experience in multi-step Synthetic Organic Chemistry including different reactions conditions. Should have Experience in process development & Technology transfer for API & Specialty Chemicals. Optimization & validations of the process, conditions for the assign project molecules as per requirements. Should have experience in regulatory approvals like REACH / FDA ...

Candidates having 2 year + expearince in formulations development can only apply. Required qualificaion is B Pharmacy/M Pharmacy. Job locaiton - Ambernath - Dist - Thane   Job Description- Handling EU/UK/ROW Market Projects.     Designs and conducts stability studies, Compatibility studies.     Responsible for process optimization, scale-up, technology transfers and process validation.     Hands on experience in handling ...