To follow safety rules in the premises according to the company norms •Monitoring of DP, RH and temperature in aseptic processing area •To maintain the BMRs and other log books in the aseptic processing area as per cGMP and SOP
Description: This role is responsible for managing and overseeing injectable manufacturing operations within a regulated pharmaceutical manufacturing environment, ensuring the production of high-quality injectable pharmaceutical products in compliance with current Good Manufacturing Practices, aseptic processing standards, and applicable
Description: This role is responsible for supporting injectable manufacturing operations by executing processing, equipment operation, and aseptic production activities within a regulated sterile pharmaceutical environment. The role operates manufacturing equipment such as autoclaves, washing machines, sterilizers, filtration systems,
Role: Engineer - Sales & Business Development (Hyderabad & Ahmedabad) Education Qualification: BE / BTech (Mechanical / Chemical / Biotechnology) with MBA (Marketing) Optional Years of Experience: 4 to 6 years in Business Development and Marketing
JOB DESCRIPTION Job title : Senior Manager– Manufacturing Operations (Biologics &Gene Therapy) Reports to : VP - Operations Job purpose We are seeking an experienced and highly motivated Senior Manager – Manufacturing Operations to support development
JOB DESCRIPTION Job title : Lead – CMC Biopharmaceuticals | (Gene Therapy) Reports to : VP - Operations Job purpose The Lead – CMC will provide technical and regulatory leadership for Chemistry, Manufacturing & Controls (CMC)
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Job Purpose To lead MSAT activities for sterile injectable products including technology transfer, scale-up, exhibit batches, process optimization, product launch, and commercial readiness while ensuring compliance with cGMP, regulatory requirements, and organizational objectives. Key Responsibilities MSAT
We are partnering with a rapidly growing biotech company to hire for multiple roles based in Bengaluru. Job Description Upstream Senior Research Associate (4 Positions) Upstream Research Associate (6 Positions) Location: Bengaluru Qualification & Experience Upstream
Job Description To follow safety rules in the premises according to the company norms. To maintain the BMRs and other log books in the aseptic processing area as per cGMP and SOP. Preparation and periodic revision of SOPs
Job Title Options (Choose One) Executive / Sr. Executive – Downstream Process ( Biologics) (Avoid Production Executive. Too small for the gravity of this work.) About the Role Join a team shaping the future of advanced
Job Overview : We are seeking a highly motivated Research Associate / Scientist to join our Cell and Gene Therapy (CGT) Projects . The role involves hands-on research in immune cell engineering , process development ,
Description JOB DESCRIPTION This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated manufacturing environment. The job role is responsible for executing and
Zotefoams plc is a world leader in cellular material technology, with facilities in Croydon, UK; Kentucky and Oklahoma, USA; Brzeg, Poland; and Jiangsu Province, China (T-FIT). We produce lightweight foams for a wide range of markets
Job description: Job Summary At Tetra Pak we commit to making food safe and available, everywhere; and we protect whats good – protecting food, protecting people and protecting the planet. By doing so we touch millions
Job Description Job Responsibility: Technical Writing & Documentation: Development Key Responsibilities Lead the preparation of comprehensive documentation for complex R&D projects, including new formulations, emerging technologies, advanced process studies, and high-priority development programs Prepare and maintain
We are looking for a skilled and experienced Microbiologist with 2–5 years of hands-on experience in microbiological processes, media optimization, and bioreactor handling. The ideal candidate will support R&D or QC functions in fermentation, strain maintenance,
Job Role : Sr.Manager / DGM - Sterility Assurance Location : Halol - Vadodara Job Summary : In this Job role we are looking for Sterility Assurance, QMS elements for Sterile manufacturing Units with experience in
Position/Job Title General Manager Department Quality Assurance Reporting To VP – Corporate Quality Assurance Location Satara Years Of Experience 15-25 Years Dosage Form Solid Oral / Liquid, Nasal is preferred Job Responsibilities/Deliverables Quality Management System (QMS):
Documentation & SOP Management Prepare and implement standard operating procedures, batch manufacturing records, protocols, cleaning procedures, and log sheets. Maintain all documentation in compliance with cGMP and regulatory requirements. Ensure timely review and revision of SOPs