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2.0 - 8.0 years
0 Lacs
tirupati, andhra pradesh
On-site
You should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of experience. Immediate joiners are preferred for this role. As a part of your role, you will be responsible for conducting HPLC analysis of solid orals/nasal products, handling QC activities related to Raw Materials, Packing, In Process, and Finished Products, and ensuring compliance with GMP/GLP Practices. The ideal candidate should have 2-8 years of experience and should have prior experience working in regulated plants approved by USFDA/MHRA. Working in this position will provide you with the opportunity to work in a fully automated world-class manufacturing facility, handle diverse dosage forms in a multi-product environment, receive attractive attendance bonuses and special allowances, and access unmatched opportunities for learning and professional growth. This is a full-time position with benefits including Provident Fund, day shifts, yearly bonus, and the requirement to commute or relocate to Tirupati, Andhra Pradesh. If you are ready to join immediately, have a minimum of 3 years of experience in 10-key typing, and are willing to work in person, we encourage you to apply before the deadline on 14/07/2025.,
Posted 1 month ago
2.0 - 8.0 years
0 Lacs
tirupati, andhra pradesh
On-site
The ideal candidate for this role should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of relevant experience. Immediate joiners are preferred for this position. As a member of our team, your responsibilities will include conducting HPLC analysis of Solid Orals and Nasal products, hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products, as well as ensuring compliance with GMP/GLP practices. The preferred candidate will have 2-8 years of experience and prior exposure to working in regulated plants, specifically those approved by USFDA/MHRA. In return, you will have the opportunity to work in a fully automated, world-class manufacturing facility. You will be involved in working with diverse dosage forms in a multi-product environment. Additionally, you will receive attractive attendance bonuses, special allowances, and unparalleled opportunities for learning and growth. This is a full-time position with benefits such as Provident Fund, yearly bonus, and day shift schedule. The ability to commute or relocate to Tirupati, Andhra Pradesh is required for this role. If you are ready to join immediately and have at least 3 years of experience in 10-key typing, we encourage you to apply. The application deadline for this position is 14/07/2025.,
Posted 1 month ago
0.0 - 1.0 years
2 - 2 Lacs
Ludhiana
Work from Office
Freshers can also welcomed for interview. QC Executive To monitor all process steps (physical, chemical & microbiological testing) and control points as per defined parameters and standards. To monitor effectiveness of overall cleaning and sanitation of the plant including all warehouses. To monitor GLP practices in lab, resources needed as per laboratory requirement. To monitor the product quality through compliance of specification for raw material, packaging material & finished products. To monitor testing plan, calendar & standard for inside & outside testing & to ensure outside testing as per schedule. To check and verify the daily deviation report, taking appropriate actions against the same. Determining and agreeing on in-house quality procedures, standards and specifications. Specifying quality requirements of raw materials with suppliers. To ensure that all the products confirm the quality specification. To identify, plan, documents and manage the practices, activities and resourced needed to meet quality goals and objectives. Responsibility for review and analyze quality index and carry out root cause analysis for failure and corrective action plan. Oversee the pre dispatch inspection related activities and ensure that the products dispatched meet the required standards. Analyze and resolve all matters related to quality issues and closure of customer complaints. Responsible for reviewing all customer complaint and provide RCA & CAPA. Continuous endeavor for zero customer complaint. Provide support to other departments in managing quality within their processes. Preparation labels for domestic and Export as per requirement. And Make data records as per buyer requirement in case of export /domestic example COA, Serial Number of Items to be dispatched etc. Provide trainings to workforce related with quality & food safety. Microbiologist Preparation of media and sterilization of media &glasswares. Microbiological analysis of raw material & finished products. Microbiological analysis of complaint samples. (whenever required) Perform hygiene tests like environment monitoring, hand swab, surface hygiene & swabs of packing material Microbiological analysis of RO & CIP water & testing Responsible for daily quality documentation & record keeping. Micro analysis of R&D & market samples with record keeping. Micro analysis of trial batches upto required time with record keeping. Assisting in calibration of laboratory equipment with documentation. To monitor & maintain incubation samples with record keeping. Validation of CIP, hygiene & environmental hygiene Preparation, Handling and destruction of media Good lab practices and arrangement of micro items. Provide trainings to workforce related with quality, microbiology & food safety. Product shelf life checking and its records. Lab Chemist / Process Controller Implementation of quality system schedule, preparation and recording Online quality control reports. In case of any deviation from standard and safety of product inform immediately to Lab In charge. Monitoring of CCPs & OPRPs and its Records and Control. Incoming Raw material ad Finished Product Testing and Records. Instrument Calibration of lab and Weighing scales. Recopies Verification and Online Parameters Check and Control if any deviation observed. Online Training to Plant Workers on Food safety/GMP/Personal Hygiene/product Parameters and Packing Parameters. Finished Product Coding Printing Verification and its records. Verification Plant GMP/ GHP . Incoming and Outgoing Vehicle checks and its records. Maintaining Keeping samples and its records. Monitoring all line labeling and Packaging of Finished product. Supervision of Plant cleaning through Housekeeping team. Ensure the PPEs monitoring wearing by Food handlers during Food Product packing. Freshers can also welcomed for interview.
Posted 2 months ago
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