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2.0 - 4.0 years
3 - 3 Lacs
amritsar
Work from Office
Role & responsibilities CARRYING OUT AHU / AUTOCLAVE / DHS / WATER SYSTEM VALIDATION COMPILING REPORTS OF VALIDATION ACTIVITIES COMPILING APQR ASSISTING QA MANAGER Preferred candidate profile CANDIDATE MUST HAVE ATLEAST 2 YEARS OF EXPERIENCE OF STERILE INJECTION MAUFACTURING FACILITY
Posted 1 week ago
4.0 - 15.0 years
0 Lacs
kochi, kerala
On-site
Role Overview: As the QC Head, you will be responsible for leading the Quality Control function in medical device manufacturing to ensure that products meet global regulatory, safety, and performance standards. Your role will involve overseeing raw material testing, in-process quality checks, stability studies, validation protocols, and final product release in compliance with applicable regulatory guidelines. Key Responsibilities: - Establish, implement, and maintain QC protocols, SOPs, testing procedures, and specifications. - Ensure batch-wise testing, documentation, and release of raw materials, intermediates, and finished products. - Oversee microbiological and biochemical testing for s...
Posted 1 month ago
8.0 - 15.0 years
0 Lacs
india
On-site
Role Summary The QC Head will lead the Quality Control function for medical device manufacturing ensuring products meet global regulatory, safety, and performance standards. The role involves oversight of raw material testing, in-process quality checks, stability studies, validation protocols, and final product release as per applicable regulatory guidelines. Key Responsibilities 1. Quality Control Management Establish, implement, and maintain QC protocols, SOPs, testing procedures, and specifications. Ensure batch-wise testing, documentation, and release of raw materials, intermediates, and finished products. Oversee microbiological and biochemical testing relevant to sterile and non-steril...
Posted 1 month ago
2.0 - 6.0 years
0 Lacs
vadodara, gujarat
On-site
As a Microbiologist at our company, your role involves performing routine microbiological analysis of raw materials, intermediates, and finished API products. You will be responsible for conducting environmental monitoring of clean rooms and production areas using methods such as settle plates, swab tests, and air sampling. Additionally, you will be required to perform water testing for PW, WFI, and purified water as per pharmacopeial standards like IP, BP, USP, and EP. Your duties will also include conducting microbial limit tests, endotoxin tests, and sterility testing following standard operating procedures. It will be your responsibility to maintain microbial culture stock, ensuring prop...
Posted 1 month ago
3.0 - 4.0 years
3 - 3 Lacs
amritsar
Work from Office
Role & responsibilities Complete knowledge of Validation ( AHU / Autoclave / Dry Heat Sterilizer etc ) and Calibration -Capable of Compiling the Validation and calibration Activities -Good Computer Skill Preferred candidate profile CLEAN SHAVEN MALE CANDIDATE WITH MINIMUM 2-3 YEARS EXPERIENCE IN STERILE INJECTION SECTION
Posted 3 months ago
10.0 - 15.0 years
9 - 12 Lacs
sikkim
Work from Office
Roles and Responsibilities Conduct microbiological testing and analysis of raw materials, in-process samples, finished products, and environmental monitoring to ensure compliance with regulatory requirements. Develop, validate, and maintain microbiology protocols for water systems, disinfection processes, and media preparation. Collaborate with cross-functional teams to investigate out-of-specification (OOS) results and implement corrective actions. Ensure timely reporting of test results to relevant stakeholders and maintain accurate records according to cGMP guidelines. Participate in audits and inspections by providing documentation support. Desired Candidate Profile 10-15 years of experi...
Posted 5 months ago
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