2 Opening(s)
5.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 6.00 LPA
Job Description: Microbiology Executive / Manager
We are looking for a dedicated Microbiology professional to manage and execute microbiological testing and related quality functions within our organization. The candidate will be responsible for conducting microbiology tests, ensuring environmental monitoring, and maintaining compliance with quality standards, with responsibilities varying based on experience.
Key ...
3 Opening(s)
1.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 6.00 LPA
Job Description: Microbiology Executive / Manager
We are looking for a dedicated Microbiology professional to manage and execute microbiological testing and related quality functions within our organization. The candidate will be responsible for conducting microbiology tests, ensuring environmental monitoring, and maintaining compliance with quality standards, with responsibilities varying based on experience.
Key ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are seeking a skilled and experienced microbiology professional to lead microbial testing and environmental monitoring activities in an API manufacturing setup. The Assistant Manager will ensure compliance with regulatory standards, supervise microbiological operations, and support quality systems in the microbiology lab.
Key Responsibilities:
Oversee routine microbiological testing of raw materials, ...
1 Opening(s)
7.0 Year(s) To 14.0 Year(s)
8.00 LPA TO 14.00 LPA
Responsible to collect the raw ingredients, EMP(Environmental monitoring program )sample, Packaging, in process samples and finished product samples as per sampling plan and conduct the test as per AN methods for salmonella, Enterobacter sakazakii, Escherichia coli, Total bacterial count, Staphylococcus aureus, shigella, Listeria monocytogen, coliforms, yeast & mold, SRC tec. ...
3 Opening(s)
1.5 Year(s) To 6.0 Year(s)
3.00 LPA TO 7.00 LPA
Key Responsibilities:
1. Method Development & Validation
Develop analytical methods for assay, dissolution, related substances, and stability testing.
Conduct method validation as per ICH guidelines (accuracy, precision, specificity, linearity, robustness).
Optimize and troubleshoot existing analytical methods.
2. Instrument Handling
Operate analytical instruments such as HPLC, GC, UV, FTIR, KF, Dissolution Apparatus, etc.
Perform daily calibration and ensure ...
2 Opening(s)
0 To 2.0 Year(s)
1.44 LPA TO 2.20 LPA
Monitors the work of manufacturing technicians and quality technicians, manages record keeping, and prepares reports for management
Works with software or websites to ensure they run properly by performing manual and automated tests during development
Ensures products meet quality standards and industry benchmarks by monitoring processes, inspecting goods and services, and proposing ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 7.00 LPA
•Electrical Supervisory license from Gujarat government
•Capable of Reading Electrical Drawings
Having knowledge of Installation and maintenance of Isolators, SF6 breakers CT, PT of Substation
•Capable of handling substation and PCC room independently.
•Inspect electrical components, such as transformers and circuit breakers (ACB, VCB and MCCB) capacitor banks.
Driving energy efficiencies improvement projects for site.
•Capable ...
1 Opening(s)
9.0 Year(s) To 11.0 Year(s)
8.00 LPA TO 10.00 LPA
Key Responsibilities:
Manage and oversee all Quality Control activities for formulation products.
Ensure compliance with cGMP, GLP, and regulatory guidelines.
Review and approve analytical reports, COA, STP, and specifications.
Handle instrument operations like HPLC, GC, UV, Dissolution apparatus, etc.
Ensure calibration, validation, and maintenance of QC instruments.
Coordinate with QA, Production, and R&D for smooth operations.
Handle ...
2 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 6.00 LPA
Position: QC Manager Location: Palanpur, Gujarat Industry: Pharma – API
Key Responsibilities:
Lead and oversee Quality Control operations in compliance with cGMP & regulatory guidelines.
Manage QC documentation, including qc document review, SOPs, and analytical records.
Supervise laboratory activities such as RM, PM, in-process, and finished product testing.
Ensure timely calibration, qualification, and maintenance of ...
30 Opening(s)
3.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Key Responsibilities:
Perform analysis and testing of Raw Materials (RM), Packaging Materials (PM), in-process samples, finished products, and stability samples as per pharmacopoeia standards.
Operate, calibrate, and maintain analytical instruments such as HPLC, GC, UV, IR, Dissolution Apparatus, etc.
Ensure timely release of materials/products with accurate and complete documentation.
Maintain records, calibration logs, data ...