90 Job openings found

1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
  Perform Extractables & Leachables (E&L) studies in line with BPOG and regulatory guidelines (USP , , ICH Q3D). Operate and maintain instruments like LC-MS/MS, GC-MS/MS, UHPLC, GC-FID. Conduct method development, optimization, and validation for targeted and non-targeted analysis. Interpret mass spectral, elemental, and chromatographic data for accurate reporting. Support wet chemistry tests (pH, conductivity, titrations) and documentation ...
1 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.40 LPA
Perform microbiological assays, including cultures, staining, and identification of bacteria, fungi, and viruses under supervision. Assist in the preparation and sterilization of culture media, glassware, and laboratory equipment. Assist in testing samples. Keep the lab clean and organized, ensuring proper storage of microbiological specimens. Record and maintain accurate data on experimental results, including microbiological ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 6.00 LPA
Position:        Manufacturing Executive Location:        Bhilad - Vapi Experience:     3 - 5 Years Industries:      Cosmetic   Responsibilities: Schedule daily production and Manufacturing work centres based on sales priorities and material availability. Resource Management To assist production head to qualify manufacturing work stations and resources. Establish and maintain quality standards for all products. strickly ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 15.00 LPA
Position:          QC Manager (Biosimilars) Location:          Bhopal Experience:       8 - 10 Year Industries:        Pharma              Responsibilities:   Manage QC activities raw materials, in-process, and finished biosimilar products. Oversee analytical and microbiological testing (e.g., HPLC, ELISA, SDS-PAGE, Western Blot). Ensure compliance with cGMP, GLP, ...
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)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
Test to a high, and continuously improving, level of GMP/GLP compliance to ensure patient safety and to minimize risk to the company business   Perform routine testing and basic GMP paperwork review with supervisor direction   Oversee the development and tracking to a plan for day-to-day testing activities to meet the daily manufacturing and ...
1 Opening(s)
0.5 Year(s) To 2.0 Year(s)
1.44 LPA TO 2.50 LPA
Documentation & Compliance: Maintain accurate and complete laboratory records in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Prepare and review Certificates of Analysis (CoAs), test reports, and deviation reports. Ensure compliance with company SOPs, safety protocols, and regulatory requirements (e.g., FDA, EPA, ISO). Process Validation & Improvement: Participate in validation of ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 7.50 LPA
  Supervise day-to-day operations in the [lab/production/QC] department. Ensure proper implementation of SOPs (Standard Operating Procedures). Manage and monitor staff/workers assigned under the respective unit. Conduct sample analysis and ensure accurate documentation of test results. Maintain records of equipment calibration, sample logs, and QC/QA reports. Ensure compliance with safety guidelines and company standards. Coordinate with internal departments ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
Test to a high, and continuously improving, level of GMP/GLP compliance to ensure patient safety and to minimize risk to the company business   Perform routine testing and basic GMP paperwork review with supervisor direction   Oversee the development and tracking to a plan for day-to-day testing activities to meet the daily manufacturing and ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
Test to a high, and continuously improving, level of GMP/GLP compliance to ensure patient safety and to minimize risk to the company business   Perform routine testing and basic GMP paperwork review with supervisor direction   Oversee the development and tracking to a plan for day-to-day testing activities to meet the daily manufacturing and ...

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