9 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.60 LPA
Job Description: Production Executive
We are looking for a Production Executive with hands-on experience in API manufacturing to join our dynamic production team. The ideal candidate will be responsible for supervising daily production activities, ensuring batch operations run smoothly, and maintaining compliance with safety and quality standards.
Key Responsibilities:
Execute and monitor day-to-day ...
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 ...
5 Opening(s)
1.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Responsibilities
Perform and supervise In-Process Quality Assurance (IPQA) OR QA checks during API manufacturing operations.
Conduct on-line review of Batch Production Records (BPR) and ensure adherence to approved procedures.
Ensure sampling, line clearance, and process compliance as per GMP/cGMP norms.
Identify, record, and support resolution of deviations, non-conformances, and quality incidents during manufacturing.
Support quality investigations and prepare required ...
1 Opening(s)
1.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The job description is as below:
To perform High Performance Liquid Chromatography analysis for various pharmaceutical tests including Related Substances, in compliance with 21 CFR Part 11 and cGMP guidelines. The role includes calibration, troubleshooting, integration, and data review activities related to HPLC.
Key Responsibilities:
Perform routine and non-routine HPLC analysis for Assay, Related Substances, Content Uniformity, and other quality ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
Key Responsibilities:
Conduct routine microbiological testing (water, environment, raw materials, in-process & finished products).
Perform environmental monitoring of cleanrooms, utilities, and aseptic areas.
Support media fill, sterility testing, endotoxin testing, and microbial limits testing.
Ensure compliance with cGMP, SOPs, and regulatory guidelines (USFDA, EU, WHO, etc.).
Review and document microbiological data, deviations, and OOS/OOT investigations.
Participate ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
To ensure the work allocation All Quality control person.
To ensure the quality of raw material, packing material and finished product are compliant with the approved specification and GMP/GLP
Maintains accurate, complete, and timely documentation (analytical reports, logbook).
Ensure compliance with cGMP, GLP and regulatory standards. participate in internal audits, external regulatory inspection ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
The ideal candidate will be responsible for overseeing formulation and production processes while ensuring compliance with Batch Manufacturing Records (BMR) and regulatory standards. This role requires a detail-oriented individual with strong organizational and communication skills to manage production activities efficiently
Job Responsibilities:
Develop and establish product formulations based on industry trends, market ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
System Operation & Monitoring:
Operate, monitor, and troubleshoot purified water, water for injection (WFI), and pure steam generation systems, including but not limited to, reverse osmosis (RO) units, deionization (DI) units, multi-effect stills, and clean steam generators.
Monitor critical parameters such as temperature, pressure, flow rate, conductivity, TOC (Total Organic Carbon), and ...
2 Opening(s)
10.0 Year(s) To 15.0 Year(s)
Not Disclosed by Recruiter
POSITION -Quality Control Manager
Location - Terre Haute. IN
Job description
The Quality Control Manager plays a crucial role in ensuring that SPI maintains high standards and consistently delivers quality products and services. This job description provides a comprehensive overview of the responsibilities and qualifications expected from the Manager of Quality Control. By effectively ...
1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
Not Disclosed by Recruiter
Lead and optimize end-to-end sterile injectable production, ensuring cGMP compliance, on-time delivery and continuous process improvement.
Production Planning and Inventory Control.
To carryout day to day production activities like Manufacturing, washing, sterilization, Powder Mixing, Filling, Visual inspection and Packing and monitoring all activities assign down line people.
To ensure that running product and produced ...