Essential Job Functions: Responsible to maintain an optimum level of manpower and over time Responsible to ensure all operation of production adherence to cGMP compliance Responsible on manpower development (training) for quality, productivity and cost consciousness To train the production personnel on cGMP Trend & regulatory requirement. Monitor the work of subordinates and ensure that the necessary assistance is provided to them for their timely, adequate and accurate completion of the assigned work Accountability to ensure production planning & timely delivery of high productivity and low cost products and with compliance to cGMP. Responsible for handling CAPA, Deviation, Change Control, URS, Contingency Plan and Investigation report. Responsible for Departmental Standard Operating Procedure update and revision execute within production in DCM. Responsible to carry out production operation as per production plan and delivery on time. Other instruction by superior. Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Application Deadline: 20/06/2025 Expected Start Date: 01/07/2025

Responsible for the safe and efficient operation of equipment and machinery used in the production of pharmaceuticals. This involves monitoring, controlling, and maintaining various processes, ensuring adherence to strict quality and safety standards. Job Type: Full-time Pay: ₹10,006.20 - ₹29,575.09 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Expected Start Date: 05/07/2025

Responsible for the safe and efficient operation of equipment and machinery used in the production of pharmaceuticals. This involves monitoring, controlling, and maintaining various processes, ensuring adherence to strict quality and safety standards. Job Type: Full-time Pay: ₹10,006.20 - ₹29,575.09 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Expected Start Date: 05/07/2025

Responsible for the safe and efficient operation of equipment and machinery used in the production of pharmaceuticals. This involves monitoring, controlling, and maintaining various processes, ensuring adherence to strict quality and safety standards. Job Type: Full-time Pay: ₹10,006.20 - ₹15,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Expected Start Date: 05/07/2025

Responsible for the safe and efficient operation of equipment and machinery used in the production of pharmaceuticals. This involves monitoring, controlling, and maintaining various processes, ensuring adherence to strict quality and safety standards. Job Type: Full-time Pay: ₹10,006.20 - ₹15,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Expected Start Date: 05/07/2025

Key Responsibilities: Media Preparation: Preparation, sterilization, and qualification of microbiological media for routine analysis and sterility testing. Environmental Monitoring: Conduct routine and alert-level monitoring of controlled areas (Grade A/B/C/D) including viable and non-viable particulate monitoring. Water Analysis: Microbiological analysis of purified water and WFI (Water for Injection) samples as per pharmacopeial standards.Carrying out microbial monitoring of cleanroom personnel to ensure aseptic practices.Performing microbial limit testing of raw materials, packaging materials, and finished products as per applicable pharmacopoeias.Conduct sterility testing using isolator/glove box/sterility test apparatus under aseptic conditions.Carry out LAL testing (gel-clot or kinetic methods) for endotoxin determination.Maintain accurate records of test results and adhere to SOPs, data integrity, and GMP documentation practices. Candidate Profile: Personnel Monitoring: Microbial Limit Test (MLT): Sterility Testing: Bacterial Endotoxin Testing (BET): Documentation and Compliance: Minimum 3–4 years of experience in a pharmaceutical microbiology laboratory. Hands-on experience in sterile manufacturing or aseptic processing environment is an added advantage. Working knowledge of cGMP, GLP, and regulatory requirements Familiar with microbiological risk assessments and aseptic techniques. Should be open to working in rotational shifts. Good communication and documentation skills. Desirable: Candidates with prior experience in regulatory inspected facilities will be preferred. Job Type: Full-time Pay: ₹30,000.00 - ₹47,050.42 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Application Deadline: 07/07/2025 Expected Start Date: 30/07/2025

Key Responsibilities: Media Preparation: Preparation, sterilization, and qualification of microbiological media for routine analysis and sterility testing. Environmental Monitoring: Conduct routine and alert-level monitoring of controlled areas (Grade A/B/C/D) including viable and non-viable particulate monitoring. Water Analysis: Microbiological analysis of purified water and WFI (Water for Injection) samples as per pharmacopeial standards.Carrying out microbial monitoring of cleanroom personnel to ensure aseptic practices.Performing microbial limit testing of raw materials, packaging materials, and finished products as per applicable pharmacopoeias.Conduct sterility testing using isolator/glove box/sterility test apparatus under aseptic conditions.Carry out LAL testing (gel-clot or kinetic methods) for endotoxin determination.Maintain accurate records of test results and adhere to SOPs, data integrity, and GMP documentation practices. Candidate Profile: Personnel Monitoring: Microbial Limit Test (MLT): Sterility Testing: Bacterial Endotoxin Testing (BET): Documentation and Compliance: Minimum 3–4 years of experience in a pharmaceutical microbiology laboratory. Hands-on experience in sterile manufacturing or aseptic processing environment is an added advantage. Working knowledge of cGMP, GLP, and regulatory requirements Familiar with microbiological risk assessments and aseptic techniques. Should be open to working in rotational shifts. Good communication and documentation skills. Desirable: Candidates with prior experience in regulatory inspected facilities will be preferred. Job Type: Full-time Pay: ₹30,000.00 - ₹47,050.42 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Application Deadline: 07/07/2025 Expected Start Date: 30/07/2025

Responsible for the safe and efficient operation of equipment and machinery used in the production of pharmaceuticals. This involves monitoring, controlling, and maintaining various processes, ensuring adherence to strict quality and safety standards. Job Type: Full-time Pay: ₹10,006.20 - ₹15,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Expected Start Date: 05/07/2025

Responsible for the safe and efficient operation of equipment and machinery used in the production of pharmaceuticals. This involves monitoring, controlling, and maintaining various processes, ensuring adherence to strict quality and safety standards. Job Type: Full-time Pay: ₹10,006.20 - ₹15,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Expected Start Date: 05/07/2025

To operate the machine in Pharma Company Job Type: Full-time Pay: ₹10,000.00 - ₹13,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Application Deadline: 19/07/2025 Expected Start Date: 19/07/2025

To operate the machine in Pharma Company Job Type: Full-time Pay: ₹10,000.00 - ₹13,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Application Deadline: 19/07/2025 Expected Start Date: 19/07/2025

Essential Job Functions: Responsible to maintain an optimum level of manpower and over time Responsible to ensure all operation of production adherence to cGMP compliance Responsible on manpower development (training) for quality, productivity and cost consciousness To train the production personnel on cGMP Trend & regulatory requirement. Monitor the work of subordinates and ensure that the necessary assistance is provided to them for their timely, adequate and accurate completion of the assigned work Accountability to ensure production planning & timely delivery of high productivity and low cost products and with compliance to cGMP. Responsible for handling CAPA, Deviation, Change Control, URS, Contingency Plan and Investigation report. Responsible for Departmental Standard Operating Procedure update and revision execute within production in DCM. Responsible to carry out production operation as per production plan and delivery on time. Other instruction by superior. Job Type: Full-time Pay: ₹25,000.00 - ₹30,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Application Deadline: 20/06/2025 Expected Start Date: 15/08/2025

Essential Job Functions: Responsible to maintain an optimum level of manpower and over time Responsible to ensure all operation of production adherence to cGMP compliance Responsible on manpower development (training) for quality, productivity and cost consciousness To train the production personnel on cGMP Trend & regulatory requirement. Monitor the work of subordinates and ensure that the necessary assistance is provided to them for their timely, adequate and accurate completion of the assigned work Accountability to ensure production planning & timely delivery of high productivity and low cost products and with compliance to cGMP. Responsible for handling CAPA, Deviation, Change Control, URS, Contingency Plan and Investigation report. Responsible for Departmental Standard Operating Procedure update and revision execute within production in DCM. Responsible to carry out production operation as per production plan and delivery on time. Other instruction by superior. Job Type: Full-time Pay: ₹25,000.00 - ₹30,000.00 per month Benefits: Food provided Health insurance Life insurance Paid sick time Provident Fund Schedule: Rotational shift Work Location: In person Application Deadline: 20/06/2025 Expected Start Date: 15/08/2025

As the Quality Control Officer, you will be responsible for ensuring the overall quality of products and compliance with GMP at the site. This includes conducting line clearance prior to dispensing, manufacturing, packing, and validation activities. You will also be involved in sampling during the manufacturing of validation, exhibit, and commercial batches, as well as in-process control, routine inspection, and online process verification and documentation. Your duties will involve the preparation, review, and approval of various documents such as SOPs, BMRs, BPRs, SMFs, VMPs, APQRs, MFR validation protocols/reports, and qualification protocols/reports. Additionally, you will be responsible for executing and evaluating qualification and validation studies, as well as evaluating and authorizing rework or reprocessing of batches. Your role will also include reviewing batch documentation and releasing batches for distribution, and ensuring quality control functions to maintain GLP and data authenticity. Furthermore, you will review and approve worksheets, COAs, raw and packing material specifications, semi-finished specifications, finished product specifications, and stability protocols. You will also review stability data generated at the site and submit it to Regulatory Affairs for dossier preparation. Additionally, you will be tasked with controlling, distributing, retrieving, and destroying master and executed documents such as BMRs, BPRs, analytical workbooks, master SOPs, protocols, reports, and logbooks. Qualifications required for this role include a Bachelor's degree in Pharmacy or Chemistry, knowledge of cGMP, and a minimum of 3 years of experience in the Pharmaceutical industry. This is a full-time position with benefits such as food provided, health insurance, life insurance, paid sick time, and Provident Fund. The work schedule involves rotational shifts, and there is a yearly bonus offered. The work location is in person, and the application deadline is 20/06/2025, with an expected start date of 20/08/2025.,