2 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 4.50 LPA
Responsible for taking ownership for safety and quality related compliance execution in respective work areas as per defined company standards.
Responsible for maintaining shift wise logbooks as per defined standard /operating procedure/ work instructions.
Responsible for maintaining excellent 5S /housekeeping standards in respective work area.
Responsible for reporting any deviation / abnormalities to ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are looking for an IPQA Executive to monitor and ensure in-process quality during manufacturing and packing operations in our API facility. The ideal candidate will be responsible for real-time quality assurance, GMP compliance, and documentation control throughout the production lifecycle.
Key Responsibilities:
Perform in-process checks during various stages of API ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 9.50 LPA
Position: Asst. Manager - Production
Location: Sarigam
Experience: 7 - 10 Years
Industries: Chemical
Responsibilities:
Accountable for controlling and monitoring of batch process parameters for smooth Plant operation.
Filling BMRs for easy access of process and time cycle of products.
Ensure that the production schedule meets quality, lead-time and ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.40 LPA TO 3.80 LPA
Instrument Technician Job Description
4.9
158 votes for Instrument Technician
Instrument technician provides troubleshooting, maintenance of controls, instrumentation, electrical and mechanical equipment of high technological level and other aspects necessary to perform the job.
Instrument Technician Duties & Responsibilities
To write an effective instrument technician job description, begin by listing detailed duties, responsibilities and expectations. We have included ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Monitoring of manufacturing related activity performed in Mfg facility.To maintain proper planning, scheduling and achievement of production with optimum utilization of resources.To preparation, review and implementation of all necessary standard operating procedure(SOP).To preparation and review of batch manufacturing record and protocol.Training given to all concern persons in their respective areas.To ...
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 10.0 Year(s)
7.00 LPA TO 8.00 LPA
Position: Executive/Sr. Executive - Production
Location: Daman
Experience: 5 - 10Years
Industries: Pharma
Responsibilities:
Manage day-to-day production operations, ensuring timely and efficient manufacturing.
Ensure compliance with GMP, safety, and environmental regulations.
Optimize production processes to improve efficiency, reduce costs, and maintain product quality.
Monitor and control production schedules, inventory ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Executive - QA
Location: Daman
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Handling of out of Specification (OOS), Out of Trend (OOT), Out of Calibration (OOC) and Lab Event investigations.
Sporadic Review of stability. PM, RM, FP, SF, SFP, in-process and process validation reports.
Review of SOPs, STPs ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
6.1 Over all responsibility of Quality Assurance Department.
6.2 Vendors approval for RM & PM.
6.3 Periodical Quality Audit.
6.4 Activities related to Drug Control Authorities.
6.5 Evaluation of Product Complaints & Product Recall.
6.6 Validation and Qualification.
6.7 GMP Training to Staff.
6.8 GMP Implementation in the factory.
6.9 Co-ordination with various departments to implement cGMP in ...
15 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 7.00 LPA
1 To work in all 3 shifts on rotation basis & take responsibility of production with desiredQuality in safe operations.2 To maintain housekeeping of plant and surrounding area, Allocation of casual manpowereffectively.3 Organize tool box talk with the subordinates & other service departments.4 Preparation and closing of work permit & ...