1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: IPQA Officer.
Location: Daman
Experience: 1 - 3 Years
Industries: Pharma
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits to assess adherence to GMP, standard operating procedures ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.00 LPA TO 3.00 LPA
Key Responsibilities:Perform analysis of raw materials, intermediates, finished products, and packing materials as per approved specifications.Conduct routine chemical testing and maintain accurate laboratory records.Operate and maintain laboratory instruments such as GC, HPLC, UV Spectrophotometer, Karl Fischer, pH Meter, and other analytical equipment.Prepare and standardize chemical reagents, solutions, and volumetric preparations.Ensure ...
2 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Quality Officer(Analytical)
Location: Dadra & Nagar Haveli - Slivassa
Experience: 3 - 4 Years
Industries: Cosmetic
Responsibilities:
Perform analytical testing of raw materials, intermediates, finished products, and stability samples.
Operate and troubleshoot instruments such as HPLC, GC, UV, FTIR, and dissolution apparatus.
Review analytical data ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
Review and approve analytical results, COAs, test reports, and raw data.
Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
Review and update SOPs, STPs, GTPs, ...
5 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 7.00 LPA
Key Responsibilities:
Perform analysis of Raw Materials, In-Process, Finished Products, and Stability Samples using HPLC.
Operate and maintain HPLC instruments as per SOP.
Preparation and standardization of reagents, volumetric solutions, and mobile phases.
Documentation of analytical records as per GMP/GLP guidelines.
Calibration and routine maintenance of laboratory instruments.
Ensure compliance with regulatory requirements and quality standards.
Handling ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The job description is as below:
Analysis: Perform quantitative and qualitative analyses of raw materials, in-process, and finished products to confirm specifications are met.
Documentation: Record test results, maintain lab notebooks, and prepare reports according to Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs).
Instrumentation: Operate, calibrate, and troubleshoot laboratory instruments such as HPLC, GC, UV-Vis, and pH ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Position: Asst. Manager - QA
Location: Daman
Experience: 8 - 15 Years
Industries: Pharma
Responsibilities:
To maintain a robust Quality Management System (QMS) aligned with regulatory expectations.
To handle internal, external, and regulatory inspections, ensuring successful outcomes and continuous compliance readiness.
To handle compliance of deviation management, change control, Market Complaint Recall, ...
1 Opening(s)
3.0 Year(s) To 15.0 Year(s)
0.50 LPA TO 10.00 LPA
We have opening for Category Manager.
Location - Delhi
Experience: 4–6 Years
Role Overview
We are looking for a strategic and execution-driven Category Manager who can own category growth, marketplace strategy, and product positioning with a strong understanding of the beauty category.
Key Responsibilities
Category Strategy & P&L Ownership
Own full P&L including revenue, margins & ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 3.00 LPA
Position: QC Officer
Location: Acchad nearby Bhilad
Experience: 0 - 1 Years
Industries: Medical Devices
Responsibilities:
Individually handling department & manpower.
Strong leadership skills to guide, supervise work activities, and help team members develop their skills.
Work allocation / Planning and Review of documents.
Preparation of SOP, Specification, Standard Test Procedures (STP), Raw Data ...
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 ...