2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
Position: QC Executive
Location: Vapi
Experience: 3 - 5 Years
Industries: Chemical
Responsibilities:
To conduct material analysis (in-process, raw material, samples, finished goods, etc) and maintain records of the same.
To maintain lab equipment’s functioning.
To maintain documentation for all lab procedures
Thorough knowledge of chemistry, analytical & ...
1 Opening(s)
0 To 1.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: Jr. Chemist - QC
Location: Sarigam, near by Vapi
Experience: 0 - 1 Years (Fresher)
Industries: Chemical
Responsibilities:
Responsible for Documentation work in QC Department.
Candidate must have knowledge of HPLC & GC.
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing.
Overall looking ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
3.50 LPA TO 4.00 LPA
Position: QC Chemist
Location: Vatva - Ahmedabad
Experience: 4 - 6 Years
Industries: Chemical
Responsibilities:
To conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods or stability samples.
To calibrate, validate, or maintain laboratory equipment.
To compile laboratory test data and perform ...
1 Opening(s)
4.0 Year(s) To 10.0 Year(s)
4.20 LPA TO 5.40 LPA
Quality Control:
Ensuring the quality of pharmaceutical intermediates and APIs through various testing and analysis methods.
Lab Analysis:
Using analytical instruments like HPLC, GC, and others to analyze samples and ensure product quality.
Documentation:
Maintaining accurate records of tests, results, and other QA-related documents.
Process Improvement:
Contributing to the improvement of QA processes and procedures.
Compliance:
Ensuring that all ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 6.00 LPA
Position: Chemist/Sr. Chemist - R&D
Location: Sarigam
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Carry out bench scale reactions, run in process tests and deliver on committed timelines
Carry out bench scale lab reactions to deliver products in expected yields and quality.
Understands safety and hazards of all ...
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)
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 3.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Sr. Officer - QC
Location: Vadodara
Experience: 2 - 3 Years
Industries: Pharma
Responsibilities:
Responsible for Documentation work in QC Department
Candidate must have knowledge of HPLC/GC
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, ...
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 ...