5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Key Responsibilities:
Documentation Management:
Review, approve, and control various quality documents, including Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), Specifications, Test Procedures (STPs), and other quality-related documentation.
Ensure proper archiving, retrieval, and revision control of all controlled documents.
Participate in the preparation and review of site master files (SMF), ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 4.20 LPA
Position: Sr. Officer/Executive - QC
Location: Vapi
Experience: 3 - 5 Years
Industries: Pharma
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), ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 15.00 LPA
Quality Control department functions for assuring the quality of all the batches manufactured,at every stage of manufacturing/processing excipients and drug products. Sampling, inspection & testing as per specifications of Raw material for release or rejection& its documentation. Sampling, inspection & testing as per specifications of packaging material for release ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.20 LPA TO 1.80 LPA
HPLC (Operation and Troubleshooting)
stability study as per ICH Guideline.
Dissolution apparatus operation and method development.
AMV analytical method validation
analyze the Raw materials, In-process and intermediates finished product and stability samples as per respective test procedures.
To perform the daily calibration of Instruments/Equipments.
To review raw materials, in process, intermediate, finished products, packing material, stability, ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
2.40 LPA TO 3.00 LPA
HPLC (Operation and Troubleshooting)
stability study as per ICH Guideline.
Dissolution apparatus operation and method development.
AMV analytical method validation
analyze the Raw materials, In-process and intermediates finished product and stability samples as per respective test procedures.
To perform the daily calibration of Instruments/Equipments.
To review raw materials, in process, intermediate, finished products, packing material, stability, ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
1.80 LPA TO 3.00 LPA
We have Urgent Opening for the following position:-
Please take it on Priority and all candidates should be from chemical and pharma background.
1) R&D Officers(Number of Opening-4)/
2) Deputy Manager/ Manager(Number of Opening-1)
Required Qualification-M.sc Organic Chemistry Compulsory
For officer minimum experience should be 3 to 7 Yrs and
for Assistant Manager /Manager minimum experience should ...
1 Opening(s)
0 To 3.0 Year(s)
1.80 LPA TO 2.40 LPA
1. Position- R&D Chemist/Officer2. Qualification- M. Sc /M. Pharm3. Experience-3-4 yrs.4. Responsibility? Handling of analytical instruments like HPLC, UV, titration, pH meter, Rheometer etc? Carry out the analytical development, analytical method validation or analytical workand prepare the reports for bulk, finish and rawmaterials.? Prepare stability protocols, schedules and carryout the ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 4.20 LPA
Position: Executive/Asst. Manager - QA
Location: Silvassa
Experience: 2 - 10 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing.
Manage quality systems, audits, documentation, validations, and batch release while leading the QA team.
Implement and maintain Quality Management ...
5 Opening(s)
5.0 Year(s) To 15.0 Year(s)
4.00 LPA TO 15.00 LPA
Job Description:* To ensure all relevant quality related documents are prepared, approved, implemented and followed.* Assuring that the right quality products reach the customer.* To ensure critical deviations are investigated and resolved.* To lead the internal audits and external periodically and follow up actions for its Compliances.* To identify gaps ...
1 Opening(s)
7.0 Year(s) To 12.0 Year(s)
7.00 LPA TO 10.00 LPA
Position: Executive/Sr. Executive - Production
Location: Daman
Experience: 7 - 12 Years
Industries: Pharma Formulation
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, ...