1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
🔑 Key Responsibilities
GMP Compliance
Ensure effective implementation of GMP guidelines across production, QA, QC, warehouse, and utilities.
Monitor day-to-day GMP activities and identify non-conformances.
Support GMP audits (internal, customer, and regulatory).
Documentation & Records
Prepare, review, and control GMP documents such as SOPs, formats, logs, and registers.
Ensure proper documentation practices (GDP) are followed.
Maintain training, deviation, ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities
Conduct routine chemical and physical tests on incoming raw materials, in-process samples, and finished products in accordance with SOPs and quality standards.
Perform analytical techniques including titration, pH measurement, and instrument-based analysis (e.g., UV-Vis, chromatography as required).
Accurately record, analyze, and interpret data; prepare test reports and maintain detailed laboratory documentation.
Ensure ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Sr. Officer - ADL
Location: Vapi
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
To follow Good Laboratory Practices.
Carry out routine analysis & Ensure documents pertaining to day to day analysis.
Calibrate instrument used for analysis as per SOP and maintain its record.
Method Transfer Activity.
Should have experience ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities:Quality Assurance & Control:ï‚· Oversee quality control activities in the Enamelling section for copper and aluminiumwires, strips, and CTC.ï‚· Ensure compliance with customer specifications, national/international standards(IEC, IS, NEMA, ASTM, etc.), and internal quality norms.ï‚· Monitor and verify raw material, in-process, and finished goods quality.ï‚· Conduct coating thickness, adhesion, flexibility, ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
6.00 LPA TO 8.00 LPA
R&D Job Responsibilities:
Conduct research to identify market trends and customer needs
Develop new products from concept to commercialization
Conduct feasibility studies and cost-benefit analysis to evaluate the viability of new product ideas.
Improve existing products through continuous research and testing
Collaborate with cross-functional teams to ensure product development meets business objectives
Monitor industry trends and ...
2 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 6.00 LPA
Position: QC Manager Location: Palanpur, Gujarat Industry: Pharma – API
Key Responsibilities:
Lead and oversee Quality Control operations in compliance with cGMP & regulatory guidelines.
Manage QC documentation, including qc document review, SOPs, and analytical records.
Supervise laboratory activities such as RM, PM, in-process, and finished product testing.
Ensure timely calibration, qualification, and maintenance of ...
30 Opening(s)
3.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Key Responsibilities:
Perform analysis and testing of Raw Materials (RM), Packaging Materials (PM), in-process samples, finished products, and stability samples as per pharmacopoeia standards.
Operate, calibrate, and maintain analytical instruments such as HPLC, GC, UV, IR, Dissolution Apparatus, etc.
Ensure timely release of materials/products with accurate and complete documentation.
Maintain records, calibration logs, data ...
2 Opening(s)
0 To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QC Lab Chemist
Location: Jhagadia nearby Ankleshwar
Experience: 0 - 3 Years
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 after ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
To ensure the work allocation All Quality control person.
To ensure the quality of raw material, packing material and finished product are compliant with the approved specification and GMP/GLP
Maintains accurate, complete, and timely documentation (analytical reports, logbook).
Ensure compliance with cGMP, GLP and regulatory standards. participate in internal audits, external regulatory inspection ...
1 Opening(s)
0.6 Year(s) To 3.0 Year(s)
Not Disclosed by Recruiter
📢 Urgent Hiring Jr. R&D ChemistQualifications: B.Sc or M.Sc with 2-3 years of experienceMinimum 2-3 years’ experience in Pharma or Chemical intermediates company.Location - Saykha
Job description:
* Execute multi step organic synthesis for target molecules as per given SOP* Optimize reaction conditions to improve yield, purity.* Purification technics by distillation, crystallization, ...