1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
12.00 LPA TO 15.00 LPA
The Section Head for Food Instrumentation & Residue Analysis will be responsible for managingadvanced instrument-based testing operations for food and agricultural products, with a focus onpesticide residues, heavy metals, toxins, and other contaminants. The role demands strong technicalexpertise in modern analytical instruments, proven leadership in NABL-accredited laboratories, andeligibility as an ...
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, ...
3 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 6.00 LPA
Job Description
Sampling and testing of raw materials, intermediates and finished products using current specification and standard test procedure for chemical testing and instrumental techniques (HPLC, IR, UV), as appropriate
Preparing Quality reports, including analytical reports (for raw materials and finished products), Certificates of Analysis (CoA) (for finished products) and stability reports
Prepare ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.60 LPA TO 4.20 LPA
24.04.25
111624
HPS/2025/301
QA/QC Analytical Chemistry
Male
1
1 to 3
BSc Chem/MSc Chem
Core Responsibilities:
Conducting Analytical Tests:
Performing chemical and physical tests on raw materials, in-process samples, and finished products using
various analytical techniques like HPLC, GC, and spectroscopy.
Data Analysis and Interpretation:
Analyzing test results, identifying deviations from quality standards, and interpreting data to ensure
compliance with regulatory requirements.
Quality ...
1 Opening(s)
0 To 2.0 Year(s)
Not Disclosed by Recruiter
Job Title: Junior Chemist – R&DDepartment: Research & Development
Location: Sayakha GIDC, Bharuch.
Reporting To: R&D ManagerJob Summary:The Junior Chemist will support the R&D team in developing, testing, and optimizingchemical formulations and processes. This role involves hands-on laboratory work,data analysis, and collaboration with cross-functional teams to drive innovation inproduct development.Key Responsibilities:• Assist ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 10.00 LPA
Position: Chemist/Executive - QC (Mundra)
Location: Mundra - Kutch
Experience: 5- 10 Years
Industries: Chemical - MNC
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 ...
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)
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 ...