2 Opening(s)
1.0 Year(s) To 7.0 Year(s)
Not Disclosed by Recruiter
Responsibilities:
Independently plan, execute, and monitor laboratory-scale reactions for new product development or process improvement.
Troubleshoot reaction-related issues and optimize parameters to achieve desired yields and purity.
Conduct analytical testing using spectroscopy techniques (IR, NMR, UV, etc.) and interpret data for structural confirmation.
Maintain detailed experiment records, observations, and analytical results in lab notebooks.
Support ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.88 LPA TO 3.00 LPA
Key responsibilities
Conduct physical and chemical tests on coal samples, including proximate analysis, ultimate analysis, and GCV (Gross Calorific Value).
Use and maintain laboratory equipment, ensuring it is calibrated and functioning correctly.
Sample and analyze other materials like input chemicals, by-products, and waste.
Prepare laboratory solutions, compounds, and reagents.
Maintain detailed records of tests, sample ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
6.00 LPA TO 7.00 LPA
Job title:Quality Assurance Chemist
Name of job holder:
Department/service:QA/QC
Signature job holder & date:
Signature hierarchical head & date:Manager - QA
Signature functional head & date:Head - QM
A. Purpose /Role of the job /: Describe in 1 phrase what contribution the job is expected toMake to the organisation’s objectives Quality Assurance of Finished Goods (SAN/ABS/ASA/PS) ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 6.00 LPA
FARMSON BASIC DRUGS PRIVATE LIMITEDNANDESARI, VADODARA.
JOB RESPONSIBILITY
Name of the Employee: Employee No.:Designation : Officer/Sr. Officer/Executive Department: QCQualification: M. Sc. Chemistry Experience: 3 to 5 YearsDate of Joining: Revision No.:Unit Effective Date:Reporting to :
FCQA-019/B/00 Page 1 of 3Sr. No. Job Responsibility1. Follow Good Laboratory Practices (GLP), safety norms, and housekeeping while ...
4 Opening(s)
1.0 Year(s) To 8.0 Year(s)
1.50 LPA TO 6.00 LPA
Key Responsibilities:
Analytical Operations:
Perform routine and non-routine analysis using HPLC, GC, UV and other instruments.
Conduct and support analytical method validations as per regulatory requirements.
Review and approve analytical data, test reports, and batch release documents.
Ensure proper calibration and qualification of laboratory instruments.
QMS & Compliance:
Manage Quality Management System (QMS) activities including:OOS, Deviations, CAPA, ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.40 LPA TO 5.00 LPA
The Project Coordinator is responsible for planning, tracking, and coordinating pharmaceutical laboratory projects across departments such as R&D, Quality Control, Regulatory Affairs, and Production. The role ensures timely execution of tasks, documentation, and compliance with industry standards and project deadlines.
🎯 Key Responsibilities:
Coordinate day-to-day activities of pharmaceutical lab projects (R&D, method ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
2.60 LPA TO 4.00 LPA
Key Responsibilities:
Perform routine and non-routine analysis using LC-MS or LC-MS/MS techniques for pharmaceutical, biological, or chemical samples.
Conduct method development, optimization, and validation as per ICH or regulatory guidelines.
Prepare standards, reagents, QC samples, and analytical test samples according to protocols and SOPs.
Operate and maintain LC-MS instruments (e.g., Agilent, Waters, Thermo, Sciex).
Interpret ...
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, ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: QC Executive
Location: Silvassa
Experience: 6 - 10 Years
Industries: Pharma
Responsibilities:
Analytical Testing:
Perform routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples using HPLC, GC, UV, IR, etc.
Conduct assay, dissolution, impurity profiling, and related substance testing as per pharmacopeial standards (USP, BP, IP, etc.).
Instrument Operation & ...
1 Opening(s)
4.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
Job Responsibilities
• Analysis of Finished products / raw materials/ in process & stability samples (Wet & Instrumentalanalysis).
• Preparing stability trend of finished products and then sharing with all stake holders.• Calibration of HPLCs & GC, Lab instruments as per defined procedure and schedule..• Method validations as per applicable guidelines.• Inventory ...