2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities
Process Development:
Design and execute multi-step organic synthesis experiments to develop new and innovative routes for API synthesis.
Conduct literature searches and patent reviews to identify non-infringing and commercially viable synthesis routes.
Optimize reaction parameters such as temperature, pressure, time, and solvent to improve yield, purity, and reduce costs.
Technology Transfer:
Prepare and document ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: QC Chemist (Dahej)
Location: Dahej
Experience: 4 - 5 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 appropriate analyses.
He should ...
5 Opening(s)
1.0 Year(s) To 2.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QC Officer
Location: Daman
Experience: 1 - 2 Years
Industries: Pharma Formulation
Responsibilities:
HPLC Analysis
Wet lab analysis
Good documentation skill
GC headspace knowledge, Installation
Sampling and testing of in-process and finished product.
Ensure all the work is performed and document accurately & complies as internal process and regulatory requirements.
Take care of daily calibration ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 17.00 LPA
Position : Associate Manager - QA/QC
Location : Vapi
Experience: 10- 15 Years
Industries: Chemical
Responsibilities:
Manage the QA and QC departments to ensure product quality, safety, and compliance with internal and external standards.
Develop, implement, and monitor Quality Management Systems (QMS) in line with ISO, and other regulatory guidelines.
Approve and review ...
3 Opening(s)
1.0 Year(s) To 4.0 Year(s)
1.80 LPA TO 3.00 LPA
Key Responsibilities
Testing and Analysis: Conduct raw material, in-process, finished product, and stability testing using HPLC, GC, UV-Vis, FTIR, and wet chemistry techniques.
Documentation & Compliance: Maintain accurate, timely records in LIMS and lab notebooks per GMP/GLP standards.
Instrument Calibration: Calibrate and maintain laboratory equipment (e.g., pH meters, refractometers, titrators).
Investigations: Investigate Out-of-Specification (OOS) results, deviations, and perform ...
3 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 4.00 LPA
Qualification: Bphama / Mpharma
Experience: Fresher
Designation: Traniee
Department: Quality Assurance
No of Vacancies: 3
CTC offered: 2.04 LPA
Gender Preference: Male / Female
Company Name: Dhyani Deva Consultancy
Company Location: bharuch
Interview Location: Panoli
Work Location: Panoli
Contact Person: dhyani Patel
Email ID of HR Person:
Any other Remarks by HR:
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 6.00 LPA
Position : Associate Manager - QA/QC(Tooling)
Location : Bharuch
Experience: 2- 5 Years
Industries: Chemical
Responsibilities:
Lead and manage the Toll Manufacturing activities to ensure product quality, safety, and compliance with SCIL specifications and guideline.
Monitor quality of raw materials, in-process, and finished product testing to ensure conformance with required specifications.
To ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Highlights
Department: Health, Safety, Environment & Quality (HSEQ)
Reporting To: Assistant Manager – QA/QC
Experience Required: 4–6 Years
Qualification: B.Sc in Quality or Engineering
Core Responsibilities:
Laboratory analysis of raw materials, finished goods & waste samples
Calibration & troubleshooting of analytical instruments
Documentation as per ISO 9001 standards
SOP, checklist & compliance management
In-process & finished product analysis
Inventory management ...
5 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 7.00 LPA
Vacancy: 01 Location: VAPI- GUJARAT Experience: 8 to 13 Years Qualification: B. Sc/ M. Sc- Micro/ Biotechnology with FDA Approval (Preference) Job Description: The ideal candidate will possess strong technical expertise in analytical instrumentation, regulatory compliance, and quality systems, with hands-on experience in RM, PM, and FG analysis. Key Responsibilities ...
5 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.50 LPA
Qualification & Experience
M.Pharm / M.S / B.S in Chemistry, Pharmaceutics or related discipline
3–5 years of experience in R&D (DQA)
Strong knowledge of GMP, GCP, GLP and 21 CFR 210/211
Experience with dermatology products or medical devices is an advantage
Key Responsibilities
Review development documents, analytical methods, R&D trials, lab notes, PDR, MFR, and batch ...