1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Store Officer
Location: Daman
Experience: 0 - 2 Years
Industries: Pharma
Responsibilities:
Stores & Inventory Management
Receive, inspect, and store raw materials, packing materials, and consumables as per SOPs.
Maintain accurate stock records and perform daily/weekly/monthly stock reconciliations.
Ensure compliance with FEFO (First Expiry First Out) / FIFO ...
1 Opening(s)
5.0 Year(s) To 6.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: Formulation & Development Executive(R&D)
Location: Daman
Experience: 5 - 6 Years
Industries: Pharma
Responsibilities:
Develop and optimize injectable dosage forms (liquid, lyophilized, suspensions).
Conduct pre-formulation and formulation studies for parenteral products.
Prepare lab-scale and pilot-scale batches for injectable formulations.
Perform technology transfer from R&D to manufacturing.
Support scale-up, validation, and exhibit ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 4.50 LPA
Position : Maintenance Engineer
Location : Vapi
Experience: 3 - 5 Years
Industries: Chemical
Responsibilities:
Maintain API manufacturing equipment (reactors, centrifuges, dryers, pumps, mills)
Perform preventive, breakdown, and shutdown maintenance
Handle utilities: boiler, chiller, HVAC, compressed air, cooling tower
Ensure GMP, EHS, and SOP compliance
Maintain maintenance records, logs, and history cards
Support audits (USFDA/WHO) and ...
4 Opening(s)
2.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
Candidate must have experience from Pharmaceutical Industry and should be ready for traveling for site work across Gujarat and India also.
Execute CSV activities as per GAMP 5, 21 CFR Part 11, and EU Annex 11
Prepare and execute validation deliverables:
Validation Plan / VMP sections
URS, FS, DS
Risk Assessments (FMEA / Risk-based)
IQ, OQ, ...
3 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 4.00 LPA
The Quality Assurance professional is responsible for ensuring that pharmaceutical products are manufactured, tested, and released in compliance with GMP and regulatory requirements. The role focuses on documentation, compliance, audits, and continuous quality improvement.
Roles and Responsibilities
GMP & Compliance
Ensure compliance with GMP, GDP, GLP, and regulatory guidelines
Review and approve SOPs, BMRs, ...
5 Opening(s)
2.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.00 LPA
Key Responsibilities
Method Validation & Development
Perform method validation as per ICH Q2 (R1/R2) guidelines
Develop, optimize, and validate analytical methods for assay, impurities, dissolution, and residual solvents
Conduct method verification and method transfer activities
Prepare and review validation protocols and reports
Instrumentation & Analysis
Operate and maintain HPLC, UPLC, GC, and related detectors (UV, PDA, FID, ...
1 Opening(s)
7.0 Year(s) To 12.0 Year(s)
Not Disclosed by Recruiter
The job description is as below:
The R&D Manager - NDDS will lead formulation and development of novel drug delivery systems, from concept to scale up and tech transfer, ensuring compliance with regulatory and quality standards and alignment with business goals. The role requires strong scientific depth in NDDS, team leadership ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
Review and approve analytical results, COAs, test reports, and raw data.
Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
Review and update SOPs, STPs, GTPs, ...
1 Opening(s)
15.0 Year(s) To 25.0 Year(s)
30.00 LPA TO 35.00 LPA
Position: Engineering & Maintenance Head
Location: Vapi
Experience: 15 - 25 Years
Industries: Pharma
Responsibilities:
Strategic Engineering
Develop and implement engineering strategies aligned with business growth, plant expansion, and regulatory expectations.
Plan and execute capex projects including equipment upgrades, facility expansions, and energy-saving ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 6.00 LPA
Key Roles and Responsibilities
In the pharmaceutical industry, a Project Engineer's main responsibilities involve ensuring the technical work is completed safely, on time, within budget, and in compliance with stringent regulatory standards (like cGMP).
Project Planning & Execution
Prepare & review project schedule, P&ID, and GA Drawing.
Co-ordinate with cross functional teams. (Civil, ...