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)
0 To 5.0 Year(s)
1.50 LPA TO 5.00 LPA
🔹 Key Responsibilities:
Execute day-to-day operations in aseptic and sterile manufacturing areas
Monitor LVP production activities in compliance with SOPs, cGMP, and regulatory guidelines
Operate and maintain critical equipment including autoclaves, filling machines, and sterilizers
Ensure strict adherence to safety, quality, and environmental standards
Prepare, review, and maintain batch production records and related documentation
🔹 Qualifications ...
5 Opening(s)
1.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 7.00 LPA
Position: QA Asst Manager ( OSD , ORAL LIQUID & OINTMENT FACILITY) Position: QA Asst. Manager Vacancy: 01 Location: VAPI- GUJARAT Experience: 10 to 15 Years Qualification: B. Pharma / M. Pharma Core Technical Expertise: ï‚· IPQA (In-Process Quality Assurance): Hands-on experience in monitoring manufacturing and packaging processes, line clearance, ...
6 Opening(s)
2.0 Year(s) To 3.0 Year(s)
4.00 LPA TO 7.00 LPA
Position: R&D Executive
Location: Ankleshwar
Experience: 3 - 5 Years
Industries: Chemical
Responsibilities:
Experience in handling chemicals and solvents at laboratory scale.
He should be conversant for preparing mass balance, SOP writing.
Good in multi step synthesis.
Good knowledge of chemistry and prepare to work independently.
Helping in Trail batch preparation, to co ...
50 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 10.00 LPA
🎯 Key Responsibilities:
Operate and monitor plant processes through Distributed Control System (DCS)
Handle continuous & batch process operations from control room
Monitor critical parameters like temperature, pressure, flow, level
Ensure safe handling of exothermic reactions / bromination processes
Maintain production targets as per shift plan
Coordinate with field operators for smooth operations
Maintain batch records & ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 6.00 LPA
🔑 Key Responsibilities:
✅ Handle complete shift production activities ✅ Monitor batch charging, reaction parameters, filtration, drying & packing ✅ Supervise operators and contract manpower ✅ Ensure adherence to SOP, BMR & safety guidelines ✅ Maintain production logbook & shift reports ✅ Coordinate with QA/QC, Maintenance & EHS departments ✅ Handle ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Urgent opening for warehouse officer in Kadodar, Jolwa location at Surat.
Experience : 2-5 years
Salary 3-4 LPA
Qualification: any graduate
Industry : from pharmaceutical & Chemical industry only
Responsible for Receiving, Storage, Dispensing / Issuance of the Raw Material,
Packing Material , General Material.
ï‚· The candidate must have hands-on experience in API industries warehouse operations ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
10.00 LPA TO 12.00 LPA
Role DefinitionManager – System Setup & Migration, Internal Audit requires to lead and manage ERP system migration and support, process automation, and system integration across departments, Internal Audit of Processes @ Plants / HOKey Skills1. Strong knowledge of ERP systems (SAP / Oracle / Tally / Finsys / etc.)2. Experience ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.50 LPA TO 4.50 LPA
Position: QA Officer
Location: Silvassa
Experience: 3 - 4 Years
Industries: Chemical
Responsibilities:
Ensuring Compliances:
Quality Assurance professionals play an important role in ensuring that all processes & product comply with QMS/IMS and other relevant regulations.
Quality Control:
Quality Assurance professionals involved in the development, maintenance & implementation of procedures ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
IPQA activities, Plant round, Online BMR review, Line clearance, Samplingof APIs, Analytical data review, Batch release, APQR preparation. People who have faced regulatory audits like EDQM would be givenpreference.
Process & cleaning validation, including cleaning matrix preparation
QMS documentation management; SOP preparation, review, and training
IPQA activities
to ensure GMP compliance during manufacturing.
Regulatory inspection exposure ...