2 Opening(s)
1.0 Year(s) To 6.0 Year(s)
0.00 LPA TO 3.00 LPA
Perform data entry, maintain databases, and update records.
Handle documentation, filing, scanning, and correspondence.
Support HR, accounts, and operations teams in administrative tasks
Manage schedules, appointments, and office communication.
Maintain confidentiality of company information.
Perform any other administrative duties assigned by management.
Good knowledge of MS Office (Word, Excel, PowerPoint).
Strong communication (written & verbal) and organizational ...
1 Opening(s)
1.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
The job description is as below:
To perform High Performance Liquid Chromatography analysis for various pharmaceutical tests including Related Substances, in compliance with 21 CFR Part 11 and cGMP guidelines. The role includes calibration, troubleshooting, integration, and data review activities related to HPLC.
Key Responsibilities:
Perform routine and non-routine HPLC analysis for Assay, Related Substances, Content Uniformity, and other quality ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: FAT Engineer
Location: Kalol - Gandhinagar
Experience: 2 - 5 Years
Industries: Engineering
Responsibilities:
Final Assembly Testing of all equipment at our factory.
Travel all over India and export for service activity of pharma lab machines.
Check job related documents like MOM, Packing list, Compliance, utility check list ,P&ID and ...
1 Opening(s)
2.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
• Responsible for piping activities & Erection activities as per P&ID, ISO & GA drawing
• Responsible for the erection of equipment like Chiller, Boiler, Reactors, Cooling tower, ANFD, Centrifuge, ETP & RO unit.
• Responsible for commissioning activities & pre start up activities: Pneumatic/ Hydro as per process requirement.
• Responsible for ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
0.00 LPA TO 3.60 LPA
Develop, review, and update QA processes, checklists, and standard operating procedures (SOPs).
Prepare and maintain quality documentation such as test plans, inspection reports, and audit findings.
Conduct inspections, audits, and product tests (manual or automated depending on industry).
Verify compliance with specifications, standards, and regulatory requirements.
Identify, document, and track defects or nonconformities.
Collaborate with ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
18.00 LPA TO 20.00 LPA
Position: Asst/Dy. Manager - R&D (Design & Development)
Location: Faridabad
Experience: 8 - 15 Years
Industries: Pharma
Responsibilities:
Product Innovation & Technical Leadership
Lead design and development of advanced orthopaedic implants and instruments, focusing on innovation, clinical performance, and patient outcomes.
Identify clinical needs and market trends, ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: QA Executive
Location: Vapi
Experience: 2 - 3 Years
Industries: Pharma API
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 ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Manager - QC
Location: Daman
Experience: 10 -15 Years
Industries: Pharma
Responsibilities:
To ensure smooth Quality & Inspection function in Incoming RM,PM & Packaging Material.
To ensure Smooth In Process Quality & Inspection function for Semi-Finished Product.
To ensure smooth Finish Good Quality & Inspection function for Finish ...
1 Opening(s)
20.0 Year(s) To 25.0 Year(s)
25.00 LPA TO 30.00 LPA
Position: Production Head
Location: Ahmedabad
Experience: 20 - 25 Years
Industries: Pharma
Responsibilities:• Responsible Accountable over all Operations. (Like Production, QA,QC,Engineering Maintenance Projects, Process, EHS Administration function)• Responsible for Profit Loss of Sites from Operations Point of View.• Responsible for handling End to end ...
3 Opening(s)
2.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
Prepare and review SOPs; ensure adherence to cGMP and QMS standards.
Receive, verify, and record materials from vendors; maintain stock registers and monthly reports.
Monitor inventory levels, reconcile discrepancies, and ensure timely stock availability.
Coordinate with purchase, QC, and production teams for smooth workflow and batch planning.
Oversee dispatches, packing, loading/unloading, and site material ...