2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Saykha near by Bharuch
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of ...
1 Opening(s)
12.0 Year(s) To 18.0 Year(s)
20.00 LPA TO 25.00 LPA
Position: Sr. Manager - QC
Location: Ahmedabad
Experience: 12 - 18 Years
Industries: Pharma
Responsibilities:
Lead and oversee the entire Quality Control department operations.
Ensure compliance with cGMP, regulatory guidelines, and company quality standards.
Review and approve analytical methods, specifications, and validation protocols.
Supervise raw material, in-process, and ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Microbiologist
Location: Sarigam near by vapi
Experience: 3 -4 Years
Industries: Pharma Formulaction
Responsibilities:
Good Knowledge OF micro
Water validation
Area monitoring
Routine analysis of sample.
Validation of micro and preparation of protocol
Required Skills
Logical thinking.
Organizing.
Good in communication.
Required Qualification: - B.Sc/M.Sc - Microbiology
Salary :- Upto ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 8.00 LPA
Position: Sr. Officer/Executive Design & Development
Location: Daman
Experience: 5 - 8 Years
Industries: Pharma - Medical Device
Responsibilities:
Minimum experience of extrusion should be 3 years.
Handling hot melt extrusion machine and management of manufacturing through extrusion process in core plastic products.
Planning the feature development.
Working ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Officer
Location: Sarigam near by Vapi
Experience: 3 -5 Years
Industries: Pharma
Responsibilities:
To perform IPQA activities at shop floor in each and every stage of manufacturing and packing.
QA overview for clean room behavior and personnel hygiene .
Review of batch processing records.
Review of all ...
1 Opening(s)
7.0 Year(s) To 8.0 Year(s)
8.00 LPA TO 9.00 LPA
Position: Sr. Executive/Asst. Manager - Quality
Location: Silvassa
Experience: 7 - 8 Years
Industry: Packaging
Responsibilities:
Ensure product quality as per customer, ISO, BIS, and company quality standards.
Handle incoming, in-process, and final product inspections.
Maintain and implement Quality Management System (QMS) documentation.
Ensure compliance with ISO 9001, BIS, customer specifications, and ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
14.00 LPA TO 15.00 LPA
Position: Manager - Process & Proposal
Location: Ahmedabad
Experience: 10 – 12 Year
Industries: Chemical
Responsibilities:
Lead process design, sizing calculations and technology selection,
Prepare and review PFDs, P&IDs, layouts, hydraulic calculations, control philosophy, load list and design reports.
Handle tender and non-tender inquiries from receipt to submission.
Prepare BOQ/BOI, CAPEX/OPEX ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: Design Engineer
Location: Vapi
Experience: 1 - 2 Years
Industries: Engineering
Responsibilities:-
Machine design
Design, develop, and optimize machines for chemical process industries using SolidWorks and AutoCAD.
Prepare machine layouts for proposal team to bid for various projects.
3d modelling & drafting
Create detailed 3D models, technical drawings, and CAD files for ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: QC Executive (Reviewer)
Location: Vapi
Experience: 4 - 6 Years
Industries: Pharma
Responsibilities:
Experience in Method Validation and Stability Studies.
Review of electronic data, audit trails, and backup systems.
Expertise in qualification and calibration of analytical instruments such as HPLC, GC, ICP-MS, AAS, FTIR, and UV.
Hands-on experience in ICP-MS operation, ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QA Officer
Location: Acchad nearby Bhilad
Experience: 1 - 2 Years
Industries: Medical Devices
Responsibilities:
Review QC raw data, BMRs, STPs, and specifications.
Monitor compliance with cGMP, GLP, and documentation practices.
Conduct GMP training sessions and maintain related records.
Handle deviations, change control, CAPA, and non-conformance.
Perform self-inspections, audits, and ensure ISO compliance.
Familiarity with ...