1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
20.00 LPA TO 25.00 LPA
A Day in the Life
One of the key deliverables of MIDC is an electromechanical product that will be used in a clinical setting. We are looking for a Lead systems engineer who will work on capturing system requirements, concept design, system modelling, risk analaysis, system. Given the entrepreneurial nature of ...
2 Opening(s)
3.0 Year(s) To 4.0 Year(s)
6.50 LPA TO 8.00 LPA
Role:
• Preparation and review of Electronic Common Technical Document (eCTD), PSUR. PADER or RMP in compliance with EU and US standards and protocols.
• Write, edit clinical study protocols. clinical study reports, summary documents, investigator brochures, portions of regulatory briefing documents and development safety update reports.
• Drafting and revising pre-clinical summaries.
• ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 9.00 LPA
We have an urgent opening for the position of Asst. Manager / Manager – Quality Assurance Auditor for a leading producer of specialty chemicals for the Ambernath location.
Designation: Asst. Manager / Manager – Quality Assurance Auditor
Job Location: Ambarnath
Education: M.Sc./ B.Sc. with any Specialization Certificate in Pharma Audit
Skills: Familiar with applicable and appropriate regional ...
1 Opening(s)
10.0 Year(s) To 16.0 Year(s)
12.00 LPA TO 15.00 LPA
Position: Civil Project Manager
Location: Ahmedabad
Experience: 10 - 16 Years
Industries: Pharma
Responsibilities:
Project Planning and Management:
Lead and manage civil engineering projects from inception to completion, including greenfield (new facility construction) and brownfield (facility renovation and upgrades) projects.
Develop detailed project plans, schedules, and budgets, ensuring ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Job Purpose
To ensure high availability, reliability, and accuracy of automation, instrumentation, and control systems in the FMCG factory by effective maintenance, troubleshooting, calibration, and continuous improvement, as well complying with safety, quality requirements.
Key Responsibilities
Automation & Control Systems
Maintain and troubleshoot PLC, HMI, SCADA, VFDs, and Servo drives (Siemens / Allen ...
1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
23.00 LPA TO 37.00 LPA
HIRING: Production Operator II / III – OSD Manufacturing
π Chantilly, VA | π Onsiteπ 2nd Shift: 4:00 PM – 12:30 AMπ 3rd Shift: 12:00 AM – 8:30 AMβ° Overtime flexibility required
We’re looking for Skilled Pharmaceutical Production Operators with strong Oral Solid Dosage (OSD) / Solid Dose Manufacturing experience.
π Must-Have Experience
β
...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
11.00 LPA TO 12.00 LPA
Position: Store Manager
Location: Bhilad near by Vapi
Experience: 10 - 15 Years
Industries: Beauty/Personal Care
Responsibilities:
Oversee complete RM & PM store operations. And approving authority of Materials receipt, issuance and returns
Ensure compliance with GMP 22716:2007 ISO Standards and FDA Guidelines for of cosmetic industry ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 7.80 LPA
Position: Store Manager
Location: Vapi
Experience: 6 - 8 Years
Industries: Plastic
Responsibilities:
Manage end-to-end storage and handling of raw materials and packing materials.
Ensure timely availability of RM and PM for production as per the production plan.
Maintain accurate inventory records using ERP or inventory management systems.
Conduct ...
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)
15.0 Year(s) To 25.0 Year(s)
19.00 LPA TO 20.00 LPA
Position: AGM/GM - Quality
Location: Daman
Experience: 15 - 25 Years
Industries: Pharma
Responsibilities:
Site Quality Leadership:
To establish and maintain a robust Quality Management System (QMS) aligned with regulatory expectations.
To represent the organization as the Quality Management Representative during internal, external,
and regulatory inspections, ensuring successful outcomes and continuous compliance readiness.
Quality ...