2 Opening(s)
1.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 6.00 LPA
Perform scheduled Preventive Maintenance (PM) and rapid troubleshooting on AHUs, Chillers, Boilers, and associated mechanical and electrical controls.
Maintain validated cleanroom conditions, including monitoring pressure cascades and supporting HEPA filter integrity checks.
Document all maintenance activities accurately within the CMMS according to cGMP/SOP requirements.
Assist in HVAC Qualification (IQ/OQ/PQ) activities.
2-6 years of HVAC ...
2 Opening(s)
5.0 Year(s) To 8.0 Year(s)
4.00 LPA TO 6.00 LPA
Job Description: Microbiology Executive / Manager
We are looking for a dedicated Microbiology professional to manage and execute microbiological testing and related quality functions within our organization. The candidate will be responsible for conducting microbiology tests, ensuring environmental monitoring, and maintaining compliance with quality standards, with responsibilities varying based on experience.
Key ...
5 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 6.00 LPA
Operate, monitor, and maintain Compression machines (e.g., Parle Elizabeth – 37 Station & 51 Station).
Handle Coating machines (e.g., Gansons – 60 Pan) for tablet coating processes.
Manage Capsule filling machines (e.g., Pacifab LLP) ensuring accuracy and compliance.
Operate Liquid Filling & Manufacturing equipment (Liquipack) for syrup, suspension, or solution formulations.
Run Granulation equipment ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
Execute preventive and breakdown maintenance of all equipment's (Plant & Utility) as per respective equipment checklist and SOP.
Predictive Maintenance to Reduce Down Time
Ensuring that all activities are performed in accordance with cGMP, cGLP, Company SOP and health & safety policies at site.
Validation and Qualification of Equipment and Facilities.
Management of the ...
2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 7.00 LPA
Key Responsibilities:
Prepare, compile, and submit CTD/eCTD dossiers for EMA and DGMED (France) including new registrations, renewals, and variations.
Coordinate with internal teams (QA, QC, R&D, Supply Chain) for document collection and compliance.
Liaise with regulatory agencies and local representatives in the EU and France for query resolution and approvals.
Ensure dossiers and product ...
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 ...