1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 18.00 LPA
B.Pharm / M.Pharm / B.Sc / M.Sc with specialization in Pharmaceutical Sciences or related
Minimum 10 years in sterile injectable manufacturing, with at least 3 years in leadership
Overall responsibility of sterile manufacturing operations including Liquid Ampoules, Liquid Vials, and Lyophilized Vials
Supervision of daily production activities ensuring compliance with GMP and regulatory ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position SummaryPlan and control material flow, production schedules and inventory to ensure seamlessoperations of all injectable lines.Key Responsibilities Prepare and maintain MRP schedules for APIs, excipients and packagingcomponents Coordinate purchase orders, expediting and vendor follow-ups to meet productiontimelines Track material consumption, buffer stocks and lead times; trigger reorders proactively Liaise ...
30 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 7.00 LPA
Responsible for Checking & distribution of approved artwork.
Responsible for colour approval of the shade card.
Responsible for the Allocation & Verification of the Pharma code.
Responsible for the Allocation & Verification of GTIN numbers as per GS1 guidelines.
Artwork management as per the product brief.
To verify artwork as per the Labelling Act.
To review ...
1 Opening(s)
15.0 Year(s) To 17.0 Year(s)
15.00 LPA TO 17.00 LPA
Sr. Manager- Quality Assurance (QA QC)
Job Responsibilities?:-
Planning and execution of daily QA, QC operation activities for production in Injectable section to smooth Functioning work culture.
To prepare and review the SOPs of QA QC departments. Ensure qualification/ validation status of equipment’s
QA, QC of Internal and external Manufacturing as per SOP.
Experience of handling ...
2 Opening(s)
4.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Production Officer (Greenfield Project)
Location: Daman
Experience: 4-5 Years
Industries: Pharma
Responsibilities:
Being a green field project, he will be part team for production department equipment’s URS and qualification documents preparation.
He will be Part of team for reviewed of technical documents for production department equipment’s.
He will ...
1 Opening(s)
8.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position : Assistant Manager Electrical (Project)
Location : Daman
Experience: 8- 12 Years
Industries: Pharma
Responsibilities:
Autoclaves, Medial fills
Vial washing filling sealing line
PFS filling and sealing line
Cartridge filling and sealing line
Lyophilizers and isolators
CIP SIP, visual inspection , Packing machines blister and cartoning, serialization, labelling
Manufacturing skid etc.
Above machine handling with multiple manufacturers.
I & Q of the ...
1 Opening(s)
7.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Project Manager – Pharma ProjectsAn Electrical or Mechanical Project Manager in the pharmaceutical industry manages theplanning, design, and implementation of formulation projects (OSD/Injectable) for newmanufacturing facilities, upgrades, or existing plants, ensuring compliance with strictindustry standards and regulations. Key responsibilities include design, contractorsupervision, cost management, and troubleshooting to support production processes, withsignificant overlap ...
1 Opening(s)
20.0 Year(s) To 25.0 Year(s)
20.00 LPA TO 25.00 LPA
Responsibilities and Duties Monitoring all purchase activities. Sourcing and procuring of all Engineering Materials ,Raw Materials & Packaging Materials for pharmaceutical formulation manufacturing plant located at Rudrapur. Developing new vendors & vendor evaluation. Inviting quotations, negotiating and finalizing pricing. Preparing comparison statements. Obtaining necessary approvals and processing purchase orders. Follow-up with ...
1 Opening(s)
12.0 Year(s) To 20.0 Year(s)
40.00 LPA TO 60.00 LPA
Position Summary
We are seeking an exceptional leader to drive operational excellence, scale manufacturing capabilities, and achieve global competitiveness while ensuring compliance with CDSCO, EMA, and EU MDR requirements.
Key Responsibilities
Oversee end-to-end manufacturing operations across all sterile/aseptic product lines
Scale production capacity to support 2X revenue growth through CMO partnerships and captive expansion
Drive ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 8.00 LPA
Oversee day-to-day production activities for formulation batches as per approved BMR/BPR.
Ensure compliance with cGMP, GDP, and regulatory guidelines (WHO, EU, USFDA, MHRA as applicable).
Monitor production planning, batch scheduling, material requirement, and manpower allocation.
Coordinate with QA, QC, Warehouse, Engineering, and RA for smooth production operations.
Review and ensure timely completion of batch ...