1 Opening(s)
15.0 Year(s) To 25.0 Year(s)
15.00 LPA TO 20.00 LPA
To review and implement a Quality Management System for cGMP compliance at the Production (Injectable) plant.
To prepare, Review and Approve BMR, BPR and related documents.
Handling of Caliber QAMS, DMS, Nichelon 5 CMS, Dynamic, Schedule and Track and trace Serialization & aggregation.
Giving the required training also Responsible for Media fill and ...
1 Opening(s)
5.0 Year(s) To 6.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Executive/Asst. Manager - Project
Location: Ahmedabad
Experience: 5 - 6 Years
Industries: Pharma
Responsibilities:
Project Management:
Lead and manage engineering projects involving mechanical and electrical systems for the injectable plant.
Develop project plans, timelines, and budgets, ensuring projects are completed on schedule and within financial constraints.
System Design and ...
1 Opening(s)
6.0 Year(s) To 7.0 Year(s)
7.00 LPA TO 8.00 LPA
Position: Sr. Executive - Project
Location: Ahmedabad
Experience: 6 - 7 Years
Industries: Pharma
Responsibilities:
Project Management:
Lead and manage engineering projects involving mechanical and electrical systems for the injectable plant.
Develop project plans, timelines, and budgets, ensuring projects are completed on schedule and within financial constraints.
System Design and Integration:
Collaborate ...
2 Opening(s)
10.0 Year(s) To 20.0 Year(s)
10.00 LPA TO 18.00 LPA
Assisting in identifying and closing sales opportunities by providing technical assistance relating to Company's products
to multi-national business teams, key development accounts and other assigned customers.
Providing product and technical support, and recommendations concerning Company's products, services, and developing
application formulation for the customers including working on product development/ formulations.
Technical interface with the ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Store Manager
Location: Ankleshwar, Gujarat Budget: ₹10 LPA
Position Summary Oversee receipt, storage, issue and custody of all raw materials, packing materials and finished goods for injectable production.
Key Responsibilities
Supervise inward inspection, material identification, labelling and storage as per storage conditions
Maintain accurate inventory records (ERP/bin cards) and conduct periodic physical audits
Manage material issue ...
2 Opening(s)
3.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Position Summary
Execute day-to-day production activities under supervision of the Production Manager,
ensuring batch integrity and documentation accuracy.
Key Responsibilities
Monitor process parameters (temperature, pressure, cycle time) and record data in
BMRs/BPRs
Accurately complete BMRs and BPRs; assist in their validation and internal audit activities
Identify and report deviations or equipment faults to Production ...
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 ...
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 ...
1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
Not Disclosed by Recruiter
Lead and optimize end-to-end sterile injectable production, ensuring cGMP compliance, on-time delivery and continuous process improvement.
Production Planning and Inventory Control.
To carryout day to day production activities like Manufacturing, washing, sterilization, Powder Mixing, Filling, Visual inspection and Packing and monitoring all activities assign down line people.
To ensure that running product and produced ...