CVC Executive

To implement and follow loading chart as per monthly packing plan.
- To co-ordinate with stores for availability of Packing Material.
- To carry out In-process checks and challenges of blister packing line, bottle packing line (CVC) and bulk packing line.
- Supervision of all Packing activity & maintain all documents related to packing area as per cGMP.
- To ensure that environmental conditions, as specified are achieved and maintained in the respective areas.
- Review **Master **documents such as **Batch Packing Records.**:

- To perform **SAP** transactions related to packing.
- To carry out** Redressing and Repacking** activity and documents of the same.
- Maintain of all document related to area as per cGmp.
- To carry out various packing activities like primary packing and secondary packing as per SOP and cGMP.
- Proper manpower allocation and utilization.
- Creation of **Product Master (Label creation) **in **Track and Trace system **and doing **Batch request **of same.
- To review documents like **BPR** and **logbooks**.
- To carry out the **Packing validation study** for the new commercial batches of **blister **and **bottle** packing line.
- To perform data integrity risk assessment of equipment **(DIRA).**:

- To Review the **Audit trial** as per planner.

To perform computer system validation **( CSV).**
- Role:_Management - Other
- Salary:_ Not Disclosed by Recruiter
- Industry:_Pharmaceutical & Life Sciences
- Department:_Production, Manufacturing & Engineering
- Role Category:_Management
- Employment Type:_Full Time, Permanent
- Key Skills
- CVCBulk packing
- OSDPackingRegulated market
- Skills highlighted with ‘‘ are preferred keyskills

Education
- UG:_B.Pharma in Any Specialization

**Company Profile**:
Marksans Pharma

Marksans Pharma Ltd has established world-class manufacturing facilities by leveraging state-of-the-art technology, incorporating best practices and adhering to stringent regulatory compliances. Our plants are approved by prestigious US FDA, UK MHRA, Australian TGA and other foreign health authorities.

Our R&D capabilities include dossier development, chemical synthesis, process optimization, formulation development, analytical development and conducting stability studies. We have a team of over 50 experienced scientists specializing in formulation development and analytical development.

We possess end-to-end capabilities from Lab scale development to Pilot scale up and from commercializing the product for large scale manufacturing to marketing globally.

The company has achieved global recognition within a very short span of time and has major global expansion plans for the near future.