Will be:
Responsible for ensuring smooth functioning of contract third party manufacturing sites for manufacturing pharma formulations for in house as well outside parties.
Production Planning & Scheduling of products as per market requirements.
Price change implementation of products.
Inform raw/packaging materials shortages to Materials department for the next accounting period and ensure released materials are available for production.
Co-ordination and follow up with Materials, Quality operation, manufacturing artwork department.
Maintain strict accountability of materials with regards to receipt, storage and dispensing.
Co-ordinate documentation at Contract Manufacture locations.
Timely availability of Finished products at all C& F depots / customers.
Inventory RM / PM / FG in ERP for LL / THP.
Handle local FDA and WHO audits along with site QA.
Optimizes efficiency of the working environment of the group.
Drives daily and weekly progress toward completion of the production schedule right first time and on time.
Makes project/work assignments with communication of the expected timeline.
Ensures adherence to personnel and equipment SOPs and other regulatory requirements.
Ensures training of the group is timely and complete.
Provides process troubleshooting support as needed.
Monitors quality performance of the group and develops and implements action plans to achieve continuous improvement.
Effectively communicates with clients and internal groups.
Ensure availability of valid master documents at site.
Ensure availability of working standards, columns and other accessories at site as part of tech transfer.
Monitoring process validation.
Batch release.
Investigation related to market complaints, root cause identification and CAPA implementation.
Monitor Implementation of changes as per designated change control and closure of document.
Deviation handling and their closure of document.
To identify new third party as per the requirement of the Company.
To develop present third parties.
Project management responsibilities with regard to timely delivery of products and services.
To assist to find partners (contract manufactures) and to support them in getting the products manufactured as per regulated market quality standards / audits.
PLEASE NOTE: THIS POSITION WILL BE BASED AT SAKINAKA, ANDHERI (EAST), MUMBAI.
Naprod Life Science Pvt. Ltd.
https://www.naprodgroup.com
Naprod Life Sciences is a fast growing pharmaceutical specialty products manufacturing company. It has a comprehensive range of Oncology (Anti Cancer) products. It operates in domestic as well as overseas markets. It exports to around 30 countries. It has a WHO cGMP approved plant located at Boisar, Tarapur. It also has a dedicated Research and Development Centre at Dahisar. It is an ISO 9001:2008 Company
Contact Details
Recruiter Name:Aditya Malvankar
Email Address:
Reference Id:NAP - Cont Mfg./ Outsourcing - Trimbakkar - 2212