General Manager - Operations

We have been retained by a fast upcoming and highly reputed Pharma company to hire a "General Manager - Operations" to be based at Baddi (Himachal Pradesh). Details of the position are mentioned below:

• Company:

  Our client operates a WHO - GMP approved liquid oral manufacturing facility at Baadi (Himachal Pradesh). The company is a third party manufactures for Most of Top 50 Pharma companies in India.

• Designation:

  General Manager Operations

• Reporting to:

  Director

• Experience:

  10 - 20 years of similar experience with a reputed Pharma company.

• Main Task:

General Manager (GM) shall have responsibilities as enumerated below:

• To manage the manufacturing element of the organization ensuring high quality business activities with maximum efficiency, service and profitability for the organization.
• Ensuring that the team understands that the organizations profits and achievements are reflected in all its operations and activities including relationships and risk management.
• To maintain overall organization responsibility for performing all duties in compliance with related manufacturing legal/statutory regulations, professional duties, responsibilities and obligations and insert as applicable e.g. Current Good Manufacturing Practices (cGMP), Best Practice Guidelines & WHO-GMP certification.
• To manage, direct and monitor the overall performance of the organization.
• To design and set up the Quality Management System.
• To maintain and improve mechanisms for manufacturing and all organization activities, including surveying and measuring the manufacturing operations, process, outcomes and profitability and disseminate feedback to the appropriate internal entities.
• Accountable for day to day activity of manufacturing and testing.
• To support all other departments in matters related to manufacturing, e.g. procurement of materials (RM & PM).
• To lead preapproval inspections and final inspections of all Regulatory authorities.
• Work allocation of all department heads and monitoring of their work.
• To discuss all observation with dept. heads and to plan the actions accordingly.
• To initiate the cGMP compliance norms.
• To conduct internal audits/self-inspection periodically, to ensure strict quality standards.
• To ensure SOP`s compliance by HODs on continuous basis.
• To set an example for team members of commitment, manufacturing process expertise, work ethics and habits and personal character.
• To interact and co-operate with all members of the organization, its suppliers and customers
• Authorizing authority for specification of equipments, instruments, systems to be procured.
• Liaison with FDA Authorities.
• Training to all subordinates.
• Authorization of all documents concerned to Production, Maintenance, Quality Control, Quality Assurance & other process.
• To ensure implementation & compliance of Quality Standards in every stage of manufacturing.
• cGMP documents Control & Monitoring.
• To ensure timely release of finished goods.
• Interaction with manufacturers, suppliers and vendors.
• To oversee validation and responsible for supervising, monitoring and ensuring all the matters related to validation.
• To ensure authorization & certification of all the validation documents.
• To provide the Price List based on mail received from party.
• Evaluation and introduction of new product.

• Other Task:

• Approving of vendor credentials of qualifications, professional competence, solvency, market standings etc.
• Ensure quality systems through management.
• Attending to market complaints through proper investigation & sorting out matters.
• To get actively involved in the design and construction of pharmaceutical manufacturing facility to comply with the regulatory agencies.
• To interact with external consultants/agencies.
• Preparation for inspection by external bodies.
• You are responsible for your allocated workload and must meet all targets as agreed with your Line Manager. You must contribute towards the smooth running of the organization generally.

• Any Other Work Assigned

  :

  Any other task assigned by the Director from time to time.

Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated resumes to sudhirvinayak@gmail.com

In case of a query, please feel free to speak to the undersigned

Sudhir Vinayak,

Director, Pharma Placements Inc.

Mobile no.: 98202 34987