Activities:
* Engages and supports Business Strategy
* Engages and supports Quality Vision and Quality Mission
* Ensures that GMP rules and regulations are followed
* Engages and supports Operations objectives
* Identifies emerging Operations-related issues and ensure communication within Operational department
* Supports cGMP manufacture based on his/her responsibilities as part of the MSAT department
Provides process know-how as well as scientific and operational
* Excellence expertise in connection with biopharma production.
Is responsible for the process transfer, production support, process
* Improvement and the correct subsequent process documentation.
* Defines Operational Manufacture Strategy and Objectives
* Implements a culture open for changes and new ideas, cooperative
* Teamwork and continuous improvement even outside the own area of responsibility
* Ensures proper execution of all people management activities including training, development
and retention of associates according to the needs of the production unit.
Leadership:
* Manages and coordinates the MSAT activities
* Responsible for recruitment, training, development, coaching, decisions and discipline issues of employees as well as resource and vacation planning
* Ensures a good information exchange from the upper management levels to his/her team and escalation of production issues.
* Accountable for the performance and the results in the area
Requirements:
* minimum of 3 years of work experience
* experience in cGMP/ GMP
* Proven experience in leadership (up to 10 people).
* experience in USP/DSP (preferred).
* experience working in Life Science companies.
