About the job
The Manufacturing Projects and Systems Senior Supervisor is responsible for the development and maintenance of production systems and software. This position assesses operational needs and provides solutions to improve efficiency and compliance. This role is also responsible for execution of production projects and tracking / reporting of performance.
Responsibilities:
· Actively searches, creatively designs and implements software applications for manufacturing operations
· Supports the maintenance and the upkeep of these computerized systems.
· Develops software to align with production needs and improvements.
· Assists operations with projects to improve efficiency, output, and quality compliance.
· Tracks general projects within manufacturing in effort to prioritize them based on workload and demand.
· Reports project progress and timelines and assists the team to ensure completion on time.
· Provides training and guidance to novice production specialists.
· Works as a liaison between production, engineering, quality, analytical services, and validation to ensure alignment.
· Trains the trainers and manufacturing operators in any new processes that are developed.
· Solicts feedback from the operators to find improvements to productions processes.
· Authors standard operating procedures (SOPs)and Management of Change (MoC) documents, as necessary.
· Manages product metric tracking and reporting.
· Interface with regulatory agencies representing manufacturing and training systems.
Set yourself apart
Skills/Qualifications:
· BA/BS degree in a relevant field (Education, Social Science or related field) and/or 5 years of experience in manufacturing roles.
· Minimum of 3 years’ experience involved with production process engineering and manufacturing systems.
· Experience with learning and development or similar experience preferred.
· Experience interpreting compliance requirements and regulations is required.
· Knowledge of DEA, FDA and state regulations pertaining to manufacturing and handling of controlled substances.
· Must possess strong organizational skills and creativity.
· Experience with QMS management platforms and practices would be required, such a Master Control.
· Must also possess working knowledge of MS Office to include Word, Excel, and PowerPoint.
· Able to work in a fast-paced environment and to multitask effectively.
· Ability to organize and manage multiple projects.
· Previous experience operating under FDA cGMP with a robust understanding of the principles and applications associated with manufacturing operations.
What’s on offer?
We offer a dynamic environment where talent and ambition can develop to its fullest. We have an open and informal organization culture, where individuals need to have strong motivation and ability to work independently. Fagron is a widely expanding, international, professional, and ambitious pharmaceutical company with multiple growth opportunities. Job opportunity includes competitive salary, comprehensive benefits, performance package, and ability to be part of an international leader in an expanding industry.