Manufacturing Supervisor - MDI

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.      Job Title : Manufacturing Supervisor - MDI  FLSA Classification : Professional, Exempt  Work Location : Fall River, MA Work Hours:  General: 8:30AM – 5:00 PM (may vary based on business needs) Reports To : Operations Manager Salary Range: $76,000 - $103,000 Purpose:   Invagen Pharmaceuticals is searching for experienced candidates for the position of Production Supervisor. This person will manage the production staff and oversee the production processes. Scope :                         The Production Supervisor ensures compliance with cGMP’s, InvaGen Pharmaceutical’s policies, standard operating procedures, and FDA requirements. The incumbent will serve as a key resource for conducting product complaints, supports packaging, packaging components within approved procedures and regulatory requirements. This position reports to the Site Lead/Operations Manager at InvaGen Pharmaceuticals, Inc, Fall River, MA.    The job duties for this position include but are not limited to the following : Schedule the production process, including setting specific targets for phases of production. Delegate responsibilities for production to team members and creating team leadership positions to oversee groups of employees. Manage performance and train assigned employees using Company systems, procedures, policies, practices, and other tools to meet established performance standards, productivity targets, and overall business requirements. Conduct performance assessments and compiling reports on the production process to identify areas where efficiency can be increased. Perform raw material and component review to ensure correct quantities, labeling and visual appearance. Perform weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging. Follow Master Batch Records for the packaging of MDIs dosage forms when required. Identify defects and report quality issues. Set up, operate, and clean in compliance with batch records and SOPs, packaging equipment. Clean and sanitize packaging equipment per SOPs. Complete accurate and timely documentation. Follow good documentation practices in accordance with cGMP. Perform in-process testing and inspections as required by Master Batch Record (weighing, visual inspection etc.). Effectively performs activities and applies knowledge in accordance with approved SOPs, company policies, regulatory requirements, schedules and provides technical expertise and direction to colleagues. Actively participate in Production team and Site communication meetings. Support GMP investigations and events. Contribute to Standard Operating Procedure (SOP) writing in…