Manufacturing Supervisor - MDI

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 technical area.
• ◆Understand and operates all necessary equipment and instrumentation to perform activities.
• ◆Maintains documentation in accordance with internal procedures and regulatory

(i.e., GMP, SOPs etc.).

• ✓Interfaces with appropriate Warehousing, Planning, Operations and Quality management to implement the procedural

as outlined and within internal operating procedures.

• ✓Performs activities for manufacturing (i.e., batch record review, packaging line clearances and manufacturing room clearances, deviations, etc.).
• ✓Comprehend and adhere to all pertinent EHS regulations, policies and procedures and the required use of all approved and issued Personal Protective Equipment.
• ✓Responsible for compliance with documentation and accountability procedures and policies, maintaining high alert to diversions.
• ✓Demonstrate a level of consciousness to safety and health related activities as evident by the daily application of

specific to job function; recognize safety and health related issues and report to management.

• ✓Independently searches, gathers, and presents information to support compliance with regulations and internal systems.
• ✓Ensure and compliance with safety, quality, productivity, and performance expectations and execution of manufacturing and packaging operations.
• ✓Follow strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Manufacturing Practices (cGMP), complying with legal regulations, monitoring environment.
• ✓Perform other duties as assigned.

• ✓Bachelor’s degree in pharmaceutical engineering, Pharmaceutical Sciences or related field of study from an accredited college/university required.
• ✓Master’s degree in Pharmaceutical Engineering,