Pharmaceutical Production Supervisor

2 weeks ago

Fall River, United States Actalent Full time

Overview:
We are seeking a highly skilled and experienced Production Supervisor to join our team. As a Production Supervisor, you will be responsible for overseeing the day-to-day operations of our production facility, ensuring that all production goals are met and quality standards are maintained. This is a critical role in our organization, and we are looking for a dedicated individual who can effectively lead and motivate a team to achieve optimal results.

**Responsibilities**:

- 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 technical area.
- Understand and operates all necessary equipment and instrumentation to perform activities.
- Maintains documentation in accordance with internal procedures and regulatory requirements (i.e., GMP, SOPs etc.).
- Interfaces with appropriate Warehousing, Planning, Operations and Quality management to implement the procedural requirements as outlined and within internal operating procedures.
- 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 technical area.
- Understand and operates all necessary equipment and instrumentation to perform activities.
- Maintains documentation in accordance with internal procedures and regulatory requirements (i.e., GMP, SOPs etc.).
- Interfaces with appropriate Warehousing, Planning, Operations and Quality management to implement the procedural requirements as outlined and within internal operating procedures.

Qualifications:

- Minimum of 3 years of experience in a supervisory role within pharmecutical manufactuing or related field
- Bachelor’s degree in pharmaceutical engineering, Pharmaceuti

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