Instructor - Pharmaceutical Sciences jobs in New Bedford, MA

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, Pharmaceutical Sciences or related field of study from an accredited college/university required.

- Master’s degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university preferred.

Schedule:

Monday - Friday, 11pm - 7:30 am

We offer competitive compensation packages, including benefits such as health insurance, retirement plans, and paid time off. If you are a dedicated professional with a passion for food production and have the skills necessary to excel in this role, we would love to hear from you. Apply today to join our team as a Production Supervisor.

Job Type: Full-time

Pay: $70,000.00 - $90,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• Night shift

Ability to Relocate:

• Fall River, MA: Relocate before starting work (Required)

Work Location: In person