MDI Manufacturing Supervisor | GMP Leadership

Aequor; Fall River (MA); On-site; USD 80,000 - 110,000; Full time

Job summary

Aequor's Manufacturing Supervisor in Fall River, MA oversees cGMP-compliant manufacturing of metered-dose inhalers and packaging operations, ensuring adherence to FDA requirements and SOPs. This Onsite, Full-Time role reports to the Site Lead/Operations Manager and leads a team to meet production targets while maintaining quality and documentation practices.

Responsibilities span production scheduling, team leadership, batch record review, quality checks, safety compliance, audits, and

Qualifications

• Bachelor's degree in pharmaceutical engineering or related field.
• Pharmaceutical industry experience.
• Master's degree in Pharmaceutical Engineering preferred.

Responsibilities

• Schedule production processes and set targets for production phases.
• Delegate production responsibilities and develop team leadership.
• Train and manage staff to meet performance and productivity standards.
• Perform material reviews, weight checks, and batch record compliance.
• Identify defects and report quality issues; maintain GMP documentation.
• Support SOP writing and participate in site communications and investigations.

Skills

Leadership

Quality Assurance

cGMP

Regulatory Compliance

Problem Solving

English

MDI Inhalation

Data analysis

SAP

Education

Bachelor's in Pharmaceutical Engineering

Master's in Pharmaceutical Engineering

Tools

SAP

Microsoft Excel

Job description

Aequor's Manufacturing Supervisor in Fall River, MA oversees cGMP-compliant manufacturing of metered-dose inhalers and packaging operations, ensuring adherence to FDA requirements and SOPs. This Onsite, Full-Time role reports to the Site Lead/Operations Manager and leads a team to meet production targets while maintaining quality and documentation practices.

Responsibilities span production scheduling, team leadership, batch record review, quality checks, safety compliance, audits, and