Pharma Manufacturing Supervisor - MDI Packaging

Cipla; Fall River (MA); On-site; USD 76,000 - 103,000; Full time

Job summary

Cipla, via its Invagen Pharmaceuticals unit, is seeking a Manufacturing Supervisor for the Fall River, MA site to oversee MDI production and staff. The role ensures cGMP and FDA regulatory compliance while coordinating production schedules and process improvements.

The candidate will lead a team, document processes, perform material checks, and support quality investigations in a fast-paced pharmaceutical manufacturing environment.

Qualifications

• Bachelor’s degree in pharmaceutical engineering or related field from an accredited college/university.
• Master’s degree preferred in related field.
• 1–3 years of direct pharmaceutical manufacturing experience.

Responsibilities

• Schedule production processes and set targets for production phases.
• Delegate responsibilities and create team leadership positions.
• Train staff and monitor performance to meet productivity targets.
• Ensure compliance with cGMP, SOPs and FDA requirements.
• Maintain documentation and support quality investigations.

Skills

Team leadership

Quality compliance

cGMP knowledge

Safety awareness

Problem solving

Data analysis

Education

Bachelor’s degree in pharmaceutical engineering, Pharmaceutical Sciences or related field

Master’s degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field

1–3 years of direct work experience in pharmaceutical manufacturing

Tools

SAP

Instrumentation knowledge

Excel

Job description

Cipla, via its Invagen Pharmaceuticals unit, is seeking a Manufacturing Supervisor for the Fall River, MA site to oversee MDI production and staff. The role ensures cGMP and FDA regulatory compliance while coordinating production schedules and process improvements.

The candidate will lead a team, document processes, perform material checks, and support quality investigations in a fast-paced pharmaceutical manufacturing environment.