Manufacturing Supervisor - MDI
$76,000–$103,000 year
On-siteFall River, Massachusetts, United States
Job Summary
Schedule production processes, set specific targets, and delegate responsibilities to team members while managing performance and training employees to meet productivity standards. Conduct raw material reviews, perform weight checks, and operate scales for incoming and dispensed materials. Follow Master Batch Records for MDI packaging, set up and clean equipment, and complete accurate documentation in compliance with cGMP. Identify defects, report quality issues, and perform in-process testing and inspections. Support GMP investigations, contribute to SOP writing, and interface with Warehousing, Planning, Operations, and Quality management. Actively participate in team meetings and ensure compliance with safety, quality, and regulatory requirements.
Required Qualifications
- Bachelor's degree in pharmaceutical engineering, Pharmaceutical Sciences or related field of study from an accredited college/university
- One (1) to three (3) years of direct work experience in pharmaceutical manufacturing
- Proficiently speak English as a first or second language
- Ability to read, write and communicate effectively
- Ability to understand and analyze complex data sets
- A strong understanding of work discipline, Chain of Command and Teamwork
- Able to apply knowledge and experience to complex problems and offer recommendations
- High standards in Safety, Environmental, and Leadership
- Self-motivated, with the ability to work in a fast-paced manufacturing environment and handle multiple tasks simultaneously
- Good basic math knowledge and excellent attention to details
- Must be willing to work in a pharmaceutical manufacturing setting
- Must be willing and able to work any assigned shift ranging from first, second, or third shift
- Work schedule may be Monday to Friday, Tuesday to Saturday, or some combination thereof based on business needs
- Must be willing to work some weekends based on business needs as required by management
- Relocation negotiable
Desired Qualifications
- Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university
- 3+ years' experience in a pharmaceutical setting
- Experience using SAP business system and applications
- Experience in Inhalation products (MDI)
- Packaging with serialization
- Knowledge of good manufacturing practices and good documentation practices
- Basic computer skills (Word and Excel) – Intermediate
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.