The Production Supervisor prepares work schedules, assigns work, and oversees the work product. Supervises and coordinates the work of employees who work on assembly-lines. Being a Production Supervisor requires a high school diploma or its equivalent. Ensures operations and employees follow proper policies and procedures. In addition, Production Supervisor typically reports to a manager. May require certain certifications in field. The Production Supervisor supervises a small group of para-professional staff in an organization characterized by highly transactional or repetitive processes. Contributes to the development of processes and procedures. Thorough knowledge of functional area under supervision. Working as a Production Supervisor typically requires 3 years experience in the related area as an individual contributor. (Copyright 2024 Salary.com)
Job Title : Production SupervisorWork Location : Fall River, MAWork Hours : General : 3rd ShiftReports To : Manager, ManufacturingClient Overview : Our client is a leading pharmaceutical company dedicated to producing high-quality products that contribute to the well-being of patients.
We are currently seeking a qualified candidate for the position of Production Supervisor at our Fall River, MA facility.
Position Overview : The Production Supervisor will play a crucial role in managing the production staff and overseeing the production processes.
This position requires a candidate with a strong background in pharmaceutical manufacturing, attention to detail, and the ability to ensure compliance with cGMPs, company policies, standard operating procedures, and FDA requirements.
Manage and train assigned employees to meet performance standards and overall business requirements.Conduct performance assessments and compile reports for process efficiency improvement.
Perform raw material and component reviews to ensure compliance with established procedures.Operate and clean packaging equipment in compliance with batch records and SOPs.
Complete accurate and timely documentation following cGMP and good documentation practices.Participate in Production team and Site communication meetings.
Support GMP investigations and events.Contribute to Standard Operating Procedure (SOP) writing in the technical area.Ensure compliance with safety, quality, productivity, and performance expectations.
Qualifications : Bachelor's degree in pharmaceutical engineering, Pharmaceutical Sciences, or related field required.Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field preferred.
1-3 years of direct work experience in pharmaceutical manufacturing.Understanding of machines used in pharmaceutical manufacturing.
Capable of conducting troubleshooting, investigations, and root cause identification and analysis.Experience in Inhalation products (MDI) is a plus.
Packaging with serialization preferred.Technical Knowledge And Computer Systems Skills : General ability to perform basic to complex mathematical computations.
Experience using SAP business system and applications is a plus.3 years' experience in a pharmaceutical setting preferred.#J-18808-Ljbffr
Last updated : 2024-03-06
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