Production/Manufacturing Supervisor
I am working with a dynamic and innovative pharmaceutical company committed to advancing healthcare through cutting-edge research, development, and manufacturing. They have state-of-the-art facilities and a dedicated team drive our mission to deliver high-quality pharmaceutical products to improve patient outcomes worldwide.
My client is seeking a passionate Production/Manufacturing Supervisors to join their expanding team at their brand new facility in New Mexico. As a Production/Manufacturing Supervisor, you will play a pivotal role in overseeing and optimizing production operations, specifically in sterile fill finish processes, to ensure the highest standards of quality, safety, and efficiency are maintained.
Main responsibilities:
Lead a team of production/manufacturing personnel in executing daily operations of sterile fill finish processes, ensuring adherence to production schedules, quality standards, and safety protocols.
Ensure timely manufacturing of all liquid and lyophilized parenteral cGMP products using aseptic processing technology to deliver high-quality sterile products to the pharmaceutical industry
Maintain and report metrics to evaluate the performance of the assigned production unit. Mentored, develop, and guide succession planning and cross-functional training of direct reports. Schedule adherence and material consumption rates relative to specific areas.
Directly supervises from 4 to15 employees in a production unit department. Carries out supervisory responsibilities following the organization's policies and applicable laws. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.
Implement and maintain standard operating procedures (SOPs) and best practices to enhance productivity, quality, and compliance in aseptic fill finish environments.
Collaborate with cross-functional teams, including Quality Assurance, Engineering, and Logistics, to address production challenges, implement process improvements, and drive continuous optimization.
Qualifications:
High School Diploma or GED and minimum of 2+ years of relevant related work in the pharmaceutical industry experience.
Minimum of 1 year experience in a supervisory role within a pharmaceutical manufacturing environment, with specific expertise in sterile fill finish operations.
Proven track record of successful leadership, team management, and performance improvement initiatives.
Strong knowledge of aseptic techniques, sterile manufacturing processes, equipment, and quality systems.
Excellent communication, interpersonal, and problem-solving skills.
Ability to thrive in a fast-paced, dynamic environment and adapt to changing priorities.
Familiarity with regulatory requirements and quality standards (e.g., FDA, cGMP) for sterile manufacturing is highly desirable.
Apply today or reach out directly to ********
#J-18808-Ljbffr
