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    Production/Manufacturing Supervisor - New Mexico, United States - Barrington James

    Barrington James
    Barrington James New Mexico, United States

    1 week ago

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    Description

    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

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