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Production Operator I

Katalyst Healthcares & Life Sciences

  • Sparks, MD
  • 30+ days ago

    Highlights

    Preferred Skills Experience working in FDA-regulated, GMP, ISO, pharmaceutical, medical device, or manufacturing environments. The Production Operator I is responsible for supporting daily manufacturing and packaging operations in a regulated production environment.

    Numbers & Facts

    LocationSparks, MD

    Description

    Job Summary
    The Production Operator I is responsible for supporting daily manufacturing and packaging operations in a regulated production environment. This role involves operating equipment, performing assembly and packaging activities, maintaining production records, and ensuring compliance with quality and safety standards.

    Key Responsibilities
    • Perform production activities such as assembly, packaging, labeling, inspection, and material handling.

    • Operate and monitor production equipment according to established procedures.

    • Complete manufacturing documentation and production records accurately and in a timely manner.

    • Follow quality, safety, and compliance requirements, including GMP, FDA, and ISO guidelines.

    • Inspect products for quality and report any defects, discrepancies, or equipment issues.

    • Support team objectives by collaborating effectively with coworkers and supervisors.

    • Maintain a clean and organized work area in accordance with company standards.

    • Adhere to standard operating procedures and work instructions while meeting productivity targets.

    • Assist with changeovers, setup activities, and other production support functions as needed.

    • Rotate between workstations and tasks based on operational requirements.

    • Qualifications

    • High School Diploma, GED, or equivalent required.

    • 1 2 years of experience in manufacturing, production, assembly, packaging, warehouse, or a related environment preferred.

    • Ability to follow written and verbal instructions and work independently on routine assignments.

    • Basic math, reading, and documentation skills.

    • Strong attention to detail and commitment to quality.

    • Effective communication and teamwork skills.

    • Ability to work flexible schedules, overtime, and additional hours when required.

    • Dependable attendance and punctuality are essential.

    • Comfortable working in a fast-paced production environment and adapting to changing priorities.

    Preferred Skills
    • Experience working in FDA-regulated, GMP, ISO, pharmaceutical, medical device, or manufacturing environments.

    • Familiarity with production documentation and quality inspection processes.

    • Ability to learn new equipment and processes quickly.

    • Strong problem-solving and organizational skills.

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