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Production Operator

Job in Sparks, Baltimore County, Maryland, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-07-04
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Production Associate / Production Line, Production QC/QA, Packaging Engineer
Job Description & How to Apply Below
Position: Production Operator I
Location: Sparks

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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