What are the responsibilities and job description for the Production Operator I position at Katalyst Healthcares & Life Sciences?
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
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.