US_Packaging Operator II_CO

Apollopros; South San Francisco (CA); On-site; USD 39,000 - 58,000; Full time

Job summary

Apollopros in California seeks a Packaging Operator II (Contract) to execute printing, labeling, and final packaging activities using automated systems in a GMP environment.

You will maintain batch records, perform inspections of packaging components, support production schedules, and collaborate with cross-functional teams to ensure quality and regulatory compliance, with overtime flexibility as needed.

Qualifications

• High school diploma or equivalent with 3–6 years in production/manufacturing, preferably regulated environments
• Bachelor's degree with 1+ year of technical/manufacturing experience
• Experience with GMP/compliance and batch records is preferred

Responsibilities

• Packaging & Production Operations: execute printing, labeling, and final packaging per procedures and quality standards
• Quality & Compliance: maintain batch records and supporting docs; perform inspections of components and materials
• Continuous Improvement: participate in quality, safety, and process improvement initiatives and support training and cross-functional teamwork

Skills

GMP operations

Documentation accuracy

Quality compliance

Communication

Team collaboration

Education

High School Diploma or equivalent

Bachelor's degree

Tools

RF devices

Automated manufacturing systems

Job description

Packaging Operator II (Contract) - Clinical Packaging & Pharmaceutical Manufacturing Join a High-Quality Pharmaceutical Packaging Team

Key Responsibilities

• Packaging & Production Operations Execute printing, labeling, and final packaging activities according to established procedures and quality standards. Receive, process, and deliver products and materials using automated systems. Safely set up, operate, monitor, and troubleshoot packaging equipment and GMP systems. Perform sample pickup and delivery activities as assigned. Support production schedules while maintaining accuracy, efficiency, and compliance.
• Quality & Compliance Complete and maintain required documentation, including batch records, forms, facility notifications, and equipment usage logs. Review batch records, forms, and supporting documentation in a timely manner. Conduct visual and dimensional inspections of packaging components, including labels, inserts, folding cartons, and container closure components. Perform documentation reviews for released components and materials. Identify process issues, collaborate with cross-functional teams, and initiate discrepancies when necessary. Ensure all activities comply with cGMP, quality, and safety standards.
• Continuous Improvement & Team Support Participate in quality, safety, and process improvement initiatives. Support departmental projects, investigations, process documentation, and solution development. Assist with change management activities and project-based assignments. Support departmental training programs and collaborate with training teams. Serve as a Subject Matter Expert (SME) or Super User for labeling and packaging operations when applicable. Foster a collaborative team environment that supports operational excellence.

Qualifications

Education & Experience One of the following is required: High School Diploma or equivalent with 3-6 years of related production or manufacturing experience, preferably in a regulated environment; OR Bachelor's degree (BS/BA) with 1+ year of technical or manufacturing experience.

Desired Skills Strong understanding of pharmaceutical manufacturing, packaging, labeling, and GMP operations. Ability to work independently while following established procedures and quality requirements. Experience resolving moderately complex production and process issues. Strong attention to detail, documentation accuracy, and regulatory compliance. Effective communication and collaboration skills. Ability to provide recommendations for operational improvements and process enhancements.

Work Environment & Physical Requirements

Work within controlled manufacturing environments requiring adherence to gowning procedures and safety protocols. Personal protective equipment (PPE) may include gloves, safety glasses, and steel-toe footwear. Ability to operate computers, RF devices, and automated manufacturing systems. Flexibility to work overtime and adjust schedules as business needs require. Ability to stand or sit for extended periods. Ability to perform repetitive packaging and visual inspection tasks for prolonged durations. Must be able to lift up to 40 pounds and push/pull loads requiring more than 75 pounds of force.

Keywords: Packaging Operator II, Pharmaceutical Packaging Operator, Clinical Packaging, GMP Manufacturing, cGMP, Labeling Operator, Pharmaceutical Production, Manufacturing Technician, Packaging Technician, Clinical Supply Packaging, Quality Compliance, Pharmaceutical Operations, Contract Manufacturing Jobs.