Manufacturing Associate I (Manufacturing/Quality) (contract)

Responsibilities

• Set up, operate, change over, and clean automated and manual packaging equipment in strict accordance with SOPs, GMP guidelines, and safety policies.
• Document all production activities accurately in batch records, log sheets, attachments, and electronic batch record systems.
• Perform manual packaging tasks on an assembly line, maintaining consistent quality and pace.
• Maintain sufficient inventory of packaging materials and manage replenishment as needed.
• Routinely and safely handle high-value product vials in various stages of packaging completion, including retrieval and storage from a 2–8°C cold room.
• Identify and promptly communicate process deviations to the supervisor or manager.
• Optimize automated packaging equipment to ensure peak performance.
• Periodically inspect and maintain flammables cabinets and satellite hazardous waste accumulation stations.
• Use computer-based systems for data collection, data analysis, timekeeping, email, and inventory management.
• Keep all required training current and complete retraining prior to expiration dates.
• Follow all written and verbal instructions provided by supervisors and managers.
• Lift up to 35 lbs. and move heavy objects such as product vial cages and pallets of packaging materials.
• Stand for extended periods of up to 3 hours during manual packaging operations.
• Adhere to all gowning requirements including hairnet, beard cover, lab coat, gloves, safety glasses, shoe covers, and task-specific PPE.

Qualifications

• Strong understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Solid mathematical and analytical skills for production documentation and data review.
• Effective written and verbal communication skills for cross-functional collaboration.
• Proficiency with Microsoft Word and Excel.
• Experience with ERP systems for inventory and production management.
• Ability to work independently and collaboratively in a fast-paced, team-oriented environment.
• Strong attention to detail and commitment to quality and compliance.
• Ability to safely handle hazardous materials in accordance with established protocols.

Skills

• Understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Basic mechanical aptitude for operating and troubleshooting packaging equipment.
• Solid mathematical and analytical skills for production documentation and data review.
• Effective written and verbal communication skills for cross-functional collaboration.
• Proficiency with Microsoft Word and Excel.
• Experience with ERP systems for inventory and production management.
• Ability to work independently and collaboratively in a fast-paced, team-oriented environment.
• Strong attention to detail and commitment to quality and compliance.
• Ability to safely handle hazardous materials in accordance with established protocols.

Benefits

This is a remarkable opportunity to contribute to life-changing work at a globally recognized pharmaceutical operations facility, where your efforts directly support patients around the world. You will gain hands-on experience in a highly regulated, cutting-edge manufacturing environment while working alongside a collaborative and knowledgeable team of industry professionals. With a structured daytime schedule, this role offers both stability and the chance to grow your expertise in pharmaceutical packaging operations.

Pay

Pay Rate Max: $29 per hour

Schedule

Monday - Friday; 7AM-3:30PM with occasional overtime (starting at 6AM and staying until 4:30PM)