Antigen Production Technician

Job Title: Antigen Production Technician
Location: Swiftwater, PA 18370
Duration: 6+ Months (Possible Extension)
 
Overview:
Performs production activities based on volume fluctuations, business needs, and effective procedures within the Biological Service Area. Responsible for manufacturing tasks in the assigned area.
 
Key Responsibilities:

• Complete sampling and corresponding documentation as required.
• Perform process order and bin-to-bin movements accurately and promptly to ensure inventory accuracy in SAP.
• Participate in inventory management activities including SAP use, cycle counting, and ordering.
• Complete assigned tasks and documentation in compliance with current Good Manufacturing Practices (cGMP).
• Collaborate with Senior and Lead Technicians and Managers to maintain efficient operations.
• Participate in team meetings; communicate improvement ideas, issues, and concerns clearly.
• Identify production issues and escalate to leadership promptly.
• Conduct environmental monitoring and water sampling tasks.
• Write and edit cGMP procedures and documents under supervision.
• Participate in deviation investigations and implementation plans to maintain product quality.
• Ensure proper process area operation through pre- and post-run setup and maintenance of lab and equipment.
• Complete quality documentation (Batch Production Records, logbooks, etc.) accurately and on time.

 
Requirements:

• Strong self-driven work ethic with excellent communication and time management skills.
• Commitment to continuous personal and professional development through training.
• Ability to adapt in a dynamic work environment where various items move across the site to meet facility demands.
• Keen attention to detail and strong documentation skills.
• Ability to work both independently and collaboratively.
• Good mechanical skills with basic mechanical aptitude.
• Proficient computer skills, good comprehension and retention, troubleshooting abilities, and manual dexterity.
• Thorough knowledge of cGMP and regulatory requirements.
• Able to stand and work efficiently for 10 hours per day.
• Capable of lifting 30+ lbs.
• Detail-oriented with clear writing ability.
• Self-motivated and proactive.
• Follow cGMP Standard Operating Procedures (SOPs) and Standard Work Instructions (SWIs) for compliance.
• Flexible to work multiple shifts including weekends.

 
Working Conditions:

• Hours may vary; employees must stay until tasks are completed.
• Must be available for weekends, holidays, and overtime as needed.
• Days off may not be consecutive and could vary weekly with rotating schedules.
• Working hours subject to change based on production demand.
• May be required to take set days off mid-week or work rotating schedules.
• Production involves active viruses with minimal exposure risk. Vaccinations required: Flu, Menactra, Yellow Fever (depending on area).
• Jewelry, makeup, and scented products (perfume, hairspray, cologne, aftershave) are prohibited on the floor.
• Artificial nails and nail polish are not allowed.
• Attire includes sterile scrubs, hairnets, beard covers, safety glasses, steel toe shoes, and Tyvek suits in some areas.

 
Experience:

• 3 to 6 years relevant production/manufacturing experience in a cGMP environment.