Technician II, Facilities (GMP Cleaner)

Job Title - Technician II, Facilities (GMP Cleaner)

Work Location – Cranbury NJ

Shift/Schedule - 4:30am - 1pm M-F, everyother weekend

WuXi Biologics is a is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop, and manufacture biologics from concept to commercial manufacturing. WuXi Biologics’ achievements are a direct result of the efforts made by our employees. We have built an extraordinary team motivated by our PROUD culture of Passion, Reward, Opportunity, Unity and Determination. WuXi Biologics offers exciting job opportunities and careers around the globe. We currently employ over 12,000 people and provide services to more than 600 customers worldwide, including all the top 20 biopharmaceutical companies.

Job Summary

This is a full-time position, reporting to the cGMP Support Supervisor. The cGMP Cleaner is responsible for the operational excellence of the cleanroom by performing daily, weekly, and monthly tasks designed to maintain the cleanrooms integrity by regulatory and industry standards. The cGMP Cleaner will clean, stock, and overall maintain the health of the cleanroom while aiding the manufacturing team to improve the flow and function of the operations onsite.

Essential Job Functions

• Strict adherence to current Good Manufacturing Practices (cGMPs).
• Strict adherence to established cleaning practices and procedures.
• Compliance with quality standards and regulations.
• Completion of all written and online trainings.
• Majority of time spent in a cleanroom, fully gowned, including a head covering, facemask, gloves, plant shoes, and safety glasses.
• Pride in delivering excellent service with high levels of energy and endurance.
• Perform all required daily, weekly, and monthly cleanings.
• Mop all floors using a variety of cleanroom disinfectants while following established cleanroom cleaning procedures.
• Completes GMP documentation, including records and logbooks.
• Comply with Health, Safety and Environmental responsibilities for the position.
• Follow relevant Standard Operating Procedures, and Site Quality procedures in ensuring 100% compliance.
  
  
  
  

Requirements

• High School Diploma or equivalent.
• Minimum experience in a GMP setting, willing to be trained
• English reading, verbal and written communications skills
• Strong attention to details.
• Excellent attendance record.
• Prior experience in a biopharmaceutical GMP controlled environment preferred.
• Strong attention to details.
• Accurate completion of area logbooks as required by SOPs.
• Ability to frequently move and lift 50 pounds.
• Working non-standard shifts, Saturdays, Sundays, and Holidays.
• Work schedule 4:30 am - 1:00 pm
• Must be able to work overtime when needed.
• Make-up, nail polish, and/or jewelry can not be worn in the GMP process areas.
• May need extended periods of standing, walking, pushing, pulling, bending, crouching, and lifting of equipment and/or materials.
  
  
  
  

The anticipated hourly rate for this job is $20-24hr

The job description does not intend to list all the duties and responsibilities assigned to this position. Employees in this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.