Job Description

GMP Cleaning Associate – Biopharm Manufacturing Associate – Level 3

1 Year

King of Prussia, PA

Max PR: $35.28/hr

Shift:

• Training “Boot Camp” 4 weeks M-F (7:30am – 4:00pm EST).
• 12-hour shifts from (12:00pm to 12:00am).
• It also includes every other weekend and Holidays.
• 100% ONSITE
• Start Date March 3rd, 2025

Required:

• High School Diploma.
• Reading and comprehension skills required to execute GMP Cleaning activities and ensure operations occur in safe, compliant and efficient manner.
• Minimum of 1 year experience in Sterile or GMP Cleaning operations within Pharmaceutical or Biotechnology industry or 5 or more years of equivalent experience.
• Prior experience with pharmaceutical manufacturing.
• Familiar with cGMP’s, regulatory guidelines, governmental codes, and standard operating procedures.
• Strong communications skills, both verbal and written.
• Basic knowledge and understanding of safety and GMP requirements.
• GMP Cleaners are responsible for providing support for the production operations. It is essential the individual have a thorough understanding of the tasks required and the repercussions of their actions.
• Demonstrate proficiency in the following systems: SAP/MERPS, VQD, Syncade, Microsoft software packages.
• Strong quality/compliance orientation and track record.

Hard Skill Sets-

• Computer Literacy. Need to know how to navigate a computer.
• Safety quality mindset.
• Punctual with the schedule. Be on time.

Interview Process:

• 30 Minute Teams Interview

Job Description

To clean the production, lab, and warehouse areas according to site procedures and complying to safety and quality requirements. Conduct GMP Cleaning operations in accordance with Biopharm Safety Procedures and cGMPs. Off-shift hours (including night work) may be required

Job Responsibilities

Safety

• Follow all EHS procedures, standards and PPE requirements.
• Notify appropriate personnel of any incident and accident in the respective area.
• Raise ZAPs for any EHS concerns.
• Attended Stop for Safety Sessions in respective shift / area

Quality

• Follow GMP procedures.
• Report any abnormalities /adverse event to FLL (OLN, Rapid Response, deviation) in a timely manner.
• Perform area cleaning and record per procedure.

Performance

• Adhere to site cleaning procedure and schedule.
• Ontime attendance.
• Maintain 5S, area cleanness and tidiness.
• Interact professionally with other staff.

Education & Qualifications

• High School Diploma.
• Reading and comprehension skills required to execute GMP Cleaning activities and ensure operations occur in safe, compliant and efficient manner.
• Minimum of 1 year experience in Sterile or GMP Cleaning operations within Pharmaceutical or Biotechnology industry or 5 or more years of equivalent experience.
• Prior experience with pharmaceutical manufacturing.
• Familiar with cGMP’s, regulatory guidelines, governmental codes, and standard operating procedures.
• Strong communications skills, both verbal and written.
• Basic knowledge and understanding of safety and GMP requirements.
• GMP Cleaners are responsible for providing support for the production operations. It is essential the individual have a thorough understanding of the tasks required and the repercussions of their actions.
• Demonstrate proficiency in the following systems: SAP/MERPS, VQD, Syncade, Microsoft software packages.
• Ensure the proper procurement of appropriate materials for tasks.
• Ensure proper documentation is completed appropriately to sufficiently document cleaning tasks.
• Strong quality/compliance orientation and track record.

Job Tags

Similar Jobs