GMP Laboratory cleaning associate - King of Prussia - 12 months contract Lisboa

GMP Laboratory cleaning associate - King of Prussia - 12 months contract
Lisboa
Lisboa, Lisboa, Portugal

Alphanumeric is hiring a GMP CLEANING ASSOCIATE - BIOPHARM MANUFACTURING ASSOCIATE - Level 3 to work in Upper Merion, King of Prussia, PA with our client of 20 years committed to improving lives through medical and pharmaceutical advancements.

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 c
GMPs. Off-shift hours (including night work) may be required.

Please note that this role is available through a 1y duration W2 contract. The compensation for this role ranges between $25 and $30 USD / hour gross.

SCHEDULE:

1. Initial training schedule of 4 weeks: MON to FRI 7:30 am to 4:30 PM EST.
2. Regular schedule: 12h rotating shifts from 12:00pm to 12:00am (it includes every other weekend).

KEY REQUIREMENTS:

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

SAFETY REQUIREMENTS:

• 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 PROCEDURES:

• 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 REQUIREMENTS:

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