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 cGMPs. 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.
Please note that we do not offer work visa sponsorships for this role. This role is not available to work through C2C agreements.
SCHEDULE:
- Initial training schedule of 4 weeks: MON to FRI 7:30 am to 4:30 PM EST.
- 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 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.
- 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.