GMP Laboratory cleaning associate - King of Prussia - 12 months contract, Lisbon
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GMP Laboratory Cleaning Associate - King of Prussia - 12 Months Contract, Lisbon
Client:
Alphanumeric Systems
Location:
Lisbon, Portugal
Job Category:
Other
EU Work Permit Required:
Yes
Job Reference:
8ded34a835dd
Job Views:
6
Posted:
09. 02. 2025
Job Description:
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 with 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 1-year 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 12:00 PM to 12:00 AM (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 a safe, compliant, and efficient manner.
- Minimum of 1 year experience in Sterile or GMP Cleaning operations within the Pharmaceutical or Biotechnology industry or 5 or more years of equivalent experience.
- Prior experience with pharmaceutical manufacturing.
- Familiar with c
GMPs, regulatory guidelines, governmental codes, and standard operating procedures. - Strong communication 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.
- Attend Stop for Safety Sessions in respective shift/area.
QUALITY PROCEDURES:
- Follow GMP procedures.
- Report any abnormalities/adverse events 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.
- Maintain 5S, area cleanliness, and tidiness.
- Interact professionally with other staff.
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