GMP Custodian

Randstad Life Sciences US; King of Prussia (Montgomery County); On-site; USD 35,000 - 55,000; Full time

Job summary

An established industry player is seeking a dedicated GMP Custodian to ensure the cleanliness and compliance of production and lab areas. This role is vital in maintaining safety and quality standards within the pharmaceutical or biotechnology sector. The ideal candidate will have a high school diploma and at least one year of experience in GMP cleaning. You will follow strict procedures while working in a dynamic environment that may require off-shift hours. Join a forward-thinking organization that values safety and quality in every aspect of its operations.

Qualifications

• Minimum of 1 year experience in Sterile or GMP Cleaning within Pharmaceutical or Biotechnology industry.
• Basic knowledge of safety and GMP requirements.

Responsibilities

• Clean production, lab, and warehouse areas according to site procedures.
• Follow GMP procedures and report any abnormalities timely.
• Maintain punctual attendance and area cleanliness.

Skills

GMP (Good Manufacturing Practice)

MS-WORD

MS-EXCEL

MS-PowerPoint

Education

High School Diploma

Job description

Join to apply for the GMP Custodian role at Randstad Life Sciences US

Location: King Of Prussia, Pennsylvania

Job type: Contract

Work hours: 9 to 5

Education: High School

Job Summary

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

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.
• Attend Stop for Safety Sessions in respective shift/area.

Quality

• 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

• Adhere to site cleaning procedures and schedule.
• Maintain punctual attendance.
• Maintain 5S, area cleanliness, and tidiness.
• Interact professionally with other staff.

Qualifications

Required:

• High School Diploma.
• Minimum of 1 year experience in Sterile or GMP Cleaning within Pharmaceutical or Biotechnology industry.
• Basic knowledge and understanding of safety and GMP requirements.

Preferred:

• Prior experience with pharmaceutical manufacturing.

Skills

MS-WORD, MS-EXCEL, MS-PowerPoint, GMP (Good Manufacturing Practice)

We are an Equal Opportunity Employer. If you require a reasonable accommodation to make your application or interview experience better, please contact [e-mail].