GMP Lab Sample Handling Specialist

SmartRecruiters, Inc.; Chesterfield (MO); On-site; USD 36,000 - 48,000; Full time

Job summary

Integrated Resources, Inc. is seeking a QC Sample Handling Technician to support a multi-discipline team with receiving, aliquoting, distributing, and documenting GMP samples for multi-site testing laboratories.

The role involves assisting with GMP data transcription and verification, handling cold samples, and maintaining shipping records in accordance with SOPs. Prior pharma/biotech experience is desired but not required.

Qualifications

• Ability to work in a highly regulated GMP environment.
• Attention to detail and strong organizational skills.
• Ability to handle cold samples for long periods of time.
• Effective interpersonal and communication skills.
• Ability to thrive in a fast-paced environment and adapt to changing priorities.
• Familiar with Microsoft Office Suite and able to learn new systems.
• Experience in pharmaceutical or biotech environment is desirable but not required.

Responsibilities

• Receive, aliquot, distribute, and handle materials for GMP labs.
• Assist with GMP data transcription and verification on paper and in electronic systems.
• Assist the sample handling team with receiving biological sample shipments.
• Inventory and shipping of in-process, reference and stability materials, including cold samples.
• Label vials with barcodes printed from a LIMS.
• Download temperature information from shipping monitors for evaluation.
• Maintain and archive shipping records in accordance with SOPs.
• The technician may also transcribe data between systems and verify accuracy.

Skills

GMP compliance

Attention to detail

Organizational skills

Interpersonal communication

Adaptability

Tools

Microsoft Office

Job description

Integrated Resources, Inc. is seeking a QC Sample Handling Technician to support a multi-discipline team with receiving, aliquoting, distributing, and documenting GMP samples for multi-site testing laboratories.

The role involves assisting with GMP data transcription and verification, handling cold samples, and maintaining shipping records in accordance with SOPs. Prior pharma/biotech experience is desired but not required.