Lab Technician I

• The QC Sample Handling Technician will assist a multi-discipline support staff with primary responsibility for receiving, aliquoting, distributing, and handling materials, as well as with documentation of GMP samples in support of multi-product and multi-site testing laboratories.

• The technician may also be expected to assist with GMP data transcription and verification on paper and in electronic systems. Must stay within GMP compliance at all times.

• Record keeping experience required. Must be familiar with general safety procedure and guidelines. Must be self-motivated and have a strong attention to detail. Good communication skills required. Years of Experience 0-2.

• Specific duties and responsibilities for this role are:

• Assist the sample handling team with receiving biological sample shipments.

• Inventory and shipping of in-process, reference and stability materials, which requires handling cold samples for long periods of time.

• Label vials with barcodes printed from a laboratory information management system (LIMS).

• Download temperature information from the shipping temperature monitors to a computer for evaluation.

• Maintain and archive shipping records in accordance with company SOPs.

• The technician may also be expected to:

• Transcribe data from one system to another.

• Perform 100% accuracy verification for previously transcribed data.

• Skills Required:

• Ability to work in a highly regulated environment and comply with GMP expectations.

• Attention to detail, strong organizational skills in order to start and complete a task.

• Ability to handle cold samples for long periods of time and cold environments for short 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 computer literate enough to quickly learn new systems.

• Ability to comply with sample handling safety instructions.

• Previous experience working in a pharmaceutical or biotech environment is desired, but not required..

All your information will be kept confidential according to EEO guidelines.