Cryo Operations Associate - Cold Chain & GMP (6 Months)

Spectraforce Technologies; Summit (NJ); On-site; USD 27,552 - 41,328; Part time

Job summary

Spectraforce Technologies is seeking an Associate Specialist for Value Stream Cryo Operations in Summit, NJ. The role focuses on cryopreservation, storage, and material tracking for patient materials in a GMP‑regulated facility.

Responsibilities include managing cold chain transfers, maintaining chain of custody, and supporting batch records and investigations. A 6‑month term is expected with overtime as needed.

Qualifications

• Bachelor's degree or related technical degree with manufacturing/operations exposure.
• Alternate qualifications include an Associate/Medical Tech degree with 0–2 years in manufacturing/operations.
• High School diploma plus 2–4 years of manufacturing/operations experience acceptable.

Responsibilities

• Handle patient material through cryopreservation, storage, distribution and disposal.
• Maintain sample tracking and chain of custody per GMP procedures.
• Destruct obsolete samples per written procedures and maintain storage reports.
• Perform sample queries and storage reports as required.
• Assist investigations and deviations related to sample management.
• Collaborate with other departments to improve processes.
• Maintain metrics for Value Stream Cryo Operations and support cold chain transfers.
• Support cGMP batch records, deviations, and CAPA closures.
• Ensure on-time cryopreservation support per production schedule.
• Record handling data clearly according to GDPs; work with trained personnel.

Skills

Cold chain storage

cGMP/FDA knowledge

Math basics

cGMP understanding

Technical writing

MS Office

Inventory control

Biology/Medical background

Education

Bachelor's degree

Associate/Medical Technical degree

High School diploma/GED

Tools

MS Office

Job description

Spectraforce Technologies is seeking an Associate Specialist for Value Stream Cryo Operations in Summit, NJ. The role focuses on cryopreservation, storage, and material tracking for patient materials in a GMP‑regulated facility.

Responsibilities include managing cold chain transfers, maintaining chain of custody, and supporting batch records and investigations. A 6‑month term is expected with overtime as needed.