Quality Control Inspector - Life Sciences (GMP/ISO)

biotechne; Newark (CA); On-site; USD 72,208,000 - 99,286,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Short-term disability

Long-term disability

401k

ESPP

Health Spending Account (HSA)

Flexible Spending Account (FSA)

Dependent Care FSA

Tuition reimbursement

Job summary

Bio-Techne is seeking a Quality Control Inspector to join our Operations team in Newark, CA. The role focuses on inspecting incoming raw materials and finished products, ensuring compliance with ISO and GMP standards, and maintaining accurate QC records.

The successful candidate will be detail-oriented, able to work with shifting priorities in a fast-paced environment, and collaborate with cross-functional teams to resolve discrepancies and improve documentation.

Qualifications

• Experience working in a Quality Control environment is strongly desired.
• Previous experience performing incoming inspections is strongly desired.
• Detail-oriented, efficient, and has excellent organizational skills.
• Excellent verbal and written communication skills
• Strong team player with the ability to work independently.
• Able to multitask and prioritize.

Responsibilities

• Receive and perform inspection of incoming raw material/components.
• Perform visual inspections on sub-assemblies and finished good products.
• Record, track, and maintain QC data in logs and spreadsheets.
• Participate in inventory counts.
• Revise/improve current incoming specification documentation.
• Initiate nonconformance/deviation/OOS as needed.
• Interact with external departments to resolve inspection discrepancies.

Skills

QC experience

Incoming inspections

Detail-oriented

Communication skills

Team player

Multitasking

Education

High School diploma or AA degree

Job description

Bio-Techne is seeking a Quality Control Inspector to join our Operations team in Newark, CA. The role focuses on inspecting incoming raw materials and finished products, ensuring compliance with ISO and GMP standards, and maintaining accurate QC records.

The successful candidate will be detail-oriented, able to work with shifting priorities in a fast-paced environment, and collaborate with cross-functional teams to resolve discrepancies and improve documentation.