Quality Control Job – Miltenyi Biotec Career in Life Sciences
Are you looking for an exciting Quality Control Job in the life sciences? Miltenyi Biotec is seeking a QC Analyst I for a swing shift in San Jose, CA. This Life Science Job is part of a Miltenyi Biotec career path that allows you to contribute to cutting-edge biomedical research, supporting the development and manufacturing of advanced cell and gene therapy products while gaining hands-on experience in GMP activities and biopharmaceutical quality control.
About Miltenyi Biotec
Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you become part of a passionate family committed to making a real impact – one breakthrough at a time. One integral division of Miltenyi Biotec is Miltenyi Bioindustry, our contract development and manufacturing organization (CDMO). As a full-scale CDMO, we provide customers with development and manufacturing services for lentiviral vectors and cell and gene therapy products. Miltenyi Bioindustry uniquely serves as both producer and service provider, using our instruments and reagents at each workflow step, controlling the supply chain, and delivering enhanced security and planning clarity to customers. Starting a Miltenyi Biotec career gives you the chance to work on innovative projects and excel in a dynamic Life Science Job environment while contributing to transformative therapies.
Job Details
- Job Title: QC Analyst I
- Job Category: Manufacturing
- Requisition Number: QCANA003385
- Location: San Jose, CA 95134, USA
- Education: Bachelor’s degree in the life sciences or related field.
- Experience: 0-2 years relevant experience in a laboratory or a cGMP/cGTP environment.
Job Description
Your role as a QC Analyst Swing Shift involves supporting day-to-day Quality Control Job activities, including GMP operations, assay development, and client or internal company projects while adhering to SOPs.
Responsibilities of QC
- Work on diverse client projects with different test methods and analysis of data.
- Communicate and collaborate effectively with colleagues, management, and departments.
- Support the execution of Quality Control Method Development and GMP release testing.
- Conduct routine and non-routine testing while compiling accurate and valid results.
- Maintain inventory of QC materials and lab supplies, including monitoring and ordering.
- Assist with developing methods and procedures for Quality Control.
Requirements
- Working knowledge of quality systems and regulations.
- Must have hands-on experience in flow cytometry and working in biopharmaceutical Quality Control.
Skills:
- Proficient in QC test methods/procedures and use of the QC lab equipment.
- Proficient in Flow Cytometry, qPCR, ELISA, and cell-based assays.
Physical Demands:
The physical demands of the job include walking, hand usage, reaching, talking, hearing, standing, balancing, and lifting up to 25 pounds, among others.
Work Environment:
This job is performed in a temperature-controlled facility without exposure to extreme temperatures. Protective equipment is required due to exposure to viruses and bacteria.
Compensation:
The hiring range for this position is $31.58 – $37.11/hour. Additional benefits and compensation may be provided based on qualifications.
