QC Specialist I - Temporary

A typical day will involve completion of testing on assigned batches and completing paperwork/data entry into SAP to document results for review/product release. This role requires communication and coordination between team members, the supervisor and the planners to ensure that we are keeping on top of priorities to avoid backorder. Besides routine testing, a day will include attending the daily Tier 1 meetings to report on safety, quality, delivery and inventory updates.

• Support Quality Control activities towards PCR reagents and consumable products.
• Perform QC testing on incoming and manufactured materials to support release into inventory.
• Document testing activities and results accurately following good documentation practices to ensure adherence to ISO13485 requirements.
• Inform supervisor of any deviations from process and perform follow up actions as needed.
• Participate in troubleshooting activities with guidance from relevant sources as needed.
• Participate in maintaining lab cleanliness, 5S and a safe work environment for self and peers.
• Cross-train across a wide variety of product portfolios and assays.

How You'll Make An Impact:

• Contribute to timely product release to meet the business goals to deliver product to customers on time by completing assigned tasks on time.
• Communicating technical issues and concerns promptly to escalate/establish root cause to move the process forward.
• Cross-training on our vast portfolio of processes to learn new lab skills while supporting equitable workload distribution and efficient product release.
• Identify areas for improvement in QC processes/procedures and execute projects to implement changes.
• Work on exciting new product implementation projects to train on and transfer robust processes for future QC testing of products.

What the Candidate Brings:

• Bachelor's degree or equivalent in a life science (Chemistry, Biology) or related field.
• 0-2 years in a general laboratory environment performing analyses in the areas of chemistry, biochemistry, or associated areas of life sciences, or equivalent combination of education and experience.
• Understands and can apply GLP (Good Laboratory Practices) and GMP (Good Manufacturing Practices).
• Strong computer skills, including Microsoft suite.
• Experience with ERP systems a plus, SAP preferred

Compensation: The estimated hourly range for this position is $32.00 to $38.84 per hour at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. As a temporary associate, your employment will be managed directly through our approved agency provider.

Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.

EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply.

Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.

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