You are responsible to inspects incoming raw materials, electronic, mechanical components as well as manufactured/ OEM products to ensure they meet design specifications before being released to production. Completes appropriate paperwork necessary for conforming and non-conforming materials.
How You’ll Make an Impact:
- Ensure the timely execution of routine QC inspection and test activities per established QC procedures.
- Perform preliminary review on NC material, QC test failures and troubleshoots for possible root cause to facilitate disposition recommendation.
- Coordinate with internal cross functions, Bio-Rad service depot on physical returned instrument process and perform verification of customer returns.
- Assist Supervisor in establishing/revising QC Inspection Plan and/ or methodology for new or existing product/ purchased material.
- Provides technical assistance to more junior QC Technicians.
- Provides weekly/ monthly reports and metrics and any other task(s), as assigned by QC Supervisor.
- Participate in in-process audit as per plan and conduct periodic reviews with cross functional process owner(s) for timely closure.
- Recommend a course of action or risk-based decision for routine QC activities.
What You Bring:
While this list of qualifications may help an employee to succeed in this position, capable candidates may have a wide range of backgrounds or skills. If you have experience that aligns with the responsibilities of this role, we encourage you to apply.
- Minimum Higher NITEC or Diploma in technical discipline is preferred.
- Minimum 7 years of QC inspection experience in similar regulated industry within min 2 years as QC team lead is desirable.
- Experience in Laboratory activities is desirable.
- Ability to read and interpret electronic and mechanical drawings.
- Capable of operating inspection tools and equipment, including the programming of automated test tools.
- Experience in laboratory activities e.g. use of pipettes.
- Ability to collect/structure/analyze and communicate data using spreadsheets and dashboards.
- Proficiency in Microsoft office tools such as Excel, Word, and PowerPoint.
- ERP system experience required, SAP desirable.
- Knowledge of ISO 9001 or 13485. ISO 14971 and MDSAP are desirable.
- Able to communicate effectively, train junior technicians and lead project teams.
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. Recently voted a Best Place to Work, 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.
Benefits: Bio-Rad's biggest asset is our people, and this is the reason why our Total Rewards deliver programs that provide value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Our offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee’s work and life cycle. We’re proud to offer comprehensive medical plans and insurance, flexible benefits, wellness programs, extensive learning and development opportunities and more.
EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with disabilities, and people of all races, ethnicities, genders, ages, and orientations 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.
