Post Market Performance Follow (PMPF) Analyst - Temporary

As a PMPF Analyst your activities involve managing and executing post-market follow-up processes. This includes reviewing scientific literature and coordinating with teams such as R&D, Clinical Affairs, Marketing, and RA/QA to collect inputs for Post Market Performance Follow-Up reports. The candidate analyzes clinical studies, marketing evaluations, and published experiences to assess product benefit-risk and draft report conclusions. You will also participates in new product development and sustaining projects, executing studies in the laboratory as required.

How You'll Make An Impact:

• Execute PMPF process and assures tasks are carried out by overseeing the generation and scheduling of Post Market Performance Follow up reports.
• Coordinates PMPFR inputs among cross-functional teams (R&D, Clinical Affairs, Marketing, RA/QA) in order to obtain deliverablesResponsible for revision of PMPF Plans and PER, as needed.
• Review and analyze scientific literature and summarize findings in applicable protocol reports.
• Guarantee all PMPF deliverables are prioritized, executed and aligned according to the Periodic Safety Update Report Publication timeline.
• Participate in new product development and sustaining projects as required, ensuring all tasks are completed accurately and on schedule.

What You Bring:

• BS in science related field (Biochemistry, Biotechnology, Chemistry or related field)
• Skill in addressing situations that need a logical, analytical, and methodical approach
• Knowledge of immunoassays, infectious diseases, bacteriology and related diagnostic techniques/instruments with a minimum of 1 year laboratory experience
• Experience in the in-vitro diagnostics industry preferred with familiarity IVDR regulation 2017/746
• Advance English level: able to communicate effectively in English and in writing
• Proficient use of applications: Word, Excel, Power Point, OneDrive, SharePoint, Teams

Compensation: The estimated hourly range for this position is $40 to $50 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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