Careers

At Micropoint, we're creating technologies that can enable rapid and accurate testing and the monitoring of serious disease, so people can have a better, longer and fuller life. We're actively involved in shaping the industry and transforming technologies so physicians have the tools to help their patients at Point of Care. Our vision requires bold leaders. If you want a career that is challenging, energizing, and rewarding, we hope you’ll consider joining us as we push the boundaries of medical technology.

We are committed to providing a work environment with great benefits to make sure that your life is satisfying as you work. The benefit package includes medical, dental and vision insurance; a retirement plan with company matching; Paid Time Off (PTO); and paid holidays.

Current Openings

Sr. Scientist/Staff Scientist in Immunoassays (R1246 & R1247)

There are two openings. These positions are responsible for participating as a team leader in a laboratory environment for research and/or development programs focused on the goal of developing and optimizing the immunoassays found in MBI in vitro diagnostic products for POC RAPID TESTS. Works independently to plan, execute and lead studies to achieve the assigned goal.

Responsibilities:

• Develop immunoassays for POC rapid tests using microfluidics, clinical biochemistry, surface chemistry, organic chemistry
• Develop novel chemistry methods for antibody and fluorescence dye conjugation, purification
• Design, carry out experiments and data analysis , and present findings with little supervision
• Proactively identify, troubleshoot and provide solutions to issues relating to development, evaluation, optimization and validation of cartridge designs and formulations
• Make sound judgment to organize and prioritize various assignments and to reach desired outcomes in a timely fashion
• Assist product transfer to manufacturing

Requirements:

• A degree in organic chemistry, biochemistry, or related disciplines
• 6 - 8 years with a B.S./M.S. or 3 – 4 years with a Ph.D. of hands-on experience with in-vitro diagnostic/medical device development and product commercialization processes (design control) for POC rapid tests
• Experiences of working with beads for immunoassay development and with dry format assays of cardiac markers such as troponin I and BNP a plus
• Highly organized with exceptional quantitative and analytical abilities
• Intermediate computer software skills including Excel, Word
• Must be able to write clear, understandable documentation
• Good organizational skills to be able to manage multiple tasks simultaneously. This includes being able to clarify and organize data in an analytical manner
• A team player with effective communication/listening skills and a proven track record of success in research or product development
• Knowledge of and the ability to apply basic biochemical principles, go through literature and plan ways forward
• Displays leadership skills, including ability to organize, clarify and influence others

 

Sr. Manager, System Integration (R1248)

This position is responsible for system integration management for MBI’s in vitro diagnostic products for POC rapid tests.  Manages complex interdisciplinary activities and teams at multiple company sites to ensure the success in the development of high quality and robust products through the integration of hardware, software, chemistry, architecture, engineering, mechanical, electrical, strip and subassembly components.  Uses technical expertise to plan and direct work intended to develop new tests, transfer new developments to manufacturing  and commercialization.   Tests and optimizes systems product performances.

Responsibilities:

• Build and manage a team of Systems Engineers in design, implementation, system integration, verification, and validation of devices in various test platforms.
• Manage product definition and design including subassembly design, architecture, software design, mechanical design, electrical design, reader covers/structural design and system Integration of assays, systems and software.
• Performs troubleshooting and finds solutions to system integration problems.
• Plans and oversees the progress of various system integration projects on going within the company
• Maintains, tracks, and modifies as necessary project work plans and timelines.
• Contributes to project budget planning, spending and reporting.
• Communicates system integration information internally to management and externally to the development partner.
• Interfaces with internal and external stakeholders to define project requirements and accomplish project objectives.
• Supports the integration of technical and business objectives to maximize project success.

Requirements:

• PhD in a scientific discipline required, experience in the field of IVD, electrochemical sensors would be advantageous
• Five to ten years experience in successful, commercial product development required
• Experience of supervising and directing engineer, scientists and research assistants required.
• Experience of giving input to product design at an early stage of development.
• A broad scientific knowledge (instrumentation, optics, chemistry, molecular biology, software, hardware design, etc).
• Experience and knowledge of the ways that changes in one part of systems can affect performance of other parts and the whole system.
• Experience of writing and executing test plans to validate systems based products performance and robustness
• Demonstrated ability to understand and successfully work across multiple disciplines such as engineering, software and manufacturing highly desired.
• Must be hands on, detail oriented and highly motivated.
• Expertise in one or more of the following areas is preferred: design control, electrochemical sensing, immunoassay, microfluidics, fluorescence dye conjugation, injection molding, reagent dispensing, diagnostic testing system integration, automation engineering.
• Must have managed the technical components of a late stage medical device project, from phase 3 clinical supply through commercial scale-up.
• A solid understanding of US and EU regulatory requirements for medical devices is necessary.
• Must have made substantial contributions to the technical sections of registration filings and post-approval inspections.
• Must demonstrate strong analytical and problem solving capabilities, excellent oral and written communication skills, and a high level of organizational ability.
• Fluent computer skills relevant to both project management and engineering are required: for example, proficiencies in MS project, Excel, and common CAD programs are necessities.
• Displays leadership skills, including ability to organize, clarify and influence others.

 

Research Associate/Scientist (R1249 & R1250)

We are looking for highly motivated Research Associates/Scientists (two openings) to join our assay development team. These positions are responsible for participating as a team member in a laboratory environment for research and/or development programs focused on the goal of developing and optimizing the immunoassays found in MBI in vitro diagnostic products for POC RAPID TESTS.

Responsibilities:

• Work with senior scientist/engineer to develop a variety of quantitative immunoassays to meet both FDA and EU regulatory requirements for clinical IVD applications
• Assist the R&D team in the POC product development including feasibility, verification and validation, manufacturing transfer and commercialization
• Working on multiple, simultaneous projects, which require you to be able to manage time flexibly and interact with a variety of people

Requirements:

• B.S. degree in organic chemistry , biochemistry, clinical lab science, biology, or related fields
• 2+ years experience in commercial POC assay and product development preferred
• Experiences in immunoassay development is a plus, including: antibody screening, reagent preparation and optimization, conjugation, purification, assay optimization utilizing DOE principles, experimental planning, execution and data analysis, verification and validation testing in conformance with CLSI guidelines
• Excellent skills in organization, record keeping and communications
• Worked in a GMP/GLP laboratory environment
• Excellent oral and written communication skills
• Collaborative and proactive attitude a must
• Able to adapt to a fast-paced work environment and must have a strong work ethic to complete assignment with high quality under tight deadlines

 

Product Manger (R1251)

As a Product Manager you will be accountable for providing primary leadership in the development and implementation of strategies and tactics to assure the commercial success of assigned product(s) for POCT rapid tests. You will also design and be responsible for sales tools, tradeshows, advertising, Key Opinion Leader (KOL) relationship development and management, clinical materials, and other programs to drive business.

Responsibilities:

• Design and implement strategic brand plan, annual marketing plans, global launch plan and promotional communication strategy
• Develop sales tools and other supports for the product line(s).
• Act as a liaison among the distribution partners, customers and internal cross-functional product teams to ensure the market trends and needs are communicated in order to translate the needs into new product design.
• Provide commercial input for clinical development and recommendations for and assist with implementing product improvements
• Forecast market demand in alignment with market needs and business focus.
• Keep up to date with competition and market trends
• Provide training for internal and external customers
• Lead commercialization activities for the product line, include sales meetings and trade shows
• Assist with maintaining and growing relationships with external partners
• Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes
• Support sales team and distribution partners to meet customer needs and growth goals.
• Other duties as assigned
• Travel as needed

Requirements:

• Bachelor’s degree in life science, business or medical technology or equivalent
• Minimum of three (3) years previous product management experience within the healthcare industry required; experience in Point of Care diagnostics and coagulation testing in clinical setting highly preferred
• Experience with both hospital and alternate site segments a plus
• Strong presentation skills, Strong written and verbal communication skills
• Strong planning, organizational and time management skills
• Must be self-motivated and have the ability to work with minimal supervision
• Are able to drive multiple projects with multiple priorities, as well as have the ability to strategically think through complex opportunities.
• Exceptional cross-functional team leadership

 

Director, Assay Development (R1252)

This position is responsible for directing and implementing policies, objectives and initiatives for research and/or development programs focused on the goal of developing and optimizing the immunoassays found in MBI in vitro diagnostic products for POC RAPID TESTS. Ensures R&D activities that will advance and maintain MBI’s competitive position and profitability.

Responsibilities:

• Direct assay development group in the development of immunoassays for POC rapid tests using microfluidics, clinical biochemistry, surface chemistry, organic chemistry
• Identify/implement reagents and novel chemistry methods for antibody and fluorescence dye conjugation, purification to develop immunoassay tests and to meet requirement for manufacturing scale up
• Work with engineering and design team to contribute to the development of the diagnostic readers
• Work with manufacturing team, including contributing to documentation to facilitate transfer to manufacturing 
• Make sound judgment to organize and prioritize various assignments and to reach desired outcomes in a timely fashion
• Lead generation of design control quality documentation and approval activities
• Assist with submissions and review of responses to notified bodies and FDA with regard to medical device directive compliance

Requirements:

• A degree in biochemistry, Biomedical engineering or related disciplines
• 6 - 8 years with a B.S./M.S. or 3 – 4 years with a Ph.D. of hands-on and management experience with in-vitro diagnostic/medical device development and product commercialization processes (design control) for POC rapid tests
• Experiences of working with beads for immunoassay development and with dry format assays of cardiac markers such as troponin I and BNP a plus
• A strategic thinker with ability to convert vision into market-driven results and track record to reduce risk in new product development through decisive, logical and disciplined actions
• Highly organized with exceptional quantitative and analytical abilities
• Intermediate computer software skills including Excel, Word
• Must be able to write clear, understandable documentation
• Good organizational skills to be able to manage multiple tasks simultaneously. This includes being able to clarify and organize data in an analytical manner
• A team player with effective communication/listening skills and a proven track record of success in research or product development
• Knowledge of and the ability to apply basic biochemical principles, go through literature and plan ways forward
• Displays leadership skills, including ability to organize, clarify and influence others

 

Manufacturing Operators (R1253 - 1254)

There are two openings. These positions are responsible for basic and routine tasks involved in the manufacture and assembly of the Company’s disposable, test cartridges.

Responsibilities:

• Responsible for following written procedures for set-up, operation, and clean up of manufacturing equipments, final assembly, and packaging
• Responsible for manual tasks including, pipette solution, pouch and box labeling, product inspection
• Prepare materials used in the cartridge production process
• Maintains records and documentation associated with producing cartridges in compliance with GMP and SOPs
• Must be able to stand for long periods of time and lift up to 40 pounds

Requirements:

• High school diploma plus 0-2 years experience in a food, pharmaceutical, medical device or diagnostics manufacturing environment
• Basic knowledge of Good Manufacturing Practices
• Familiar with wet chemical handling and solution preparation
• Good skill in pipette use preferred
• Basic math skills including addition, subtraction, multiplication and division
• Detail-oriented with ability to recognize deviations from accepted standard
• Must be able to read, write and speak English

 

Submit your resume at: HR@micropointbio.com.