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ADAPTED_NOW

In addition, bioMérieux offers a competitive Total Rewards package that may include: · A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options · Company-Provided Life and Accidental Death Insurance · Short and Long-Term Disability Insurance · Retirement Plan including a generous non-discretionary employer contribution and employer match. The role drives innovation in assays and biomolecule development, supports product and method advancement through biological sample management, and ensures robust analytical verification and validation to meet regulatory requirements.

YEAR

<h2><strong>Position Summary</strong></h2><p>The IVD Diagnostic Development Manager leads the design, development, optimization, and lifecycle management of antimicrobial susceptibility testing (AST) diagnostic assays and reagents within a regulated environment. The role drives innovation in assays and biomolecule development, supports product and method advancement through biological sample management, and ensures robust analytical verification and validation to meet regulatory requirements. This position also provides technical expertise for sustaining and improving existing diagnostic products while identifying and integrating emerging technologies and trends in IVD diagnostics.</p><h2><strong>Primary Duties</strong></h2><ol><li><p>Builds, leads and oversees a medium-sized team of individual contributors responsible for antimicrobial susceptibility testing (AST) reagent and assay development.</p></li><li><p>Manages day-to-day operations of complex laboratory activities, including reagent formulation, assay optimization, and performance characterization within a regulated IVD environment.</p></li><li><p>Maintains organizational strategy and AST product development goals relevant to team objectives, technical deliverables, and execution timelines.</p></li><li><p>Oversees local budgets, resource planning, and staffing to support development, verification, and support activities.</p></li><li><p>Provides technical leadership and training to staff members, while fostering cross-functional collaboration with quality, regulatory, manufacturing, and systems teams.</p></li><li><p>Ensures consistent application of quality systems, design controls, and best practices in compliance with FDA, MDR, and internal quality standards.</p></li><li><p>Ensure compliance with applicable regulatory requirements (IVDR/MDR).</p></li><li><p>Identify and implement operational process optimization and efficiency improvements, including development and application of SOPs and best practices.</p></li><li><p>Perform all work in compliance with company quality procedures and standards.</p></li></ol><div> </div><h2><strong>Qualifications</strong></h2><h3><strong>Required Education, Training and Experience</strong></h3><ul><li><p>Bachelor's degree required — Microbiology or related field.</p></li><li><p>Minimum of 6 years' experience in industry and product development, including demonstrated ability to lead a team.</p></li></ul><h3><strong>Preferred Education, Training and Experience</strong></h3><ol><li><p>Advanced degree preferred; PhD in microbiology or related field.</p></li><li><p>5+ years of relevant industry experience in microbiology or diagnostic assay development, including a minimum of 3 years in a managerial role within a regulated medical device or diagnostics environment.</p></li></ol><div> </div><h2><strong>Knowledge, Skills, and Abilities (KSAs)</strong></h2><ul><li>Consistently upholds and reflects the core ethical principles and values that bioMérieux promotes.</li><li><p>Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared deliverables.</p></li><li><p>Effective Presentation Skills.</p></li><li><p>Comfortable giving clear, direct, and actionable feedback.</p></li><li><p>Strong analytical and problem-solving skills.</p></li><li><p>Demonstrated ability to make sound decisions using data to guide decision-making and manage complex information.</p></li><li><p>Demonstrates strong core knowledge; manages complex tasks and integrates multiple tools and technologies.</p></li><li><p>Demonstrated expertise in microbiological resistance mechanisms and antimicrobial susceptibility testing methodologies.</p></li><li><p>Experienced supporting verification and validation activities for IVD products, including assays built around ID/AST or CE-IVD.</p></li><li><p>Strong data analysis and troubleshooting skills, with demonstrated ability to interpret complex datasets and drive technical decision-making.</p></li><li><p>Strong proficiency with technical data analysis tools, including JMP, Tableau, or equivalent analytical tools.</p></li></ul><div> </div><h2><strong>Supervisory Responsibilities</strong></h2><ul><li><p>Direct supervision: 1–5 employees</p></li><li><p>Indirect supervision: 0 employees</p></li></ul><h2><strong>Working Conditions </strong></h2><ul><li><p>Travel requirement: up to 10% domestically and 5% internationally</p></li><li>Typical Lab/office environment</li></ul><p> </p><div>The estimated salary range for this role is between $105,000-$140,000. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux’s bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate’s experience and will be presented in writing at the time of the offer. </div><div>In addition, bioMérieux offers a competitive Total Rewards package that may include: </div><div>·        A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options </div><div>·        Company-Provided Life and Accidental Death Insurance </div><div>·        Short and Long-Term Disability Insurance </div><div>·        Retirement Plan including a generous non-discretionary employer contribution and employer match. </div><div>·        Adoption Assistance </div><div>·        Wellness Programs </div><div>·        Employee Assistance Program </div><div>·        Commuter Benefits </div><div>·        Various voluntary benefit offerings </div><div>·        Discount programs </div><div>·        Parental leaves </div><p> #LI-JS1</p><p> </p>

Biofire

Sr. Manager, R&D Microbiology

Biofire jobs

In addition, bioMérieux offers a competitive Total Rewards package that may include: · A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options · Company-Provided Life and Accidental Death Insurance · Short and Long-Term Disability Insurance · Retirement Plan including a generous non-discretionary employer contribution and employer match. Skilled in MS Office tools to include but not limited to Outlook, Teams, Word, and Excel — Intermediate: applies skills independently in most situations; handles moderately complex tasks with occasional guidance.

<h2>Job Posting: Associate Staff Scientist </h2><p><strong>Department:</strong> R&D Microbiology</p><h3>Position Summary</h3><p>Contributes, with technical and scientific expertise to the design and development of high-quality products on time, within budget, and with a high degree of customer satisfaction. Acts as a team leader for new product development or current product improvement projects.</p><h3>Primary Duties</h3><ol><li><p>Collaborate closely with the software, hardware development and system engineering teams.</p></li><li><p>Contribute to development of tools for analyzing large performance data sets generated from (AST/ID/molecular) experiments.</p></li><li><p>Support biological testing needed for assay development and system verification activities.</p></li><li><p>Troubleshoot technical issues that may arise in the (AST/ID/Molecular Biology) tests/system, record and report these issues cross-functionally, and provide suggestions and resolutions for improvement.</p></li><li><p>Perform experiments in the lab according to good lab practice.</p></li><li><p>Collaborate with other scientists and managers to optimize testing protocols and workflows within the lab.</p></li><li><p>Maintain accurate records of experiments and results, write work instructions (WIs), standard operating procedures (SOPs), protocols, reports, process flows etc...</p></li><li><p>Ensure compliance with regulatory standards (e.g., FDA, ISO) and comply with biohazard safety standards.</p></li><li><p>Participate in product risk assessment, technical design reviews and critically evaluate design and implementation plans.</p></li><li><p>Summarize findings and present results to cross-functional teams.</p></li><li><p>Mentor and train new and existing team members and be a technical advisor for data analysis problems.</p></li><li><p>Perform all work in compliance with company quality procedures and standards.</p></li><li><p>Perform other duties as assigned.</p></li></ol><div> </div><h3>Qualifications</h3><ul><li><p>Bachelor's degree required </p><ul><li>Specific Field: Life Sciences, Biomedical, Microbiology, related science field</li></ul></li><li><p>5 years of professional experience with data visualization/analysis software such as Tableau, JMP or RStudio and regulatory and the compliance requirements for IVD products (e.g., QSR, ISO, GLP).</p></li><li><p>Preferred: Experience in product development in regulated environment; proficient in good laboratory safety, aseptic technique, and basic Microbiology/Molecular technique</p></li><li>2 years of proficiency with using Python, R, or similar for data analysis</li><li>Advanced use and understanding of Excel</li></ul><div> </div><h3>Knowledge, Skills, and Abilities</h3><ul><li><div>Consistently upholds and reflects the core ethical principles and values that bioMérieux promotes</div></li><li><div>Comfortable giving clear, direct, and actionable feedback</div></li><li><div>Demonstrates assertiveness and confidence in the face of a challenge</div></li><li><div>Written communications – including the ability to communicate technical data in written form</div></li><li><div>Informing others by sharing clear, timely information to ensure alignment</div></li><li><div>Manage and meet competing deadlines, requiring careful prioritization and time management to ensure all tasks are completed on time</div></li><li><div>Skilled in MS Office tools to include but not limited to Outlook, Teams, Word, and Excel — Intermediate: applies skills independently in most situations; handles moderately complex tasks with occasional guidance</div></li><li><div>Teamwork and collaboration across diverse teams and fast-paced projects</div></li><li><div>Achievement orientation, analytical thinking, flexibility, information seeking</div></li></ul><div> </div><div>Working Conditions</div><ul><li><p>Stationary position (sitting or standing) for prolonged periods: Yes</p></li><li><p>Ascend/descend stairs, ladders, ramps: Yes</p></li><li><p>Wear PPE correctly most of the day: Yes</p></li><li><p>Operate repetitive motions: Yes</p></li><li><p>Adjust or move objects up to 50 pounds: No</p></li><li><p>Work in high places: No</p></li><li><p>International travel required: 5%</p></li><li><p>National travel required: 10%</p></li><li><p>Other physical requirements: Lab-based position; follows work practices for laboratory biohazards and chemical hazards. Hybrid work schedule - with ~60% of time in office.</p></li></ul><div> <div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">The estimated salary range for this role is between $92,000-$135,000. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux’s bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate’s experience and will be presented in writing at the time of the offer. </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">In addition, bioMérieux offers a competitive Total Rewards package that may include: </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Company-Provided Life and Accidental Death Insurance </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Short and Long-Term Disability Insurance </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Retirement Plan including a generous non-discretionary employer contribution and employer match. </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Adoption Assistance </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Wellness Programs </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Employee Assistance Program </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Commuter Benefits </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Various voluntary benefit offerings </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Discount programs </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">·        Parental leaves </div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px"></div><div style="background-repeat:no-repeat;outline:none;color:rgb( 51 , 51 , 51 );font-family:'open sans' , 'helvetica';font-size:14px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px">#LI-US</div></div>

Associate Staff Scientist

OTHER

FEED

Successful completion of a course study which meets all academic requirements for a bachelor's, or higher, degree in one of the chemical or biological sciences from an accredited institution, and in addition, at least six months of acceptable supervised experience and/or relevant training. Be capable of identifying problems that may adversely affect test performance or reporting of test results, and either must correct the problems or immediately notify the General Supervisor, Technical Supervisor, or Laboratory Director.

<p>Clinical Laboratory Scientist II</p><p><em>This is an onsite, in-office position at Geneoscopy HQ in St. Louis, Missouri.</em></p><p>The <strong>Clinical Laboratory Scientist II</strong> will be responsible for performing day-to-day routine patient testing within a high-complexity clinical laboratory.<br/><br/></p><p><strong>RESPONSIBILITIES</strong></p><ul><li>Perform work under general supervision, navigating moderately complex issues.</li><li>Each individual performs only those high-complexity tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training, or experience, and technical abilities.</li><li>Each individual performing high complexity testing must:<ul><li>Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting, and maintaining records of patient test results.</li><li>Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens.</li><li>Adhere to the laboratory's established quality assurance procedures, documenting all quality control activities, instrument and procedural calibrations, and maintenance performed.</li><li>Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.</li><li>Be capable of identifying problems that may adversely affect test performance or reporting of test results, and either must correct the problems or immediately notify the General Supervisor, Technical Supervisor, or Laboratory Director.</li><li>Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.</li></ul></li><li>Perform high complexity testing only under the on-site, direct supervision of a qualified General Supervisor.</li><li>Other duties as assigned.</li></ul><p> </p><p><strong>EDUCATION REQUIREMENTS</strong></p><ul><li>Minimum education requirements:<ul><li>Successful completion of a course study which meets all academic requirements for an bachelor's, or higher, degree in medical technology or laboratory science from an accredited institution; or</li><li>Successful completion of a course study which meets all academic requirements for a bachelor's, or higher, degree in one of the chemical or biological sciences from an accredited institution, and in addition, at least six months of acceptable supervised experience and/or relevant training.</li></ul></li></ul><p> </p><p><strong>QUALIFICATIONS</strong></p><ul><li>Possess a minimum of two years of clinical laboratory experience in a high-complexity, molecular diagnostic laboratory setting.<ul><li>Knowledge of CAP/CLIA regulations is preferable.</li></ul></li><li>Exemplify solid knowledge of the subject matter.</li><li>Exemplify the ability to multitask and thrive in an agile, fast-paced, deadline-driven environment while remaining flexible, proactive, resourceful, and efficient.</li><li>Possess proficient verbal and written communication skills, while willing to share and receive information and ideas from all levels of the organization to achieve the desired results.</li><li>Possess high ethics and conduct business in the most professional manner.</li><li>Seek inclusiveness and collaboration but step up to responsibility, make tough decisions, and be accountable for those decisions.</li><li>Act as a results-oriented team player with strong interpersonal and communication skills, capable of working collaboratively with colleagues.</li></ul><p> </p><p><strong>SCHEDULE<br/></strong>This is an hourly position with overtime for hours worked beyond 40 per week. There may be projects that require activities beyond the standard hours.</p><p> </p><p><strong>COMPENSATION & BENEFITS</strong></p><ul><li>Hourly rate determined based on the candidate's experience, knowledge, and abilities.</li><li>Benefits: health, vision, dental, life insurance, 401(k), and accrued paid time off.</li></ul><p> </p><p><strong>ADDITIONAL INFORMATION</strong></p><p><strong>Geneoscopy's Core </strong><strong>Values</strong><br/>Ability to embody Geneoscopy's beliefs, philosophies, and principles:</p><ul><li>Integrity - we do the right thing through our words, actions, and behaviors</li><li>Courage - step up, speak up, stand out</li><li>Agility - think and act fast, embracing change</li><li>Passion - for our customers, our people, our work, and for excellence</li><li>Collaboration - our differences are assets</li></ul><p><strong><br/>Physical Demands</strong></p><ul><li>Employees may be required to lift routine office supplies and use standard office equipment.</li><li>Must possess the ability to sit and/or stand for long periods.</li><li>Must possess the ability to perform repetitive motion.</li></ul><p><br/><strong>Work Environment</strong></p><ul><li>May have exposure to fumes and bio-hazardous material in the laboratory environment.</li><li>May be required to handle blood-borne pathogens and general laboratory reagents.</li></ul><p> </p><hr/><p><em>By completing this online employment application, you certify that the information on this application is true and complete to the best of your knowledge. You understand that any misrepresentation or omission of fact in response to any inquiry made in this application may result in the rejection of the application or if hired, dismissal whenever it is discovered. You authorize and release all parties from any liability or damage that may result from seeking, furnishing, or using such information. You understand and agree that, if hired, your employment is for no definite period and may, regardless of the date of payment of compensation, be terminated by Geneoscopy at any time, for any or no reason, with or without notice. You understand that no representation to the contrary is valid unless in writing, setting a definite term of employment, and signed by the company's CEO. You further understand and agree that any job offer is contingent upon your passing, to the company's satisfaction, a criminal background check, reference checks, and other possible screenings. You understand that this application is active for 90 days only, and if you do not hear from the company but still wish to be considered for employment after 90 days, you will need to fill out a new application.</em></p>

Geneoscopy, Inc.

Clinical Laboratory Scientist II

Analysis Skills

Background Investigation

Biology

Clinical Laboratory

Communication Skills

Compensation and Benefits

Corrective Action

Hazardous Materials/Substances

Identify Issues

Insurance Documentation

Interpersonal Skills

Laboratory

Laboratory Techniques

Medical Records

Molecular Analysis

Multitasking

Performance Analysis

Performance Management

Performance Testing

Presentation/Verbal Skills

Procedure Development

Quality Assurance

Quality Control

Record Keeping

Reference Verification

Regulations

Sample/Specimen Processing

Team Player

Technical Leadership

Testing

Time Management

Writing Skills

Talent Acquisition

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Sr. Manager, R&D Microbiology Biofire

Associate Staff Scientist Biofire

Clinical Laboratory Scientist II Geneoscopy, Inc.

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