Careers

Even if you don’t match one of our job descriptions, we always want to hear from anybody who is passionate about diagnostics and patient healthcare – drop us your resumé and a cover letter if you’re interested!

  • Position Title: Director of Operations and Project Management
    Department: Operations
    Location: San Diego

    Company Overview:
    Beacon Scientific is a new CDMO for immunodiagnostics specializing in the research, development, and manufacturing of cutting-edge lateral flow assays. We are a company of scientists, for scientists, and preach data driven decision making to guide our clients to success. We emphasis close collaboration across departments, and open communication with our clients so they are involved and informed throughout the development process. We are seeking driven, highly motivated, and detail-oriented individuals who enjoy close collaboration with their peers and interested in building positive and productive work environment.

    Position Summary:
    The Director of Operations and Project Management will oversee all operational aspects of the company, ensuring that projects are delivered on time, within scope, and budget. This role is pivotal in driving the company's operational strategy, optimizing processes, and leading cross-functional teams to achieve business objectives.

    Key Responsibilities:

    • Lead and manage the operations team to ensure efficient production processes, resource allocation, and project delivery.

    • Oversee the planning, execution, and delivery of all projects, ensuring alignment with company goals and client expectations.

    • Develop and implement operational strategies, policies, and procedures to optimize efficiency and scalability.

    • Monitor and report on key performance indicators (KPIs) to track project progress, operational efficiency, and resource utilization.

    • Collaborate with the R&D, Quality, and Manufacturing teams to ensure seamless project transitions from development to production.

    • Manage relationships with clients, vendors, and stakeholders to ensure project alignment and satisfaction.

    • Ensure compliance with industry regulations, including GMP, FDA, and other relevant standards.

    • Lead continuous improvement initiatives to enhance operational performance and project management practices.

    • Provide leadership and mentorship to the operations and project management teams, fostering a culture of accountability, innovation, and collaboration.

    Required Skills and Qualifications:

    • Educational Background: Bachelor’s degree in Engineering, Life Sciences, Business Administration, or a related field. An MBA or advanced degree is preferred.

    • Experience: Minimum of 10 years of experience in operations and project management within the pharmaceutical, biotech, or CDMO industries.

    • Technical Expertise:

      • Strong understanding of manufacturing processes, quality control, and regulatory requirements.

      • Proven track record in managing complex projects from inception to completion.

      • Experience with Lean, Six Sigma, or other process improvement methodologies.

    • Leadership and Management:

      • Demonstrated ability to lead and inspire cross-functional teams.

      • Excellent organizational and time-management skills with the ability to manage multiple priorities.

      • Strong problem-solving and decision-making abilities.

    • Communication and Interpersonal Skills:

      • Excellent communication skills, with the ability to effectively interact with clients, stakeholders, and team members.

      • Ability to build and maintain strong working relationships.

    • Financial Acumen:

      • Strong understanding of budgeting, cost management, and financial analysis.

      • Experience managing operational budgets and project financials.

    • Regulatory Knowledge:

      • In-depth knowledge of GMP, FDA, and other relevant regulatory requirements in the pharmaceutical and biotech industries.

    Preferred Qualifications:

    • PMP (Project Management Professional) certification or equivalent.

    • Experience in a leadership role within a Contract Development and Manufacturing Organization (CDMO).

    • Familiarity with ERP systems and project management software.

    Application Process:
    Interested candidates should submit their resume and a cover letter detailing their relevant experience to HR@beacon-sci.com or apply using the form on this page.

  • Position Title: Lateral Flow Research Associate
    Department: Research & Development (R&D)
    Location: San Diego

    Company Overview:
    Beacon Scientific is a new CDMO for immunodiagnostics specializing in the research, development, and manufacturing of cutting-edge lateral flow assays. We are a company of scientists, for scientists, and preach data driven decision making to guide our clients to success. We emphasis close collaboration across departments, and open communication with our clients so they are involved and informed throughout the development process. We are seeking driven, highly motivated, and detail-oriented individuals who enjoy close collaboration with their peers and interested in building positive and productive work environment.

    Position Summary:
    The Lateral Flow Research Associate will play a critical role in the development and optimization of lateral flow assays, and will work closely with both research scientist and senior scientists across cross-functional teams. The ideal candidate will perform laboratory experiments, document findings, and contribute to the successful development of high-quality diagnostic products. The role will also include presenting data both internally and externally, and will require strong oral and written communication skills.

    Key Responsibilities:

    • Assist in the development and optimization of lateral flow immunoassays, including reagent preparation, membrane selection, and assay assembly.

    • Perform routine laboratory tasks such as buffer preparation, antibody conjugation, and membrane coating.

    • Conduct experiments to evaluate assay performance, sensitivity, and specificity, and assist in troubleshooting assay issues.

    • Record experimental data meticulously, maintain laboratory notebooks, and generate technical reports.

    • Collaborate with the R&D team to support the transfer of assays from development to manufacturing.

    • Ensure compliance with laboratory safety protocols and quality standards.

    Required Skills and Qualifications:

    • Educational Background: Bachelor’s degree in Biochemistry, Molecular Biology, Chemistry, or a related field.

    • Experience: Minimum of 1 years of hands-on experience in a laboratory setting, preferably with exposure to lateral flow assay development or immunoassays.

    • Technical Expertise:

      • Basic knowledge of lateral flow assay principles and techniques.

      • Experience with routine lab procedures, including reagent preparation, pipetting, and data recording.

      • Familiarity with data analysis tools and techniques.

    • Attention to Detail: High level of accuracy in conducting experiments and recording data.

    • Teamwork: Ability to work collaboratively with scientists and other team members.

    • Communication: Strong verbal and written communication skills, with the ability to follow protocols and document results clearly.

    Preferred Qualifications:

    • Experience working in a contract development and manufacturing environment.

    • Knowledge of GMP (Good Manufacturing Practices) and quality management systems (QMS).

     Application Process:
    Interested candidates should submit their resume and a cover letter detailing their relevant experience to hr@beacon-sci.com or apply using the form on this page.

  • Position Title: Lateral Flow Research Scientist
    Department: Research & Development (R&D)
    Location: San Diego

    Company Overview:
    Beacon Scientific is a new CDMO for immunodiagnostics specializing in the research, development, and manufacturing of cutting-edge lateral flow assays. We are a company of scientists, for scientists, and preach data driven decision making to guide our clients to success. We emphasis close collaboration across departments, and open communication with our clients so they are involved and informed throughout the development process. We are seeking driven, highly motivated, and detail-oriented individuals who enjoy close collaboration with their peers and interested in building positive and productive work environment.

    Position Summary:
    The Lateral Flow Research Scientist are the backbone of the company. The role will be responsible for the design, development, and optimization of lateral flow immunoassays from prototype through to manufacturing. This role involves conducting experiments, analyzing data, and collaborating with cross-functional teams to ensure the successful development of high-quality diagnostic products. The role will be customer facing and require strong communication skills and organization.

    Key Responsibilities:

    • Conduct research and development activities focused on lateral flow immunoassay design and optimization.

    • Develop and validate new lateral flow assays, including reagent formulation, membrane selection, and antibody conjugation.

    • Perform experiments to evaluate assay performance, sensitivity, and specificity, and troubleshoot any issues that arise.

    • Collaborate with cross-functional teams, including manufacturing, quality, and regulatory, to ensure smooth transition from R&D to production.

    • Document research findings, prepare technical reports, and present data to internal teams and external stakeholders.

    • Stay updated on the latest advancements in lateral flow technology and apply new techniques to improve assay performance.

    Required Skills and Qualifications:

    • Educational Background: Bachelor or Master’s degree in Biochemistry, Molecular Biology, Chemistry, or a related field with a focus on immunoassays or diagnostics.

    • Experience: Minimum of 3 years of experience in lateral flow assay development or a related field, with hands-on experience in process development and scale-up. 5+ years of experience preferred.

    • Technical Expertise:

      • Strong understanding of lateral flow assay design, development, and troubleshooting.

      • Expert in bioconjugation and protein chemistry

      • Experience with reagent preparation, antibody conjugation, and reagent selection.

      • Proficiency in data analysis and interpretation, with experience using statistical software such as JMP and MATLAB.

    • Problem-Solving: Demonstrated ability to troubleshoot assay issues and optimize processes for improved performance.

    • Communication: Excellent verbal and written communication skills, with the ability to effectively present scientific data to diverse audiences.

    • Teamwork: Ability to work collaboratively within cross-functional teams and contribute to project goals.

    Preferred Qualifications:

    • Expert in affinity reagent and material screening and selection.

    • Experienced in product development for qualitative, semi-quantitative, and quantitative immunoassays.

    • Experienced in immunoassay platform development that includes, but not limited to, fluorescent or colorimetric reader integration and consumable evaluation.

    • Experience in transferring assays from R&D to manufacturing.

    • Knowledge of regulatory requirements, including ISO 13485 and FDA guidelines, for medical diagnostics.

    Application Process:
    Interested candidates should submit their resume and a cover letter detailing their relevant experience to hr@beacon-sci.com or apply using the form on this page.

  • Position Title: Senior Scientist – Lateral Flow Development
    Department: Research & Development (R&D)
    Location: San Diego

    Company Overview:
    Beacon Scientific is a new CDMO for immunodiagnostics specializing in the research, development, and manufacturing of cutting-edge lateral flow assays. We are a company of scientists, for scientists, and preach data driven decision making to guide our clients to success. We emphasis close collaboration across departments, and open communication with our clients so they are involved and informed throughout the development process. We are seeking driven, highly motivated, and detail-oriented individuals who enjoy close collaboration with their peers and interested in building positive and productive work environment.

    Position Summary:
    The Senior Scientist - Lateral Flow Development will play a critical role in the design, development, and optimization of lateral flow immunoassays for diagnostic applications. We seek individuals capable and comfortable being on the bench and desk, who enjoy leading both teams and projects. This position involves being the technical lead on projects, collaborating with cross-functional teams across the company, and ensuring that all development activities align with industry standards, regulatory requirements, and our clients needs. This role is customer facing so strong communication and organization skills are required.

    Key Responsibilities:

    • Lead the development and optimization of lateral flow immunoassays, including reagent formulation, assay design, and process development.

    • Manage and execute experiments to evaluate and improve assay performance, sensitivity, specificity, and any analytical or clinical requirements.

    • Collaborate with manufacturing, quality, and regulatory teams to ensure seamless transfer of assays from development to production.

    • Analyze experimental data, generate reports, and present findings to internal and external stakeholders.

    • Provide technical leadership and mentorship to junior scientists and laboratory staff.

    • Ensure compliance with regulatory standards such as ISO 13485 and FDA guidelines throughout the development process.

    • Stay current with industry trends, advancements, and emerging technologies in lateral flow and diagnostic assay development.

    Required Skills and Qualifications:

    • Educational Background: Ph.D. in Biochemistry, Molecular Biology, Chemistry, or a related field with a strong focus on immunoassays or diagnostics. A Bachelor or Master’s degree with significant relevant experience may also be considered.

    • Experience: Minimum of 5 years of hands-on experience in lateral flow assay development, including experience in a CDMO or diagnostics company.

    • Technical Expertise:

      • Deep knowledge of lateral flow assay principles, design, and troubleshooting.

      • Experience with reagent selection, antibody conjugation, and membrane selection.

      • Proficiency in assay optimization techniques and statistical data analysis.

    • Project Management: Demonstrated ability to lead projects from concept to completion, managing timelines, resources, and deliverables effectively.

    • Communication: Excellent verbal and written communication skills, with the ability to present complex scientific concepts to diverse audiences.

    • Regulatory Knowledge: Experience with ISO 13485, FDA QSR, and other relevant regulatory requirements for medical diagnostics.

    Preferred Qualifications:

    • Experience in the transfer of assays from R&D to manufacturing.

    • Knowledge of automated assay development and high-throughput screening techniques.

    • Previous experience in a leadership or supervisory role.

     Application Process:
    Interested candidates should submit their resume and a cover letter detailing their relevant experience to hr@beacon-sci.com or apply using the form on this page.

  • Position Title: Process Development Scientist
    Department: MSAT
    Location: San Diego

    Company Overview:

    Beacon Scientific is a new CDMO for immunodiagnostics specializing in the research, development, and manufacturing of cutting-edge lateral flow assays. We are a company of scientists, for scientists, and preach data driven decision making to guide our clients to success. We emphasis close collaboration across departments, and open communication with our clients so they are involved and informed throughout the development process. We are seeking driven, highly motivated, and detail-oriented individuals who enjoy close collaboration with their peers and interested in building positive and productive work environment.

    Position Summary:
    The Lateral Flow Process Development Scientist will be responsible for the development, optimization, and validation of lateral flow assay manufacturing processes. This is a critical role that bridges development and manufacturing and will requires familiarity with the processes associated with both. This role involves working closely with cross-functional teams to scale up processes from bench to production, ensuring consistency, quality, and compliance with regulatory standards. This role can be customer facing so strong oral and communication skills will be required.

    Key Responsibilities:

    • Develop and optimize lateral flow assay processes from lab-scale to manufacturing-scale production.

    • Design experiments to evaluate and improve the performance and robustness of lateral flow assays.

    • Collaborate with the R&D, quality control, and manufacturing teams to ensure seamless process transfer and scalability.

    • Analyze and interpret data, providing recommendations for process improvements.

    • Document all development work, including protocols, data, and reports.

    • Ensure compliance with industry regulations and standards, including ISO 13485 and FDA guidelines.

    • Troubleshoot process issues and implement corrective actions as needed.

    • Stay updated on the latest advancements in lateral flow technology and apply relevant innovations to current processes.

    Required Skills and Qualifications:

    • Educational Background: Minium bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related field. Ph.D. or Master’s degree preferred but not required.

    • Experience: Minimum of 3 years of experience in lateral flow assay development or a related field, with hands-on experience in process development and scale-up. 5+ years of experience preferred.

    • Technical Expertise:

      • Strong understanding of lateral flow assay design, development, and manufacturing.

      • Proficiency in analytical techniques such as ELISA, chromatography, and spectroscopy.

      • Experience with manual, semi-automated, and automated diagnostic manufacturing equipment

      • Experience with statistical analysis and Design of Experiments (DOE) methodologies.

      • Familiarity with statistical software such as JMP, Analyse-IT, or MATLAB.

    • Problem-Solving: Demonstrated ability to troubleshoot complex technical issues and optimize processes for consistency and efficiency.

    • Attention to Detail: High level of accuracy in experimental design, data analysis, and documentation.

    • Communication: Excellent verbal and written communication skills, with the ability to collaborate effectively across teams.

    • Project Management: Experience managing multiple projects simultaneously, with strong organizational and time-management skills.

    • Personnel Management: Desire and/or experience directly managing teams and building teams through new hires.

    • Regulatory Knowledge: with industry standards and regulatory requirements, including ISO 13485 and FDA regulations for diagnostic products.

    • Teamwork and Leadership: Ability to work effectively in a collaborative, team-oriented environment. A willing leader to motivate and support cross functional teams.

    Preferred Qualifications:

    • Experience with automated manufacturing processes and equipment.

    • Knowledge of lean manufacturing principles and practices.

    • Experience with quality management systems (QMS) and good manufacturing practices (GMP).

    Application Process:
    Interested candidates should submit their resume and a cover letter detailing their relevant experience to HR@beacon-sci.com or apply using the form on this page.

  • Position Title: Production Chemist
    Department: MSAT
    Location: San Diego

    Company Overview:

    Beacon Scientific is a new CDMO for immunodiagnostics specializing in the research, development, and manufacturing of cutting-edge lateral flow assays. We are a company of scientists, for scientists, and preach data driven decision making to guide our clients to success. We emphasis close collaboration across departments, and open communication with our clients so they are involved and informed throughout the development process. We are seeking driven, highly motivated, and detail-oriented individuals who enjoy close collaboration with their peers and interested in building positive and productive work environment.

    Position Summary:

    The Lateral Flow Production Chemist is an essential role at Beacon Scientific that both develops and executes manufacturing processes for lateral flow and other immunodiagnostics. The role will be responsible for the preparation, formulation, and production of lateral flow immunoassays. This role requires a strong background in chemistry and biochemistry experience with lateral flow technology and/or immunodiagnostics. The Production Chemist will work closely with the development teams and process development teams to scale up processes and ensure consistent, high-quality production.

    Key Responsibilities:

    • Prepare and formulate reagents, buffers, and solutions for lateral flow immunoassay production.

    • Optimize and scale up lateral flow assay production processes from R&D to manufacturing.

    • Perform quality control tests and assays to ensure product consistency and compliance with industry standards.

    • Troubleshoot and resolve production issues in a timely manner.

    • Collaborate with the R&D team to improve existing products and develop new formulations.

    • Maintain accurate records of production processes, formulations, and test results.

    • Ensure compliance with all safety and regulatory requirements during production activities.

    • Operate and maintain production equipment, ensuring it is in good working order.

    • Participate in continuous improvement initiatives to enhance production efficiency and product quality.

    Required Skills and Qualifications:

    • Educational Background: Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related field. Advanced degrees are a plus but not required.

    • Experience: Minimum of 1 year of experience in lateral flow assay development or production, or a related field in the diagnostic or pharmaceutical industries.

    • Technical Expertise:

      • Strong understanding of lateral flow immunoassay principles and technology.

      • Proficiency in the preparation of reagents, buffers, and solutions.

      • Familiarity with analytical equipment such as DLS and UV-Vis.

      • Experience with production equipment used in lateral flow assay manufacturing.

    • Quality Control: Knowledge of quality control principles and experience in conducting QC assays.

    • Problem-Solving: Strong analytical and problem-solving skills, with the ability to troubleshoot production issues effectively.

    • Attention to Detail: Meticulous attention to detail in all aspects of production and record-keeping.

    • Communication: Excellent verbal and written communication skills, with the ability to collaborate effectively across teams.

    • Regulatory Knowledge: Familiarity with industry regulations and standards (e.g., ISO 13485, FDA regulations) applicable to diagnostic product manufacturing.

    • Teamwork: Ability to work effectively in a team-oriented environment and contribute to continuous improvement efforts.

    • Time Management: Strong organizational skills with the ability to manage multiple tasks and prioritize workload effectively.

    Preferred Qualifications:

    • Experience with process development in a manufacturing environment.

    • Knowledge of automated production equipment.

    • Familiarity with GMP (Good Manufacturing Practices) and cleanroom environments.

    Application Process:
    Interested candidates should submit their resume and a cover letter detailing their relevant experience to HR@beacon-sci.com or apply using the form on this page.

  • Position Title: Senior Quality Engineer
    Department: Quality Assurance
    Location: San Diego

    Company Overview:
    Beacon Scientific is a new CDMO for immunodiagnostics specializing in the research, development, and manufacturing of cutting-edge lateral flow assays. We are a company of scientists, for scientists, and preach data driven decision making to guide our clients to success. We emphasis close collaboration across departments, and open communication with our clients so they are involved and informed throughout the development process. We are seeking driven, highly motivated, and detail-oriented individuals who enjoy close collaboration with their peers and interested in building positive and productive work environment.

    Position Summary:
    The Senior Quality Engineer will be responsible for leading quality engineering activities across all phases of product development and manufacturing. This role will an essential part of both the development and manufacturing arms of the company. The role will involve working closely with cross-functional teams to ensure that quality is built into our processes from design through production, and that all products meet regulatory requirements and industry standards.

    Key Responsibilities:

    • Develop, implement, and maintain quality engineering methodologies and systems to support product development and manufacturing.

    • Lead risk management activities, including FMEA (Failure Modes and Effects Analysis) and other risk assessment tools.

    • Conduct root cause analysis and implement corrective and preventive actions (CAPA) for quality issues.

    • Collaborate with R&D, manufacturing, and regulatory teams to ensure product quality and compliance with ISO 13485, FDA, and other relevant standards.

    • Oversee validation and verification activities, including process validation, design verification, and test method validation.

    • Lead internal and external quality audits and ensure timely resolution of audit findings.

    • Provide technical guidance and mentorship to junior quality engineers and other team members.

    • Ensure proper documentation and record-keeping in compliance with QMS (Quality Management System) requirements.

    • Continuously drive improvements in quality systems and processes to enhance product quality and operational efficiency.

    Required Skills and Qualifications:

    • Educational Background: Bachelor’s degree in Engineering, Life Sciences, or a related field. A Master’s degree or equivalent experience is preferred.

    • Experience: Minimum of 7 years of experience in quality engineering, with at least 5 years in the medical device or diagnostics industry.

    • Technical Expertise:

      • In-depth knowledge of ISO 13485, FDA QSR (Quality System Regulation), and other relevant regulatory standards.

      • Experience with risk management tools, including FMEA, and CAPA processes.

      • Strong understanding of validation and verification processes.

      • Proficiency in quality engineering methodologies such as Six Sigma, Lean, and statistical process control (SPC).

    • Problem-Solving: Demonstrated ability to lead root cause analysis and drive continuous improvement initiatives.

    • Leadership: Proven leadership skills with the ability to guide and mentor junior staff.

    • Communication: Excellent verbal and written communication skills, with the ability to work effectively across departments.

    • Attention to Detail: High level of accuracy in quality documentation, data analysis, and process validation.

    Preferred Qualifications:

    • Certified Quality Engineer (CQE) or Six Sigma Black Belt certification.

    • Experience in a contract development and manufacturing organization (CDMO) environment.

    • Experience with lateral flow and immunodiagnostic principles, design, and capabilities.

    • Familiarity with electronic QMS (eQMS) tools and software.

    Application Process:
    Interested candidates should submit their resume and a cover letter detailing their relevant experience to hr@beacon-sci.com or apply using the form on this page.