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Reports to: CEO
Supervises: Visiting Scholars; Event Management Staff; Vendors, Volunteers, Program Support Consultants
Location: Sarasota, Florida (on-site)
OUR MISSION
The Elling Eide Center is a nonprofit research library, nature preserve, and scholarly retreat located on 72 acres of rare coastal habitat in Sarasota, Florida. Named after sinologist and preservationist Elling Oliver Eide (1935–2012), the Center’s mission is to advance scholarly research in the humanities and environmental sciences with a particular emphasis on Asian studies. The Center is home to one of the most significant private collections of East Asian literature, history, and related fields in the United States, as well as one of the last remaining reserves of biodiversity in an increasingly urbanized Florida coastline. Our scholarly programs going forward will thus highlight our Center’s strengths in pre-modern Chinese Studies while finding new ways to connect with the Center’s landscape and living collections.
POSITION SUMMARY
The Director of Scholarly Programs and Education is responsible for shaping and helping to lead the overall research identity and multi-year research agenda of the Elling Eide Center in Sarasota, Florida.
We are seeking a rare individual to help us advance our approach to scholarship that provides students and scholars with unique opportunities to address critical questions that advance knowledge in fields connected to the Center’s mission. The successful candidate’s research and program interests will enable them to lead scholarly programs focused on Elling Eide’s own strong interests in sinology and ecology, as well as the pre-history and languages of the Native American people who once lived on our preserve. We seek a director who can strengthen the Center’s goal of making broad contributions to human knowledge.
To achieve so ambitious a mandate over the next five to ten years, this role will likely need to grow a whole education department and at first will coordinate the work of others more than produce original research. The Director of Scholarly Programs and Education is thus responsible for ensuring timely implementation, logistical coordination, and smooth delivery of all Center-led activities. The Director will work closely with the Director of the Eide Library and the Director of Land Management and Environmental Programs to facilitate engaging, mission-aligned programs and experiences both online and in person that expand community engagement and scholarly participation while contributing new insight to those arts and sciences so loved by Elling Eide.
DUTIES AND RESPONSIBILITIES
- Design, develop, coordinate, and execute our Visiting Scholars programs, residencies, and other fellowships
- Develop partnerships with other leading research institutions to promote all areas of our research agenda
- Recruit, train, and supervise new team members and volunteers as needed
- Coordinate, recruit, and manage volunteers to support our programs both in-person and online
- Establish and enforce standard operating procedures for our various kinds of scholarly programs
- Create and manage the departmental budget and align it with the organization’s annual budget
- Provide contractor oversight for remote broadcast and promotion of our programs online
- Participate in public outreach. Develop materials for public education/interpretation. Represent and promote the Elling Eide Center and our research agenda at offsite meetings and outreach events
REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES
- Ph.D. in Chinese Studies or related academic field
- Proficiency in classical Chinese including romanization systems
- Broad knowledge of Chinese history and culture, including scholarly resources and bibliographic tools as demonstrated in own research and publications
- Native proficiency in both English and modern Chinese complemented by excellent interpersonal, verbal, and written communication skills for collaborative work as a member of the Eide Center leadership team
- Leadership experience designing, developing, and delivering outstanding scholarly programs that command the international respect of academics in the field, attract media attention, and advance mission
- Ability and willingness to build and maintain good working relationships with a variety of national and international organizations to bring together people, projects, and resources in service of our mission
- Excellent problem-solving skills and organizational skills, with attention to detail and good records
- Self-starter, flexible, and able to work under pressure
- Highly competent with computer software, including Word, Excel, and PowerPoint
- Project management skills that extend to online portals and project management platforms
- Programs through social media, such as Instagram and Facebook
- Valid driver’s license (or ability to obtain one within 30 days)
DESIRABLE QUALIFICATIONS
- Reading ability in Japanese, Korean, and relevant European languages especially Russian, French, German
- Bachelor’s degree in the liberal arts or a life science preferred
SCHEDULE
- Full Time, 40 hours per week
- Occasionally will be required to work weekends/holidays as requested.
- Attend special events (as needed)
OTHER CONSIDERATIONS
Perform slightly strenuous work in varying or adverse weather conditions. Able to lift 50 pounds occasionally and/or up to 20 pounds frequently. Required to drive light-duty vehicles e.g. car, golf cart, truck.
BENEFITS
- Annual performance bonus (up to 20 percent of salary) for achieving departmental and organizational goals
- Ability to dedicate up to 20 percent of time on the job to original research — to write, publish, and contribute to the research of others — with the incentive to help drive the Eide Center research agenda
- Healthcare (company pays 90% of the annual cost), Dental and Vision, and 3% company contribution to a Fidelity Simple IRA account with employee participation
- 14 paid holidays and three weeks additional PTO
- Time and budget to participate in other professional development activities both for your own professional growth and to help with the Eide Center’s public visibility and outreach
SALARY
Negotiable based on experience and vision for the job
Join Our Client’s Team as a Scientist-II – Analytical R&D and be at the forefront of pioneering pharmaceutical innovations! In this dynamic role, you'll develop and establish cutting-edge analytical methods to support FDA-approved drug development, focusing on oral solids, liquids, and semi-solids. As a key contributor, you'll work hands-on in the lab, manage complex projects, and collaborate across departments to ensure scientific excellence and regulatory compliance. Your expertise will directly impact the safety and efficacy of vital healthcare products, making a meaningful difference in patients' lives.
What You'll Bring To The Table
- Bachelor’s Degree (BA/BS) in Chemistry or a related pharmaceutical science, with at least 5+ years of experience in analytical method development and validation, or
- Master’s Degree (MS/MA) with a minimum of 3+ years of relevant industry experience
- Extensive knowledge of cGMP, FDA/ICH guidelines, and regulatory standards (USP, Ph. Eur.)
- Hands-on experience with analytical instruments such as HPLC, GC, and familiarity with data acquisition software (Empower, Chemstation)
- Proficiency in laboratory management systems (Labvantage or equivalent) and Microsoft Office Suite
- Strong communication skills, with the ability to write clear reports and collaborate effectively with teams
- Experience with method transfer, stability studies, and troubleshooting
- Knowledge of DEA regulations and controlled substances handling
- Prior mentorship or training experience in analytical sciences
- Additional familiarity with reverse engineering, compatibility, and degradation studies
- Bachelor’s or Master’s degree in Chemistry or relevant pharmaceutical sciences
- 3 to 5+ years in a pharmaceutical analytical R&D setting, focusing on method development, validation, and regulatory compliance
- Ability to perform physical tasks including walking, standing, lifting up to 50 pounds, and working at various elevations
- Commitment to maintaining a safe, compliant laboratory environment and adhering to SOPs and regulatory guidelines
How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to and tell us why you’re interested. Or feel free to email your resume. Please include Job#19687.
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Company
Myrias Optics, Inc. is a fast-growing startup using proprietary nanoimprint technology to revolutionize the way optical components and systems are conceptualized, designed, and manufactured. The company is positioned to disrupt markets across a wide range of applications including consumer electronics, AR, 3D scanners and LiDAR, imaging systems, optical communications, medical equipment, optical computing and more. Our unique all-inorganic imprinted optics enable metalenses, diffractive optics, waveguides all manufactured using wafer level process. By removing any organic material, we not only eliminate environmental and reliability issues but at the same time enable more complex designs with unmatched optical performance and highly cost-effective manufacturing.
Website:
POSITION – Process Engineer
Reporting to the Technical Director, the Process Engineer will collaborate with a talented team of engineers and scientists to help develop and manufacture cutting-edge Myrias Optics components and systems. Specifically, this position will support Myrias’ nanoimprint ink development efforts, working with our process and characterization teams to optimize the formulations and process conditions to enable imprinted optical devices with high performance, high yield and new functionality. This position will also be responsible for transitioning the technology to our manufacturing team whose goal will be to bring a high volume, high yield nanoimprint process to market for our optical components and subsystems. This is an exciting opportunity for a highly motivated and capable engineer to gain expertise in the growing fields of meta-optics, waveguides, and diffractive optics. Together, we can shape next-generation optical systems for consumer devices, AR, medical instrumentation, automobiles, robotics, and more.
POSITION TYPE: Full time, on-site
SALARY RANGE: $70,000 - $90,000
LOCATION: Amherst, MA
RESPONSIBILITIES
Process and formulation development:
- Work closely with the Myrias process, characterization and manufacturing teams to develop and optimize ink formulations meeting product requirements and production standards
- Work with our manufacturing team to transitioning fabrication knowledge and processing techniques for all-inorganic nanoimprinting to high volume production, including formulations, stamp making and imprint processes
- Assist with fabrication of components and systems based on Myrias’ proprietary materials and processes meeting quality and optical performance specifications
- Conduct comprehensive nanoimprint ink tests and optimization, including formulation, imprinting, and post processing (calcination, ashing, etching, atomic layer deposition and/or overcoating)
- Performing metrology for fabricated components by top-down and cross-sectional scanning electron microscopy, variable angle spectroscopic ellipsometry, UV-Vis-NIR spectrometry and contact angle measurements
- Work with Myrias optical characterization team to feedback optical test results into process optimization efforts to enabling a closed loop process
- Familiarity with characterization and testing of optical devices, including the use of lenses, mirrors, light sources, fiber optics, cameras, lasers, and other optical devices is a strong plus
- Establish detailed and thorough documentation for all operating procedures and production processes
- Assist in expand Myrias’ fabrication capabilities by identifying and implementing new process improvements
- Development and maintain comprehensive database of research data, sample/product travelers, characterization and yield data, and sample histories
- Provide technical guidance and feedback to management for more efficient workflow
- Create detailed internal reviews and customer product reports
- Assist in providing customer support for new designs and products
- Monitor and participate in safe clean room practices
QUALIFICATIONS
- Bachelor’s degree in chemical engineering, material science, electrical engineering or equivalent technical discipline. A Master’s degree is a plus, Ph.D. Preferred
- 5+ years of industrial experience working with optical materials
- Strong understanding of chemical engineering, processing and optical testing and metrology
- Expertise in imprint or nanofabrication processes
- Experience with atomic layer deposition systems, high temperature oven, etching tools, ashers and evaporation tools
- Expertise with standard characterization tools like scanning electron microscopy, variable angle spectroscopic ellipsometry, UV/Vis/NIR spectroscopy and laser table characterization
- Ability to analyze and interpret complex datasets and validate system performance
- Experience with document control best practices
- Strong interpersonal and technical communication skills
- Experience with polymers, inorganic materials and chemicals with strong understanding of nanoparticle composites and binding chemistry
- The ability to problem-solve and trouble shoot complications safely
- Experience collaborating within and between personnel with multi-disciplinary backgrounds
- Familiar with the startup or early-stage business environment
- Entrepreneurial spirit, with a hands-on, roll-up-the-sleeves mentality
WHAT WE OFFER
- Competitive Compensation Package, including equity
- Full Medical, Vision and Dental plans
- Insurance: Company paid disability insurance
- Paid time off: Vacation and sick time
EEO Statement
Myrias Optics is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
If you are interested in the role, please submit your resume in .pdf format with a title of “[First name] [last name] Resume” to
About PFX™
We engineer leading fluid solutions that keep the world moving and we’re building a better future while we do it. As a vertically integrated global powerhouse, we operate 17 manufacturing facilities and 4 R&D centers across the world, delivering performance from lab to road in over 40 countries.
PFX Group™ brings together a family of trusted companies including Recochem, Prestone, Adam’s Polishes, B&B Blending, Kost USA, Ultra Clear, POR and Auto-Chem, each with deep expertise, regional insight, and a shared commitment to engineering excellence.
From automotive and heavy-duty thermal management systems to household and industrial solutions, our products are built for performance, reliability, and a commitment to sustainability. Join us and be part of a team that’s redefining what’s possible in fluid technology.
Job Summary:
The Analytical Lab Intern plays an integral role in product development and growth of the PFX /Prestone Organization. The responsibilities include the setup, testing, and documentation of analytical testing including physical properties and wet chemistry testing, based out of the PFX/Prestone Danbury, CT site. The PFX/Prestone Technology Center Analytical laboratory also performs ICP, HPLC/UHPLC, and GC/GC-MS testing on automotive consumer products. The Analytical Intern will be expected to run a variety of analytical tests in a demanding fast-paced environment with the internal R&D team as well as external partners to support the development of products, and solve problems based on the needs of the business.
Position Description:
We are currently seeking an applicant interested in an internship position in the Prestone Technology Center conducting analytical testing to support research activities, production, product stewardship, and technical growth. A person who is pursuing a chemistry undergraduate degree is preferred. Job assignments are varied; thus, flexibility is essential.
This is a fully on-site position based at our Danbury, CT location that will be offered during the Summer 2026, lasting for approximately 10-12 weeks. Work schedule is Monday-Friday, 40 hours/week. No housing or relocation assistance provided.
As part of the Research and Development team an intern must be able to work on multiple R&D or Development test items simultaneously. Duties include but are not limited to running and monitoring analytical laboratory testing equipment, and conducting wet chemistry tests to evaluate automotive products, with supervision. An interest in automobile technology is highly desirable.
Minimum Requirements:
- Current enrollment in undergraduate program.
- Must be able to follow instructions, work independently and safely in a laboratory environment and work on several projects at the same time.
- Completion of an analytical instrumentation course is a plus.
- Ability to work well with peers is required.
Principal Duties and Responsibilities:
Job assignments are varied, and flexibility is essential. Basic requirements include
- Conducts activities following established Corporate and Site Safety procedures and notifies the Supervisor of any unsafe conditions or practices in the area.
- Operates analytical equipment for samples submitted to the PTC Analytical laboratory, including pH, Refractive Index and Specific Gravity meters.
- Records and tabulates data in laboratory notebook in legal form following defined procedures.
- Observes irregularities, unusual behavior, or trends in tests, and communicates observations to Supervising Managers.
- Communicates the results of work to Supervisors following prescribed procedures.
Key Responsibilities
- Plan, schedule and carry out to completion, sample testing in accordance with PTC Analytical Laboratory Management system with supervision. Communicates results, conclusions and recommendations in person and in formal written reports.
- Must be able to safely follow detailed Analytical test procedures, making observations, recording test data into spreadsheets and laboratory notebooks, and summarizing data into presentable form.
- Ensure that samples are reported on time, meeting quality and turnaround targets.
- Possess good oral communication skills and a flexible approach to work. Conducts self in a professional manner and exerts a positive impact upon the morale and attitude of other team members.
UII America, Inc., a subsidiary company of Shanghai United Imaging Intelligence Healthcare Co. Ltd. (UII), is building an organization of highly-motivated, talented and skillful AI experts and software developers to strengthen our R&D power and address the need of our innovative products in the USA market. United Imaging Intelligence (UII) is committed to providing AI solutions for medical devices, imaging, and diagnosis – to helping clients better understand and embrace AI. United Imaging Intelligence is led by two world-renown leaders in the AI industry. Together, they will lead UII in focusing on “empowerment” and “win-win.” UII empowers doctors and equipment in order for doctors and hospitals to win, for research institutions to win, and for third-party companies to win. UII America, Inc. is building a world-class research and development team in Boston, MA.
We have immediate openings for Computer Vision and Robotics Research Interns with the following qualification requirements:
· Ph.D./M.S student in Computer Science, Electrical Engineering, Robotics, Data Science, Biomedical Engineering, Statistics, Applied Mathematics, or other related fields;
· Self-motivated and demonstrated problem solving and critical thinking skills;
· Familiar with at least one mainstream deep learning toolkit, e.g., Pytorch, Tensorflow;
· Familiar with Python, C++ and OpenCV;
· Proven track record of publications in the top computer vision, machine learning and robotics venues such as CVPR, ICCV, ECCV, NeurIPS, ICML, ICLR, AAAI, ICRA, IROS, RSS, TPAMI, IJCV, T-RO, and IJRR is a plus;
· Experience with 6D pose estimation, 3D visual perception, video understanding, efficient neural reconstruction, and embodied AI is a plus;
· Excellent communication skills and team-work spirit.
Main Responsibilities
· Conduct top-tier research in the area of Computer Vision and Robotics in a collaborative team-working environment;
· Working closely with full-time employees to come up with, implement, and verify research ideas;
· Fast prototyping, and developing cutting edge AI assets for the company;
· Contribute to intellectual properties, strong publications and transferring technologies into practical product solutions;
· Be ambitious to change future Healthcare with innovations.
The Program Associate, NS, functioning as the Community Engagement Liaison, will serve as a liaison to internal and external stakeholders including but not limited to victims, government agencies, hospitals, and community organizations in order to develop a more robust outreach, engagement, and evaluation function as it relates to the provision of OVS services to victims of crime in New York State. Specific duties include but are not limited to:
- Assist in the development and maintenance of a robust network of statewide connections for effective interaction with community leaders, allied professionals, and other community stakeholders in the victim services field.
- Serve as the primary liaison with the OVS Advisory Council, including coordinating the logistics of quarterly and ad hoc Council meetings.
- Lead the development of the OVS Mass Violence Response Council and oversee the implementation of regional training initiatives and events to enhance agency preparedness and collaboration with community stakeholders.
- Work collaboratively with staff in other OVS units to develop comprehensive relationships with regional and statewide victim assistance coalitions and advocacy groups.
- Act as a bridge between OVS, other State-based nongovernmental organizations (NGOs), and other State and local government agencies to improve and increase access to resources for victims of crime.
- Research and identify gaps in target populations who can benefit from OVS services including but not limited to victims, community associations, community stakeholders, schools, and non-profits.
- Develop recommendations and policy proposals to enhance services to crime victims and increase awareness of OVS programs.
- Meet with stakeholders to identify the community needs of crime victims and develop strategies to address those needs, specifically, the targeting of services to underserved populations.
- Elicit experiences and perspectives of victims of crime, stakeholders, and victim service providers that are directly impacted by the effects of victimization.
- Represent OVS at events where target populations and stakeholders are present, including but not limited to meetings, panels, conferences, and public events.
- Administer and manage applicable state operation contracts and oversee all contract compliance, reporting, and deliverables.
- Perform the full range of supervisory responsibilities.
Minimum Qualifications: Bachelor’s degree and three years of relevant experience.*
*Substitutions: Four years of specialized experience or associate’s degree and two years of specialized experience may substitute for bachelor’s degree; J.D. or master’s degree may substitute for one year of specialized experience; Ph.D. may substitute for two years of specialized experience.
Preferred Qualifications:Master's Degree in Public Administration, Social Work, or a related field; experience with stakeholder engagement, experience working with victim service providers and/or allied professionals; and familiarity with NYS procurement requirements.
Location: South San Francisco, CA (Onsite)
Key Responsibilities
- Design and synthesize small-molecule analogs to support SAR campaigns.
- Develop and execute efficient synthetic routes, including multi-step syntheses and late-stage diversification strategies.
- Utilize parallel or high-throughput approaches to generate focused compound libraries.
- Troubleshoot and optimize challenging reactions with scientific rigor and independence.
- Scale synthesis of intermediates and final compounds from milligram to decagram quantities.
- Collaborate closely with Medicinal Chemistry and cross-functional project teams to advance program goals.
- Coordinate with external CRO partners to plan and troubleshoot synthetic activities.
- Purify and characterize compounds using NMR, LC-MS, and related analytical techniques.
- Maintain high-quality electronic lab documentation suitable for IP and regulatory standards.
- Clearly communicate experimental rationale, progress, and results to internal and external stakeholders.
- M.S. or Ph.D. in Organic Chemistry or related discipline with 4+ years of pharmaceutical or biotechnology industry experience.
- Strong foundation in modern synthetic organic chemistry with demonstrated application of enabling technologies (e.g., photocatalysis, electrochemistry, transition metal–mediated transformations).
- Experience with parallel synthesis, high-throughput experimentation, or automated reaction platforms preferred.
- Proven ability to design and execute robust, scalable multi-step syntheses.
- Experience delivering high-quality compounds across varying scales.
- Prior experience working effectively with CRO partners.
- Excellent documentation practices and strong analytical interpretation skills.
- Strong communication skills and collaborative mindset.
Estimated Min Rate: $65.00
Estimated Max Rate: $77.00
What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
- Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
- Health Savings Account (HSA) (for employees working 20+ hours per week)
- Life & Disability Insurance (for employees working 20+ hours per week)
- MetLife Voluntary Benefits
- Employee Assistance Program (EAP)
- 401K Retirement Savings Plan
- Direct Deposit & weekly epayroll
- Referral Bonus Programs
- Certification and training opportunities
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:
The position of Technical Manufacturing Chemist is within the Infectious Disease (ID) business unit located at Scarborough, Maine. In this role you will produce material for use in immunology-based chromatography and enzyme tests.
(This job description is reviewed periodically and is subject to change by management.)
RESPONSIBILITIES:
• Maintains and supports the production schedule
• Investigates problem areas and areas of desirable improvement
• Undertakes new procedures and observes proper safety precautions
• Responsible for in-process QC testing of manufacturing material as it relates to
qualifications, quality inspections and titration.
• Maintains quality systems and proper GMP/GLP
• Creates and follows protocols designed around product improvement
• Responsible for making critical and non-critical bioreagents for use in product and manufacturing processes using Standard Operating Procedures (SOPs).
• Works in a team setting and coordinates manufacturing efforts based upon a set
production schedule and maintaining the raw bioreagent supply as needed to support this schedule.
BASIC QUALIFICATIONS | EDUCATION:
• Bachelors Degree in a Chemistry, Life Sciences, or related field or equivalent
combination of education and experience.
• Prior Experience in the following areas:
o Pipette
o Spectrophotometry
o HPLC
o pH meters
o Gel Electrophoresis o SDS Page
o ELISA assays
COMPETENCIES:
• Ability to work successfully as a member of a team and independently with moderate supervision.
• Skill in using computer applications including spreadsheet, database, manufacturing, and word processing software Provides reasonable accommodation to qualified individuals with disabilities.
The Scientific Affairs Director will perform duties in accordance with the performance expectations as well as Workplace Health and Safety Policies and Procedures.This will be ideally an On-site role.
The Scientific Affairs Director plays a key role in the scientific affairs strategic plan, the management of clinical research projects, the organization of the scientific assets developed by M2 Ingredients using their strong scientific expertise, leadership skills, and the ability to communicate findings effectively. Partnering with colleagues in the Scientific Affairs Team, the Scientific Affairs Director will support overall research and scientific communication to ensure M2 Ingredients is the leader in functional mushrooms health solutions.
The Scientific Affairs Director has the responsibility of managing the research project portfolio and assist with robust communications to increase the distribution of M2 Ingredients products globally through distribution partners in various geographies. They will help to create scientific dossiers and marketing assets intended for distribution to the M2 customers and key stakeholders to showcase M2 as the industry leader in manufacturing full spectrum mushroom mycelium products.
Essential Duties and Responsibilities:
- Responsible for coordinating and managing research projects with external clinical research organizations and universities, including study synopsis creation, study designs, managing timelines, payment schedules, progress reporting to internal stakeholders and final consolidation of research findings for the internal and external audiences.
- Contribute to manuscripts for publication in scientific journals when needed in collaboration with contract research organizations, the Chief Science Officer, and the scientific affairs team.
- Support the M2 Ingredients marketing team by generating guidance documents for various product formats, customer presentations, website copy, white paper write-ups, & other research commercialization assets.
- Generate nutrition science content and scientific communications in partnership with the cross functional team to enhance our brand presence.
- Build external networks (key experts, allies) to scope and facilitate new studies on M2 portfolio of products that will highlight their performance, support claims and thus, create a positive impact on the business.
- Lead grant writing to support research efforts when relevant
- Proactively monitor the scientific literature, research and new studies in the mushroom and dietary supplements industry as it relates to our business.
- Support the Director of Regulatory Affairs in collecting relevant data, as required, for regulatory submissions. This would include sample management, sample submissions to labs and collation of data.
- Respond to questions from internal teams and customers on synopsis of key research studies carried out, and their impact on product claims, as needed.
Qualifications:
- M.Sc./ Ph.D. in Preventative Health, Toxicology, Biology, Biochemistry, Chemistry or other relevant fields
- At least 5 yrs of experience in a scientific affairs role in the food or dietary supplement industry
- Scientific writing experience a must
- Experience with project management best practices and tools
- Previous experience working in the food, dietary supplement industry or for an ingredient company
- Experience with planning clinical trials and managing their timely execution
- Ability to work cross functionally and to manage external contractors and CROs
- Ability to travel in the US and internationally approximately 10% of the time
Company
Myrias Optics, Inc. is a fast-growing startup using proprietary nanoimprint technology to revolutionize the way optical components and systems are conceptualized, designed, and manufactured. The company is positioned to disrupt markets across a wide range of applications including consumer electronics, AR/VR, 3D scanners and LiDAR, imaging systems, optical communications, medical equipment, optical computing and more. Our unique all-inorganic imprinted optics enable metalenses, diffractive optics, waveguides all manufactured using wafer level process. By removing any organic material, we not only eliminate environmental and reliability issues but at the same time enable more complex designs with unmatched optical performance and highly cost-effective manufacturing.
Website:
POSITION – Lead Optical Characterization Engineer
Reporting to the CTO, the Lead Optical Characterization Engineer will collaborate with a talented team of engineers and scientists to test and evaluate cutting-edge Myrias Optics components and systems. Specifically, this position will lead experimental characterization of optical components, define and set up optical characterization systems, establish test and characterization procedures, develop efficient data acquisition and analysis methodologies, and grow and manage the optical characterization team. This role is ideal for someone with strong system-level thinking and hands-on optical experience, who is eager to lead complex interdisciplinary projects and mentor junior staff. You will serve as a bridge between software, hardware, and optical domains, ensuring our systems meet stringent performance and quality benchmarks. This is an exciting opportunity for a highly motivated and capable engineer to gain expertise in the growing fields of meta-optics, waveguides, and diffractive optics. Together, we can shape next-generation optical systems for consumer devices, AR/VR, medical instrumentation, automobiles, robotics, and more.
POSITION TYPE: Full time, on-site
SALARY RANGE: $125,000 - $145,000
LOCATION: Amherst, MA
EXPERIENCE LEVEL: Senior (5+ years)
Key Responsibilities
Technical Leadership & Systems Engineering
- Lead cross-functional efforts in the development and integration of optical test systems.
- Define and enforce system-level requirements, test procedures, and verification protocols.
- Coordinate resources and timelines for optical characterization projects from concept to execution.
- Provide technical mentorship and guidance to a growing team of engineers and technicians.
Optical Characterization and Metrology
- Design optical systems for high volume screening and characterization of wafer level optics operating in mass production environments.
- Execute precise optical measurements and characterization utilizing systems involving lasers, fiber optics, cameras, and power meters.
- Establish designs and processes for alignment and integration of optical components into custom assemblies.
- Develop calibration and validation methods to ensure high measurement fidelity and reproducibility.
Software and Automation Integration
- Oversee or contribute to development of software tools for machine control, data acquisition, and image processing.
- Drive system automation strategies for scalable and repeatable test and metrology setups.
Quality Control and Troubleshooting
- Establish quality assurance workflows, analyze measurement data, and resolve systemic performance issues.
- Manage root cause analysis and continuous improvement for metrology tools and setups.
Cross-Functional Collaboration
- Work closely with design and fabrication teams to influence product and measurement fixture development for testability.
- Maintain detailed technical documentation, review reports, and communicate project updates across teams.
Qualifications and Requirements
Experience
- Minimum 5 years in optical engineering, systems engineering, or optical characterization roles.
- Demonstrated leadership or mentorship experience in a technical setting.
Technical Expertise
- Strong proficiency with optical instruments such as cameras, lasers, power meters, and fiber optics.
- Familiarity with machine control programming in Python, LabVIEW, MATLAB, or similar.
- Experience integrating hardware/software in optical test setups.
Education
- Bachelor’s degree in Optical Engineering, Physics, Electrical Engineering, Mechanical Engineering or a related field.
- Master’s or Ph.D. preferred.
Skills
- Deep understanding of optical principles (reflection, refraction, alignment, metrology).
- Strong systems thinking and analytical skills for debugging and optimization.
- Excellent communication skills for technical collaboration and leadership.
Preferred Qualifications
- Experience with real-time control systems and/or machine vision.
- Familiarity with optical design tools (e.g., Zemax) and mechanical design tools (e.g., SolidWorks).
- Background in fast-paced R&D, manufacturing, or laboratory environments.
WHAT WE OFFER
- Competitive Compensation Package, including equity
- Full Medical, Vision and Dental plans
- Insurance: Company paid disability insurance
- Paid time off: Vacation and sick time
EEO Statement
Myrias Optics is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
APPLY
If you are interested in the role, please submit your resume in .pdf format with a title of “[First name] [last name] Resume” to