NanoComposix is a privately-held R&D and manufacturing company that develops innovative nanomaterials for research and commercial markets. We manufacture hundreds of different variants of metal and metal-oxide core/shell nanocomposites for a wide range of applications including biosensors, medical devices, clinical diagnostics, and optical effects. Our mission is to help our clients bring nano-enabled products to market. We’re passionate about what we do and are looking for smart, energetic, and self-motivated individuals who take pride in their work to join our fun and innovative team in this exciting industry.
Benefits include medical and dental insurance, paid vacation and personal days, retirement plan with company-match, and an annual bonus program with opportunity for stock ownership in this employee-owned business.
You can see a list of our open opportunities below or go directly to our career application portal in the table.
+ Important notice for recruiters
Recruitment and the employment process is managed through the Human Resources Department and all candidates must be presented through this avenue. Recruiters are requested not to contact our hiring managers or employees directly to inquire about open positions or to present candidates. Complying with this request will be a factor in determining any initial or ongoing professional working relationship with nanoComposix.
To protect the interests of all parties involved, nanoComposix requires a signed agreement to be in place prior to the presentation of any candidates. Nanocomposix does not accept unsolicited resumes from any source other than directly from candidates for either current or future positions. Submission of unsolicited resumes in advance of a signed agreement between nanoComposix and the recruiter does not create any implied obligation on the part of nanoComposix. If and when a signed agreement is in place, the recruiter is responsible for following all submission policies set forth by nanoComposix as well as ensuring their candidates apply through the company website.
Updated August 12, 2020
The Quality Assurance Manager (IVD/POCT) will support the In-vitro Diagnostics and Lateral Flow Point-of-Care Testing department by leading hands-on the IVD/POCT Design Control process from feasibility through manufacturing / EUA release, while ensuring procedural and regulatory compliance. The QA Manager (IVD/POCT) will support continuous improvement, and on-going development of the Quality Management System, and support ISO 13485 certification. The QA Manager (IVD/POCT) will be responsible for IVD/POCT Quality reporting, CAPAs, validations, specification development, NCM reporting, internal and external audits, and IVD/POCT regulatory reporting and compliance domestically and internationally with cross-functional support.
Key Responsibilities
- Oversee aspects of the quality management system and support documentation and processes specific to IVD/POCT
- Lead IVD/POCT Design Control
- Report to Management on the performance of the quality management system and any need for improvement
- Recruit, lead, manage, and develop the Quality Assurance (IVD/POCT) staff including responsibilities for selection, coaching, performance management, and talent development of the team
- Evaluate and sign off on IVD/POCT CAPAs, quality plans, documentation, customer complaints, audits, validations, training, NCMRs and other quality feedback mechanisms
- Review product documentation and records, including quality control test results, as needed for the release of product
- Develop product and process inspection plans and criteria
- Recognize and handle product, process and quality system nonconformities
- Maintain an in-depth understanding of the quality and documentation systems, applicable standards and requirements
- Monitor process controls associated with all IVD/POCT business functions to ensure compliance with the requirements and intent of the established ISO quality system
- Maintain an awareness of Regulatory Affairs (FDA EUA, relevant domestic and international regulations) as it relates to and impacts IVD/POCT manufacturing and distribution, including the requirements for vigilance reporting
- Support and approve audits: internal, external, and supplier
- Conduct quality system training for company and IVD/POCT department personnel as required to comply with quality system requirements
- Review IVD/POCT product documentation and records, including quality control test results, as needed (for the release of product
- Recognize and handle product, process and quality system nonconformities
Education, Experience, & Skills
- Bachelor’s degree in business, science, or related technical field
- 7 years’ In-vitro Diagnostics / Point-of-Care Testing industry experience a must
- 7 years’ experience in Quality related systems
- At least 3 years of experience managing a team
- Ability to collaborate and communicate effectively within cross-functional teams
- Solid knowledge and experience with electronic quality system management software
- Ability to effectively prioritize, managing multiple projects with overlapping timelines
- Solid communication, decision-making, and organizational skills
- Ability to think critically and problem solve
- Ability to think strategically, and work tactically on multiple concurrent projects
- Computer proficiency with Microsoft Office products required
- Work Remotely: temporarily as a result of COVID-19; 50% required on-site
Application Process
Qualified candidates should create a pdf with both a cover letter and resume and apply online here. The cover letter should include information on how your previous experience relates to the job requirements and your availability. Specific examples are of interest. You will not be considered without a cover letter.
All your information will be kept confidential according to EEO guidelines.
This job is located in San Diego, California.
Updated May 6, 2019
A research associate is needed to assist with developing next-generation lateral flow tests based on both fluorescent and plasmonic particles. We are seeking a highly motivated individual with ability to design and conduct robust and efficient experiments to solve difficult technical problems. Must be able to work independently under supervision of a project manager, and be able to clearly document and communicate results. The applicant should be familiar with optimizing lateral flow assays and bioconjugation in general.
Responsibilities will include the functionalization of nanoparticles with antibodies and other targeting agents, assembling and running of lateral flow strips, and optimizing these devices to increase sensitivity and minimize non-specific background.
Requirements
- Bachelor's or master's degree in chemistry, biochemistry, bioengineering, or related field
- Experience with bioconjugation to surfaces or particles
- Experience with analytical, physical, inorganic, and organic chemistry laboratory procedures, techniques and equipment.
- Research experience in a relevant field of study.
- Ability to multi-task, handle frequently changing job functions, and rapidly learn new techniques and approaches.
- Good organizational skills
- Excellent verbal and written communication skills
- Must work well in a fast-paced, start-up environment.
- Due to government contractual obligations, US citizenship or green card is a requirement for this position
Desired Skills
- Lateral flow development
- Bioassays, antibody conjugation, fluorescent labeling
- Experience fabricating, functionalizing, and processing nanomaterials
- Strong instrumentation background including optical microscopy, UV-Vis, DLS, Zeta-Potential, DLS, TEM, or SEM
- Experience with analytical, physical, inorganic, and organic chemistry laboratory procedures, techniques and equipment.
- Familiar with cGMP or ISO 13485 compliant quality systems
Application Process
Qualified candidates should create a pdf with both a cover letter and resume and apply online here. The cover letter should include information on how your previous experience relates to the job requirements and your availability. Specific examples are of interest. You will not be considered without a cover letter.
Updated Jan 13, 2020
NanoComposix is searching for Project Managers and Senior Scientists to lead projects, manage scientific staff, and to bring lateral flow assays to market. This is a unique opportunity to leverage nanoComposix’s innovations in lateral flow R&D including ultra-bright reporter particles, covalent chemistry, and next-generation mobile point of care readers. The candidate will be expected to lead technical teams for assay development as well as support commercialization activities for both nanoComposix’s proprietary assays and assays developed for external clients.
A number of open positions at the senior level are available. The specific job description will depend on the candidate’s prior experience. Responsibilities include managing a highly motivated and innovative team of assay developers, transitioning R&D assays into an ISO 13485 compliant quality system, and coordinating regulatory and manufacturing activities for commercialization. The candidate will work closely with senior management to develop strategic plans for product development and expanding operations.
Requirements
- Bachelor’s, master’s, or PhD degree in chemistry, biochemistry, bioengineering, or a related field
- 5+ years of experience of immunoassay development
- Demonstrated track record of solving challenging issues with assay design, development, and optimization
- Excellent organizational and project management capabilities to facilitate internal and external scientific interactions
- Experience managing direct reports
- Strong verbal and written communication skills for generating high-quality proposals, presentations, and reports for clients
- Ability to multi-task, manage multiple projects and rapidly learn new techniques and approaches.
- Ability to work effectively in a cross-disciplinary environment.
- Must excel in a fast-paced, start-up environment
- Due to government contractual obligations, US citizenship or green card is a requirement for this position
Desired Skills
- Demonstrated track record of bringing point-of-care diagnostics from feasibility through transfer to manufacturing
- Direct, hands-on experience generating analytical assay development, optimization, and validation data packages in accordance with regulatory requirements
- Previous experience with ELISAs, antibody conjugation, protein purification, and fluorescent labeling
- Experience with cGMP / ISO 13485 compliant quality systems and the 510k approval process
- Drafting and release of standard operating procedures and batch production records
- Highly motivated and innovative problem solver able to independently design, execute, troubleshoot, and interpret experiments within a co-operative matrixed team environment.
- Experience working directly with clients
Application Process
Qualified candidates should create a pdf with both a cover letter and resume and apply online here. The cover letter should include information on how your previous experience relates to the job requirements and your availability. Specific examples are of interest. You will not be considered without a cover letter.
This job is located in San Diego, California.
Updated November 19, 2019
A Research Scientist position is available at nanoComposix. Responsibilities include working on a wide range of projects for government, academic and commercial clients (start-ups to Fortune 50). The applicant will leverage their nanoparticle synthesis background to fabricate stock products, custom products, and to develop new products that provide order-of-magnitude increases in performance or enable products that would not be possible without nanotechnology. At nanoComposix we are helping accelerate many different technologies to market and the applicant will participate in all aspects of commercialization including project planning, research, and development, scale-up, transfer to manufacturing, quality, marketing, and commercial production.
Requirements
- Masters or PhD degree in chemistry, biochemistry, chemical engineering or nanoengineering with experience in nanoparticle fabrication
- Experience with analytical, physical, inorganic, or organic chemistry laboratory procedures, techniques, and equipment.
- Ability to multi-task, handle frequently changing job functions, and rapidly learn new techniques and approaches.
- Great communicator and writer. Will be responsible for brainstorming new ideas for products and pitching early stage concepts both internally and externally.
- Must work well in a fast-paced, start-up environment.
- Must hold US citizenship or US green card
Desired Skills
- Fabrication of sol-gel, quantum dot, metal/metal oxide, polymer, core-shell nanoparticles, and composites.
- Synthesis of unagglomerated, low coefficient of variation metal and metal oxide nanoparticles (e.g. gold, silver, copper, platinum, magnetite, TiO2, SiO2, nanoparticles).
- Strong analytical background including experience with TEM, DLS, Zeta Potential, and optical microscopy and spectroscopy.
- Nanoparticle surface functionalization for transfer between organic and aqueous dispersions.
- Pilot or production scale chemistry including reactor design, production scale manufacturing, or continuous flow processes.
- Experience with the bioconjugation of targeting molecules to surfaces or particles
Application Process
Qualified candidates should create a pdf with both a cover letter and resume and apply online here. The cover letter should include information on how your previous experience relates to the job requirements and your availability. Specific examples are of interest. You will not be considered without a cover letter.
This job is located in San Diego, California.
Updated November 5, 2019
A nanoparticle synthesis research associate position is available at nanoComposix. Responsibilities include working with the product team to fabricate and characterize nanoparticles, prepare specification sheets, and carefully follow standard operating procedures for the large-scale production of nanoparticles. For candidates that have recently graduated, there are internship opportunities available with the possibility of converting to a full-time position.
Requirements
- Bachelors or Masters degree in chemistry, biochemistry or nanoengineering with a strong chemistry background or minor in chemistry.
- Experience with analytical, physical, inorganic, or organic chemistry laboratory procedures, techniques, and equipment.
- Research experience in a relevant field of study.
- Ability to multi-task, handle frequently changing job functions, and rapidly learn new techniques and approaches.
- Pays significant attention to detail and carefully documents all experimental procedures, observations, and methodology.
- Ability to keep organized data and records.
- Excellent oral and written communication skills.
- Strong computer skills including MS word, excel, and powerpoint.
- US citizenship or green card
Desired Skills
- Experience fabricating, functionalizing, and processing nanomaterials
- Experience with the bioconjugation of targeting molecules to surfaces or particles
- Experience with optical microscopes, UV-Vis, DLS, Zeta-Potential,TEM, or SEM.
Application Process
Qualified candidates should submit a resume and cover letter online here. The cover letter should include information on how your previous experience relates to the job requirements and your availability. Specific examples are of interest. You will not be considered without a cover letter. Candidate should be prepared to demonstrate their chemistry knowledge during the interview process.
Internship opportunities are available for recent graduates.
All of your information will be kept confidential according to EEO guidelines.
Updated July 29, 2020
A Production Chemist position is available at nanoComposix. This is a highly collaborative and hands on opportunity. Responsibilities include working with the team to ensure that the nanomaterial production schedule is maintained, all quality control measures are in place and followed, all nanomaterials are manufactured, processed and characterized as specified under a formal quality system, all team members are trained and have all of the tools necessary for success. See full list of responsibilities below.
Duties/Responsibilities
- Execute formulation and other lab activities
- Participates in Lean Initiatives and Activities.
- Assist in nonconforming and customer complaint investigation
- Ensuring that the manufacturing area is compliant with all required FDA, ISO and other applicable regulatory agency standards and documentation.
- Ensuring that the manufacturing area is compliant with the requirements associated with EHS, HR, Facilities, Housekeeping, etc.
- Maintains appropriate inventory levels of raw materials and supply items used in manufacturing.
- Develop and initiate policies and/or procedures for continual metric improvement.
- Assist when needed in both external and internal inventory audits.
- Review manufacturing records for accuracy and completeness in accordance with GMP.
- Coordinate lab shutdown activities to prevent production disruption.
- Actively contribute to team discussion, project planning and project execution
- Maintain an organized, safe and efficient work area at all times.
- Review batch records for accuracy and completeness.
- Resolve routine issues and escalate non-standard or critical issues
- Support new product transfer and validation and implementation of process improvements.
- Perform other duties and projects as assigned.
- Demonstrates commitment to the development, implementation and effectiveness of the Quality Management System per ISO, FDA and other regulatory agencies.
- Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
- Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.
Requirements
- BS in Chemistry or Biological Sciences
- 0-2 years’ experience in GMP chemistry manufacturing.
- Knowledgeable of federal and other regulations, e.g. QSR’s, ISO, ISO 13485.
- Ability to perform laboratory operations with a high degree of skill, efficiency and professionalism.
- Basic understanding of manufacturing systems (documentation, compliance, inventory control, production scheduling/controls, etc.).
- Must be very detail oriented.
- Must work well in a fast-paced, start-up environment.
- Solid understanding of the product and manufacturing processes.
- Excellent written and verbal communication skills.
- Occasional safe lifting of up to 45 pounds
- US citizenship or green card.
- Candidates must be local to San Diego County
Application Process
Qualified candidates should create a pdf with both a cover letter and resume and apply online here. The cover letter should include information on how your previous experience relates to the job requirements and your availability. Specific examples are of interest. You will not be considered without a cover letter.
This job is located in San Diego, California.
Updated July 29, 2020
A Research Scientist position is available at nanoComposix. Responsibilities include working on a wide range of projects for government, academic and commercial clients (start-ups to Fortune 50). The applicant will leverage their knowledge of molecular biology to help build rapid pathogen detection systems based on isothermal amplification. The role is a hands-on in the lab. At nanoComposix we are helping accelerate many different technologies to market and the applicant will participate in all aspects of commercialization including project planning, research, and development, scale-up, transfer to manufacturing, quality, marketing, and commercial production.
Requirements
- Masters or PhD degree in chemistry, biochemistry, chemical engineering or nanoengineering with specific expertise in optimization of isothermal amplifications, LAMP in particular. Candidates with extensive experience, but bachelor’s degrees are also encouraged to apply.
- Ability to multi-task, handle frequently changing job functions, and rapidly learn new techniques and approaches.
- Great communicator and writer. Will be responsible for brainstorming new ideas for products and pitching early stage concepts both internally and externally.
- Must work well in a fast-paced, start-up environment.
- Must hold US citizenship or US green card
- Must be able to start work in a very short time frame.
Desired Skills
- Familiarity with the challenges of point of care diagnostics
- Experience in working in a BSL-2 facility
- An understanding of the regulatory path for diagnostics
- Experience working in compliance with an iso13485 quality system is desirable
Application Process
Qualified candidates should create a pdf with both a cover letter and resume and apply online here. The cover letter should include information on how your previous experience relates to the job requirements and your availability. Specific examples are of interest. You will not be considered without a cover letter.
This job is located in San Diego, California.
