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.
Updated May 6, 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
- Bachelor's 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.
- Due to government contractual obligations, US citizenship or green card is a requirement for this position
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 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. Candidate should be prepared to demonstrate their chemistry knowledge during the interview process.
Updated May 6, 2019
nanoComposix Inc., has an immediate need for a Quality Assurance Manager (Part-Time)experienced in the medical device and/or pharmaceutical industries. This is a unique opportunity to support nanoComposix bring a wide variety of medical devices, topical therapeutics, and nanomedicines through clinical trials to commercialization.
Position Summary
The Quality Assurance Manager (Part-Time) will be responsible for Quality department management and supporting various aspects of the Quality Management System, including: document control, non-conforming materials program management, calibration program management, batch record/device history records reviews, training program management, quality record management, internal audit / external audit management, developing and measuring Key Quality Initiatives. The position is part-time with approximately 20 hours a week on-site.
Key Duties and Responsibilities include the following:
- Manage the Quality Department.
- Manage the Document Control function and maintain all Quality Management System records.
- Support Manufacturing in generating and revising Bill of Materials, Raw Material Specifications, Labels, Finished Good Specifications, and Batch Records.
- Support R&D and Manufacturing Product Development in the Design Control process through Clinical Trials, and Commercialization. Transfer of methods to Manufacturing Batch Records.
- Manage the Calibration & Preventive Maintenance Program activities and maintain related records.
- Manage the Employee Training Program.
- Manage non-conforming material (NCR) & CAPA activities.
- Manage the Approved Supplier Program.
- Perform Batch Record/Device History Records reviews for product release.
- Coordinate and Manage Internal Audit activities, External Audit activities, Key Quality Initiatives.
Requirements
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Minimum – Associates Degree
- Working knowledge of GDP; FDA 21 CFR, Part 820, Quality System Regulations; and ISO 13485.
- Working knowledge of: FDA 21 CFR, Part 210 & 211; ISO 9001 a plus.
- Exceptional organizational skills
- Excellent written and verbal communication skills
- Capable of supporting cross-functional project goals with a Quality focus
- Ability to work effectively in a positive, fast-paced, start-up, team environment
Desired Skills
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Medical Device Experience – 10 years minimum in an application requiring chemical, biological, or nanomaterial reagent manufacturing.
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SOP and Batch Record Experience – 10 years minimum drafting and releasing standard operating procedures and batch production records
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Management Experience– 10 years minimum
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Quality Assurance/Quality System Experience – 10 years minimum
- Scientific background in biology or chemistry
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 May 6, 2019
nanoComposix Inc., has an immediate need for a Document Control/Quality Assurance Specialist with experience in the medical device and/or pharmaceutical industries. This is a unique opportunity to help nanoComposix bring a wide variety of medical devices, topical therapeutics, and nanomedicines through clinical trials to commercialization.
Position Summary
The Document Control / Quality Assurance Specialist will be responsible for day-to-day administration and supporting various aspects of the Quality Management System, including: document control, receiving inspection, non-conforming materials program, calibration program, batch record/device history records reviews, training records, quality record management, etc. The Document Control / Quality Assurance Specialist coordinates and participates in Internal Audit activities, and Key Quality Initiatives.
Key Duties and Responsibilities include the following:
- Administrate the Document Control function and maintain all Quality Management System records.
- Support Manufacturing in generating and revising Bill of Materials, Raw Material Specifications, Labels, Finished Good Specifications, and Batch Records.
- Support R&D and Manufacturing Product Development in the Design Control process through Clinical Trials, and Commercialization. Transfer of methods to Manufacturing Batch Records.
- Coordinate Calibration & Preventive Maintenance Program activities and maintain related records.
- Maintain employee training records.
- Coordinate non-conforming material (NCR) & CAPA activities.
- Initiate Supplier Qualification process and follow-up with suppliers on product issues.
- Perform Batch Record/Device History Records reviews for product release.
- Coordinate and Participate in Internal Audit activities, External Audit activities, Key Quality Initiatives.
Requirements
-
Minimum – 2 year college degree
- Working knowledge of GDP; FDA 21 CFR, Part 820, Quality System Regulations; and ISO 13485.
- Working knowledge of FDA 21 CFR, Part 210 & 211; ISO 9001 a plus.
- Exceptional organizational skills
- Excellent written and verbal communication skills
- Capable of supporting cross-functional project goals with a Quality focus
- Ability to work effectively in a positive, fast-paced, start-up, team environment
- Scientific background in biology or chemistry
Desired Skills
-
Medical Device Experience – 3 years minimum in an application requiring chemical, biological, or nanomaterial reagent manufacturing.
-
SOP and Batch Record Experience – 3 years minimum drafting and releasing standard operating procedures and batch production records
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Document Control Experience – 3 years minimum
-
Quality Assurance/Quality System Experience – 3 years minimum
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. Candidate should be prepared to demonstrate their chemistry knowledge during the interview process.
Updated May 6, 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.
- Due to government contractual obligations, US citizenship or green card is a requirement for this position
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. Candidate should be prepared to demonstrate their chemistry knowledge during the interview process.
Updated May 6, 2019
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 bioassay development with a focus on lateral flow immunoassays
- Demonstrated track record of solving challenging issues with lateral flow assay design, development, and optimization
- Direct, hands-on experience generating analytical assay development, optimization, and validation data packages in accordance with regulatory requirements
- Excellent organizational and project management capabilities to facilitate internal and external scientific interactions
- 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
- 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.
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 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.
