Cell Inspector Job Description Sample
Manager, Cell Chemistry Design
The Manager of Cell Chemistry Design will be responsible for development of new lithium-ion battery designs for lithium-iron-phosphate (LFP) and Nickel/Manganese/Cobalt (NMC) chemistries. This person will manage a team of 4-6 scientists and engineers, including BS, MS, and PhD level contributors. The team will be responsible for developing the cell chemistry and layer design. In addition, the Cell Development team will be responsible for generating material, subassembly, and assembly level specifications for all cell components (cathode, anode, electrolyte, and separator), often working with materials vendors and/or other internal stakeholders to align on material and component characteristics. The preferred candidate will have a track record of leadership in product development, an understanding of Tier-1 automotive, the battery industry, as well as the research community.
This person and their team will also interface closely with other functions in cell development and the larger organization. The group will interface frequently with peers in Fundamental R&D to evaluate new materials, Modeling to define requirements, and Validation to test new designs. The group will work with Cell Mechanical Design, defining the cell bill of materials (BOM) as well as all critical chemical and mechanical design parameters. The team will also be responsible for developing and maintaining a product DFMEA and support development of PFMEA and manufacturing control plans, working with Manufacturing teams to transfer processes and designs.
Travel up to 25% (including international) required.
This position will report to Director, Cell Design.
MS in chemistry, chemical engineering, materials science, or related field of study. PhD preferred.
Minimum 4+ years of experience in battery industry
3+ years in a product development role
3+ years in a management role
Demonstrated record of launching products successfully.
Experience with concept, design, and product validation (CV, DV, and PV) as part of a product development environment
Understanding of Failure Mode Effects Analysis (FMEA, DFMEA, PFMEA)
Experience maintaining effective technical relationships with suppliers and internal departments
Demonstrated record of technical innovation, including publications, presentations, and/or patents
Excellent oral and written communication skills.
Experience working in the automotive industry (Tier-1 supplier particularly)
Understanding of design-for-cost and value-added value-engineering (VA/VE)
Familiarity with Advanced Product Quality Planning (APQP) or similar product development process
Experience with formal root cause analysis (Ishikawa, Six Sigma) and design of experiments (DOE) tools
Experience with Design for Manufacturing (DFM)Document cell designs and maintain design concept iterations in Agile Documentation System
Good tolerance stack up calculation ability
Assembly Cell Operator Job
Primary responsibility is for the assembly of light fixtures, packing items into cartons, or other assembly work
Additional responsibilities may include:
Function as area spider (including manual movement of materials & product or with walkies/hand trucks)
Perform inventory control procedures/paperwork/computer work
Responsible for safety and general housekeeping
Support, Sustain, Participate in Lean Manufacturing/process improvement events
Perform similar or assigned duties as required by department
Must be a self-motivated individual and work well in a team environment
Basic math skills
Must be competent in the use of hand tools
Assure compliance with appropriate quality standards/requirements
Must be able to work overtime
- High School Diploma or Equivalent
- Medium work
Equal Opportunity Employer/Minorities/Women/Veterans/Disabled/Sexual Orientation/Gender Identity
We endeavor to make this site accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact (770) 922-9000.
Any unsolicited resumes sent to Acuity Brands from a third party, such as an Agency recruiter, including unsolicited resumes sent to an Acuity Brands mailing address, fax machine or email address, directly to Acuity Brands employees, or to Acuity Brands resume database will be considered Acuity Brands property. Acuity Brands will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Acuity Brands will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor, but does not have the appropriate approvals to be engaged on a search.
Assistant Scientific Editor, Cell Stem Cell
We are looking for a stem cell scientist to join the Cell Stem Cell editorial team as a full-time, in-house, scientific editor.
As a member of the Cell Stem Cell editorial team, you would be responsible for a broad range of contributions to the journal, including recruiting exciting studies; assessing submitted research papers; selecting and collaborating with top notch referees; identifying timely, emerging topics to commission for review articles; and promotion of our content online and through social media. The job also entails traveling to scientific conferences and research institutions where you will directly interact with the scientific community and hear about cutting-edge research developments.
This is an exciting opportunity to be engaged in shaping and guiding the leading edge of basic and translational stem cell research, as well as an opportunity to facilitate the process of scientific discourse and communication.
The position is based in Cambridge, MA, where the Cell Press offices are located, and will report to the Editor-in-Chief of Cell Stem Cell.
Your responsibilities will include:
assessing submitted research papers across all areas of stem cell biology
selecting and collaborating with referees
Engaging with scientists and recruiting exciting studies within the journal'
commissioning and editing "front matter" (commentaries, reviews etc. )
regular travel to scientific conferences and research institutions
The qualified candidate is expected to have:
- a Ph.D. in any area of biomedical research
- postdoctoral and/or editorial experience (not required but would be an advantage)
- specific expertise in the areas of stem cell research, cell fate plasticity and/or regenerative medicine
- broad interest in all areas of stem cell biology, with a sophisticated understanding of the basic principles as well as the ethical, legal and social issues
- ability to think critically about a wide range of scientific issues
- strong communication and organizational skills
- interest in engaging with the scientific community
- talent for distilling complex concepts and communicating them
- the ability to work well in diverse team settings
Applications will be considered on a rolling basis until July 1st. All applications must include a resume and cover letter describing your interest in the position.
An assessment or business case could be part of our selection procedure. A pre-employment screening will be part of our recruitment procedure.
Elsevier is a global information analytics business that helps institutions and professionals progress science, advance healthcare and improve performance for the benefit of humanity. We help researchers make new discoveries, collaborate with their colleagues, and give them the knowledge they need to find funding. We help governments and universities evaluate and improve their research strategies. We help doctors save lives, providing insight for physicians to find the right clinical answers, and we support nurses and other healthcare professionals throughout their careers.
Elsevier provides digital solutions and tools in the areas of strategic research management, R&D performance, clinical decision support, and professional education; including ScienceDirect, Scopus, SciVal, ClinicalKey and Sherpath. Elsevier publishes over 2,500 digitized journals, including The Lancet and Cell, more than 35,000 e-book titles and many iconic reference works, including Gray's Anatomy. Elsevier is part of RELX Group, a global provider of information and analytics for professionals and business customers across industries.
Elsevier employs over 7,000 people in more than 70 offices worldwide. We are an employer of choice, attracting and developing talented and creative people who thrive in a challenging and fast-paced environment. We offer an excellent compensation and benefits package as well as a real opportunity for career growth in a growing organization. Elsevier is an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law. If a qualified individual with a disability or disabled veteran needs a reasonable accommodation to use or access our online system, that individual should please contact 1.877.734.1938 or firstname.lastname@example.org.
Stem Cell Research Associate 2
The Astellas Institute of Regenerative Medicine (AIRM) is a wholly-owned subsidiary of Astellas Pharma and focused on the development and commercialization of stem cell and regenerative medicine therapies. Astellas is an R&D-driven global pharmaceutical company whose philosophy is to contribute to the improvement of people's heath around the world through the provision of innovative and reliable pharmaceutical products.
Developing innovative therapies is one of the most challenging, most essential and personally rewarding fields in science. This is the most exciting time to be a part of Astellas, a company with a uniquely collaborative and patient-focused culture. There's something special about working at Astellas. It's reflected in our focus on the people we serve, the way we treat each other and the results we achieve together as a company.
AIRM has a world-class R&D team, and is pursuing a diverse range of disease indications, ranging from macular degeneration (currently in clinical trials) and other ocular indications to vascular and autoimmune disease. AIRM's intellectual property portfolio includes pluripotent stem cell platforms -- both embryonic and induced pluripotent stem cells as well as other cell based therapy research programs. AIRM is headquartered in Marlborough, Massachusetts.
We are seeking a highly motivated and energetic Research Associate to join the Translational Development team. This person will assist with process development projects in collaboration with other members of our group, maintain accurate records and perform routine laboratory duties such as restocking supplies, ordering and equipment maintenance. On-the-job training for specific operations will be provided, but a strong background in mammalian cell culture as well as a high level of scientific curiosity are a must.
Essential Job Responsibilities:
Understands and effectively conducts biological laboratory experiments utilizing internal and published procedures
Assists with cell culture of various cell lines including pluripotent cells using specified protocols
May design and independently conduct experiments with minimal guidance from manager
Maybe involved in developing new process or assays using cell culture and analytical methods
Maintains records in notebook and electronic format according to Company policies
Contributes to preparation of technical reports and result summaries
Ensures availability of all experimental materials
Understands the proper use and maintenance of laboratory equipment and record keeping
Contributes to general laboratory and equipment maintenance
BS degree with a minimum of three years of relevant experience or equivalent
Impeccable aseptic techniques
Solid working knowledge of cell culture with adherent mammalian cell lines
Working knowledge of RNA isolation, PCR, immunostaining, flow cytometry, microscopy
Proven ability to efficiently learn new skills
Ability to maintain accurate records and effectively manage multiple projects
Excellent communication skills
Attention to detail
Ability to work flexible schedule including weekends
Experience with stem cells including pluripotent cells
Experience with primary cells
Experience with process or assay development
Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled
Engineering Technician – R&D Cell Assembly
Position: Engineering Technician – R&D Cell Assembly
Reports To: Supervisor, Cell Assembly
Location: Waltham, MA
A123 Systems, LLC is a leading developer and manufacturer of lithium-ion batteries and battery systems for the transportation and commercial markets.
The Engineering Technician will work under the direction of the Cell Assembly Supervisor. Primary responsibilities of this position include operating process equipment and basic technical analysis and documentation development.
Conduct analytical tests including but not limited to high potential tests, leak/ hermetic seal test, Karl Fischer moisture analysis and physical property measurements.
Operate various process equipment used in the development of cells. Ability to cross train and be competent in multiple work areas. Independently document standard data for every production run in standard format.
Work on assignments that are semi-routine in nature. Recognize the need for deviation from accepted practice and develop solutions. Can facilitate process/equipment corrections independently for prime responsibility.
Contribute proactively to process improvements by independently documenting learning and data, analyzing using basic math and computer software.
Confront & resolve issues in a positive way. Implement simple solutions to reduce operator variation & potential quality defects.
Focus on work area safety, cleanliness, material usage and organization.
Perform other functions as required to support the R&D operation.
Successful candidates will be both quality and detail oriented, be team oriented and flexible. They will possess good interpersonal skills, be proficient in written and verbal communication and be able to interface with co-workers and management.
- The position requires the ability to grasp basic technical concepts and language and the ability to communicate in a data-driven manner. Attention to detail is critical and the ability to work with a minimum amount of supervision.
High school diploma required with assembly, chemical processing and/ or relevant battery experience preferred.
Proficient with Microsoft Excel, Word, Outlook and general computer use
Professional written and verbal communication skills required.
Strong interpersonal, organizational skills and attention to detail.
Ability to work independently with minimal direction, and also as part of team.
Senior Research Investigator II, Cell Line And Gene Therapy Process Development
Senior Research Investigator II, Cell Line and Gene Therapy Process Development
The Senior Research Investigator II in Cell Culture Process development will be responsible for cell line creation and selection activities for research and cGMP purposes, for cell banking activities, and for support of cell culture process and technology development for a portfolio of early and late stage gene therapies.
Roles and Responsibilities
Responsible for cell line selection and cell banking for viral vector production
Evaluate multiple producer cell line types for various gene therapy programs
Oversee manufacturing of MCB/ WCB
Support developing efficient, robust, scalable, and transferable cell culture processes for the production of gene therapies that span AAV, Lentivirus and other viral-vector manufacturing platforms
Serve as technical expert and SME on a cross-functional team to provide guidance on process development and characterization of gene therapy production processes
Author and/or review method development reports, SOPs, and relevant sections of regulatory submissions and updates
Adhere to all relevant compliance regulations
Train and mentor junior scientists
- Ph.D. in biochemical engineering, bioengineering, molecular biology, biochemistry, cell biology or related field with 4+ years of relevant experience or an MS with 7+ years relevant experience
Experience and Skills
Experienced in cell line creation and selection procedures.
Experienced in cell banking for research and GMP operations
Experience with mammalian cell culture both with adherent and suspension formats including maintenance and expansion, transfection. Fixed bed bioreactor performance knowledge is a plus
Experience in the development of mammalian cell culture processes for manufacture of gene therapy products and/or viral vectors for gene therapy is desirable, in particular, knowledge of AAV manufacturing.
Demonstrated experience with DOE execution and data interpretation
Knowledge of process transfer and experience managing CMOs/CROs
Excellent problem solving skills
Able to manage multiple projects across various development stages
Detail-oriented with excellent verbal and written communication
- 10 - 15%
Stem Cell Transplant Coordinator
Cancer Care Northwest is the premier cancer center in the Inland Northwest providing comprehensive, innovative, compassionate care by a team of integrated cancer specialists. We are seeking a Part-time Stem cell Transplant Coordinator, this positions Coordinates the transplant department and provides comprehensive nursing care to patients and families during all phases of the transplant program. Supports and adheres to the Cancer Care Northwest Compliance Program, to include the Code of Ethics and Business Standards.
MINIMUM JOB QUALIFICATIONS: To perform this job successfully, an individual must meet the minimum qualifications listed below. These qualifications are representative of the knowledge, skill and/or ability required to perform this job.
Formal Education, Certification/Licensure, and Prior Experience: to perform this job successfully, an individual must have:
Bachelors of Science in Nursing (BSN), from an accredited program for professional nursing education from four-year college or university.
Minimum five years actively practicing as a registered nurse,
including at least two years oncology and chemotherapy administration experience.
Current oncology certification required. (Certification must be obtained within one year of employment and maintained.)
Experience and knowledge of the purpose and use of chemotherapy in the treatment of cancer and hematopoietic stem cell transplant.
Current RN state license.
Current OCN and Basic Cardiac Life Support (BCLS) certification.
This position is at our South Clinic
Scientist L, CHO Cell Line Development
The Process Sciences Department at the AbbVie Bioresearch Center in Worcester, MA is seeking a highly motivated and experienced Scientist to join the CHO Cell Line Development team. The Scientist will advance AbbVie's biotherapeutics pipeline through the development and characterization of highly-productive CHO cell lines suitable for cGMP protein manufacturing. The selected candidate will have a primary role in the genetic characterization of CHO cell lines. A strong candidate will have in-depth experience in CHO cell line genetic testing techniques used in the biopharmaceutical industry and demonstrated laboratory skills in methods development. The position is based in AbbVie Bioresearch Centre, Worcester, MA.
Key Responsibilities Include:
Develop and/or characterize highly-productive stable CHO cell lines suitable for cGMP biotherapeutic manufacturing within project timelines.
Experimental design and bench experience with Southern blot, Northern blot, qPCR and ddPCR techniques.
Experience with vector design and construction and with sequence analysis software.
Experience in CHO cell line development and cell engineering/gene editing techniques including ZFN, CRISPR/Cas9 etc.
Author and review technical reports detailing genetic characterization protocols and results. Effectively present scientific data and concepts to various audiences.
Maintain a high level of productivity in the lab, with clear and accurate documentation of experiments.
Contribute to team performance and process improvement in a climate of scientific excellence. Work collaboratively on projects across multiple Process Science groups.
Proactively seek out new information and opportunities to advance our technologies.
Contribute to the smooth and effective operation of the CHO cell line development labs through our 5S program.
Understand and adhere to corporate standards regarding code of conduct, documentation, safety, appropriate handling of materials, and GxP compliance.
Position will be hired based on level of experience.
MS degree in Molecular Biology or related discipline with 0-2+ years of relevant experience in the biopharmaceutical industry, or Bachelor's Degree with 3-5+ years of experience.
Enable cGMP biotherapeutics manufacturing and associated areas of expertise (e.g., cell and molecular biology, genetic characterization, gene editing, process development, recombinant protein production).
Excellent interpersonal and communication skills. Strong scientific curiosity with a passion for problem-solving and optimization.
Self-motivated with excellent attention to detail and ability to multi-task. Strong organizational, planning and trouble-shooting skills.
Skilled in using common software packages such as Microsoft Office.
Ability to work effectively in a highly collaborative and dynamic environment.
- Proven track record in one or more of the following: CHO cell line development, cell line genetic characterization, vector construction, gene editing such as gene knock-out/knock-in.
Key Leadership Competencies:
Builds strong relationships with peers and cross-functional team members.
Learns quickly, grasps the 'essence' and can change the course quickly where indicated.
Raises the bar and is never satisfied with the status quo.
Embraces a learning environment, open to suggestions and experimentation for continuous improvement.
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.
Significant Work Activities and Conditions: N/A
Job Type: Experienced
Global Strategic Marketing Leader- Cell And Gene Therapy
Role Summary:The Global Strategic Marketing Leader – Cell & Gene Therapy is responsible for continued evaluation of current marketplace dynamics including market potential, competitor activity and disruptive technologies within the rapidly changing global cell and gene therapy market. This position also has responsibility to identify and evaluate potential key growth areas, recommending potential new opportunities for the current product portfolio and overall GE capabilities.
• Performs industry trend analysis, customer segment analysis, market share and competitive analysis
Identifies and determines the market opportunity/size in adjacent spaces to cell processing, viral vectors, cord blood banking or point-of-care market where the current product portfolio can be
Provides market insights and analysis for market and business development opportunities including exploration and piloting of new business models
Supports business case development for organic and inorganic priorities
Develops and executes on market research plans to evaluate market opportunities for the Cell & Gene Therapy business
Works closely with Regional Field Marketing and Commercial teams to closely track market place trends, competitive activity and customer needs
Works closely with Global Marketing, Product Management and R&D to provide input to the product development roadmap
Deliver strategic business priorities and execute tactical plan on time, on budget and communicate across business while ensuring plan is driving business impact
The ideal candidate has past experience and passion for the Life Science industry
Bachelor's Degree in Business Management, Marketing, Engineering, Science
5+ years experience in marketing, sales, R&D, technical functions or related field
Marketing expertise in market & customer insights, product commercialization and branding
Strategic thinking – able to independently design/identify ideal approach to answering complex business questions
Proven record of accomplishment of establishing and delivering analytical projects, adjusting to changing circumstances. Prioritizes and effectively controls key milestones.
Ability to interpret large amounts of data to commercially insightful & objective competitive and business analysis
Strong project management skills and cross functional collaboration - able to collaborate effectively with various functional partners
Strong influencing skills – ability to motivate individuals and demonstrate organizational influence
Excellent oral, written communication and presentation skills
Strong data analytical and business process expertise.
Ability to work effectively within matrix environment
The ability to manage multiple projects and to adapt to changing priorities
High attention to detail is critical
A curious mind with an ability to quickly learn technical and scientific aspects of various products and application areas
Customer focus and the ability to build strong ties with stakeholders and peers
Ability to energize, develop, and build rapport, collaboration and influence at all levels within an organization
Proficient in MS Office, email and online communication tools
Desired Characteristics:• Advanced Degree in Business Management (MBA), Marketing, Engineering, Science
Innovation – develop new ideas through collaboration and execute on creative ideas
Independence – able to manage workload with limited guidance and support in prioritization
Previous experience working in large multinational corporations
Project management experience
About Us:GE (NYSE:GE) drives the world forward by tackling its biggest challenges. By combining world-class engineering with software and analytics, GE helps the world work more efficiently, reliably, and safely. GE people are global, diverse and dedicated, operating with the highest integrity and passion to fulfill GE's mission and deliver for our customers. www.ge.com
GE offers a great work environment, professional development, challenging careers, and competitive compensation. GE is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, gender (including pregnancy), sexual orientation, gender identity or expression, age, disability, veteran status or any other characteristics protected by law.
GE will only employ those who are legally authorized to work in the United States for this opening.Additional Locations:Switzerland, United Kingdom, United States;Massachusetts;Marlborough, Eysins, Cambridge;
Lead Scientist Cell Therapy Process And Technology Development
At CRISPR Therapeutics, we are focused on developing transformative gene-based medicines for serious human diseases.
We are rapidly translating our specific, efficient and versatile CRISPR/Cas9 gene-editing platform into therapies to treat hemoglobinopathies, cancer, diabetes and other diseases
Our multi-disciplinary team of world-class researchers and drug developers works every day to translate our CRISPR/Cas9 technology into breakthrough human therapeutics. Our lead program targeting the blood diseases β-thalassemia and sickle cell disease has entered clinical testing, and our immuno-oncology programs, focused on CRISPR/Cas9-edited allogeneic CAR-T cell therapies, have the potential to deliver a new generation of cancer therapies to patients.
We are seeking a Scientist II/Senior Scientist, Cell Therapy Process Development to join an exciting, fast-growing and well-financed company to develop novel gene editing therapies for serious diseases. This role is within the Technical Operations department (Tech Ops) at CRISP Therapeutics, reporting to the director of late stage and clinical manufacturing. The successful candidate will be a key technology leader in the development of late-stage CAR-T cell manufacturing novel technologies and processes for Phase III readiness and commercialization. The ideal candidate will be a process scientist with extensive knowledge of T-cell biology, immunology, stem cell biology, and gene editing cell therapies. Knowledge of late-stage process development, BLA-enabling study designs is a plus.
The successful candidate will have significant experience in designing and performing experiments in process development studies. Additionally, he or she will:
Provide technical leadership to the cross-functional staff in the lab at the start with the opportunity to lead projects and direct reports as the programs expand;
Plan and execute late stage process development activities for manufacturing process optimization, characterization and validation of CRISPR's autologous and/or allogeneic CAR-T cell programs to ensure Phase III readiness;
Lead and execute both cell processes and in-process assays including trouble-shooting; report data and articulate impacts both internally and externally to stakeholders;
Apply knowledge of T-cell biology, immunology, stem cell biology, and gene editing cell therapies to establish unit operation robustness and improve manufacturing technologies for commercial success;
Evaluate new technologies and drive scientific innovation in CAR-T cell process platform development;
Lead and execute both cell processes and in-process assays including trouble-shooting; report data and articulate impacts both internally and externally to stakeholders;
Optimize manufacturing processes including cell selection, cell culture, gene editing and gene transfer with electroporation and viral vectors;
Collect, analyze and present experimental data while maintaining clear and complete experiment records;
Maintain high-level technology knowledge in allogeneic CAR-T cell therapy process development and manufacturing;
Write and review technical documentation, including SOPs, batch records, protocols, development reports, and pre-validation plans, to facilitate tech transfer, clinical manufacturing, and regulatory submissions (i.e. IND to BLA);
Serve as the subject matter expert and represent Process Development in cross-functional project teams;
PhD in Immunology, Cell biology or related biomedical science disciplines with the level-appropriate experience in cell therapy with cell-based assay experience;
Scientist II: Ph.D. and 5+years overall experience, with >2 years in relevant biotech/pharma experience
Senior Scientist: Ph.D. and 8+ years overall experience, with >4 years in relevant biotech experience including leading projects and/or teams.
MS/BS with 12+ years of relevant industrial experiences may be considered
Demonstrated extensive knowledge of T-cell biology, immunology, and/or stem cell biology, with experience of applying them to gene edited cell therapy process development; Demonstrated track record in leading and driving innovative ideas from proof of concept through implementation;
Working knowledge of GXPs and generation/review of GMP documents; (Recommend making this a requirement)
Experience with editing and cell selection technologies for primary human cells;
Excellent oral and written communication skills;
Highly organized with significant attention to detail;
Positive interpersonal and management skills with the ability to interact with individuals from different levels and functions;
Demonstrated leadership to manage projects in a matrix environment; and,
The ideal candidate enjoys working in a fast-paced environment and breaking new ground in the gene and cell therapy space.
Experience in late-stage development activities such as process characterization, process validation, and commercial regulatory submission;
Knowledge of cell therapies, viral vectors, Cas9, and gRNA GMP manufacturing is a plus;
Experience with formulation development;
Experience operating bioreactors (e.g. AMBR), benchtop to 100Lscale;
Experience developing processes using single-use disposables;
Experience with Design of Experiments (DOE) for process development and optimization.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy
Making better hires starts with building better job descriptions
- Browse 100s of templates across 40+ industries
- Customize your template with your company info & job requirements
- Post it to 20+ job boards in seconds – for FREE!