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field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
New England Cryogenic Center (NECC), affiliate of New England Cord Blood Bank, Inc., was founded in 1971 and is considered one of the pioneers in processing and cryopreservation of human cells and tissue. Our goal is to continue to be a premiere worldwide leader in cryopreservation of human cells, tissue, and cellular therapies. In addition, we aim to educate the public and medical communities on the availability of cryogenic storage of cells and tissue, along with their current and potential benefits for future use in treating disease and injury. 
This position requires that you perform all necessary duties of the Lead-Laboratory, Cryogenics, and laboratory personnel, while also supporting and monitoring departmental workflows to ensure smooth and efficient operations. This position's responsibilities are primarily in the Cryogenics department with some cross-over to laboratory.
We are seeking a full-time Lead-Laboratory to join our Marlborough, MA team. The schedule is working Monday-Friday 8:30am-5:00pm, with every 4 week weekend rotation and at least 1-2 holidays per year.
What You'll Do:
<ul>
<li>Assign, pull and verify orders</li>
<li>Perform daily and weekly QM/QC</li>
<li>Receive products and verify them via packing slips to ensure correct amount received</li>
<li>Check-in shipping tanks and perform shipping procedures for specimen orders</li>
<li>Maintain a high level of cleanliness in the Cryogenic area</li>
<li>Assist Manager in drafting and reviewing SOPs as needed</li>
<li>Attend meetings when necessary</li>
<li>Convey any non-compliances and difficulties to upper management</li>
<li>Perform and assist in all duties pursuant to the betterment of NECC and related companies</li>
<li>Maintain and update inventory locations by using paper records and computerized specimen inventory software</li>
<li>Coordinate specimen pick-ups and deliveries with courier and sales department</li>
<li>Review and approve client reports, client test results, and report results to appropriate staff</li>
<li>Maintain electronic cord blood client files</li>
<li>Respond to emails and requests from the cord blood processing laboratory in a timely manner</li>
<li>Processing andrology specimens as needed</li>
<li>Responsible for being an “on call” person for the cryogenic alarm monitoring system, once or twice per month</li>
<li>Responsible for alarming/disarming the building security system</li>
<li>Perform other related duties as assigned by management</li>
</ul>
What You'll Bring:
<ul>
<li>Bachelor’s degree in a chemical, physical, biological, clinical laboratory science, or medical technology from an accredited institution is preferred</li>
<li>At least one year of related laboratory experience preferred</li>
<li>High attention to detail</li>
<li>Must be capable of performing, evaluating, and reporting cryogenics procedures by following standard operating procedures</li>
<li>Strong written and oral communication skills</li>
<li>Weekend rotation: once or twice per month</li>
<li>Holiday coverage rotation once or twice per year</li>
<li>Occasional overtime</li>
<li>Working knowledge in a variety of computer software applications in word processing, database, and Microsoft Applications (Outlook, Word, Excel)</li>
<li>Computer proficiency required</li>
<li>Have skills to access, input, and retrieve information from a computer</li>
<li>Have understanding of SOPs, OSHA and HIPAA</li>
<li>Flexibility and willingness to learn at all times</li>
<li>Excellent multi-tasking abilities</li>
<li>Excellent interpersonal skills and ability to work as part of a multi-disciplinary team, and build and maintain effective working relationships</li>
<li>Ability to effectively provide technical and knowledge training to staff</li>
<li>Ability to develop continuous quality improvement</li>
<li>Results orientation; highly responsive to requests</li>
<li>Verbal and written communication skills</li>
<li>Excellent organizational skills</li>
<li>Ability to maintain the highest level of confidentiality and accuracy</li>
<li>Must have the aptitude to learn to make appropriate judgments about the clinical significance of laboratory data</li>
<li>Ability to troubleshoot and test equipment issues, problem solve by identifying issues, and proposing solutions</li>
</ul>
More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful. 
What We Offer:
We are proud to provide a comprehensive and competitive benefits package tailored to support the needs of our team members across all employment types:
<ul>
<li>Full-Time Employees (30+ hours/week): Medical, dental, and vision insurance, 401(k) with company match, tuition assistance, performance-based bonus opportunities, generous paid time off, and paid holidays</li>
<li>Part-Time Employees: 401(k) with company match and performance-based bonus opportunities</li>
<li>Per Diem Employees: 401(k) with company match</li>
</ul>
How To Get Started:
To have your resume reviewed by someone on our Talent Acquisition team, click on the “Apply” button. Or if you happen to know of someone who might be interested in this position, please feel free to share the job description by clicking on an option under “Share This Job” at the top of the screen.
To learn more about our company and culture please visit our website.

Lead - Laboratory

<h3>Job Description</h3>
In this vital role you will be developing, qualifying and transferring innovative and fit-for-purpose quantitative assays for the measurement of DNA, proteins and other biological analyzes for manufacturing process development. The Senior Associate in Process Development is instrumental in designing, developing, and optimizing manufacturing processes. They are involved in conducting experiments, analyzing results, and implementing process improvements to enhance efficiency and product quality.
 
Responsibilities:
<ul>
<li>Routine testing support for PD DS process related impurity analysis</li>
<li>Preparation of lab buffers and reagents</li>
<li>Lab reagent and materials inventory</li>
<li>Maintenance of critical reagents stocks</li>
<li>General lab upkeep and equipment maintenance support</li>
<li>Provides critical evaluation of analytical data and results to support product development analytical testing activities.</li>
<li>Documentation of assays and laboratory activities in electronic notebook documentation system</li>
<li>Generating, analyzing, and interpreting analytical data</li>
<li>Supporting analytical projects involving method development, qualification, and transfer</li>
<li>Analyzing routine samples by qPCR and ELISA, data interpretation and reporting,</li>
<li>Documentation of results and peer review of electronic notebooks.</li>
<li>Preparation of lab buffers and reagents, maintenance of critical reagents stocks</li>
<li>Sample, reagent and materials inventory tracking and re-stocking</li>
<li>General lab upkeep and equipment maintenance support</li>
<li>To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.</li>
</ul>
Requirements / Qualifications:
<ul>
<li>Associate’s degree in Biology, Chemistry, Biochemistry, Analytical Chemistry, or a related field and 2 years of Scientific experience OR</li>
<li>Bachelor’s degree in Biology, Chemistry, Biochemistry, Analytical Chemistry, or a related field</li>
<li>Experience and expertise with protein assays, especially immunoassays, ELISAs or qPCR.</li>
<li>Experience in GMP lab setting.</li>
<li>Experience and expertise with Microsoft Office software: Word, PowerPoint and Excel.</li>
<li>Enjoys participating in a cohesive, high performing team, establishes effective and adaptable relationships with colleagues, while contributing as an effective independent contributor.</li>
<li>Communication – establishes and maintains effective communication mechanisms to keep colleagues appropriately advised; bridges communication between individuals, team and other organizational units as necessary.</li>
<li>Social skills – communicates optimally, using appropriate tact and sensitivity; makes others feel respected, valued and understood.</li>
<li>ELISA, immunoassays and qPCR technologies</li>
<li>Familiarity with electronic laboratory notebook/record keeping system(s)</li>
<li>Familiarity with working in a GMP/GxP environment</li>
<li>Strong Communication skills</li>
<li>Team player</li>
</ul>

Associate Scientist

<h3>Job Description</h3>
Job Description
Discover Veranova
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focuses on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
The Analytical/QC Lab Metrologist is responsible for the timely installation, maintenance, repair, calibration, and IQ/OQ of instruments, balances, and other equipment used by the Analytical Development (AD) and Quality Control (QC) groups. This role also ensures Standard Operating Procedures are technically sound and provide full regulatory compliance. This position is critical to supporting high-quality science, operational excellence, and regulatory compliance across both sites.
Core Responsibilities: 
<ul>
<li>Revises and reviews metrology-related protocols and IQ/OQ to ascertain proper functioning of the instrumentation. Ensures that appropriate documentation for the instrument calibration program is in place for compliance with regulatory expectations.</li>
<li>Schedules, executes and supports instrument calibrations and preventative maintenance in such a way so as not disrupt the analysts using the instruments. Responsible in the assignment of instrument custodians, assuring instrument maintenance and usage logbooks have been maintained. Trouble shooting or judging the issue for chromatographic systems mainly LC/GC.</li>
<li>Negotiates and manages contracts with external vendors and contracted services as required. Oversees the work of contracted personnel to install/modify equipment and systems in accordance with the specific needs of the AD and QC groups while meeting all cGMP and USP requirements.</li>
<li>Keep abreast of instrument validation requirements to ensure compliance with respect to USP and cGMP requirements.</li>
<li>Provides assistance in internal and customer audits by providing relevant, up to date documentation related to calibration, qualification and maintenance of appropriate analytical instrumentation used by the analytical groups. </li>
<li>Leads the process to evaluate, purchase and install new instrumentation. Interacts with internal and external vendors to ensure the proper instrumentation is identified to support the needs of the business. Evaluates and recommends appropriate application of new software packages as well as upgrades of software/firmware/hardware.</li>
<li>Directly involved with and supports investigations that are instrument related. Conducts all work in compliance with USP and cGMP standards and all other appropriate Federal, state and local regulations.</li>
</ul>
Qualifications: 
Required
<ul>
<li>Bachelor’s Degree in chemistry or a related science with a minimum of 5 years’ related experience </li>
<li>Familiarity with LC/GC trouble shooting.</li>
<li>Experience in a cGMP environment</li>
<li>Ability to exercise independent judgment in the application of scientific principles pertaining to analyses as related to this business and operation </li>
<li>Proficiency with computers and other software packages relevant to installation, modification, calibration and qualification of instrumentation systems and equipment</li>
<li>Strong communication skills; written and verbal. </li>
<li>Possess strong organizational skills</li>
</ul>
Preferred
<ul>
<li>Experience in lab equipment such as analytical balance, micro balance, KF, OVEN-KF, NMR, ICP-MS, PSD, XRPD, TGA, DSC, etc. </li>
<li>Experience or familiarity with Labware LIMS and the Instrument Manager module</li>
<li>Experience or familiarity with Master Control and Veeva</li>
<li>Recent relevant experience in bulk pharmaceutical/API manufacturing or specialty chemicals</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a misson to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship. 
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.
#LI-Onsite

Analytical/Quality Control Lab Metrologist

<h3>Job Description</h3>
Job Description
Title: Spring Drug Discovery Biology Co-Op/Internship
Location: Downtown Boston, MA (on-site 5 days/week)
Duration: January-June 2026
Hourly Rate: $20-$30/hr, dependent on experience 
Weekly Hours: 30-40 hours/week
Job Summary: 
Antares Therapeutics is seeking a highly motivated co-op/intern student to join the Drug Discovery Biology team for the Spring semester of 2026. This candidate will serve a critical role in helping establish cell-based assays to inform target biology, in addition to supporting translational biology efforts. This position is ideal for a talented, highly motivated and results driven individual who will thrive in a fast-paced, innovative, start-up environment.
Key Responsibilities:
<ul>
<li>Maintain human tumor cell lines in tissue culture (thawing, freezing, splitting cell lines). New CRISPR and lentiviral engineered cell lines are regularly being developed (e.g. knockout and knock-in mutation/insertions) that require maintenance such as pools and sub-cloning.This will be a great opportunity for the co-op/intern student to gain valuable TC experience and exposure to cell line engineering.</li>
<li>The co-op/intern student will assist in cellular assays and studies to help elucidate mechanism of action (MoA), with a focus on cell growth (proliferation) and biomarkers (TR-FRET, AlphaLISA, Western blot, ELISA).</li>
<li>The co-op/intern student will gain experience with the design, optimization, and execution of cellular assays, data analysis and communication of results in a team environment.</li>
<li>The co-op/intern student will learn documentation of experimental results in an electronic notebook and the use of data analysis and data archive systems.</li>
<li>The co-op/intern candidate will learn automation workflow procedures that support programs across the portfolio.
<ul>
<li>The co-op/intern student will gain exposure to using equipment such as the Echo, PHERAstar, Bravo, and MultiDrop Combi.</li>
</ul>
</li>
<li>The co-op/intern student will gain valuable experience working in a collaborative team environment and interactions that contribute to a positive work environment, including safety, lab hygiene, and general lab duties such as stocking and reagent preparation.</li>
</ul>
Basic Requirements:
<ul>
<li>Current undergraduate student studying Biology or a related field</li>
<li>Fundamental understanding of basic biology concepts realized through lab work or relevant coursework</li>
<li>Experience with basic lab techniques is a plus (preparing buffers/solutions and dilutions, pipetting, and sterile technique; experience with PCR, gel electrophoresis, western blotting, and/or tissue culture is a plus); such experience may have been realized through a lab course or a prior internship.</li>
</ul>

Spring Drug Discovery Biology Co-Op/Internship

<h3>Job Description</h3>
Job DescriptionTitle: Research Associate, Antibody &amp; Protein Engineering
 Adimab is the leading technology provider for therapeutic antibody drug discovery, focusing solely on our partnerships without pursuing an internal product pipeline. Since 2009, we have partnered with over 130 pharmaceutical and biotechnology companies, generating more than 600 therapeutic programs, of which more than 75 have entered clinical trials.&nbsp;&nbsp;
Role Overview: We are seeking a focused and enthusiastic protein engineer to join our Platform Technologies group. In this role, the Research Associate will work in a small, collaborative team to execute Adimab’s platform for the discovery, optimization and characterization of protein-based therapeutics.
Responsibilities:&nbsp;
<ul>
<li>Designing and executing protein engineering experiments</li>
<li>Constructing yeast display libraries and performing FACS selections</li>
<li>Basic protein/DNA sequence and structural analysis</li>
<li>Basic yeast handling and propagation</li>
<li>Collecting, organizing, and analyzing antibody characterization data</li>
<li>Collaborating with colleagues and external partners &nbsp;</li>
</ul>
Needed Upon Hire:
<ul>
<li>B.S., or equivalent practical experience, with training in molecular biology, chemical engineering, or biochemistry</li>
<li>At least 2 years of lab experience in an academic or industry setting&nbsp;</li>
<li>Knowledge of molecular biology, protein engineering, structural biology, and/or flow cytometry</li>
<li>Meticulous approach to benchwork and data analysis &nbsp;</li>
</ul>
Value-added Experience:
<ul>
<li>Experience with protein display technologies (yeast, bacterial and/or ribosomal) desired</li>
<li>Knowledge of protein sequence analysis and next-generation sequencing workflows desired</li>
<li>Experience with protein structural analysis or computational design methods desired</li>
<li>Demonstrated ability to evaluate, interpret, and present scientific data</li>
<li>Internally motivated with proven track record of operating independently at the bench and bringing projects to completion</li>
<li>Excellent organization skills and the ability to manage multiple projects simultaneously</li>
<li>Adaptable and productive in a fast-paced environment</li>
<li>Communicates effectively and openly with colleagues and supervisors</li>
<li>Resourceful with outstanding execution and problem-solving skills</li>
<li>Excellent quantitative skills with a mastery of Excel</li>
</ul>
 Come join us! Our integrated antibody discovery and engineering platform provides unprecedented speed from antigen to purified, full-length human IgGs with exquisite specificity and biophysical behavior. We offer&nbsp;fundamental advantages by delivering diverse panels of antibodies that meet the most demanding standards for affinity, epitope specificity, species cross-reactivity, and developability. We enable our partners to rapidly expand their biologics pipelines through a broad spectrum of technology access arrangements.
As a profitable privately-held biotech company, we take a long-term view on value creation and make substantial investments in technology development, research, and our people. We offer individually tailored compensation packages comprised of a competitive salary, meaningful equity, a 2:1 401(k) match, and comprehensive health care benefits.
Located in New Hampshire’s beautiful Upper Connecticut River Valley, we are minutes from Dartmouth College, the Geisel School of Medicine, the Thayer School of Engineering, the Tuck School of Business, and the Dartmouth Hitchcock Medical Center. We are fortunate to be situated in an area that is renowned for its premier skiing, hiking, kayaking, and biking.
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Research Associate, Antibody & Protein Engineering

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Bioprocess Development at the AbbVie Bioresearch Center in Worcester, MA is seeking a highly motivated junior 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 good experience in mammalian cell culture and demonstrate good aseptic technique history, following standard protocol to generate and analyze precise, reliable, and reproducible data in a timely manner. The candidate will also need to demonstrate good communication, presentation, and technical writing skills, team-working spirit, and strong scientific thinking approach in problem solving. The position is based in AbbVie Bioresearch Centre, Worcester, MA.
Key Responsibilities includes:
<ul>
<li>Develop a highly productive stable CHO cell line suitable for cGMP biotherapeutic manufacturing for various Biologics projects following standard protocols</li>
<li>Participate and contribute to cross functional CMC team as CLD lead to ensure the success of CMC timeline</li>
<li>Participate new technology improvement projects</li>
<li>Perform routine tasks competently, independently and generate reliable and consistent results.</li>
<li>Author technical reports detailing standard procedures used and results. Effectively present scientific data and concepts to various audiences Analyze and critique results, noting significant deviations.</li>
<li>Learn and effectively implement new experimental protocols and/or techniques. Maintain laboratory equipment and optimize laboratory operations for efficient use of time and laboratory supplies and reagents, when appropriate.</li>
<li>Consult literature to understand scientific purpose of assignments. Impact projects predominantly through lab activity.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree, or equivalent education, with typically 3 or more years’ experience or Master’s Degree or equivalent education (no additional experience).</li>
<li>Attention to details, careful record-keeping, strong time management skills with executing multi-step experiments</li>
<li>Strong interest in working in a highly collaborative environment</li>
<li>Ability to prioritize and multi-task across projects while keeping deliverables within timelines</li>
<li>Good verbal and written communication skills.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist, Process Development II

<h3>Job Description</h3>
About Simcere:
Simcere Pharmaceutical Group is an innovation-driven pharmaceutical company committed to "For patience, for life." Our core therapeutic areas include oncology, central nervous system (CNS) disorders, autoimmunity, and infectious diseases. We are continuously expanding into areas with significant unmet medical needs. Our Cambridge, MA site is dedicated to cutting-edge research aligned with the company strategic directions.
 
Job Summary:
We are seeking a highly motivated PhD-level researcher to join our dynamic Neuroscience Discovery team. This role focuses on investigating cellular mechanisms underlying Alzheimer’s disease, Parkinson’s disease, Stroke and other CNS disorders. The successful candidate will lead and execute translational research to identify disease-relevant targets and develop therapeutic candidates with enhanced CNS delivery.
The ideal candidate will have deep expertise in antibody engineering, ideally for CNS indications, with a proven track record of applying these technologies to achieve development milestones. This position requires a strategic thinker who can integrate molecular engineering with functional disease biology. It offers a unique opportunity to contribute to impactful discoveries in a highly collaborative and innovative environment.
 
Responsibilities:
<ul>
<li>Lead target discovery efforts by identifying and validating novel therapeutic candidates for CNS diseases.</li>
<li>Provide scientific and technical leadership and execution in the design, and development of novel biologics, including antibodies and/or AOCs, for CNS indications.</li>
<li>Drive innovation in CNS delivery, including the design and validation of blood-brain barrier crossing technologies.</li>
<li>Design and execute in vitro and/or in vivo studies to validate therapeutic targets and to assess target engagement, mechanism of action, and therapeutic efficacy. </li>
<li>Contribute to the establishment of advanced cellular models, such as iPSC-derived CNS cell types, to elucidate mechanisms of action and evaluate therapeutic responses.</li>
<li>Analyze and interpret complex experimental data, troubleshoot technical challenges, and ensure scientific rigor across all research activities.</li>
<li>Stay current with emerging scientific literature and technological advancements, actively contributing to project development, and innovation initiatives.</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. in Neuroscience, Molecular Biology, Biochemistry, or a related field, with a minimum of 5 years of post-doctoral or industry experience in drug discovery.</li>
<li>Proven expertise in protein/antibody engineering, and/or AOC development. </li>
<li>A track record of successfully contributing to or leading drug discovery programs.</li>
<li>Demonstrated proficiency in neurological disease biology and with relevant experience in cellular and in vivo models (e.g., iPSC-derived neurons, astrocytes, microglia; AD/PD animal models).</li>
<li>Familiarity with cellular function analysis techniques, such as microscopy and biochemical assays.</li>
<li>Experience with CNS delivery strategies and platform technologies is preferred.</li>
<li>Expertise in bioinformatics analysis of high-dimensional datasets (e.g., transcriptomics, proteomics) is highly valued.</li>
</ul>

Senior/Principal Scientist, Biologics drug discovery for Neuroscience indications

<h3>Job Description</h3>
About Protobrand
Protobrand is a technology powered market research consultancy that empowers brands with game-changing insights. With a strong culture of innovation, we apply behavioral science to build cutting edge technology research methods and reveal true consumer motivations. We are dedicated to bringing our core values into everything that we do, and we take pride in our diversity, social responsibility, and dedication to positive environmental change. With offices in Boston, Toronto, Amsterdam and Stockholm, Protobrand is committed to building value-centric relationships with our clients around the world.
 
Role Overview:
Protobrand is seeking an enthusiastic and talented individual to join the growing research team. This position is based in Boston. As a Senior Research Manager at Protobrand, you will play a pivotal role in being a member of the research function, ensuring the successful delivery of high-quality, data-driven insights that meet the strategic objectives of our clients. This role demands a blend of leadership skills, research expertise, and project management abilities.
 
The ideal candidate has a strong background and interest in market research and consumer behavior and is expected to contribute to the forward-thinking and innovative nature of our firm. In this role, the senior research manager will primarily lead client research projects but will also collaborate with our client services and product development teams. The individual should be a strategic thinker and problem solver, with the ability to turn data into insights and develop story-driven recommendations and strategy.
 
Key Responsibilities:
- Responsible for the design, execution, and delivery of end-to-end market research projects, including survey development, fielding operations, data analysis, insight development and report creation.
- Conduct both qualitative and quantitative analyses, applying robust methodologies to extract meaningful insights.
- Collaborate with cross-functional teams, including Client Delivery and Business Development, on study design and to ensure alignment with client objectives and timelines.
 
Qualifications:
- 5+ years of experience in market research.
- Proven track record of managing complex research projects from inception to completion, balancing multiple priorities while ensuring high-quality outcomes.
- Bachelor's or advanced degree in business, statistics, psychology, or a related field.
- Strong foundation in both qualitative and quantitative research methods.
- Experience with survey analysis software (e.g., SPSS, MarketSight) is preferred.
- Excellent project management, communication, and organizational skills, with the ability to work effectively across teams.
- A proactive, innovation-driven mindset with a focus on continuous improvement and client satisfaction.

Senior Research Manager / Director

<h3>Job Description</h3>
WHO WE ARE
ODDITY is a consumer tech company that builds and scales digital-first brands to disrupt the offline-dominated beauty and wellness industries. The company serves over 40 million users with its AI-driven online platform, deploying data science to identify consumer needs, and developing solutions in the form of beauty and wellness products. ODDITY owns IL MAKIAGE and SpoiledChild.
ODDITY LABS is our cutting-edge biotechnology R&amp;D center, powering science-backed product innovation through the discovery and development of new molecules, probiotics, peptides, and other biological modalities. Unlike pharmaceuticals, ingredient innovation in the beauty and wellness industry has remained stagnant for decades. We are deploying patented, proprietary technologies and capabilities, including AI-based molecule discovery and advanced phenotypic databases, to understand the biological mechanisms that drive cellular behavior and develop uniquely efficacious products for beauty and wellness applications. Innovations from the ODDITY LABS will power game-changing products through ODDITY’s current brands, as well as future brands.
ODDITY operates with business headquarters in New York City, an R&amp;D center in Tel Aviv, Israel, and a biotechnology lab in Boston. Our culture is fast-paced, innovative, agile, and offers every team member the opportunity to drive a big impact.
 
THE ROLE
We’re looking to hire a Research Associate in Bioengineering for ODDITY LABS. In this role, you will:
<ul>
<li>Design, prepare, execute, and analyze various experiments to support research &amp; development (R&amp;D) projects in our pipelines.</li>
<li>Support an environment that enables a staff of highly skilled and specialized peers to perform biological and computational experiments and promote trust and decision-making.</li>
<li>Help develop and standardize standard operating procedures (SOPs).</li>
<li>Refine and continuously evolve existing pipelines to enable data-driven decision-making, acceleration through the proof-of-concept to product stages, and product validation pipelines.</li>
<li>Keep and maintain all laboratory-related documentation, including but not limited to laboratory notes, experimental records, safety data sheets, regulatory documents, and SOPs.</li>
<li>Help manage and coordinate instrument and equipment maintenance as necessary. This can include both internal maintenance and external third-party procurement. Help perform regular calibration and QA/QC checks on instrumentation and equipment.</li>
<li>Stay apprised of trends across beauty and biotechnology and implement new technologies that may further enhance the capabilities of ODDITY LABS.</li>
<li>Contribute to promoting a unified office/laboratory culture by organizing and assisting in planning community-building activities.</li>
<li>Ensure a clean and safe environment for all laboratory personnel. Enforce and support universal precautions and use of personal protective equipment for all laboratory personnel.</li>
<li>Assist in laboratory ordering, inventory, regulations, and permits.</li>
</ul>
 
WHO YOU ARE
<ul>
<li>B.S. or higher in Biology, Bioengineering, Biochemistry, or related major, with biological laboratory experience with 2 – 3 years of industry experience in biotech or pharma.</li>
<li>You have extensive experience (3+ years) with mammalian cell culture, particularly experience with handling primary human cells and immortalized cell lines. Experience with stem cells, iPSC differentiation, various culture substrates, and/or 3D models is ideal.</li>
<li>You have prior experience with genetic manipulation of mammalian cells (using either viral vectors, RNAi, CRISPR, etc) and molecular biology techniques, such as nucleic acid preparation, primer design, cloning and Western Blot.</li>
<li>Previous experience with ELN/LIMS systems and compound/plasmid management preferred.</li>
<li>Proven expertise with functional assays including reporter cell lines, flow-cytometry, ELISA, cytokine profiling, enzymatic activity assays, and fluorescence imaging.</li>
<li>You have strong project management and organizational skills, with an ability to create structure in ambiguous situations. You can balance multiple projects at once and know how to prioritize required tasks.</li>
<li>You have excellent written and verbal communication skills with experience working with a diverse range of stakeholders.</li>
<li>You are proficient in MS Office software, especially Excel.</li>
<li>You have a strong attention to detail and are committed to maintaining ODDITY LABS’ high standards and scientific rigor.</li>
<li>You are willing to learn new skills as needed to help the team be as successful as it can be.</li>
<li>You are an independent problem solver, consistently thinking out of the box and taking the initiative to take the next step without instruction.</li>
<li>You are a hard worker with a high level of accountability. You hold yourself to high standards but also expect those around you to as well.</li>
<li>You are excited about being a part of a world-class team that is growing and achieving incredible heights every single day. You have a desire to be in the laboratory and engage with our teams.</li>
<li>You believe good enough never really is good enough. You want to always improve, both personally and professionally.</li>
<li>You are adaptable and a team player, willing to go the extra mile and jump in on ad hoc tasks to support the overall company growth.</li>
</ul>
 
WHAT WE OFFER
<ul>
<li>Competitive compensation and benefits package.</li>
<li>This position will consider and sponsor candidates on a visa (OPT, STEM OPT, H1B, TN).</li>
<li>This position is in-office in our Cambridge, Massachusetts office and laboratory.</li>
<li>The salary for this position is negotiable and commensurate with experience.</li>
</ul>
Note: We’re currently hiring for many roles! Not the right fit, but interested in another position? Contact us <a href="mailto:olabs.jobs@oddity.com" target="_blank">olabs.jobs@oddity.com</a>

Research Associate, Bioengineering

<h3>Job Description</h3>
WHO WE ARE
 
ODDITY is a consumer tech platform transforming the global beauty and wellness market. We deploy advanced technology, including molecular discovery, synthetic biology, artificial intelligence, machine learning, and computer vision to develop exceptional products and deliver consumers a superior experience. Our digital-first brands, IL MAKIAGE and SpoiledChild, are rapidly disrupting the offline-dominated beauty and wellness industries around the world. Brands 3 and 4 will launch next year, replicating the playbook of our existing brands in adjacent spaces to take a step change in our growth and impact.
ODDITY Labs is our cutting-edge biotechnology R&amp;D center, powering product innovation through the discovery of new molecules that will power game changing products through ODDITY's current and future brands. Our exceptional team is passionate about using biology, chemistry, and technology to disrupt consumers' product expectations and shopping journeys, shifting millions of consumers from offline to online along the way. Our culture is fast-paced, innovative, agile, and offers every team member the opportunity to drive a big impact.
We are seeking an Advanced Topical Delivery Principal Scientist to lead innovation and development of advanced skin and hair delivery systems. This individual will drive strategy and execution of topical formulation and delivery technologies - including but not limited to encapsulation systems (e.g., liposomes, polymersomes, nanoemulsions), microneedle arrays, and patch-based delivery platforms - to maximize the effectiveness, bioavailability, and sensory profile of our novel active ingredients.
You are a scientific expert with deep hands-on experience across diverse topical delivery systems. You thrive in interdisciplinary teams, can independently drive complex programs from concept to prototype, and bring strategic vision alongside scientific rigor. This is a key role with direct impact on multiple R&amp;D and commercial pipelines across ODDITY’s consumer-facing brands.
 
WHAT YOU WILL DO
 
<ul>
<li>Lead the development, optimization, and characterization of advanced topical delivery systems (including encapsulated actives, microneedling devices, dissolvable microneedles, and transdermal patches)</li>
<li>Evaluate and select delivery technologies based on target product profiles, skin/hair penetration requirements, and consumer preferences.</li>
<li>Drive innovation in formulation strategies to enhance stability, penetration, controlled release, and sensory attributes.</li>
<li>Collaborate cross-functionally with chemistry, biology, product, and clinical testing teams to ensure delivery systems align with active properties and intended use.</li>
<li>Design and interpret in-vitro and ex-vivo assays to assess penetration, retention, release kinetics, and efficacy of delivery systems.</li>
<li>Manage internal and external partners, including CROs and technology vendors, for advanced delivery development and scale-up.</li>
<li>Stay abreast of new delivery technologies, materials, and regulatory trends, and assess their potential for ODDITY’s product lines.</li>
<li>Contribute to IP strategy and support patent filings for novel delivery technologies.</li>
</ul>
 
WHO YOU ARE
 
<ul>
<li>Ph.D. or M.S. in Pharmaceutical Sciences, Biomedical Engineering, Material Science, Chemical Engineering, or related field</li>
<li>7+ years of industry experience in topical/transdermal delivery, formulation, or drug delivery development</li>
<li>Proven expertise in encapsulation (e.g., lipid- or polymer-based), microneedling systems, patch technologies, or related delivery platforms</li>
<li>Experience with skin biology, in-vitro/ex-vivo models, and performance characterization</li>
<li>Deep understanding of material selection, formulation scale-up, and delivery-system manufacturing processes</li>
<li>Familiarity with regulatory considerations for cosmetic and/or drug-based delivery systems</li>
<li>Strong project management and communication skills; ability to work in cross-functional teams</li>
<li>Creative, execution-focused, and comfortable working in a fast-paced environment</li>
</ul>
 
WHAT WE OFFER
 
<ul>
<li>Competitive compensation and benefits package.</li>
<li>This position will consider and sponsor candidates on a visa (OPT, STEM OPT, H1B, TN).</li>
<li>This position is in-office in our Cambridge, Massachusetts office and laboratory.</li>
<li>The salary for this position is negotiable and commensurate with experience.</li>
</ul>
 
Note: We’re currently hiring for many roles! Not the right fit, but interested in another position? Contact us <a href="mailto:olabs.jobs@oddity.com" target="_blank">olabs.jobs@oddity.com</a>

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