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<h3>Job Description</h3>
工作地点：济南、成都、连云港、南京
岗位职责：
1. 负责改良型新药/一类创新药的立项评估、剂型设计开发、处方筛选和工艺开发及优化工作；
2. 跟踪重要治疗领域的临床需求，进行制剂的改良和创新，实现增效减毒的目的；
3. 密切关注和学习国内外上市和临床研究阶段的改良型新药相关的创新制剂技术、研究思路和相关文献资料，并深入思考、转化和运用；
4.不断加强对制剂相关专业知识的深入学习，并补充跨学科专业知识，如临床药学、药物化学、生物药剂学等，以临床需求为导向，科学设计和开发改良型新药；
5. 深入分析思考和总结药学和体内试验数据，不断建立和完善制剂特性、体内药动学行为和临床疗效之间的关联；
6.记录和整理原始试验记录及相关文件，完成注册申报资料的撰写，并保证其真实性和完整性；
7.完成领导安排的其它相关工作，如引进项目评估、新技术平台调研、新药资讯相关文献查询、内部电子期刊编辑、相关专业技术培训等。
任职要求：
1. 博士，有复杂制剂研（如复杂注射剂、口服缓控释制剂、吸入剂等）发经验者优先，药学、药物制剂等相关专业；
2. 在制药领域拥有广博而扎实的知识和较高的制剂专业技术水平，并具有清晰的科研思路以及较强的分析和解决技术问题的能力；
3. 具有较强的检索和阅读外文资料和文献能力，并可有效提取、梳理和转化文献中的核心专业技术；
4．具有强烈的求知欲望，以及较强的自我学习与探索的能力，乐于接受创新性、挑战性的知识和任务；
5. 熟悉各类药物制剂仪器设备的使用、处方筛选、试验总结报告撰写等日常相关工作；
6. 具有良好的道德修养、心理素质、抗压能力及团队合作精神，能够与同事进行良好的沟通协作。
 
Job Responsibilities:
1.Lead feasibility assessment, dosage form design, formulation screening, process development, and optimization for 505(b)(2) NDAs and first-in-class innovative drugs.
2.Track clinical needs in key therapeutic areas to drive formulation innovations achieving enhanced efficacy/reduced toxicity.
3.Monitor global innovations in clinical-stage modified-release drugs; translate novel technologies/research concepts into R&amp;D strategies.
4.Deepen expertise in formulation science while integrating cross-disciplinary knowledge (clinical pharmacology, medicinal chemistry, biopharmaceutics) for clinically driven drug development.
5.Establish in vitro-in vivo correlations (IVIVC) by analyzing pharmaceutical data and PK studies to link formulation properties with clinical outcomes.
6.Document experimental records; author regulatory submission documents ensuring data integrity and ALCOA+ compliance.
7.Execute assigned tasks: due diligence for in-licensed projects, novel technology platform assessments, literature reviews, e-journal editing, and technical training.
Qualifications:
1.Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related field. Preferred: Experience with complex dosage forms (e.g., complex injectables, modified-release oral systems, inhalation products).
2.Comprehensive expertise in drug development with advanced technical proficiency; demonstrated ability to design scientifically sound studies and solve complex formulation challenges.
3.Proficient in literature mining (English journals/patents) with strong capability to extract, synthesize, and implement technical insights.
4.Intellectual curiosity and self-driven learning agility; embraces innovative/high-challenge tasks.
5.Hands-on experience with:Formulation equipment (e.g., fluid bed dryers, hot-melt extruders)、DoE-based formulation screening、Technical report writing.
6.Strong ethics, resilience in fast-paced environments, and collaborative mindset with excellent cross-functional communication skills.

制剂科学家 -- 恒瑞-全球精英计划

<h3>Job Description</h3>
COMPANY OVERVIEW
AIRNA is a biotechnology company with a mission to be the leading RNA editing company delivering precision therapies to patients with rare and common diseases.
AIRNA is harnessing advances in genetics to develop transformative RNA-editing medicines that improve human health. Our proprietary platform is based on groundbreaking research by pioneers of the field and company co-founders Thorsten Stafforst (University of Tübingen) and Jin Billy Li (Stanford University) and enables optimal potency, safety, and delivery. AIRNA is advancing a robust pipeline of therapeutic candidates that are designed to provide functional cures for severe or chronic diseases by repairing harmful genetic variants or introducing beneficial variants promote optimal health.
AIRNA has raised $245 million in financing from a world-class syndicate of investors including Arch Venture Partners, Forbion, Venrock Healthcare Capital Partners, RTW Investments, Nextech Invest, and ND Capital. We value teamwork, resilience, excellence, human, and health, and have a diverse team at both our headquarters in Cambridge, MA and our research operations in Tübingen, Germany.
 
JOB OVERVIEW
We are seeking a dynamic and experienced Principal Scientist, Biomarker Lead to join our Translational Medicine team. This individual will play a critical role in designing and executing biomarker strategies to support the clinical development of our oligonucleotide-based therapeutics. The ideal candidate will bring deep scientific expertise across proteomics, metabolomics, and molecular biology, along with demonstrated hands-on experience in clinical trial settings and assay development. This is a high-impact, cross-functional role with significant visibility and strategic input across R&amp;D and Clinical.
 
RESPONSIBILITIES
<ul>
<li>Lead the development and execution of biomarker strategies for clinical programs, with a focus on mechanism-of-action, pharmacokinetic and pharmacodynamic biomarkers, and patient stratification markers.</li>
<li>Design and oversee the development, qualification/validation, and implementation of fit-for-purpose biomarker assays (e.g., ELISA, LC-MS/MS, immunoassays, NGS, etc.) in alignment with regulatory and clinical timelines.</li>
<li>Apply multi-omics approaches (proteomics, metabolomics, transcriptomics) to uncover disease biology and drug response signals that inform clinical decision-making.</li>
<li>Partner closely with Clinical Development, Bioinformatics, Regulatory, and external CROs to ensure high-quality data generation and integration.</li>
<li>Serve as the scientific lead for biomarker-related activities in clinical trials, including protocol development, sample collection plans, and data interpretation.</li>
<li>Collaborate with Discovery, Preclinical, and Regulatory to ensure continuity of biomarker strategy throughout all phases of development.</li>
<li>Maintain awareness of emerging technologies and regulatory guidance in the biomarker space.</li>
<li>Represent the company in external collaborations, scientific meetings, and regulatory interactions as needed.</li>
</ul>
 
QUALIFICATIONS 
<ul>
<li>PhD in Molecular Biology, Biochemistry, Pharmacology, or related field with 8+ years of industry experience in translational medicine, biomarker development, or related function.</li>
<li>Proven track record of biomarker leadership in clinical-stage therapeutic programs, ideally in the context of oligonucleotide therapeutics.</li>
<li>Deep hands-on experience in proteomics and metabolomics, including data interpretation and technology selection.</li>
<li>Strong assay development and validation experience, including managing external vendors and CROs.</li>
<li>Demonstrated experience with central lab management and clinical sample management.</li>
<li>Demonstrated experience translating preclinical insights into clinical biomarker strategies and endpoints.</li>
<li>Strategic thinker with excellent problem-solving skills and the ability to operate effectively in a fast-paced, matrixed environment.</li>
<li>Outstanding communication and collaboration skills with a demonstrated ability to lead cross-functional initiatives.</li>
</ul>
 
LOCATION:
AIRNA has a hybrid work model, and the role will be based in AIRNA’s corporate headquarters in Cambridge, MA ~3 days per week.

Principal Scientist, Biomarker Lead

<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 Assistant

<h3>Job Description</h3>
Nabla Bio is building AI capable of generating biomolecules on demand to probe and treat disease. By combining cutting-edge AI with experimental systems that reflect how drugs behave in humans, we’re designing new kinds of medicines — targeting biology conventional tools can’t reach, and in drug formats built for disease precision, safety, and human impact. Backed by premier investors like Radical and Khosla Ventures, we have forged significant partnerships with leading pharma companies such as AstraZeneca, Takeda, and Bristol Myers Squibb.
 
The Role
Fueled by partnerships and increasing demand for internal R&amp;D, we will be looking to you to help scale our antibody expression, purification, and developability measurement pipeline and apply it toward solving hard antibody design problems. This will include:
<ul>
<li>Developing high-throughput HEK and CHO-based antibody expression and purification protocols.</li>
<li>Prioritizing top development candidates by characterizing antibodies for key biophysical traits, including but not limited to, affinity, cross-reactivity, stability, polyspecificity, aggregation, and hydrophobicity</li>
<li>Performing and improving molecular biology workflows including cloning, PCR, Gibson/Golden Gate assembly, DNA sequencing, and bacterial transformation.</li>
<li>Working together with our dry-lab and other wet-lab scientists to establish a rapid and seamless production and testing pipeline for characterizing machine learning generated antibody designs</li>
<li>This role has a strong focus on process development and workflows.</li>
</ul>
 
Qualifications
You are a strong candidate if you have led successful multi-month/year projects featuring direct experience in the above.
<ul>
<li>Life science-focused MS or BS with 1-2 years research/industry experience are highly desirable.</li>
<li>You must like to work quickly with precision. High aptitude, tenacity, and the foundational knowledge to solve problems outside of your comfort zone is critical.</li>
<li>We will invest heavily in training you, and are committed to helping you grow within Nabla and beyond.</li>
</ul>
 
What We Offer
<ul>
<li>A fast-moving environment where you can build and ship tools that impact real drug programs</li>
<li>A small, focused team where your scientific and engineering decisions have outsized impact</li>
<li>Highly competitive salary, equity, and benefits package</li>
</ul>
 
Nabla Bio is an equal opportunity employer. We welcome applicants from all backgrounds and experiences, and strongly encourage candidates from underrepresented groups in science and technology to apply. Reach out at <a href="mailto:hiring@nabla.bio" target="_blank">hiring@nabla.bio</a>.

Protein Production & Characterization (RA/Scientist, entry)

<h3>Job Description</h3>
A client of Innova Solutions is immediately hiring for a&nbsp;Associate Scientist Position type: Full-time– Contract Duration: 12 Months Location:&nbsp;Cambridge, MA AsAssociate Scientist,&nbsp;you will: Job&nbsp;Description: 
<ul>
<li>Performs analytical testing and lab support activities for the analysis of process related impurities to support development of large molecules in the pipeline.&nbsp;</li>
<li>We provide essential data to purification scientists regarding clearance of process related impurities and develop methods and transfer them to various analytical&nbsp;laboratories for release testing of clinical and commercial materials. </li>
</ul>
Preferred Qualifications: 
<ul>
<li>Experience with protein assays, especially immunoassays, ELISAs, or qPCR</li>
<li>Experience&nbsp;in GMP lab setting</li>
<li>Experience&nbsp;with Microsoft Office software: Word, PowerPoint, Excel </li>
</ul>
Responsibilities: 
<ul>
<li>Routine testing support for PD DS process related impurity analysis</li>
<li>Preparation&nbsp;of lab buffers and reagents</li>
<li>Lab reagent&nbsp;and materials inventory and maintenance of critical reagent stocks</li>
<li>General lab&nbsp;upkeep and equipment maintenance support</li>
<li>Documentation&nbsp;of assays and laboratory activities in electronic notebook documentation system</li>
<li>Generating, analyzing, and interpreting analytical data</li>
<li>Supporting analytical&nbsp;projects involving method development, qualification, and transfer </li>
</ul>
Skills: 
<ul>
<li>ELISA, immunoassays, and qPCR technologies</li>
<li>Familiarity&nbsp;with electronic laboratory notebook/record keeping systems</li>
<li>Familiarity&nbsp;with working in a GMP/GxP environment </li>
</ul>
Day to Day: 
<ul>
<li>Analyzing routine samples by qPCR and ELISA, data interpretation and reporting</li>
<li>Documentation&nbsp;of results and peer review of electronic notebooks</li>
<li>Sample,&nbsp;reagent, and materials inventory tracking and re-stocking </li>
</ul>
Additional: 
<ul>
<li>Perform experiments, organize data, and analyze results under minimal supervision</li>
<li>Plans, conducts, or monitors experiments; records and organizes data; generates robust and reliable data</li>
<li>Ensures&nbsp;contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. </li>
</ul>
Qualified candidates should&nbsp;APPLY NOW&nbsp;for immediate consideration! &nbsp;Please hit APPLY to provide the required information, and we will be back in touch as soon as possible. We are currently interviewing to fill this and other similar positions. If this role is not a fit for you, we do offer a referral bonus program for referrals that we successfully place with our clients, subject to program guidelines. &nbsp;&nbsp;ASK ME HOW. &nbsp; Thank you!&nbsp; Harish Yadav Phone: 213-797-4030 <a href="mailto:harish.yadav@innovasolutions.com" target="_blank">harish.yadav@innovasolutions.com</a>&nbsp; &nbsp; PAY RANGE AND BENEFITS:&nbsp; Pay Range*:&nbsp;$28.00-$32.00 per hour.&nbsp; *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc.&nbsp; &nbsp; Benefits:&nbsp;Innova Solutions offers benefits( based on eligibility) that include the following: Medical &amp; pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident &amp; Critical illness coverage, Pre-paid legal &amp; ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). &nbsp; ABOUT INNOVA SOLUTIONS:&nbsp;Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: 
<ul>
<li>Named One of America’s Best Employers for New Grads by Forbes (2024</li>
<li>Named One of the Best Companies to Work for by U.S. News &amp; World Report (Private Companies List, 2024-2025)</li>
<li>One of the Largest IT Staffing Firms in the US – Ranked #3 by Staffing Industry Analysts (SIA, 2024)</li>
<li>One of the Largest Staffing Firms in the US – Ranked #13 by Staffing Industry Analysts (SIA, 2024; includes Innova Solutions, Volt, &amp; HireGenics)</li>
<li>Named One of the Top Ten Private Companies in Atlanta by the Atlanta Business Chronicle (2023)</li>
<li>One of the Largest Certified Minority Business Enterprises (MBEs) in the United States (NMSDC, 2024)</li>
<li>AWS Advanced&nbsp;Tier Services Partner with 100+ certifications </li>
</ul>
Website:&nbsp;<a href="https://www.innovasolutions.com/" target="_blank">https://www.innovasolutions.com/</a> Innova Solutions offers a referral bonus for qualified Ambassadors who refer eligible referrals. Submit referrals at&nbsp;<a href="https://innovasolutions.workllama.com/atsuser/anonreferafriend&nbsp;&nbsp;and" target="_blank">https://innovasolutions.workllama.com/atsuser/anonreferafriend&nbsp;&nbsp;and</a> earn $250-$1,000 per referral. Innova Solutions&nbsp;is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. &nbsp;If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at&nbsp;<a href="mailto:hr@innovasolutions.com" target="_blank">hr@innovasolutions.com</a>&nbsp;or (770) 493-5588. Please indicate the specifics of the assistance needed. &nbsp;Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. &nbsp; Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

Associate Scientist

<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 looking for the ideal Medicinal
We are seeking an experienced and strategic Principal Scientist to lead our efforts in translational skin biology, driving the development and validation of novel approaches across our discovery and development pipeline. You will work cross-functionally with chemistry, pharmacology, and formulation teams to advance programs from target validation through preclinical studies. You are a strategic thinker who excels in designing and executing translational biology studies, applying in vitro and ex vivo, and integrating complex data into actionable insights. This individual thrives in fast-paced, results-driven environments, is highly collaborative across disciplines, and brings a proactive approach to managing multiple projects under tight timelines.
 
 
WHAT YOU WILL DO
 
<ul>
<li>Lead and execute translational biology studies with a focus on skin biology, using in vitro and in vivo models to evaluate efficacy, mechanism of action, and safety.</li>
<li>Design, implement, and optimize assays for skin-relevant endpoints, including collagen, elastin, hyaluronic acid, pigmentation, inflammation, and barrier function.</li>
<li>Develop and validate biomarkers of skin health and aging to support target validation and preclinical proof-of-concept.</li>
<li>Collaborate with cross-functional partners (chemistry, pharmacology, formulation, and clinical) to align biological strategy with program goals.</li>
<li>Manage and guide external CRO relationships for biological assays, skin models, and advanced analytical testing.</li>
<li>Contribute to program strategy by interpreting biological data and translating findings into actionable insights for compound advancement.</li>
<li>Ensure rigorous experimental design, data analysis, and clear communication of results to internal stakeholders and external collaborators.</li>
<li>Maintain awareness of emerging technologies in skin biology and dermatological research, driving innovation in models and methodologies.</li>
<li>Advance projects from target validation through preclinical development, ensuring delivery of high-quality data packages that support decision-making and regulatory readiness.</li>
</ul>
 
WHO YOU ARE
 
<ul>
<li>Ph.D. (or equivalent experience) in Biology, Dermatology, Pharmacology, or a related life science field with a strong focus on skin biology and translational research.</li>
<li>7+ years of industry experience in translational biology, preclinical research, or related areas, ideally within dermatology, cosmetics, or skin-focused therapeutics.</li>
<li>Proven expertise in designing and executing in vitro and in vivo skin models to assess efficacy, safety, and mechanism of action.</li>
<li>Hands-on experience with skin-relevant endpoints such as collagen, elastin, hyaluronic acid, pigmentation, inflammation, and barrier integrity.</li>
<li>Strong knowledge of biomarkers for skin health, aging, and disease, with the ability to integrate biological data into development strategies.</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>

Principal Scientist

<h3>Job Description</h3>
COMPANY OVERVIEW
AIRNA is a biotechnology company with a mission to be the leading RNA editing company delivering precision therapies to patients with rare and common diseases.
 
AIRNA is harnessing advances in genetics to develop transformative RNA-editing medicines that improve human health. Our proprietary platform is based on groundbreaking research by pioneers of the field and company co-founders Thorsten Stafforst (University of Tübingen) and Jin Billy Li (Stanford University) and enables optimal potency, safety, and delivery. AIRNA is advancing a robust pipeline of therapeutic candidates that are designed to provide functional cures for severe or chronic diseases by repairing harmful genetic variants or introducing beneficial variants promote optimal health.
 
AIRNA has raised $245 million in financing from a world-class syndicate of investors including Arch Venture Partners, Forbion, Venrock Healthcare Capital Partners, RTW Investments, Nextech Invest, and ND Capital. We value teamwork, resilience, excellence, human, and health, and have a diverse team at both our headquarters in Cambridge, MA and our research operations in Tübingen, Germany.
 
JOB DESCRIPTION
AIRNAis seeking a highly motivated Research Associate/Senior Research Associate to join our Preclinical Development team in Cambridge, MA and assist in executing activities associated with AIRNA's drug development programs advancing novel therapeutics to the clinic.
 
As a member of AIRNA’s Preclinical team, you will be involved in the development and execution of biochemical and cell-based assays for-RNA-modifying oligonucleotides. Your responsibilities will include:
 
<ul>
<li>Working independently or with minimal supervision to develop, and qualify biochemical and next generation sequencing-based assays.</li>
<li>Preparing RNA and proteins from cell or animal samples and analyzing these samples by qPCR, ELISA, MSD, next-generation sequencing, or Western blot analysis.</li>
<li>Generating detailed study summaries and preparing reports for regulatory submission.</li>
<li>Performing general lab duties such as maintenance of lab equipment and reagent preparations.</li>
<li>Maintaining accurate and complete records in an electronic notebook; preparing and updating documentation as needed (SOP, Batch Records, etc.).</li>
<li>Ensuring compliance with company policies, procedures, and safety regulations.</li>
<li>Being a positive, collaborative, and committed team member.</li>
</ul>
 
QUALIFICATIONS
<ul>
<li>Bachelor's degree in Biological Sciences, Biochemistry, Molecular Biology, or Pharmaceutical Sciences.</li>
<li>1 - 5 years of relevant working experience in industry. Experience in the field of oligonucleotide therapies is highly desirable.</li>
<li>Previous experience in oligonucleotide PK and PD assays.</li>
<li>Demonstrated ability to execute next generation sequencing-based assays, including primer design, PCR optimization, RT-qPCR, operation of a benchtop sequencer, and QC and basic processing of sequencing data.</li>
<li>Experience with aseptic laboratory technique required.</li>
<li>Timely and detailed experimental documentation.</li>
<li>Being detail-oriented with strong analytical and trouble-shooting skills.</li>
<li>Working familiarity with command line, Python, Microsoft Office, and PRISM.</li>
<li>Demonstrated ability to work as part of a team and to adapt within a fast-changing environment.</li>
</ul>
 
REQUIREMENTS
<ul>
<li>Biotechnology or pharmaceutical industry experience.</li>
<li>Experience in bioanalytical assay development and qualification based on regulatory guidelines.</li>
<li>Experience in using automatic liquid handlers and performing assays in 96+ plate formats.</li>
<li>Experience in sequencing library preparation and data processing.</li>
</ul>
 
LOCATION
AIRNA has a hybrid work model, and the role will be based in AIRNA’s corporate headquarters in Cambridge, MA ~4 days per week.

Research Associate / Senior Research Associate, Preclinical Development

<h3>Job Description</h3>
Job Description
Our client, a leading innovator in the food industry, is seeking a Research &amp; Development Tech to join their team. As a Research &amp; Development Tech, you will be part of the R&amp;D department supporting product development and process optimization teams. The ideal candidate will have curiosity, problem-solving skills, and a collaborative mindset which will align successfully in the organization.
Job Title: Research &amp; Development Tech
Location: Quincy, MA
Pay Range: $20 - $23 per hour
Shift: 8:00am to 5:00pm Monday to Friday
What's the Job?
<ul>
<li>Conduct research including new product development and food formulation</li>
<li>Develop new and improved methods for food processing, quality control, and packaging</li>
<li>Support pilot plant activities and assist with production scale-ups and commercialization efforts</li>
<li>Address customer requests from conceptualization through troubleshooting and commercialization</li>
<li>Collaborate with culinary and subject matter experts to develop standards and optimize formulations</li>
</ul>
What's Needed?
<ul>
<li>Basic understanding of food science and processing techniques</li>
<li>Strong communication skills for technical and culinary presentations</li>
<li>Ability to troubleshoot and understand customer processes</li>
<li>Experience in research documentation and process improvement</li>
<li>Motivation to innovate and contribute to product excellence</li>
</ul>
What's in it for me?
<ul>
<li>Opportunity to work in a dynamic and innovative environment</li>
<li>Engage in meaningful research that impacts product quality and customer satisfaction</li>
<li>Collaborate with cross-functional teams and industry experts</li>
<li>Develop your skills in food science and product development</li>
<li>Be part of a company committed to nourishing and delighting customers</li>
</ul>
Upon completion of waiting period associates are eligible for:
<ul>
<li>Medical and Prescription Drug Plans</li>
<li>Dental Plan</li>
<li>Supplemental Life Insurance</li>
<li>Short Term Disability Insurance</li>
<li>401(k)</li>
</ul>
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
About ManpowerGroup, Parent Company of: &nbsp;Manpower, Experis, Talent Solutions, and Jefferson Wells
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells –&nbsp;creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.

Research & Development Tech

<h3>Job Description</h3>
Job Description
For more than 50 years, EdgeTech has been the industry leader in the design and manufacture of advanced underwater sonar systems for applications involving seabed survey, target detection, object identification, mooring instrumentation, and acoustic tracking/positioning.&nbsp; Our products are used to support a variety of customers, from offshore oil and gas to fisheries/science/underwater research, defense, and police/fire search and rescue
We’re looking for an engineer/scientist with interest in applying signal processing to develop algorithms that enable new capabilities in next-generation sonar systems. Typical assignments include algorithm design, analysis, and implementation; sonar system analysis; involvement in software and hardware prototyping and test activities; documentation and planning; as well as sea testing, data collection, and post-trial analysis.
Job Responsibilities
<ul>
<li>Design algorithms for processing of sonar signals including waveform design, beamforming, broadband processing, and detection.</li>
<li>Develop processing algorithms and assess their performance. Interpret results.</li>
<li>Collaborate with real-time code developers and modeling/simulation analysts to develop and integrate system software.</li>
<li>Develop simple and reliable signal processing algorithms for a variety of processors, to include ARM’s, SoC’s/SoM's and FPGAs</li>
<li>Assist with the development of signal processing specifications and their implementation</li>
<li>Test software, firmware and full sonar solutions in simulation, hardware-in-the-loop, and field demonstrations</li>
<li>Collaborate with a cross-functional team testing your contributions and analyzing performance</li>
<li>Support the engineering, production, and sales/marketing teams with productization of technologies and solutions</li>
<li>Understand broad product objectives to develop and maintain relationships with major customers.</li>
<li>Collaborate with other engineers, customers and the technical community to advance sonar capabilities for current and future applications</li>
</ul>
Job Requirements
<ul>
<li>This job can be filled at multiple levels, depending upon the successful candidate’s education and experience. Minimum education required is an M.S. degree in an engineering or science related discipline plus five year’s related experience or an equivalent combination of education and experience.</li>
<li>Experience with signal processing theory and applications</li>
<li>Experience with scripting and analysis tools such as Matlab and Python</li>
<li>Experience with planning and conducting sea trials and surveys.</li>
<li>Highly effective written and verbal communication skills</li>
<li>Ability to work effectively in a team and set priorities</li>
<li>Work with sonar imaging technologies or hydrographic applications is a big plus.</li>
<li>Familiarity with hardware (amplifiers, antennas/transducers, filters), and digital processing with FPGAs, GPUs, CPUs, is desirable but not required.</li>
<li>Work will include a mix of field and office assignments, with domestic and international travel as part of the job.</li>
</ul>
If interested, please contact:
Kevin Igo
<a href="mailto:Kevin.Igo@edgetech.com" target="_blank">Kevin.Igo@edgetech.com</a>
Company DescriptionEdgeTech is a leading manufacturer of underwater technology solutions. The company is known worldwide for its high quality products which include: side scan sonars, sub-bottom profilers, bathymetry systems, AUV and ROV-based sonar systems, combined and customized solutions. In addition to the full line of underwater survey products, EdgeTech provides reliable USBL systems, transponder beacons, deep sea acoustic releases, shallow water and long life acoustic releases, MRUs and customized underwater acoustic command and control systems. 
<h3>Company Description</h3>
EdgeTech is a leading manufacturer of underwater technology solutions. The company is known worldwide for its high quality products which include: side scan sonars, sub-bottom profilers, bathymetry systems, AUV and ROV-based sonar systems, combined and customized solutions. In addition to the full line of underwater survey products, EdgeTech provides reliable USBL systems, transponder beacons, deep sea acoustic releases, shallow water and long life acoustic releases, MRUs and customized underwater acoustic command and control systems.

Applied Research Scientist

<h3>Job Description</h3>
Job DescriptionWho We Are
TetraScience is the Scientific Data and AI Cloud company. We are catalyzing the Scientific AI revolution by designing and industrializing AI-native scientific data sets, which we bring to life in a growing suite of next gen lab data management solutions, scientific use cases, and AI-enabled outcomes. 
TetraScience is the category leader in this vital new market, generating more revenue than all other companies in the aggregate. In the last year alone, the world’s dominant players in compute, cloud, data, and AI infrastructure have converged on TetraScience as the de facto standard, entering into co-innovation and go-to-market partnerships: Latest News and Announcements | TetraScience Newsroom: 
In connection with your candidacy, you will be asked to carefully review the Tetra Way letter, authored directly by Patrick Grady, our co-founder and CEO. This letter is designed to assist you in better understanding whether TetraScience is the right fit for you from a values and ethos perspective. 
It is impossible to overstate the importance of this document and you are encouraged to take it literally and reflect on whether you are aligned with our unique approach to company and team building. If you join us, you will be expected to embody its contents each day. 
Who You Are
You are a strategic, analytically minded professional with a passion for bridging scientific insights and cutting-edge technology. You thrive in environments where you can collaborate with scientists, product managers, and engineers to transform complex scientific data into actionable outcomes.
With deep domain knowledge in drug discovery/preclinical development, CMC, or Quality, you are skilled at uncovering innovative use cases that drive AI and machine learning applications. Your ability to engage with scientists and business leaders alike makes you a key player in maximizing the value of scientific data.
You will need to be a high clock speed and forward-thinking individual with a passion for developing requirements for complex solutions targeted to R&amp;D and Quality personas inside of Life Sciences. 
You will need to be a high clock-speed, forward-thinking individual with a passion for developing requirements for complex solutions targeted to R&amp;D and Quality personas inside Life Sciences. You embody extreme ownership and have a demonstrated history of deriving maximum value from data through enrichment, analysis, and integration with AI and machine learning applications.
You should also be energized by regularly working onsite with customers. You thrive in dynamic, high-impact, face-to-face collaborative environments where you can build deep relationships and drive scientific transformation firsthand.
Requirements
What You Have Done
<ul>
<li>PhD with 15+ years of industry experience in life sciences, preferably across pharma, biotech, or health tech, with deep domain expertise in discovery, preclinical, CMC, and/or Quality.</li>
<li>Extensive hands-on experience or direct oversight in one or more of the following areas: high throughput screening, preclinical toxicology, materials engineering, analytical development, drug substance (DS) synthesis and manufacturing.</li>
<li>Delivered requirements for AI/ML-driven solutions in operational or productized environments that improved efficiency, reduced cost, and enhanced data utilization.</li>
<li>Extensive hands-on experience with scientific data workflows and lab automation; exposure to FAIR principles and modern data architecture is a plus.</li>
<li>Strong coding or scripting background (e.g., Python, Nextflow, AWS, SDKs) and familiarity with scientific tools, databases, and ontologies is preferred.</li>
<li>Exceptional communication and storytelling ability to engage technical and executive stakeholders.</li>
<li>Prior experience in customer-facing, consulting, or commercial-scientific interface roles.</li>
</ul>
What You Will Do
<ul>
<li>You will be a critical team member in a unique partnership to industrialize Scientific AI. As such, you will engage directly with customers onsite up to 4-5 days per week in the Boston Region</li>
<li>Customer Data Exploration: Investigate diverse customer datasets, identifying enrichment and AI-readiness opportunities.</li>
<li>Scientific Use Case Development: Collaborate with customers to define, iterate, and implement innovative scientific AI/ML use cases.</li>
<li>Stakeholder Engagement: Conduct onsite interviews and workshops to deeply understand customer challenges and data landscapes.</li>
<li>Data Analysis and Enrichment: Perform exploratory data analysis and define transformation workflows that enable scientific AI.</li>
<li>Workflow Documentation: Develop visual documentation including workflow diagrams, ERDs, and ontology definitions.</li>
<li>AI Model Evaluation: Provide practical scientific input on model output, with suggestions to improve real-world performance.</li>
<li>Customer Enablement: Deliver onsite demonstrations, conduct working sessions, and act as a trusted advisor in AI adoption.</li>
<li>Strategic Insight: Propose new directions, experiments, or platforms that can amplify scientific discovery and development.</li>
</ul>
Benefits
<ul>
<li>100% employer-paid benefits for all eligible employees and immediate family members</li>
<li>Unlimited paid time off (PTO)</li>
<li>401K</li>
<li>Remote working opportunities, when not at customer sites </li>
<li>Company paid Life Insurance, LTD/STD</li>
<li>A culture of continuous improvement where you can grow your career and get coaching</li>
</ul>

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