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<h3>Job Description</h3>
Pay Range: $34 - $39/hour
 
Position Details:
Industry: Pharmaceutical
Title: Biologist II
Duration: 12 Months (++Possibility of Extension)
Location: Worcester, MA 01605

Responsibilities (include but are not limited to):
<ul>
<li>Basic understanding of LC-MS, SEC_MALS, Western blotting and other protein characterization techniques</li>
<li>Sample handling and preparation of sample for peptide mapping and proteomics</li>
<li>Basic instrument operation and maintenance.</li>
<li>Documentation : Accurate record-keeping of experiments and results</li>
<li>Data analysis and interpretation of the data.</li>
<li>The Protein Science group within Biologics and Genetic Medicine seeks a talented scientist to develop advanced and robust LC-MS analytical methods for the bioanalysis of various molecular formats, such as peptides and proteins. The successful candidate will develop and implement innovative, high-resolution mass spectrometry-based methods for peptide mapping and intact protein analysis.</li>
<li>Responsibilities include sample preparation for mass spectrometry and other related analytical techniques, such as Western blotting, SEC-MALS, ELISA, and spectroscopic methods. The candidate will also maintain and troubleshoot laboratory instruments, including biological sample extraction systems, HPLC, and LC-MS.</li>
<li>Education -Bachelors degree, Masters preferred. PhD would be overqualified.</li>
</ul>
 
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)

Biologist (LC-MS)

<h3>Job Description</h3>
Job Description
Be Part of a High-Performing Team
This innovative biopharmaceutical company is dedicated to advancing therapies for rare diseases, with a strong focus on next-generation gene therapy solutions. The R&amp;D team in Lebanon, NH, operates in a collaborative, fast-paced environment where experimental and computational scientists work side by side to drive discovery and innovation. The lab fosters creativity, scientific rigor, and mentorship, providing an opportunity to contribute directly to groundbreaking advancements in biologics research.
What’s In Store For You
<ul>
<li>Hands-on role in a state-of-the-art research lab, supporting cutting-edge gene therapy programs</li>
<li>Opportunity to lead projects and mentor junior scientists</li>
<li>Exposure to novel discovery efforts with real-world impact on rare disease treatment</li>
<li>Long-term career trajectory, with conversion from contract to full-time employee after 6 months</li>
</ul>
How You Will Make an Impact
<ul>
<li>Lead research efforts focused on engineering and discovery of viral vectors for gene therapy</li>
<li>Design and optimize molecular and cellular assays for high-throughput screening</li>
<li>Conduct viral vector development, transfection, transduction, and sequencing-based analysis</li>
<li>Build and characterize viral vector libraries using advanced molecular biology methods</li>
<li>Perform mammalian cell culture, primary cell work, and provide in vivo study design support</li>
<li>Prepare and analyze Next-Generation Sequencing (NGS) libraries, with exposure to long-read sequencing (PacBio)</li>
<li>Document protocols, deliver reports, and present results to cross-disciplinary teams</li>
<li>Mentor junior scientists and support lab operations while maintaining high-quality standards</li>
</ul>
Are You an Accomplished Scientist Ready to Drive Innovation in Gene Therapy?
<ul>
<li>PhD in cell biology, virology, immunology, molecular biology, bioengineering, or related field with 2+ years of industry experience (academic considered), OR Master’s with 8+ years hands-on experience</li>
<li>Proven expertise in viral vectors; direct AAV experience strongly preferred</li>
<li>Strong foundation in molecular biology (cloning, PCR/qPCR/ddPCR, DNA/RNA workflows)</li>
<li>Skilled in mammalian and primary cell culture</li>
<li>Background in viral vector engineering, library preparation, and screening</li>
<li>NGS sample preparation experience required; PacBio or long-read sequencing strongly desired</li>
<li>In vivo study design experience is a plus</li>
<li>Prior leadership or mentorship experience preferred, with potential to transition into a leadership role after conversion</li>
<li>Strong communication, problem-solving, and organizational skills</li>
</ul>

Senior Associate Scientist #3443550

<h3>Job Description</h3>
Job DescriptionJob Title: Manufacturing Chemist II
Job Description
We have multiple openings for the position of Manufacturing Chemist II across 1st, 2nd, and 3rd shifts. This role offers a dynamic opportunity for career growth within a thriving Contract Manufacturing Organization (CMO) in the biotech industry.
Responsibilities
<ul>
<li>Maintain a clean, organized, and safe work environment in compliance with GMP standards and safety protocols.</li>
<li>Proactively identify and report safety hazards and incidents.</li>
<li>Accurately complete GMP documentation and review basic records such as logbooks.</li>
<li>Assist in revising procedures under direct supervision.</li>
<li>Participate in investigations and support execution of CAPA (Corrective and Preventive Actions).</li>
<li>Contribute to small-scale continuous improvement initiatives.</li>
<li>Perform assigned production activities, ensuring all required training is completed and compliant prior to operations.</li>
<li>Apply basic problem-solving skills to identify abnormal results and escalate issues appropriately.</li>
<li>Demonstrate proficiency in designated process areas.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in pH testing, aseptic technique, buffer preparation, UV Vis spectrophotometry, and general Chemistry.</li>
<li>Experience with GMP, UV Vis, and pH Meter operations.</li>
<li>Knowledge of purification, chromatography, and biotechnology processes.</li>
<li>Two plus years of experience in a cGMP manufacturing environment.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Minimum education requirements: high school diploma or equivalent.</li>
<li>Preferred: college-level Chemistry degree or equivalent work experience.</li>
<li>A biotechnology certificate or college degree is preferred.</li>
<li>Knowledge of basic laboratory instrumentation such as use of pH meter, UV instrumentation, and solution delivery systems (process skids).</li>
</ul>
Work Environment
You will be working in a GMP-based environment with a team that values teamwork and camaraderie. The atmosphere is easygoing yet focused on productivity, allowing for a balance of fun and professionalism. Shifts available are: 1st Shift, 2nd Shift with a 15% shift differential, and 3rd Shift with a 20% shift differential. Our close-knit team is committed to making a difference in the biotech industry, offering a chance to be part of an innovative and exciting work setting.
Pay and Benefits
The pay range for this position is $61700.00 - $75600.00/yr.
Health insurance, 401k, PTO, 12 Paid holidays
Workplace Type
This is a fully onsite position in Milford,MA.
Application Deadline
This position is anticipated to close on Sep 26, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Manufacturing Chemist II

<h3>Job Description</h3>
Job Description
Family owned and operated, Joseph's Bakery is the country's premier CPG manufacturer of Pita Bread, Flat Breads &amp; Lavash. Established in 1972 by Joseph Boghos, Joseph's Bakery is proudly owned and managed by the third generation of our founding family. A majority female owned business, we bake a diverse variety of Joseph's Branded and private label flat bread items that are widely distributed to grocery retailers throughout the United States, Central &amp; South America, and the Caribbean Islands. Joseph's Bakery is a high growth environment with ten processing lines and approximately 150k square feet of manufacturing space. We operate twenty-four hours per day, five days per week, with dedicated production lines for Pita Breads, Tortillas, Flat Breads, Lavash, and Frozen Pancakes. 
Joseph's is the number one national brand of Pita Bread, Flatbread &amp; Lavash, and is seeking candidates to join our family legacy! 
Position Summary
The R&amp;D Technician supports the Research &amp; Development team in the creation, testing, and improvement of new and existing products, processes, and equipment. This role involves hands-on experimentation, data collection, sample preparation, and collaboration with cross-functional teams to help bring innovative products from concept to commercialization.
Key Responsibilities
<ul>
<li>Assist in developing, testing, and evaluating new product formulations and process improvements.</li>
<li>Prepare samples for internal testing, customer evaluation, and sensory panels.</li>
<li>Operate lab and pilot plant equipment, ensuring proper setup, use, and cleaning.</li>
<li>Collect, record, and analyze data accurately, preparing reports and documentation for review.</li>
<li>Maintain R&amp;D lab organization, inventory, and supplies.</li>
<li>Follow established protocols, standard operating procedures (SOPs), and safety guidelines.</li>
<li>Collaborate with Quality, Production, and Operations teams to support trials and scale-up activities.</li>
<li>Troubleshoot issues during product testing and provide feedback to the R&amp;D team.</li>
<li>Stay informed about industry trends, ingredients, and technologies relevant to product innovation.</li>
</ul>
Qualifications
<ul>
<li>Associate or Bachelor's degree in Food Science, Chemistry, Biology, Engineering, or related field (or equivalent experience).</li>
<li>Prior experience in a laboratory, pilot plant, or food manufacturing environment preferred.</li>
<li>Strong attention to detail with the ability to follow precise instructions and protocols.</li>
<li>Basic knowledge of food safety, GMP, and laboratory practices.</li>
<li>Proficiency in Microsoft Office (Excel, Word, PowerPoint); ability to learn data collection software.</li>
<li>Strong organizational and time management skills.</li>
<li>Effective communication and teamwork abilities.</li>
</ul>
Physical Requirements
<ul>
<li>Ability to stand for extended periods and lift up to 30 lbs.</li>
<li>Ability to work in a lab, pilot plant, or production environment with varying temperatures.</li>
</ul>
Work Environment
<ul>
<li>Laboratory and pilot plant setting with exposure to food ingredients, allergens, and processing equipment.</li>
<li>May occasionally require flexible hours to support testing and production trials.</li>
</ul>
Equal Employment Opportunity Policy:
Joseph's Bakery provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

R&D Technician

<h3>Job Description</h3>
Job Description
We are currently seeking a Scientist, Oligonucleotide Synthesis for a prominent Pharmaceutical client of ours. This position is in Waltham, MA. Details for the position are as follows: Job Description:
<ul>
<li>Pay: 51.00/hr. No flexibility in pay.</li>
<li>Length of Assignment: 1 year to start with potential for extension or conversion. </li>
<li>Manager is open to candidates willing to relocate at their own expense. </li>
<li>MUST HAVE Oligonucleotide Synthesis experience. </li>
<li>MUST HAVE Ph.D degree. Academic only experience is acceptable.</li>
<li>Experience with any of the following: sequence design, gene assembly, NGS library prep, analysis, and process optimization. Hands-on molecular biology skills in oligo synthesizer, PCR, Gibson and Golden Gate Assembly, Illumina and nanopore NGS platform, automated liquid handler Hamilton etc., nucleic acid sequence analysis software (Geneious, SnapGene, Benchling etc.). </li>
<li>Analytical and molecular biology methods relevant to DNA work is a plus.. </li>
<li>Experience in programing such as Python, SQL, R is a plus.</li>
<li>Independently plan, design, and execute synthetic biology experiments to construct and prepare high quality of nucleic acid material for mRNA vaccine production. Take part in mRNA vaccine target development, DNA template production, QC, and data analysis.</li>
</ul>
#LI-DB1 #Zip

Now Hiring - Scientist, Oligonucleotide Synthesis

<h3>Job Description</h3>
Job DescriptionJob Title: Manufacturing Chemist IIJob Description
We offer multiple openings for the Manufacturing Chemist II position across 1st, 2nd, and 3rd shifts, providing an opportunity to join a growing company in the biotech industry.
Responsibilities
<ul>
<li>Maintain a clean, organized, and safe work environment in compliance with GMP standards and safety protocols.</li>
<li>Proactively identify and report safety hazards and incidents.</li>
<li>Accurately complete GMP documentation and review basic records such as logbooks.</li>
<li>Assist in revising procedures under direct supervision.</li>
<li>Participate in investigations and support execution of CAPA (Corrective and Preventive Actions).</li>
<li>Contribute to small-scale continuous improvement initiatives.</li>
<li>Perform assigned production activities, ensuring all required training is completed and compliant prior to operations.</li>
<li>Apply basic problem-solving skills to identify abnormal results and escalate issues appropriately.</li>
<li>Demonstrate proficiency in designated process areas.</li>
</ul>
 Essential Skills
<ul>
<li>Proficiency in pH testing, aseptic techniques, buffer preparation, UV-Vis spectroscopy, and general chemistry.</li>
<li>Experience with GMP standards.</li>
<li>Knowledge of basic laboratory instrumentation, including the use of pH meters, UV instrumentation, and solution delivery systems.</li>
<li>Two or more years of experience in a cGMP manufacturing environment.</li>
</ul>
 Additional Skills &amp; Qualifications
<ul>
<li>A high school diploma or equivalent is required, with college-level coursework in Chemistry or equivalent work experience preferred.</li>
<li>A biotechnology certificate or college degree is preferred.</li>
<li>Performance and other experience can be considered pending discretion.</li>
</ul>
 Work Environment
The position is based in a GMP environment with a team-oriented and supportive atmosphere. Employees enjoy a collaborative and intimate setting, encouraging both fun and productivity. Current openings include 1st shift, 2nd shift with a 15% differential, and 3rd shift with a 20% differential. Our team is dedicated to teamwork and making a positive impact in the biotech industry.
Job Type &amp; Location
This is a Contract to Hire position based out of Milford, Massachusetts.
Pay and Benefits
The pay range for this position is $30.00 - $31.25/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Milford,MA.
Application Deadline
This position is anticipated to close on Oct 6, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Manufacturing Chemist

<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 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 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>

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