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<h3>Job Description</h3>
Job DescriptionBiological Technicians – NOAA Fisheries Sea-Going Surveys (Levels I–III)
Remote/Offshore within Massachusetts or Rhode Island – accessible to Falmouth/Woods Hole, MA, and Narragansett, RI (with assignments on NOAA and partner vessels throughout the Northeast U.S.)
@Orchard LLC has been awarded the PEMAD sea-going support contract through NOAA Fisheries. We are actively hiring Biological Technicians (Levels I–III) to support NOAA Fisheries’ Ecosystem Surveys Branch (ESB). Technicians collect and process biological samples and environmental data during fishery-independent resource surveys. Work includes at-sea survey participation (5–140+ days annually), data QA/QC, sample processing, and equipment support. This is a hands-on science role that directly supports stock assessments and ecosystem-based fisheries management.
Responsibilities 
<ul>
<li>Participate in sea-going surveys aboard NOAA and partner vessels (sorting, identifying, weighing, measuring fish/invertebrates, collecting biological samples for age, growth, maturity, genetics, diet). </li>
<li>Stand scientific watches of up to 12 hours/day at sea.</li>
<li>Operate electronic data acquisition systems for fisheries and oceanographic sampling. </li>
<li>Assist with deployment, calibration, and maintenance of survey gear, acoustics, and optical/video equipment. </li>
<li>Conduct QA/QC of survey data using NOAA protocols; prepare documentation of sampling procedures and metadata. </li>
<li>Annotate benthic imagery and optical survey data as directed. </li>
<li>Maintain, repair, and inventory sampling hardware (measuring boards, motion-compensated scales, barcode systems, touch screens). </li>
<li>Support cruise staging/de-staging, equipment prep, and vessel logistics. </li>
<li>Contribute to laboratory analysis of biological samples and assist with database management. </li>
<li>Train new staff (Levels II &amp; III) and provide leadership of field parties/watches at sea (Level III). </li>
<li>Summarize survey data, assist with reports, and contribute to outreach materials (manuals, protocols, blogs, newsletters). </li>
</ul>
Qualifications
Your background will include (all levels): 
<ul>
<li>Experience working aboard research or commercial vessels.</li>
<li>Ability to work 12-hour shifts at sea for trips lasting up to 3 weeks.</li>
<li>Strong teamwork and communication skills in challenging field environments.</li>
<li>Must meet NOAA OMAO sea duty health criteria and provide proof of a recent TB test.</li>
<li>Proficiency with Microsoft Office; familiarity with data entry and QA/QC practices.</li>
<li>Valid driver’s license. </li>
</ul>
Level I (Entry/Seasonal Technician):
<ul>
<li>Basic familiarity with marine species ID in the Northwest Atlantic (fish/invertebrates).</li>
<li>Coursework or experience in biological sciences preferred.</li>
<li>Able to assist with sampling, data recording, and shipboard organization under supervision.</li>
</ul>
Level II (Experienced Technician): 
<ul>
<li>Minimum 2 years’ experience identifying fish and invertebrates in the Northwest Atlantic.</li>
<li>At least 1 year of experience with survey bottom trawls or shellfish dredges.</li>
<li>Experience with fishery sampling hardware (electronic boards, scales, barcode systems).</li>
<li>Strong written and verbal communication skills; ability to work independently.</li>
</ul>
Level III (Senior Technician): 
<ul>
<li>Minimum 200 days at sea (Bottom Trawl Survey) or 100 days (Shellfish/Advanced Tech Surveys). </li>
<li>At least 2 years’ experience with electronic data acquisition systems.</li>
<li>Experience leading watches/field teams of up to 7 at sea. </li>
<li>Familiarity with acoustic net mensuration systems (Scanmar, Simrad, Marport). </li>
<li>Experience querying/analyzing fishery-independent data from relational databases (e.g., Oracle). </li>
<li>Ability to train staff, conduct QA/QC, and contribute to protocol development.</li>
</ul>
To learn more about this opportunity to serve the NOAA Fisheries mission of advancing Fisheries science, please apply.
Compensation will be based on experience and qualifications, and is expected to be in the range of $58-62k
Established in 2010, @Orchard has an exceptional reputation, providing staffing solutions to time-sensitive, talent scarcity issues to deliver better talent management ROI. Our specialty lies in the critical area of program talent acquisition and resource management, not in one narrow skillset, but across many areas of technical and functional delivery. To learn more about our other exciting opportunities, visit our Jobs Page at <a href="http://www.atorchard.com" target="_blank">www.atorchard.com</a>.

Biological Technician - Fisheries Survey Support

<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>

Research Assistant

<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.

<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>
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>
We are a Boston-area biomedical diagnostics startup company seeking a Clinical Blood Biochemist/Microbiologist to join our team.
Your mission will be to apply your biochemistry and microbiology expertise in support of developing rapid clinical diagnostics. Working closely with a multidisciplinary team spanning many fields of expertise, from medical microbiology to machine learning, you will take the lead designing, executing, and interpreting experiments involving blood-borne pathogens and biochemical growth conditions—helping advance diagnostics that improve patient outcomes around the globe.
Required Qualifications
<ul>
<li>Master’s degree or PhD in biochemistry, microbiology, or a related life sciences field</li>
<li>2+ years of wet-lab experience, ideally in a BSL2 and/or clinical laboratory setting</li>
<li>Hands-on experience with microbial culturing, gram staining, and antimicrobial susceptibility testing</li>
<li>Experience designing and conducting experiments involving growth of bacteria and fungi in blood and/or blood-derived growth media</li>
<li>Deep understanding of blood chemistry, including pH, blood additives (e.g. anticoagulants), and blood components (molecular and cellular)</li>
<li>Skilled in preparing and managing blood cultures and growth assays for clinically relevant organisms</li>
<li>Excellent documentation habits and experience writing and maintaining SOPs and lab protocols</li>
<li>Strong organizational and communication skills, both written and verbal</li>
<li>Commitment to accuracy, quality control, and laboratory safety standards</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience supporting or working alongside clinical microbiologists in a diagnostic or research setting</li>
<li>Familiarity with laboratory instrumentation for microbial growth and analysis (e.g. incubators, anaerobic chambers, spectrophotometers)</li>
<li>Experience with fungal identification or culturing in clinical matrices</li>
<li>Exposure to automated microbial identification tools or molecular platforms (e.g. MALDI-TOF, BioFire)</li>
<li>Familiarity with basic programming or data analysis tools (Python, R, Excel macros, etc.)</li>
</ul>
Particulars
<ul>
<li>Company headquarters: Beverly, MA; on-site work preferred</li>
<li>Competitive salary and equity compensation package</li>
<li>Comprehensive health benefits and flexible paid time off</li>
</ul>
Why Join Us?
You could take your training and experience to a big-name institution or multinational—but if you’d rather be on a close-knit team of innovators who actually build and ship life-saving technologies, you might find your home here. You’ll be a core part of a team that values creativity, urgency, precision, and purpose.
If that resonates, please send a short (~250-word) cover letter and resume/CV to <a href="mailto:careers@astradx.com" target="_blank">careers@astradx.com</a>. Feel free to include any links to lab notebooks, GitHub, protocols you’ve authored, or other relevant work.
Note: Your cover letter should include:
<ul>
<li>Why you’re interested in this particular role and company (~100 words)</li>
<li>One experiment, technique, or scientific idea you’ve come across recently that you found fascinating (~100 words)</li>
</ul>
Let me know if you'd like a version for internal use (e.g. hiring manager spec) or edited for a different platform like LinkedIn or academic job boards.

Clinical Blood Biochemist/Microbiologist at Biomedical Diagnostics Startup

<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>

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