field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<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>
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>

Spring Drug Discovery Biology Co-Op/Internship

<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>
Job Descriptionjob summary: 
The Chemist is an individual contributor responsible for performing a variety of tests on samples within a Quality Control (QC) laboratory. This role involves operating and maintaining various instruments, ensuring data integrity, and adhering to strict cGMP and documentation practices. The specific duties and responsibilities may vary based on the assigned department, group, as well as the individual's education, training, and level of experience. This position requires a strong working knowledge of analytical techniques and equipment to ensure the quality and compliance of all tested materials. 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab is required. 
FLSA Classification: Full-Time
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
 location: Fall River, Massachusetts job type: Permanent salary: $70,000 - 90,000 per year work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Execute a full range of analytical testing, including routine, advanced, and critical analysis, with a working knowledge of raw materials testing and release.</li>
<li>Operate and maintain a variety of specialized instruments, such as Karl Fischer, HPLC, GC, Particle Size, and ICP, and coordinate with vendors for their installation and qualification.</li>
<li>Ensure strict compliance with all cGMP (current Good Manufacturing Practices), data integrity, and good documentation practices.</li>
<li>Lead investigation activities to address testing deviations or other issues as they arise.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelor's degree (BS or BA) in scientific discipline</li>
<li> 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab </li>
</ul>
Preferred:
<ul>
<li> Experience in Inhalation products (MDI)</li>
</ul>
 #LI-AB1 
 skills: High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay 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. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

QC Chemist II

<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 Description
Discover Veranova:
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
The Analytical/QC Lab Metrologist is responsible for the timely installation, maintenance, repair, calibration, and IQ/OQ of instruments, balances, and other equipment used by the Analytical Development (AD) and Quality Control (QC) groups. This role also ensures Standard Operating Procedures are technically sound and provide full regulatory compliance. This position is critical to supporting high-quality science, operational excellence, and regulatory compliance across both sites.
Core Responsibilities: 
<ul>
<li>Revises and reviews metrology-related protocols and IQ/OQ to ascertain proper functioning of the instrumentation. Ensures that appropriate documentation for the instrument calibration program is in place for compliance with regulatory expectations.</li>
<li>Schedules, executes and supports instrument calibrations and preventative maintenance in such a way so as not disrupt the analysts using the instruments. Responsible in the assignment of instrument custodians, assuring instrument maintenance and usage logbooks have been maintained. Trouble shooting or judging the issue for chromatographic systems mainly LC/GC.</li>
<li>Negotiates and manages contracts with external vendors and contracted services as required. Oversees the work of contracted personnel to install/modify equipment and systems in accordance with the specific needs of the AD and QC groups while meeting all cGMP and USP requirements.</li>
<li>Keep abreast of instrument validation requirements to ensure compliance with respect to USP and cGMP requirements.</li>
<li>Provides assistance in internal and customer audits by providing relevant, up to date documentation related to calibration, qualification and maintenance of appropriate analytical instrumentation used by the analytical groups. </li>
<li>Leads the process to evaluate, purchase and install new instrumentation. Interacts with internal and external vendors to ensure the proper instrumentation is identified to support the needs of the business. Evaluates and recommends appropriate application of new software packages as well as upgrades of software/firmware/hardware.</li>
<li>Directly involved with and supports investigations that are instrument related. Conducts all work in compliance with USP and cGMP standards and all other appropriate Federal, state and local regulations.</li>
</ul>
Qualifications: 
Required
<ul>
<li>Bachelor’s Degree in chemistry or a related science with a minimum of 5 years’ related experience </li>
<li>Familiarity with LC/GC trouble shooting.</li>
<li>Experience in a cGMP environment</li>
<li>Ability to exercise independent judgment in the application of scientific principles pertaining to analyses as related to this business and operation </li>
<li>Proficiency with computers and other software packages relevant to installation, modification, calibration and qualification of instrumentation systems and equipment</li>
<li>Strong communication skills; written and verbal. </li>
<li>Possess strong organizational skills</li>
</ul>
Preferred
<ul>
<li>Experience in lab equipment such as analytical balance, micro balance, KF, OVEN-KF, NMR, ICP-MS, PSD, XRPD, TGA, DSC, etc. </li>
<li>Experience or familiarity with Labware LIMS and the Instrument Manager module</li>
<li>Experience or familiarity with Master Control and Veeva</li>
<li>Recent relevant experience in bulk pharmaceutical/API manufacturing or specialty chemicals</li>
</ul>
Salary Range: $90,000 - $105,000 annual base salary
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship. 
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.
#LI-Onsite

Analytical/Quality Control Lab Metrologist

<h3>Job Description</h3>
Job DescriptionWho We Are
TetraScience is the Scientific Data and AI 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>

810 Science Jobs