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<h3>Job Description</h3>
POSITION SUMMARY 
Manomet Conservation Sciences is a mission-driven conservation NGO seeking a Senior Shorebird Scientist with a strong background in shorebird ecology to lead applied research and conservation efforts focused on shorebirds.&nbsp;This is a senior-level position for a scientist who combines deep ecological expertise with a passion for protecting migratory birds and their habitats.
The ideal candidate has a PhD. in conservation research and is a skilled field biologist, analytical thinker, and collaborative leader, with demonstrated success in shorebird research, conservation partnerships, and science communication. The Senior Shorebird Scientist manages a program of research related to the conservation of shorebirds throughout the Western Hemisphere, with a special focus on the flagship species identified in Manomet’s current Strategic Plan, and with a special focus on arctic breeding shorebirds and their habitats.&nbsp;The major focus of the research is to identify factors limiting populations of these species, so that conservation action can be targeted to reverse declines and recover populations.&nbsp;
 
ABOUT MANOMET:
Manomet is a 501(c)(3) organization that empowers stakeholders through science and works with partners to make a world where ecosystems and human communities thrive. Since Manomet’s beginnings as a bird banding operation in 1969, its science and research have expanded to focus on ecosystem management and resilience, shorebird conservation, and educating tomorrow’s leaders about the importance of the natural world. Workplace diversity, science, and climate change are the fundamental principles driving Manomet’s work today.
 
ESSENTIAL JOB FUNCTIONS
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Design and lead research and field studies on shorebirds, including demographic monitoring, migration ecology, habitat use, and climate-related impacts, and lead project planning, research design, project implementation, and data analysis and reporting
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Oversee and conduct data collection and analysis using techniques such as nest monitoring, bird banding, remote sensing, and tracking technologies (e.g., GPS, geolocators, satellite tags).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Maintain long-term datasets and publish high-impact research in peer-reviewed journals.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Secure and manage funding through grant writing and reporting, donor proposals, and institutional partnerships.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Lead project teams and partnerships, manage budgets, and ensure timely completion of deliverables.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Mentor early-career scientists, technicians, and Indigenous youth interested in conservation science.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Support staff across Manomet’s shorebird conservation programs with field research planning, research design, and data analysis and reporting
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Work collaboratively with other scientists and conservation specialists across multiple projects
 
OTHER DUTIES AND RESPONSIBILITIES
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proficiency with wildlife tracking technologies, remote sensing, or climate-related modeling preferred.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Excellent leadership, communication, and collaboration skills.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Manage science and conservation grants for other flagship species
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Perform other duties as directed by the Vice President of Science
 
PREPARATION, KNOWLEDGE, SKILLS &amp; ABILITIES
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Advanced degree (Ph.D. preferred) in Ornithology, Ecology, Wildlife Biology, or a closely related field, with a strong publication record. 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Minimum 7 years of relevant experience, including Arctic fieldwork and shorebird research
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Advanced knowledge of Arctic ecosystems and shorebird ecology.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proficiency in ecological data analysis (R, Python, or similar) and GIS tools.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with wildlife tracking technologies, remote sensing, or climate-related modeling preferred.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Excellent leadership, communication, and collaboration skills.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Track record of publication in scientific journals related to bird conservation
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Familiarity with demographic modeling and statistical analysis of field data
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Successful history of raising grant funding to support research and conservation
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability to effectively supervise other staff, and manage multiple grant projects simultaneously
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience working respectfully with Indigenous communities and integrating Traditional Knowledge with Western science.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Familiarity with North American Flyway conservation frameworks (e.g., Atlantic, Pacific, Mid-continent, East Asian–Australasian).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proven success in grant writing and managing complex, multi-stakeholder projects.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Multilingual capability preferred, especially Spanish or French for migratory shorebird research partnerships
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Must have reliable method of transportation, valid driver’s license and passport
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Must successfully pass a background check
 
WORKING CONDITIONS/PHYSICAL DEMANDS 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability and willingness to travel to various locations in the US as necessary to complete job duties, such as travel to scientific meetings and conferences.&nbsp;Travel may also be international. Travel is reimbursed. (If applicable)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Extensive field work required in many different environments, including arctic, temperate, and tropical field sites
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Comfortable working in remote and challenging field conditions and working remotely in bear country
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability to cover long distances on foot over difficult terrain in challenging weather conditions, and camp in wilderness settings for many weeks
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Willingness to travel extensively for field work in remote locations, sometimes by small aircraft 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Close work (paperwork, visual examination).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Occasionally walking up and down stairs, standing, and bending. 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Fully remote/Hybrid remote work possible. Attendance at Manomet headquarters for meetings, special events, and staff retreats.

SALARY RANGE: &nbsp;$89,000 – $109,000
Compensation commensurate with experience. Manomet offers excellent benefits including health insurance, dental, 403b match, life insurance, and several other benefits. 
 
HOW TO APPLY:
Please email a resume and cover letter to <a href="mailto:jobs@manomet.org" target="_blank">jobs@manomet.org</a> by September 30th, 2025.&nbsp;Please reference the job title Senior Shorebird Scientist in the subject line.

The above statements are intended to describe the general nature and level of work being performed by people assigned to do this job.&nbsp;The above is not intended to be an exhaustive list of all responsibilities and duties required.
 
External and internal applicants, as well as position incumbents who become disabled as defined under the Americans with Disabilities Act must be able to perform the essential job functions (as listed) either unaided or with the assistance of a reasonable accommodation to be determined by management on a case-by-case basis.&nbsp;
 
Manomet 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.&nbsp;

Senior Shorebird Scientist

<h3>Job Description</h3>
Responsibilities
<ul>
<li>Synthesize complex, non-routine, and routine target compounds containing isotopes such as 15N, 18O, D, and/or 13C, utilizing established SOPs where applicable</li>
<li>Design and develop new synthetic routes when required to achieve optimal results</li>
<li>Contribute to the optimization of chemical processes for targeted molecules, intermediates, and scalable, cost-effective production methods</li>
<li>Analyze and interpret data using various techniques, including Nuclear Magnetic Resonance (NMR), Ultraviolet (UV) Spectroscopy, Mass Spectrometry (MS), High-Performance Liquid Chromatography (HPLC), and Infrared (IR) Spectroscopy</li>
<li>Employ a variety of purification techniques, including chromatography, distillation, recrystallization, and sublimation</li>
<li>Maintain accurate and detailed records in the laboratory notebook</li>
<li>Mentor and assist junior team members, offering guidance on experimental techniques and troubleshooting</li>
<li>Ensure all work is conducted with strict adherence to safety protocols and good laboratory practices</li>
<li>Perform additional related duties as needed</li>
</ul>
 
Requirements
 
<ul>
<li>Ph.D. in Synthetic Organic Chemistry or a closely related field, or a Master's degree with significant relevant experience (e.g., 5+ years in organic chemistry and/or synthesis)</li>
<li>Alternatively, a Bachelor's degree in Chemistry or a related field with extensive hands-on experience in organic synthesis and chemical processes may be considered</li>
<li>1-3 years of professional experience in organic chemistry and/or synthesis, or equivalent practical training as a Research Assistant or Postdoctoral Researcher</li>
<li>Expertise in organic synthetic methods, chemical separation, and compound identification, with strong analytical skills</li>
<li>Proficiency in laboratory techniques, including synthesis, purification, and characterization of organic compounds</li>
<li>Excellent verbal and written communication skills. Additionally, strong documentation and collaboration skills are essential</li>
<li>Ability to perform hands-on bench chemistry, which may involve standing, bending, and stooping</li>
<li>Familiarity with working in a controlled, hooded lab environment, as required by safety protocols</li>
<li>Comfortable working with both hazardous and non-hazardous chemicals</li>
<li>Physical ability to lift 50 lbs regularly and transport drums of chemicals, including up to 55-gallon drums, using appropriate equipment (e.g., drum dolly)</li>
</ul>

Sr. Chemist

<h3>Job Description</h3>
Job Description
Job Title: Clean Room Assembler
As a Clean Room Assembler, you will be responsible for assembling product parts on the assembly line in accordance with production guidelines. You will also perform spot checks of products to ensure adherence to approved quality standards.
Responsibilities
<ul>
<li>Assemble assigned product parts on the assembly line following production guidelines.</li>
<li>Perform spot checks of products to ensure adherence to approved quality standards.</li>
<li>Notify management of product discrepancies or equipment malfunctions.</li>
<li>Adhere to established company policies and procedures, paying special attention to safety regulations.</li>
<li>Wear personal protective equipment in accordance with training guidelines.</li>
<li>Perform other related duties as assigned.</li>
</ul>
Essential Skills
<ul>
<li>Must have microscope experience </li>
<li>Must have previous manufacturing experience </li>
<li>Comfortable using tweezers, cutters, wire strippers, and adhesives.</li>
<li>Strong attention to detail and mechanical assembly skills.</li>
</ul>
Pay and Benefits
The pay range for this position is $22.00 - $24.00/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 NASHUA,NH.
Application Deadline
This position is anticipated to close on Oct 15, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<h3>Job Description</h3>
Job DescriptionPay: $17.50 per hourJob description:
Now Hiring: Chemical Mixer – Manufacturing Location: Holyoke Ma Schedule: Monday to Friday 8am-4:40pm Pay: $17.50
Are you detail-oriented, safety-conscious, and ready to work in a hands-on manufacturing environment? We’re looking for a Chemical Mixer to join our team and help produce high-quality products in a fast-paced facility!
What You’ll Be Doing:
<ul>
<li>Measure, mix, and blend chemicals according to precise formulas and safety protocols</li>
<li>Operate and maintain mixing equipment and machinery</li>
<li>Follow batch records and production schedules</li>
<li>Perform quality checks and report any inconsistencies</li>
<li>Maintain a clean, safe, and organized work area</li>
</ul>
What We’re Looking For:
<ul>
<li>Experience in chemical mixing or manufacturing preferred</li>
<li>Strong attention to detail and commitment to safety</li>
<li>Ability to read and follow instructions and production documentation</li>
<li>Physically able to lift up to 50lbs and stand for extended periods</li>
<li>Team player with a positive attitude and good communication skills</li>
</ul>

Chemical Mixer

<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 
AbbVie is seeking an innovative scientist to join our Discovery Research team, specializing in pre-clinical research and development of antibody oligonucleotide conjugates (AOCs), as well as antibody drug conjugates (ADCs).
Key Responsibilities:
<ul>
<li>Synthesis, purification, and characterization of AOCs and ADCs on mg to gram scale under minimal supervision.</li>
<li>Development, optimization, and validation of conjugation protocols specifically for antibody oligonucleotide conjugates.</li>
<li>Optimization and validation of formulation buffers for AOCs and related bioconjugates.</li>
<li>Application and refinement of automated techniques for AOC/ADC synthesis and purification.</li>
<li>Collaboration with cross-functional teams to advance AOC discovery programs from conceptualization to early development.</li>
</ul>
Qualifications 
<ul>
<li>B.S. degree with typically 5-10+, M.S. degree with typically 2-8+, or PhD with typically 0+ years of experience in Analytical Chemistry, Biochemistry, Molecular Biology, or related field.</li>
<li>Demonstrated hands-on expertise in laboratory-scale protein purification using Hydrophobic Interaction Chromatography (HIC), Size Exclusion Chromatography (SEC), Ion-Exchange (IEX), mixed-mode chromatography, and/or affinity chromatography. Experience with GE AKTA FPLC and Unicorn software is preferred.</li>
<li>Strong experience in the discovery, design, synthesis, and purification of Antibody Oligonucleotide Conjugates (AOC), including familiarity with associated chemistries and analytical methods.</li>
<li>Hands-on experience with relevant analytical techniques such as HIC-HPLC, SEC, IEX, RP-HPLC, and capillary electrophoresis techniques (e.g., CE-SDS, icIEF).</li>
<li>Proven problem-solving skills, motivation, enthusiasm, attention to detail, and the ability to thrive in a fast-paced, cross-disciplinary team environment.</li>
<li>Superior written and oral communication skills, with a strong record of collaboration and innovation.</li>
</ul>
Preferred:
<ul>
<li>Previous experience with linker chemistry and payload conjugation strategies specific to oligonucleotide therapeutics.</li>
<li>Experience troubleshooting or optimizing the stability and delivery of antibody-oligonucleotide conjugates.</li>
</ul>
Position will be filled at level commensurate with extent of education, experience, and accomplishment – Scientist I, Scientist II, or Senior Scientist I. 
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;ofthis posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location,and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.&nbsp;​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;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&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;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>

Scientist or Senior Scientist I, Antibody Oligonucleotide Conjugation (AOC)

<h3>Job Description</h3>
Job Description
Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve. Analytical Sciences &amp; Technology (AS&amp;T) Scientist
<ul>
<li>Job Location: Boston, MA (Hybrid, 3 days onsite)</li>
<li>Schedule: &nbsp;M–F standard hours</li>
</ul>
 
Description: We’re seeking an experienced&nbsp;Analytical Sciences &amp; Technology (AS&amp;T) Scientist&nbsp;to join a leading biotech organization in Boston supporting the Cell and Gene Therapy (CGT) portfolio. This role focuses on analytical assay lifecycle management for&nbsp;late-stage and commercial programs, making it ideal for scientists with strong GMP and commercialization experience. Key Responsibilities
<ul>
<li>Lead and support analytical lifecycle activities, including method validation and transfer.</li>
<li>Author, review, and contribute to technical documents such as method SOPs, study protocols, and regulatory reports.</li>
<li>Act as Subject Matter Expert (SME) for analytical troubleshooting, quality events, deviations, CAPAs, and change controls.</li>
<li>Perform data trending, analytical assessments, and lab-based experiments as needed.</li>
<li>Partner cross-functionally with internal stakeholders and external testing organizations.</li>
</ul>
Required Qualifications
<ul>
<li>Strong knowledge of&nbsp;ICH and GMP regulations.</li>
<li>Hands-on experience with&nbsp;protein and/or oligo mass spectrometry (MS).</li>
<li>Reference Standard lifecycle management&nbsp;experience is highly preferred.</li>
<li>Proficiency in&nbsp;HPLC, UPLC, and/or flow cytometry.</li>
<li>Excellent technical writing and documentation skills.</li>
<li>Proven ability to collaborate effectively with internal teams and contract organizations.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience in&nbsp;cell and gene therapy&nbsp;and/or&nbsp;CRISPR gene editing.</li>
<li>Prior exposure to&nbsp;late-stage or commercial biologics&nbsp;support.</li>
<li>Familiarity with&nbsp;critical reagent management&nbsp;and&nbsp;JMP/statistical tools.</li>
<li>Ability to manage multiple priorities and maintain flexibility in a fast-paced environment.</li>
</ul>
Education &amp; Experience
<ul>
<li>B.S. or higher in Biology, Biochemistry, Analytical Chemistry, or a related field.</li>
<li>Minimum&nbsp;8 years of experience&nbsp;in the pharmaceutical or biopharmaceutical industry, or an equivalent mix of education and experience.</li>
</ul>
Company DescriptionConnexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve. 
<h3>Company Description</h3>
Connexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve.

AS&T Scientist - Late Stage and Commercial experience

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, a place to call home, apply with us today!
Job Description 
The incumbent will participate in the formulation and process development of biotherapeutics. This position will be responsible for performing particle characterization of candidate molecules by using various biophysical, biochemical and particulates characterization techniques as well as supporting laboratory operations and maintenance. This is a laboratory-based position performing formulation and process development activities specifically for biotherapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. Furthermore, this position will assist in data compilation, data presentations, report authoring, and department documentation support.
 RESPONSIBILITIES: The responsibilities of this position include, but are not limited to:
<ul>
<li>Support the development of parenteral formulations for biotherapeutic modalities such as monoclonal antibodies, antibody drug conjugates, proteins, mRNA and vaccines.</li>
<li>Perform rapid, comprehensive characterization of candidate molecules to determine the stability profile. This will be achieved by applying various biophysical, biochemical, particulates characterization techniques such as DLS, DSC, SEM, HPLC (SE-HPLC, IEX, HIC, RP-HPLC), Capillary Gel electrophoresis (CGE), imaged Capillary Electrophoresis (iCE), Spectroscopy techniques, light obscuration, microflow imaging and additional characterization techniques.</li>
<li>Provide general laboratory support, including ordering/replacement of reagents and consumables, general maintenance of equipment, continuous improvement activities, and participating in periodic lab inspections.</li>
<li>The incumbent must be able to interact effectively with a multidisciplinary team of scientists for formulation optimization and overall candidate progression.</li>
<li>This position will be responsible for preparing data summary presentations, providing data verification support, compiling data, and using lab-based systems for data collection such as Empower and electronic laboratory notebooks.</li>
<li>Effective communication skills are required for interactions with laboratory scientists, project managers and colleagues from numerous functions.</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>At least a BS in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, Biology or equivalent&nbsp;</li>
<li>1+ years of industry experience utilizing particle characterization techniques such as microflow imaging (flowcam, HIAC, etc.), DLS, DSC, etc.</li>
<li>Familiarity with biologics such as proteins, enzymes, monoclonal antibodies, vaccines, mRNA, or antibody drug conjugates and how to characterize them with analytical techniques</li>
<li>Must be eligible to work in the United States indefinietly without restriction or sponsorship (OPT, H1B, etc.)</li>
</ul>
Preferred:&nbsp;
<ul>
<li>Familiarity with HPLC, Capillary electrophoresis, and other analytical techniques</li>
<li>Strong computer skills and experience with lab-based computer systems</li>
<li>Ability to collect and analyze data sets</li>
</ul>
 Additional Information 
Position is&nbsp;Full Time, Monday – Friday 8am-5pm.&nbsp;Candidates currently living within a commutable distance of&nbsp;Andover, MA&nbsp;are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holiday</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
<li>Compensation: $25.00-$30.00&nbsp;per hour</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Particle Characterization Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
Eurofins is seeking a highly motivated and detail-oriented lab associate who will be responsible for qualifying and performing analytical methods to support particulate testing of drug products. This individual will work directly on a client site in Boston, MA, supporting a multidisciplinary team of scientists and engineers. The candidate will contribute to a variety of CMC activities in a fast-paced, agile, and highly collaborative environment.
Key Responsibilities:
<ul>
<li>Routinely perform batch and stability testing of drug products using qualified methods.</li>
<li>Troubleshoot and resolve testing-related issues.</li>
<li>Maintain accurate records and documentation of test results.</li>
<li>Regularly perform analytical data review and reporting of results.</li>
<li>Participate in internal and external audits.</li>
<li>Stay current with the latest industry developments and regulatory requirements.</li>
<li>Aid in the development and qualification of particulate assays.</li>
<li>Support the technology transfer of analytical methods to external parties.</li>
<li>Maintain safe laboratory working conditions following GLP and EHS guidelines.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree with 0-2 years of industry experience, in Chemistry or a related field.</li>
<li>Hands-on experience with microscopy techniques such as: Flow Imaging Microscopy (FIM), Scanning Electron Microscopy (SEM), Fluorescent Microscopy preferred.</li>
<li>Experience with other methods for particle characterization (e.g. Raman) and counting (e.g. light obscuration) is also desirable.</li>
<li>General knowledge of cGMP, GLP, and regulatory requirements for biotech and pharmaceutical industries is highly desirable.</li>
<li>Strong attention to detail and ability to document experimental work with electronic laboratory notebooks (ELN) is a must.</li>
<li>Experience performing analytical data review and historical data evaluations.</li>
<li>Experience with writing SOPs and technical documents.</li>
<li>Familiarity with standard office software (MS Office, Teams, SharePoint).</li>
<li>Ability to work in a fast-paced, agile and highly collaborative environment is essential.</li>
</ul>
 Additional Information 
Position is full-time, Monday - Friday, 8:00 am - 5:00 pm.&nbsp; Candidates currently living within a commutable distance of Cambridge, MA, are encouraged to apply.
<ul>
<li>Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Compensation is between 23.00-29.00 per hour, depending on education and experience&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Particulates Lab Associate

<h3>Job Description</h3>
Job DescriptionCompany Description 
About Mote Therapeutics
Are you a scientific leader with a passion for advancing RNA therapeutics and the drive to make a difference in the world? Do you want to be a part of a dynamic and innovative team at the forefront of RNA medicines? If so, join our new RNA Venture and be a part of the revolution in RNA therapeutics!
Backed by Fapon Biotech, an international leader in in vitro diagnostics, biologics, and precision medicines, Mote Therapeutics is an innovative Lexington-based biotechnology startup building the RNA medicines of tomorrow. Led by a pioneer in the field of RNA therapeutics and supported by Fapon’s Greater Boston R&amp;D Center of Excellence, we’re pulling together a team of talented scientists, leaders, and operations specialists to solve some of the major barriers to success that RNA therapeutics face.
About Fapon Biotech
Founded in 2001 and headquartered in Guangdong, China, Fapon Group is mainly engaged in product R&amp;D and services of in vitro diagnostics (IVD), biological therapies, and precision diagnostics and treatments. With our core value of "foresee and prepare for what the future demands", Fapon has historically focused on three major businesses: raw material solutions, IVD ecosystem platform service, and intelligent digital diagnosis and treatment. Fapon’s recent expansion into therapeutics was recently marked by success with the receipt of IND approval from the FDA for a differentiated CD47 antibody drug, the first in a rapidly expanding therapeutics effort.
With a global footprint, Fapon has established major production and sales (R&amp;D) bases in Beijing, Shenzhen, Shanghai, the United States, Germany, India and other locations throughout the world, forming a global R&amp;D, production, marketing, and service network with products being widely sold in 61 countries and regions.
You can learn more about us by visiting <a href="https://en.faponbiotech.com" target="_blank">https://en.faponbiotech.com</a>
An equal-opportunity employer, Fapon welcomes and encourages diversity in our workforce.
Job Description 
We are seeking a scientific contributor to lead and execute in vivo studies using novel LNP formulations designed to cross the BBB and target cells within the brain. This role will spearhead our CNS program and would be responsible for designing and executing in vivo studies using rodent models as well as downstream bioanalytic methods. The candidate would have the opportunity to work in a collaboration-oriented role in which they would coordinate with other teams, plan and run animal studies with a cross-functional group of scientists, and support the growth and career development of junior scientists. The ideal candidate is a life sciences major with strong in-vivo and ex-vivo analytic techniques who is excited by the idea of being a core participant in building an early startup and guiding the scientific vision of the company. They would be engaged in science and driven by our mission to create therapies that help people in ways that are currently impossible.
Key Responsibilities
<ul>
<li>Design, plan and execute in vivo experiments to support LNP based targeted delivery across the blood brain barrier through systemic administration</li>
<li>Develop bioanalytical assays (cell-based, flow cytometry, ELISA, biomedical imaging) to assess the delivery efficiency of RNA cargo in rodent tissue to facilitate development of neuroscience focused therapeutics pipeline</li>
<li>Conduct studies in small animals models for brain characterization, biodistribution (qualitative/quantitative), disease model development, efficacy and toxicity assessment</li>
<li>Contribute to patent applications related to the neuroscience program</li>
<li>Perform CRO outreach including experimental planning, work coordination and data interpretation for neuroscience program</li>
<li>Support technology transfer to Industry Partners</li>
<li>Foster collaborative relationships across the team and company and engage in a positive and exciting work environment</li>
<li>Contribute to hiring, training, and collaborating with scientists (as needed) to support assessment of efficacy in relevant in vivo models</li>
<li>Plan and coordinate animal studies with formulations team members</li>
<li>Author technical documents, including SOPs for analytical methods, maintain diligent records and demonstrate proficiency in scientific communication</li>
<li>Support high-quality documentations to support regulatory filings</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>PhD/MS in life sciences, pharmaceutical sciences, or related field, preferably with 1-3/6+ years of relevant experience. The title will be commensurate with experience.</li>
<li>Experience working with murine animals, including animal handling, dosing (IV, IP, PO, SC), blood collection (submandibular and cardiac) and tissue necropsy</li>
<li>Prior experience in neuroscience focused research is a must</li>
<li>Knowledge in brain physiology and cell biology</li>
<li>Experience in biomolecular analytics (ELISA, PCR, Flow Cytometry)</li>
<li>Must be eligible to work in the United States</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience in brain tissue dissection, histology and imaging is a plus</li>
<li>Strong communication skills and ability to present complex technical topics to diverse audiences with varying technical depth.</li>
<li>Strong collaborative instinct with good time and resource management skills to match the fast-paced start-up work culture.</li>
<li>Able to collaborate on and execute multiple parallel studies</li>
</ul>
 Additional Information 
What We Offer:
At our RNA Venture, we aim to outmatch the typical benefits you might see in an early startup. We offer:
<ul>
<li>Financial security through competitive compensation, incentives, and retirement plan</li>
<li>Health care and well-being programs including competitive medical, dental, vision &amp; medical benefits</li>
<li>Generous paid time off including vacation, sick time, holidays, and winter shutdown</li>
<li>401(k) retirement savings with a generous company match</li>
<li>Commuter benefits</li>
<li>Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more</li>
<li>We continue to optimize our benefits &amp; wellness programs as we grow our organization to make sure they meet our diverse workforce needs</li>
<li>The stability of a startup backed by a company with a record of strong financial performance year over year</li>
</ul>

Senior Scientist, In Vivo Discovery

<h3>Job Description</h3>
Job ID: 705582BR Date posted: Oct. 07, 2025 Description: You will be the Metrologist Senior for the Measurement Science team. Our team is responsible for advancing precision measurement capabilities and ensuring the reliability of calibration systems across diverse applications. What You Will Be Doing As the Metrologist Senior you will be responsible for designing, evaluating, and refining calibration systems that quantify physical and chemical properties with high accuracy. Your responsibilities will include not limited to: 
<ul>\n
<li>Develop and validate calibration methods rooted in measurement‑science principles.</li>
\n 
<li>Identify and quantify error sources to assess uncertainty and reliability.</li>
\n 
<li>Perform hands‑on calibration of electronic, electromechanical, optical, pneumatic, and pressure‑type instruments.</li>
\n 
<li>Analyze measurement problems and recommend technical solutions to meet precision requirements.</li>
\n 
<li>Document procedures, results, and recommendations for continuous improvement.</li>
\n</ul>
\n Why Join Us The ideal candidate is a collaborative, detail‑oriented professional who thrives on solving complex measurement challenges. This role offers the chance to impact critical programs, work with cutting‑edge instrumentation, and influence the future of precision engineering. We are committed to supporting your work‑life balance and overall well‑being, offering flexible scheduling options. Learn more about Lockheed Martin's comprehensive benefits package here. Further Information About This Opportunity This position is in Chelmsford. Discover more about our Chelmsford, Massachusetts location. MUST BE A U.S. CITIZEN - This position is located at a facility that requires special access. The selected candidate must be able to obtain a secret clearance. Basic Qualifications: - Ability to follow general instructions without supervision - Experience with the use and operations of general test equipment from a variety of disciplines. - Ability to utilize computer controlled automatic software and associated test equipment. - Experience in using computer programs for word processing and document generation, I.E. Microsoft Office products. - Proven ability to work as a member of a team. Desired Skills: - Physical Dimensional calibration experience. - Experience with multiple disciplines of calibration (Phys/D, Torque, Pressure, RF, etc.) - Familiarity with following Quality Processes, and participating in audits - Experience with automated calibration software: Met/CAL, SureCal, Agilent VEE, etc. - 3-6 years direct calibration/metrology experience. Security Clearance Statement: This position requires a government security clearance, you must be a US Citizen for consideration. Clearance Level: Secret Other Important Information You Should Know Expression of Interest: By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings. Ability to Work Remotely: Onsite Full-time: The work associated with this position will be performed onsite at a designated Lockheed Martin facility. Work Schedules: Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits. Schedule for this Position: 4x10 hour day, 3 days off per week Pay Rate: The annual base salary range for this position in California, Massachusetts, and New York (excluding most major metropolitan areas), Colorado, Hawaii, Illinois, Maryland, Minnesota, New Jersey, Vermont, Washington or Washington DC is $85,500 - $150,765. For states not referenced above, the salary range for this position will reflect the candidate's final work location. Please note that the salary information is a general guideline only. Lockheed Martin considers factors such as (but not limited to) scope and responsibilities of the position, candidate's work experience, education/ training, key skills as well as market and business considerations when extending an offer. Benefits offered: Medical, Dental, Vision, Life Insurance, Short-Term Disability, Long-Term Disability, 401(k) match, Flexible Spending Accounts, EAP, Education Assistance, Parental Leave, Paid time off, and Holidays. (Washington state applicants only) Non-represented full-time employees: accrue at least 10 hours per month of Paid Time Off (PTO) to be used for incidental absences and other reasons; receive at least 90 hours for holidays. Represented full time employees accrue 6.67 hours of Vacation per month; accrue up to 52 hours of sick leave annually; receive at least 96 hours for holidays. PTO, Vacation, sick leave, and holiday hours are prorated based on start date during the calendar year. This position is incentive plan eligible. Pay Rate: The annual base salary range for this position in most major metropolitan areas in California, Massachusetts, and New York is $98,300 - $170,315. For states not referenced above, the salary range for this position will reflect the candidate's final work location. Please note that the salary information is a general guideline only. Lockheed Martin considers factors such as (but not limited to) scope and responsibilities of the position, candidate's work experience, education/ training, key skills as well as market and business considerations when extending an offer. Benefits offered: Medical, Dental, Vision, Life Insurance, Short-Term Disability, Long-Term Disability, 401(k) match, Flexible Spending Accounts, EAP, Education Assistance, Parental Leave, Paid time off, and Holidays. This position is incentive plan eligible. Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics. The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration. At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work. With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility. If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs, and apply for roles that align with your qualifications. Experience Level: Experienced Professional Business Unit: MISSILES AND FIRE CONTROL Relocation Available: Possible Career Area: QA/Test and Inspection Type: Full-Time Shift: First

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