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<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

Metrologist Senior (Calibration) - Chelmsford, MA

<h3>Job Description</h3>
Job Description
At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases. 
Why Choose Editas?
At Editas Medicine, we’re a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and become an Editor!
Decoding The Role:
The Process Development team within the Technical Operations Group is seeking a highly motivated scientist to support the development and production of critical RNA-based gene editing components. The successful candidate will contribute to advancing in vivo LNP programs from preclinical through to clinical stages by producing mRNA materials at small scale to support research and development efforts.
This role requires hands-on experience across both upstream and downstream aspects of the mRNA manufacturing process, as well as proficiency in analytical testing of mRNA intermediates and final products. A strong background in in-vitro transcription and nucleic acid analytics is essential. Additionally, the candidate will serve as a subject matter expert (SME) in interactions with external suppliers (both research-grade and GMP) and collaborate closely with the research team on molecule design and optimization.
Characterizing Your Impact:
As the mRNA scientist, you will:
<ul>
<li>Manage external vendor activities to supply mRNA (research and GMP grades)</li>
<li>Provide subject expertise internally and externally regarding plasmid DNA and mRNA design, quality characteristics, and production processes. </li>
<li>Prepare DNA templates for IVT e.g. pDNA linearization, purification, and analysis.</li>
<li>Perform IVT reactions to produce mRNA.</li>
<li>Analyze final products and intermediates.</li>
<li>Purify mRNA, as needed, using automated or semi-automated preparative FPLC/HPLC systems</li>
<li>Desalt and concentrate final mRNA material using LiCl precipitation/tangential flow ultra-filtration (TFF) or similar technique(s).</li>
<li>Coordinate with members of other teams and manage material requirements, priorities, and timelines. </li>
<li>Adapt as needed to meet the needs of the most critical project(s).</li>
<li>Assist with the coordination of instrument preventative maintenance and repairs.</li>
<li>Maintain an electronic laboratory notebook and miscellaneous documentation.</li>
<li>Maintain reagent inventory.</li>
</ul>
Requirements
The Ideal Transcript:
To thrive in this role, you’ll need:
<ul>
<li>Bachelor’s degree in Chemical Engineering, Biology, Pharmacy, Biochemistry or related discipline with 7+ years of relevant industry experience, Master’s degree with 5+ years of relevant industry experience, or PhD with 1+ years’ experience.</li>
<li>In-depth knowledge of RNA and mRNA design, production methods, impurities, and analytics. </li>
<li>Experience with enzymatic reactions such as in vitro transcription (IVT)</li>
<li>Experience with AKTA purification and instrumentation</li>
<li>Experience with TFF and instrumentation a plus.</li>
<li>Experience with nucleic acid analytics, including running gel and capillary electrophoresis and interpreting data.</li>
<li>Experience with aseptic / RNase-free handling and operation</li>
<li>Excellent time and project management.</li>
<li>Ability to work effectively in a cross-functional team environment.</li>
<li>Excellent oral and written communication skills.</li>
<li>Technical troubleshooting and organizational skills.</li>
<li>Proficient with Microsoft Office programs.</li>
<li>Prior experience managing external CRO and CDMO vendors is a plus</li>
<li>Experience in high throughput processing methodologies and automation is a plus</li>
</ul>
Benefits
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy
Salary Range: 
$115,000 - $135,000
Pay Transparency
Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices.
.
Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.

mRNA Scientist I, Process Development

<h3>Job Description</h3>
Job Description
About Mass Audubon Mass Audubon is the largest nature-based conservation organization in New England. Founded in 1896 by two women who fought for the protection of birds, Mass Audubon carries on their legacy by focusing on the greatest challenges facing the environment today: the loss of biodiversity, inequitable access to nature, and climate change. With the help of our 160,000 members and supporters, we protect wildlife, conserve and restore resilient land, advocate for impactful environmental policies, offer nationally recognized education programs for adults and children, and provide endless opportunities to experience the outdoors at our wildlife sanctuaries. Explore, find inspiration, and take action at massaudubon.org. 
About This Position Mass Audubon is looking for two energetic, team-oriented, seasonal Wildlife Care Technicians to perform the day-to-day care for non-releasable wildlife at Drumlin Farm, with its diverse collection of exhibit and program animals consisting of mammals, birds (including raptors), amphibians, and reptiles. Position responsibilities include feeding and diet preparation, maintaining and cleaning animal enclosures, behavioral observation, record keeping, exhibit maintenance, and providing environmental enrichment. Application Instructions Please submit a resume and cover letter with your ADP application.
Responsibilities
<ul>
<li>Care for wildlife:
<ul>
<li>Feed approved diets,</li>
<li>Clean and disinfect cages and enclosures</li>
<li>Assist with response to medical needs of wildlife and consult with veterinarians as needed,</li>
<li>Transport animals,</li>
<li>Create and provide daily animal enrichment,</li>
<li>Perform lab work as needed,</li>
<li>Assist in socializing and conditioning animals for use in programs.</li>
</ul>
</li>
<li>Support compliance with all applicable state and federal permits relating to the possession of program and display animals.</li>
<li>Train and supervise volunteers.</li>
<li>Participate in education programs on caring for wildlife in captivity and wildlife rehabilitation, including developing curriculum, leading tours, and answering questions from the public.</li>
<li>Perform various building, exhibit, and grounds maintenance projects required to support the Wildlife Care unit.</li>
</ul>
Qualifications At Mass Audubon, our highest priority is finding the best candidate for the job. Research has shown that people of color and women are less likely to apply for jobs if they don’t believe they meet every one of the qualifications described in a job description. We encourage you to apply, even if you don't believe you meet every one of our described qualifications or you have a less traditional background. We are looking for applicants with the following qualifications:
<ul>
<li>At least 18 years of age</li>
<li>High school diploma minimum, preferred college degree in Biology, Zoology, Ecology, Veterinary Technician, Wildlife biology, or a related field</li>
<li>Prior animal care experience required</li>
<li>Knowledge of wildlife biology and related natural history topics</li>
<li>Demonstrate a sincere passion for working with captive wildlife</li>
<li>Ability to communicate easily with staff and the public</li>
<li>Responsible and self-driven with the ability to work independently and as a team player</li>
<li>Ability to relate to a diverse range of people and exercise cultural competence and inclusion</li>
</ul>
Compensation, Benefits and Perks This position’s pay range is $18.48-$20.79/hour; actual salary will reflect level of experience and qualifications relative to position requirements. This position may be eligible for health insurance benefits.
Work Schedule This is a temporary, full-time seasonal position starting in January 2026 and ending in June 2026. The schedule for this position is either Tuesday through Saturday or Sunday through Thursday, 40 hours per week.
Other Requirements Employees must successfully complete a CORI and SORI Background Check and a Motor Vehicle Record (if applicable) is required.
Mass Audubon’s Commitment to Diversity, Equity, Inclusion, &amp; Justice Mass Audubon embraces diversity and equal opportunity in a serious way. We are dedicated to forming a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be. People of color are strongly encouraged to apply.
Mass Audubon’s mission is to “protect the nature of Massachusetts for people and for wildlife” by building a strong coalition of employees, volunteers, and community members. We recognize that the environmental movement and field of conservation have been affected by societal systems that have limited opportunity and access for many people. As a result, Mass Audubon is committed to creating an inclusive environment for all employees and applicants. We are engaged in an ongoing process of organizational assessment and change, designed to remove barriers and create a workplace where all forms of diversity are recognized and valued.
Equal Employment Opportunity Statement Mass Audubon is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and applicants. Mass Audubon prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Wildlife Care Technician

<h3>Job Description</h3>
Job DescriptionCompany Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview We are seeking an experienced Associate Director, Scientific Communications as part of the North America Medical Affairs team to lead the strategic planning and execution of scientific publications and communications for our rare neuroendocrine portfolio across North America. This role requires a scientific expert who can distill complex clinical and translational data into impactful publications that support medical, clinical, and commercial objectives for both approved therapies and pipeline candidates. As a key member of the North America Medical team, reporting to the Senior Medical Director, North America, you will be accountable for advancing Rhythm’s scientific leadership in Rare Neuroendocrine Diseases including marketed and other pipeline indications. You will thrive in this role if you are a self-starter and a highly collaborative individual who cares to have impact on patients in rare disease space. Responsibilities and Duties
<ul>
<li>Develop and implement a comprehensive scientific communications and publication strategy for rare neuroendocrine diseases, encompassing all approved and pipeline indications with focus on North America priorities. </li>
<li>Lead the creation, review, and dissemination of high-quality scientific manuscripts, abstracts, posters, and presentations targeted at key US medical conferences and peer-reviewed journals in strong collaboration with Global Scientific Communications team. </li>
<li>Serve as a scientific thought leader and subject matter expert on neuroendocrine disease biology ensuring scientific accuracy and relevance in all communications for cross-functional teams. </li>
<li>Collaborate closely with Value and Evidence, Clinical development, Global Scientific Communications, Commercial, International teams and external partners to ensure alignment and integration of scientific messaging across functions and materials. </li>
<li>Contribute to Global Scientific Platform development and serve as the North America representative on the Global Publication Planning team for strategic planning, and review of manuscripts and posters. </li>
<li>Monitor emerging scientific literature, competitive landscape, and publication trends in neuroendocrine diseases to identify and leverage publication opportunities. </li>
<li>Ensure all scientific communications adhere to industry codes, ethical standards, and regulatory requirements. </li>
</ul>
 Qualifications and Skills
<ul>
<li>Advanced degree (PhD, PharmD or equivalent) in a relevant scientific or medical discipline.</li>
<li>At least 5+ years of experience across scientific communications and/or medical affairs functions within biotech, pharma, or medical communications agency.&nbsp; Rare disease preferred.</li>
<li>Familiarity with publication guidelines such as ICMJE, GPP, and PhRMA Code is strongly preferred. </li>
<li>Proven track record of developing and executing publication strategies for complex therapeutic areas, preferably within rare diseases or oncology/neuroendocrine space. </li>
<li>Strong ability to interpret and communicate complex clinical and translational data clearly and accurately.&nbsp; Extensive experience in writing, reviewing, and publishing scientific materials and the ability to appraise scientific literature and raw data critically for potential development of new publications. </li>
<li>Experience managing external vendors and ensuring compliance with timelines and quality standards. </li>
<li>Expertise in publication guidelines and industry standards, including Good Publication Practices, ICMJE requirements, and PhRMA guidelines </li>
<li>Knowledge of scientific, statistical, and research principles and guidelines </li>
<li>Experience with and knowledge of publication management software/tools and a demonstrated ability to seek out and learn new technology </li>
<li>Excellent interpersonal and communication skills, with demonstrated success collaborating in cross-functional teams.</li>
<li>Ability to travel up to 30% of the time, in alignment with business needs.</li>
</ul>
 Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs. This role involves travel. The expected salary range for this position is $160,000 - $240,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units. More about Rhythm We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause.&nbsp; Our team is passionate about&nbsp;expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism. At Rhythm our core values are:
<ul>
<li>We are committed to advancing scientific understanding to improve patients’ lives</li>
<li>We are inspired to tackle tough challenges and have the courage to ask bold questions</li>
<li>We are eager to learn and adapt</li>
<li>We believe collaboration and ownership are foundational for our success</li>
<li>We value the unique contribution each individual brings to furthering our mission</li>
</ul>
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Associate Director, Scientific Communications

<h3>Job Description</h3>
Job Description
Duties &amp; Responsibilities:
<ul>
<li>
Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures.
</li>
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Utilize small hand tools (both manual and electric), manual presses, assembly fixtures, calibrated instruments, measurement equipment, microscopes, and test fixtures.
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Utilize documentation such as Bill of Materials, product flow charts, work orders, check sheets, visual aids, production reports and assembly drawings to assemble product and record results.
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May perform soldering, fabricating, crimping, mechanical assembly, sealing, ultra-sonic welding, bonding and gluing with adhesives, Epoxy or RTV.
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Kitting assemblies using a parts list, scanner and inventory software as required.
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Participates in any routine start up or end of day equipment inspections or verifications.
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Inspects work throughout the assembly process and communicates any quality or operational issues to appropriate leader.
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Maintain neat, orderly and clean work area to ensure efficiency and no safety hazards. Participate in safety programs, meetings, and trainings as required. Bring safety concerns to the attention of management.
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Participate in continuous improvement activities as part of a cross-functional team.
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Meet all quality, quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Read and/or understand operating procedures for specific products where training has been completed.
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Show constant attention to detail, and immediately inform supervisor of anything out of the ordinary, or anything which does not conform to the approved process sheets.
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Work with Engineers and line leads to resolve issues and correct procedures to ensure quality and efficiency.
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Maintain Clean Room integrity by using proper attire and adherence to Clean Room environment practices and procedures as applicable.
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Maintain accurate records/documentation related to quality, work in progress, test results, labor (e.g. timecards), and special projects.
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<li>
Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations.
</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.

Assembler (Cleanroom)

<h3>Job Description</h3>
Job Description
Position: Medical Technologist / Medical Laboratory Scientist – General Supervisor We are a small, independent laboratory within a Rheumatology clinic seeking a full-time Medical Technologist or Medical Laboratory Scientist to serve as General Supervisor under the direction of the Laboratory Director. Position Overview The Laboratory Supervisor will oversee daily laboratory operations, ensuring compliance with CLIA, CMS, and DPH requirements as well as established safety and quality standards. This role requires both technical expertise and leadership skills to guide a small team of technicians while maintaining efficiency, accuracy, and regulatory compliance. This is a generalist position with primary responsibilities in: ● Clinical chemistry ● Hematology ● Synovial fluid analysis ● Manual differentials Additional duties include developing and maintaining standard operating procedures (SOPs), performing venipuncture for sample collection, conducting assays, and ensuring timely and accurate reporting of results. Key Responsibilities ● Supervise and support daily laboratory operations under the Laboratory Director ● Ensure adherence to quality assurance, quality control, and safety standards ● Write, review, and update SOPs in alignment with regulatory requirements ● Perform and oversee testing in chemistry, hematology, and synovial fluid analysis ● Conduct and review manual differentials with accuracy and efficiency ● Perform venipuncture and specimen collection as needed ● Prepare for and maintain readiness for regulatory inspections (CLIA, CMS, DPH) ● Train and mentor laboratory staff, fostering professional growth and development Qualifications ● ASCP or AMT certification preferred, or certification-eligible within 6 months and certified within 1 year ● Associate’s or Bachelor’s degree in Medical Laboratory Technology, Medical Laboratory Science, or equivalent with at least 24 credit hours of academic science (minimum of 8 hours in biological sciences and 8 hours in chemical sciences) ● Minimum of 3 years of laboratory experience (including clinical rotations) ● Proficiency in manual differentials required ● Commitment to ongoing continuing education as required by certifying agency ● Strong organizational, communication, and leadership skills

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