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<h3>Job Description</h3>
Job Description
MERL is seeking highly-qualified Ph.D. interns passionate about robotic research to contribute to the fundamental research of perception and control algorithms for loco-manipulation tasks. The work will involve extensive validation in both simulation and hardware, using a legged robot equipped with a manipulator arm with mounted cameras. Depending on the intern's expertise and the agreed project scope, research topics may include one or more of the following: Human-robot collaboration, LLM/VLM-based Active SLAM, and state estimation. The internship is expected to lead to a publication in a top-tier robotics, machine learning, or computer vision conference and/or journal. The internship has a flexible start date (Spring/Summer 2026), with a duration of 3-6 months.
Required Specific Experience 
<ul>
<li>Current/Past Enrollment in a Ph.D. Program in Computer Engineering, Computer Science, Electrical Engineering, Mechanical Engineering, or a related field.</li>
<li>Exposure to core subjects from robotics curriculum including planning, control, and estimation (e.g., motion planning, feedback control, sensor fusion, Kalman filtering, kinematics, dynamics, etc).</li>
<li>Expertise in at least one or more areas: LLM fine-tuning, SLAM, graph-based optimization (e.g, factor graphs with GTSAM), generative models (e.g., diffusion, flow-matching), 3D computer vision, whole-body control.</li>
<li>Excellent programming skills in Python and/or C++, with prior knowledge of ROS2 and high-fidelity simulators such as Isaac Sim and/or MuJoCo.</li>
</ul>
The pay range for this internship position will be 6-8K per month.

Internship - Perception and Control for Legged Loco-Manipulation

<h3>Job Description</h3>
Job Description
At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands—including Curaleaf, Select, and Grassroots—offer premium products and services in both medical and adult-use markets.
Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our Rooted in Good initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis.
Job Title: Confections Formulation Scientist Location: Lexington, KY or Webster, MA (Relocation may be provided for the right candidate) Job Type: Full Time | Exempt Travel: Up to 50–75% to support our confection production facilities across the country
Who You Are:
You're a product development scientist with experience in confections, gummies, or candy formulation. You understand how hydrocolloids, pectin/gelatin systems, sugars, and emulsions work together to create consistent flavor, texture, and stability — and you know how to translate bench-top trials into scalable production. You bring deep knowledge of ingredient functionality, emulsions, and hydrocolloids, paired with the technical skill to scale formulations from the lab bench to full production. Whether running shelf-life studies, managing formulation data, or collaborating with cross-functional partners, you approach each challenge with precision, organization, and a problem-solving mindset. Above all, you're excited to push boundaries in the growing cannabis edibles space while upholding the highest standards of quality, safety, and compliance.
What You'll Do:
As a Confections Formulation Scientist, you'll play a central role in developing and scaling innovative cannabis-infused products. You'll conduct formulation trials, lead product testing, and support commercialization to bring new concepts to market. Your work will span from sensory evaluations to regulatory compliance, ensuring each product is safe, consistent, and high-quality. On any given day, you might be:
<ul>
<li>Supporting the development, optimization, and scaling of cannabis-infused edibles through bench trials, pilot runs, and full-scale production</li>
<li>Conducting sensory testing, shelf-life studies, and technical evaluations of texture, flavor, and stability using industry tools like viscometers and texture analyzers</li>
<li>Maintaining SOPs, batch records, and technical documentation to streamline operations and support audits</li>
<li>Ensuring compliance with GMP, food safety, labeling, and cannabis regulations, including coordinating third-party lab testing and interpreting results</li>
<li>Managing formulation and ingredient data using MRP systems and formulation software for efficiency and accuracy</li>
<li>Sharing data-driven insights that influence innovation, continuous improvement, and collaboration across the team</li>
</ul>
What You'll Bring:
<ul>
<li>5–8 years of experience in confectionery formulation and/or food manufacturing</li>
<li>A bachelor's degree in Food Science, Chemistry, Food Chemistry, or a related field</li>
<li>Hands-on experience in confection formulation and scale-up, with knowledge of production equipment</li>
<li>Strong understanding of ingredient functionality, food chemistry, emulsions, and hydrocolloids to design stable formulations</li>
<li>Familiarity with GMPs, food safety, and regulatory requirements, with direct experience in sensory testing and shelf-life evaluations</li>
<li>Excellent communication and documentation skills, paired with attention to detail and strong organizational abilities</li>
<li>Proficiency with Microsoft Office and formulation software</li>
<li>Willingness to travel for trials, production support, and industry events</li>
</ul>
Even Better If:
<ul>
<li>You have experience in the cannabis or hemp industry</li>
<li>You're familiar with ERP/MRP systems for managing formulations and ingredient tracking</li>
<li>You bring experience applying data science or analytics to product development</li>
<li>You've supported R&amp;D trials and helped scale products from concept to commercialization</li>
</ul>
Physical Requirements:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this Job, the employee is regularly required to stand, walk, sit, talk or hear, use hands to finger or feel, reach with hands and arms, and lift up to 25 lbs. The employee is occasionally required to climb and balance, stoop, kneel, crouch, or crawl and lift up to 50 lbs. This position requires close vision, distance vision, peripheral vision, depth perception and the ability to adjust focus.
Work Environment:
This position has allergen warnings, potential exposure to dust, pollen, and plant pathogens, requires exposure to cleaning solvents, such as high volumes of isopropyl alcohol, requires daily use of provided PPE, such as masks, hair nets, beard covers, respirators, boot covers, scrubs, non-slip shoes, and Tyvek suits as necessary, requires the ability to work in confined spaces, has exposure to loud noises, including but not limited to air compressors, packaging equipment, and alarms, has exposure to CO2 manufacturing procedures at OSHA approved CO2 levels and requires a high stress tolerance, adaptability, and flexibility. Ability to work in an ever-changing environment.
Curaleaf Pay Transparency$78,000—$87,000 USD
What We Offer:
<ul>
<li>Career Growth Opportunities</li>
<li>Competitive Pay and Benefits</li>
<li>Generous PTO and Parental Leave</li>
<li>401(K) Retirement Plan</li>
<li>Life/ Disability Insurance</li>
<li>Community Involvement</li>
<li>Referral Bonuses and Product Discounts</li>
</ul>
Benefits vary by state, role type, and eligibility. 
Follow us on Social Media: Instagram: @curaleaf.usa Twitter: @Curaleaf_Inc LinkedIn: Curaleaf LinkedIn
Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence
Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis. 
Our Values:
<ul>
<li>Lead and Inspire. </li>
<li>Commit to Win. </li>
<li>ONE Curaleaf. </li>
<li>Driven to Deliver Excellence. </li>
</ul>
Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Individuals adversely impacted by the war on drugs are encouraged to apply.
Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.

Confections Formulation Scientist

<h3>Job Description</h3>
Job Description
Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We've built a mammalian synthetic biology platform – from cells to software – to enable the design and manufacture of next-generation therapeutics.

We are seeking a Head of Cell Line Development (CLD) to lead Asimov’s biologics CLD team and help push the boundaries of biologics manufacturing. The successful candidate will be responsible for managing direct reports and lab activities in support of the generation and characterization of cell lines expressing the highest quantity and quality of protein therapeutics. We have experienced rapid growth in both our project portfolio and CLD team, and we expect that growth trajectory to continue for the foreseeable future. This role will be central to scaling capabilities, workflows, and leadership structures accordingly.

This role requires a strategic leader with a deep technical foundation in biologics cell line development and a proven track record of growing and managing high-performing teams. Working closely with Asimov’s synthetic biology, process development, computational modeling, and software teams, this role will shape Asimov’s CLD vision and contribute as a thought leader to advance the state of the art in biologics cell line development. The role will also partner with commercial, program management, and technical teams to support customer-facing communications, including scientific discussions with prospective clients and collaborators. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology company.
 
About the Role:
<ul>
<li>
As the Head of CLD, you’ll lead and develop Asimov’s CLD team, managing scientists and research associates focused on CHO-based biologics CLD.
</li>
<li>
You’ll guide individuals and the team towards personal and professional development milestones, all in support of Asimov's vision and goals.
</li>
<li>
You’ll drive excellence in execution, ensuring robust, high-throughput workflows for stable clone generation, screening, and characterization to deliver production cell lines meeting titer, quality, and regulatory expectations.
</li>
<li>
You’ll address complex cell line development challenges by demonstrating and applying cross-functional knowledge and industry best practices.
</li>
<li>
You’ll foster cross-functional collaboration with Synthetic Biology, Process Development, Process Modeling, Computational Biology, and Software teams to integrate design, data, and automation capabilities.
</li>
<li>
You’ll serve as a scientific and technical thought leader, identifying and implementing emerging technologies in expression vector design, gene integration, host engineering, productivity optimization, and workflow improvements.
</li>
<li>
You’ll represent Asimov externally, contributing to industry conferences, industry forums such as AMBIC and BioPhorum, filing patents, and publishing peer-reviewed manuscripts.
</li>
</ul>

About You:
<ul>
<li>
You have a Ph.D. in Biological Engineering, Cell Biology, Molecular Biology, or a related field.
</li>
<li>
You have 10+ years of experience in CHO-based cell line development supporting IND-enabling and/or GMP manufacturing activities.
</li>
<li>
You have a deep understanding of cell biology, expression system design, gene integration technologies, and process-relevant analytics.
</li>
<li>
You have a track record of strategic thinking and innovation, translating R&amp;D advances into scalable, manufacturable platforms.
</li>
<li>
You have proven experience managing a team of scientists, with a track record of developing scientists and supporting rigorous scientific execution.
</li>
<li>
You are comfortable engaging with internal and external stakeholders and can clearly communicate scientific and strategic considerations to prospective partners or clients.
</li>
</ul>

We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.
Compensation Range: $220K - $280K

Head of Cell Line Development

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
The Bioresearch Center is seeking a dedicated and talented full-time contractor for the position of Biologist I or II to join the Immunology Discovery Dermatology team in Worcester, MA.
</li>
<li>
The role involves the design and execution of in vitro and ex vivo pharmacology experiments aimed at defining the activity and mechanism of action of novel biotherapeutics and small molecules in mammalian cell lines and primary human immune cells.
</li>
<li>
The individual will be responsible for experimental planning and execution, data analysis and presentation, and detailed data documentation.
</li>
<li>
Assist in the design and execution of in vitro/ex vivo studies using mammalian cell lines and primary immune cells to evaluate target biology.
</li>
<li>
Perform primary immune cell and stable cell culture to support in vitro studies.
</li>
<li>
Support downstream analysis, including flow cytometry, MSD, and/or ELISA as needed.
</li>
<li>
Maintain accurate records of experimental procedures and data in laboratory notebook.
</li>
<li>
Additional responsibilities include data analysis, interpretation, and communication of experimental results to cross-functional team members, as well as working in a strong collaborative atmosphere.
</li>
</ul>
Qualifications:
<ul>
<li>
BS or MS in Biology, Molecular Biology, Immunology or related field with 1+ years relevant experience in academia or industry (Required) Biologist II = 3+ years of experience
</li>
<li>
Experience in aseptic tissue culture techniques involving immune cell isolation/culturing and mammalian cell lines culturing (Required)
</li>
<li>
Experience with flow cytometry and/or protein detection methods (ELISA and/or MSD), (required)
</li>
<li>
Strong organizational skills, attention to detail and good communication skills (oral and written) (required)
</li>
<li>
Capable of working independently as well as collaboratively within project teams (required)
</li>
<li>
Ability to develop and implement quality control measures for experimental procedures to ensure robust and reproducible datasets that support reaching project milestones.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Immunology Discovery Biologist

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
We are currently seeking a highly motivated and passionate scientist to join our team in Immunology Discovery department based in Cambridge MA.
</li>
<li>
The candidate will focus on generating biology data packages to help advance target identification and validation within GI immunology.
</li>
<li>
The position offers a unique opportunity for a talented scientist to work in a dynamic, innovative, and multi-disciplinary environment to develop their career at the interface of basic research and early drug discovery.
</li>
<li>
The scientist will focus on developing and optimizing cellular/molecular assays to generate reliable and reproducible data in a timely manner.
</li>
<li>
The scientist is expected to read and adapt scientific literature and internal protocols to accomplish assignments and demonstrate broad and versatile technical expertise within immunology.
</li>
<li>
Develop and execute cell-based functional assays using cell lines and mammalian tissue primary cells, for key readouts including cell activation, differentiation and effector molecule secretion
</li>
<li>
Perform advanced molecular and cellular biology techniques (including but not limited to FACS, ELISA, MSD, HTRF)
</li>
<li>
Isolate and culture immune cells (T cells, myeloid cells) from human and mouse tissues
</li>
<li>
Work independently on the design, execution and interpretation of experimental results to validate hypotheses related to the project need
</li>
<li>
Implement and innovate new experimental protocols/techniques as needed
</li>
<li>
Analyze, interpret, document and report data consistently, concisely and rigorously, both to individual stakeholders and in group settings
</li>
<li>
Demonstrate scientific excellence through dedication to multiple projects in a fast-paced multi-disciplinary environment
</li>
<li>
Impact projects mostly through lab-based activities
</li>
</ul>
Qualifications:
<ul>
<li>
Master's degree in Biological Science or related field with 2-3 years of experience in biotech or pharma set up.
</li>
<li>
Experience in in vitro cell culture (sterile techniques, handling challenging cell types) and cell-based assays development is required.
</li>
<li>
Experience with human PBMC functional assays and/or immune cells (T cells and myeloid cells) is required.
</li>
<li>
Experience in immunoassays including multi-color flow cytometry and ELISA (or MSD, HTRF) is required.
</li>
<li>
Experience with mouse tissue processing for immune profiling (not direct mouse handling) is a plus but not required.
</li>
<li>
Knowledge of DNA/RNA handling and other molecular biology techniques like PCR and qPCR is a plus but not required.
</li>
<li>
Ability to learn new skills and apply them in a fast-paced research environment.
</li>
<li>
Creativity, problem-solving, and attention to details.
</li>
<li>
Excellent oral and written communication and collaboration skills.
</li>
<li>
Ability to work independently as well as in a team.
</li>
<li>
Proven flexibility to deal with changing timelines and shifting work priorities.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientist, Immunology Discovery

<h3>Job Description</h3>
Job DescriptionCompany Description 
Why Join Eurofins?
At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits.
Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries—from food and water to pharmaceuticals and advanced materials. We help the world’s top companies ensure their products are safe, authentic, and accurately labeled.
Why Relocate to Rensselaer, NY?
<ul>
<li>Be part of a thriving biopharma and life sciences hub.</li>
<li>Enjoy a lower cost of living compared to Boston and other major metro areas.</li>
<li>Benefit from relocation assistance and onboarding support for a smooth transition.</li>
</ul>
Job Description 
We’re seeking a Microbiology Operations Supervisor to lead second-shift operations in a GMP-regulated environment at our Rensselaer, NY site. This is a full-time leadership role with relocation support provided.
What You’ll Do
<ul>
<li>Oversee environmental monitoring (EM) activities, including sampling of cleanrooms, compressed gases, and water systems.</li>
<li>Conduct microbial identification and acceptance testing of microbiological culture media.</li>
<li>Maintain microbiology productivity databases and generate trend reports.</li>
<li>Lead investigations into microbiological deviations and prepare detailed reports.</li>
<li>Ensure calibration and maintenance of lab equipment and compliance with GMP standards.</li>
<li>Supervise and mentor microbiology analysts and group leaders.</li>
<li>Manage onboarding, training, and scheduling for second-shift operations.</li>
<li>Apply Lean principles to optimize workflows and drive continuous improvement.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Microbiology, Life Sciences, or related field.</li>
<li>Minimum 3 years of microbiology lab experience, including EM in a GMP setting.</li>
<li>At least 3 years of leadership experience in technical or lab environments.</li>
<li>Strong understanding of microbiological testing, EM protocols, and compliance standards.</li>
<li>Proven ability to coach and develop staff while managing operations.</li>
<li>Authorized to work in the U.S. without restriction or sponsorship.</li>
<li>Willingness to relocate to Rensselaer – relocation support is available.</li>
</ul>
 Additional Information 
<ul>
<li>Full-time, onsite position based on second-shift schedule (Mon–Fri, 2:30pm–11:00pm), with occasional weekends and overtime as needed.</li>
<li>Candidates within a commutable distance to Rensselaer, NY, are strongly encouraged to apply.</li>
<li>Relocation assistance may be available for qualified candidates seeking to relocate.</li>
</ul>
Benefits include:
<ul>
<li>Comprehensive medical, dental, and vision coverage</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Hourly pay ranges from&nbsp;$33–$38/hour + 10% shift differential</li>
</ul>
Ready to make an impact? Join a team where your scientific skills matter and your growth is supported. If you're passionate about quality, collaboration, and continuous improvement, we want to hear from you. Apply today and take the next step in your career with Eurofins PSS!
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Microbiology Operations Supervisor - Relocation to Rensselaer, NY Provided!

<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 
This scientist will develop formulations for oral solid dosage forms (tablets and capsules) on high-priority programs with accelerated timelines. Key responsibilities include designing and executing formulation and process development experiments, interpreting scientific data, and communicating findings to stakeholders. The role requires close coordination with cross-functional teams to meet tight project deliverables and authoring technical reports and CMC sections for regulatory submissions.
Position Responsibilities:
<ul>
<li>Understand project timelines and deliverables and plans/coordinates project work accordingly with stakeholders.</li>
<li>Contribute significantly and independently to project work which may include multiple projects within functional area.</li>
<li>Review, interpret and communicate data within project teams. &nbsp;</li>
<li>Plan and implement resolutions to technical problems/issues.</li>
<li>Independently design and execute experiments and report results.</li>
<li>Proactively analyze manufacturing issues and coordinate potential resolution with the drug substance team.</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>A degree in chemistry, biology, pharmacy, engineering, or a related pharmaceutical science with at least 4 years of formulation development experience</li>
<li>BS with at least 6 years of industry experience, MS with at least 4 years of industry experience, or PhD with at least 6 months of industry experience in formulation development</li>
<li>Must have experience specificially with oral solid dosage formulation development</li>
<li>Strong knowledge of CMC pharmaceutical development, including hands-on operation manufacturing equipment and laboratory instruments (compression, wet/dry granulation, capsule filling, etc.)</li>
<li>Sound knowledge of current Good Manufacturing Practices</li>
<li>Technical writing experience</li>
<li>Experienced working in a multi-disciplinary team environment</li>
<li>Must be eligible to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
Position is&nbsp;Full Time, Monday – Friday, 8am-5pm with overtime as needed.&nbsp;Candidates currently living within a commutable distance of&nbsp;Cambridge, 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>Base Compensation: $90,000 to $99,000 per year based on experience and education</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Formulation Development Scientist - Oral Solid Dosage

<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 individual will join a team of scientists and engineers focused on developing and optimizing mammalian cell culture processes for recombinant proteins and biologics for early-phase and late-phase clinical trials. He or she will be responsible for executing mammalian cell culture experiments in bench-top bioreactors and associated scale-down equipment with the goal of developing robust, scalable, high productivity processes that produce therapeutic proteins with the appropriate product quality attributes for use in treating human disease. The work will also involve working with clinical production facilities to ensure accurate technology transfer and successful large-scale production.
Responsibilities
<ul>
<li>Plan and execute experiments in shake flasks and bench-top bioreactors.</li>
<li>Ensures timely, effective, and high-quality documentation in electronic laboratory notebooks.</li>
<li>Communicate results and findings to stakeholders on a regular basis; presents data/strategy to colleagues and management as appropriate.</li>
<li>Work collaboratively with colleagues both within the group and cross-functionally contributes to maintaining and improving upon our safe, effective, and efficient lab operations.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree with 2–5 years of relevant experience, OR</li>
<li>Master’s degree with 0–2 years of relevant experience in Biotechnology, Microbiology, Cell Biology, Chemical/Biochemical Engineering, or a related field.</li>
<li>Strong aseptic laboratory technique (required)</li>
<li>Exceptional attention to detail</li>
<li>Excellent organizational skills</li>
<li>Clear and effective oral and written communication</li>
<li>A collaborative, team-oriented mindset</li>
<li>Must be authorized to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>45-60 Minute In-Person Meeting to Meet the Team&nbsp;</li>
</ul>
Additional Details:&nbsp;
This is a full-time, onsite position based on a first-shift schedule Monday through Friday, with overtime required as needed. Candidates located within a commutable distance to&nbsp;Andover, MA,&nbsp;are strongly encouraged to apply.&nbsp;
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 holidays</li>
<li>Hourly rate is between $26.00-$30.00,&nbsp;depending on education and experience&nbsp;</li>
</ul>
Ready to take the next step in your career? Apply today and join a team that’s making a difference in science every day.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Upstream Process Development Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
About Mote Therapeutics:&nbsp;
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 
Key Responsibilities:
We are seeking a scientific contributor to lead and execute novel LNP formulation process development activity for the delivery of circular RNA therapeutic at scale. This role will spearhead LNP process development/scale up activity and would be responsible for designing and executing DOE-based formulation process optimization. They would engineer and functionalize LNPs, develop analytics for formulation quality control, and develop processes to improve formulation at scale. 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 chemical engineer/pharmaceutical major with strong LNP formulation, optimization, and process development experience, 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.
<ul>
<li>Establish, execute and document protocols for preparation and characterization of targeted LNP formulations with nucleic acid cargo for in vitro and in vivo studies</li>
<li>Design and execute DOE-driven studies for LNP composition, mixing parameters and process optimization to improve formulation quality, stability, delivery efficiency and functional activity</li>
<li>Develop cell and molecular biology assays to assess the delivery efficiency of RNA cargo in mammalian primary cells to facilitate development of therapeutics drugs pipelines</li>
<li>Assist in the buildout of formulation and analytical capabilities with focus on delivery with nanoparticle technology, lyophilization and process development for scale up/production</li>
<li>Contribute to patent applications related to the delivery technology</li>
<li>Support technology transfer to CDMOs and 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 formulate, characterize, develop, and support assessment of efficacy</li>
<li>Plan and coordinate animal studies with in vivo team</li>
<li>Author technical documents, including SOPs for formulation processes and 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>BS/MS in chemical engineering, chemistry, pharmaceutical sciences, or related field, preferably with industry experience of 2-5 years for MS or 5-8 years for BS candidates.</li>
<li>Strong track record of productivity in nanoparticle research with an understanding of key challenges in nanoparticle/formulation scale-up and translation</li>
<li>Prior experience in developing lyophilization protocols for nanoparticle formulation, and stability testing is a plus</li>
<li>Technical proficiency with LNP formulation of RNA and analytical assays for particle characterization</li>
<li>Technical proficiency in developing cell and molecular biology assays to support drug product development</li>
<li>A minimum of 3-4 years of experience working with lipid nanoparticles for RNA delivery in any capacity</li>
</ul>
Preferred Qualifications:
<ul>
<li>Demonstrated capability in LNP formulation for nucleic acid delivery is must</li>
<li>LNP process development and scale-up experience is desired</li>
<li>Experience with tissue-specific targeted delivery of LNP-nucleic acid formulation is a plus</li>
<li>Demonstrated ability to present complex technical topics to a wide range of audiences with varying technical depth</li>
<li>Demonstrated proficiency in record keeping and documentations to support SOP generation, technology transfer and preferably regulatory filings</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/Principal Research Associate, LNP Discovery/PD

<h3>Job Description</h3>
Job Description
At the Center for Health Information and Analysis (CHIA), we serve as stewards of Massachusetts health data, employing multifaceted datasets and&nbsp;cutting-edge&nbsp;analytics to ensure transparency in our health care system. By joining CHIA,&nbsp;you'll&nbsp;dive into health care data, revealing invaluable trends and insights, and play a pivotal role in evidence-based decision-making.   &nbsp;
Our work directly&nbsp;impacts&nbsp;the health care system, supporting the development of data-driven policies that aim to improve the quality and equity of care, while keeping costs affordable for Massachusetts families. We foster a flexible, collaborative environment, offering a hybrid model that balances in-person and remote work. Our hybrid approach allows you to work alongside your colleagues in our vibrant Boston office at 501 Boylston Street for at least two designated days per week, with the flexibility to work remotely on others.   &nbsp;
Join us at CHIA and be a driving force&nbsp;in&nbsp;health policy impact! We&nbsp;are seeking&nbsp;a&nbsp;Research Analyst&nbsp;to&nbsp;contribute to&nbsp;our growing research projects within the dynamic Strategy and Research team.   &nbsp;
The Research&nbsp;Analyst&nbsp;will work closely with the research team and other colleagues at CHIA, vendors,&nbsp;and stakeholders such as sister agencies,&nbsp;providers,&nbsp;payers etc.&nbsp;The Research&nbsp;Analyst&nbsp;will help lead and support&nbsp;analytic work and product development&nbsp;in addressing ongoing and emerging health care information and data gaps, particularly in areas such as health care&nbsp;workforce, health care&nbsp;utilization,&nbsp;and emerging issues.&nbsp;&nbsp;
As a&nbsp;Research Analyst, you will have the opportunity to: &nbsp;
<ol>
<li>
Drive Data-Backed Insights: Seize the opportunity to work with an extensive range of data on health care&nbsp;utilization, access, and&nbsp;equity&nbsp;related issues. You will be at the forefront of producing and reviewing clear and comprehensive written analyses, graphics,&nbsp;tables&nbsp;and presentations using CHIA's rich data sources to unearth crucial insights that will inform and shape health care policies and initiatives.  &nbsp;
</li>
</ol>
<ol>
<li>
Shape&nbsp;Data Management and Analysis:&nbsp;Take an active role in shaping data projects&nbsp;by&nbsp;implementing&nbsp;data management&nbsp;tasks for&nbsp;large datasets such as&nbsp;the&nbsp;All&nbsp;Payer Claims&nbsp;Database&nbsp;(APCD),&nbsp;hospital discharge data&nbsp;(Case&nbsp;Mix),&nbsp;and other&nbsp;data&nbsp;assets&nbsp;to facilitate and deliver&nbsp;insightful analyses that drive real change in Massachusetts health care, all while expanding your skills in a dynamic, mission-driven environment.&nbsp;
</li>
</ol>
<ol>
<li>
Champion Data Integrity:&nbsp;Participate&nbsp;in quality assurance (QA) and documentation processes to ensure that reported data is reliable and&nbsp;accurate. Work both independently and collaboratively with team members in developing analytical plans&nbsp;and documentation&nbsp;appropriate for&nbsp;each project.&nbsp;
</li>
</ol>
<ol>
<li>
Become&nbsp;a Technical and Subject Matter Expert: Provide technical support to&nbsp;the&nbsp;research&nbsp;team in programming and data analytics using&nbsp;APCD,&nbsp;Case Mix, and other&nbsp;data&nbsp;assets. Use your critical thinking skills to conduct literature searches and synthesize findings&nbsp;on topics of interest.&nbsp;&nbsp;
</li>
</ol>
Here are the important qualifications we are looking for:  &nbsp;
<ol>
<li>
Data&nbsp;Programming and Visualization&nbsp;Expertise:&nbsp;At least&nbsp;1&nbsp;year of experience&nbsp;and knowledge of&nbsp;data management and analysis using SAS, R, STATA, and/or any other major statistical packages.&nbsp;Knowledge of/experience with&nbsp;PowerBI,&nbsp;Tableau for data visualization&nbsp;preferred&nbsp;
</li>
</ol>
<ol>
<li>
Research Background: Knowledge of and experience with research methods&nbsp;and processes&nbsp;
</li>
</ol>
<ol>
<li>
Health Care Knowledge: Experience working with&nbsp;hospital&nbsp;discharge&nbsp;data and&nbsp;previous&nbsp;experience working with&nbsp;health&nbsp;care claims&nbsp;data strongly&nbsp;preferred.&nbsp;&nbsp;
</li>
</ol>
<ol>
<li>
Effective Communication: Demonstrate&nbsp;excellent written and verbal communication skills, with an ability to articulate complex technical issues clearly and persuasively.  &nbsp;
</li>
</ol>
<ol>
<li>
Educational Background:&nbsp;Bachelor’s degree in social sciences, public policy, public health, or quantitative field&nbsp;required;&nbsp;Advanced degree in health services research, statistics, epidemiology, or related&nbsp;field&nbsp;strongly&nbsp;preferred.&nbsp;&nbsp;
</li>
</ol>
Minimum Entrance Requirements:&nbsp; &nbsp; Analyst I: Applicants must have at least (A) two years of full-time, or equivalent part-time professional experience in business administration, health care planning or administration, public health policy or administration, human services policy analysis or administration or economics, the major duties of which included financial analysis of costs, expenses and revenue and/or the development, implementation and monitoring of financial reimbursement systems, or (B) any equivalent combination of the required experience and the substitutions below.&nbsp; &nbsp; Substitutions:&nbsp; I. A&nbsp;Bachelor's&nbsp;or higher degree with a major in health care administration, hospital administration, public health or health services administration, accounting, business administration, business management, public policy, public&nbsp;administration&nbsp;or economics may be substituted for the required experience.&nbsp; &nbsp; Analyst II: Applicant must have at least (A) three years of full-time, or equivalent part-time professional experience in business administration, finance, accounting, health care planning or administration, public health policy or administration, human services policy analyses or administration, economics, or a similar field; or (B) any equivalent combination of the required experience and the substitutions below.&nbsp;
Substitutions:&nbsp;
I. A Bachelor's degree with a major in health care administration, hospital administration, public health or health services administration, finance, accounting, business administration, business management, public policy, public administration, economics, or similar degree may be substituted for a maximum of two years of the required&nbsp;experience.*&nbsp;
II. A graduate degree with a major in health care administration, hospital administration, public health or health services administration, finance, accounting, business administration, business management, public policy, public administration, economics, or a similar degree may be substituted for a maximum of three years of the required&nbsp;experience.*&nbsp;
Analyst III: Applicant must have at least (A) four years of full-time, or equivalent part-time professional experience in business administration, health care planning or administration, public health policy or administration, human services policy analyses or administration, economics, the major duties of which included financial analysis of costs, expenses and revenue and/or the development, implementation and monitoring of the health care service delivery system and pricing methods. In addition, applicant must have a working knowledge of CHIA’s administration of nursing and residential care facility rate setting operations, including&nbsp;determining&nbsp;revised capital rates, setting rates for existing and new facilities, ownership changes, realty and management companies, and CHIA’s systems used to&nbsp;maintain&nbsp;nursing and residential care facility operations and rates.&nbsp;
Substitutions:&nbsp;
I. A Bachelor's degree with a major in health care administration, hospital administration, public health or health services administration, accounting, business administration, business management, public policy, public administration, economics, or similar degree may be substituted for a maximum of two years of the required&nbsp;experience.*&nbsp;
II. A graduate degree with a major in health care administration, hospital administration, public health or health services administration, accounting, business administration, business management, public policy, public administration, economics, or a similar degree may be substituted for a maximum of three years of the required&nbsp;experience.*&nbsp;
*Education toward such a degree will be prorated&nbsp;on the basis of&nbsp;the proportion of the requirements&nbsp;actually completed.&nbsp;
NAGE: Reimbursement Systems Analyst I (RSA I) and Reimbursement Systems Analyst II (RSA II)&nbsp;
The full&nbsp;salary band: &nbsp;
&nbsp;
Analyst I/&nbsp;RSA I: $61,551.88&nbsp;- $87,921.34&nbsp;annually.&nbsp; Analyst II/&nbsp;RSA II: $70,757.18&nbsp;- $102,269.96&nbsp;annually.
Analyst II/&nbsp;RSA III: $81,166.28&nbsp;- $118,145.56 annually. &nbsp;
Total Compensation: &nbsp;
We value the talent and&nbsp;expertise&nbsp;you bring to the table. We offer a competitive salary range&nbsp;of $61,551.88 - $118,145.56&nbsp;annually&nbsp;for this position. Salary is&nbsp;commensurate&nbsp;with experience. CHIA may adjust title, responsibilities, and salary depending on the experience and&nbsp;expertise&nbsp;of the individual selected.  &nbsp;
Comprehensive Benefits  &nbsp;
When you embark on a career with the Commonwealth, you are offered an outstanding suite of employee benefits that add to the overall value of your compensation package. We take pride in providing&nbsp;a work&nbsp;experience that supports you, your loved ones, and your future.  &nbsp;
Want the specifics? Explore our Employee Benefits and Rewards!  &nbsp;
Together,&nbsp;let's&nbsp;embark on a journey of meaningful impact&nbsp;in&nbsp;healthcare. We invite you to&nbsp;join CHIA, where your&nbsp;expertise&nbsp;will shape the future of healthcare in Massachusetts. Likewise,&nbsp;we're&nbsp;eager to take a chance on you - to welcome a dedicated professional who shares our passion for making a difference. Join us in this collaborative endeavor, where&nbsp;we'll&nbsp;forge new paths, innovate, and lead the way toward a healthier Commonwealth. &nbsp;
Apply now and be part of our transformative journey at CHIA! &nbsp;

An Equal Opportunity / Affirmative Action Employer. Females, minorities, veterans, and persons with disabilities are strongly encouraged to apply.
The Commonwealth is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, disability, national origin, veteran status, or any other basis covered by appropriate law. Research suggests that qualified women, Black, Indigenous, and Persons of Color (BIPOC) may self-select out of opportunities if they don't meet 100% of the job requirements. We encourage individuals who believe they have the skills necessary to thrive to apply for this role.
Information submitted by applicants is collected through the JazzHR Platform, your submission of application materials constitutes your express consent for this information to be provided to JazzHR for processing. Please do not include any personally identifiable information with your application materials other than that specifically requested by CHIA. CHIA requests basic information such as name, address, telephone number, and email address. You may also self-identify with your race/ethnicity, gender, disability and/or veteran status. However, you should not provide more detailed personal information such as your date of birth or Social Security Number with your application materials.

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