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<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: $22.00-$32.00&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 
Canam Bridges designs, manufactures and installs steel bridges for major infrastructure contractors across North America. Canam Bridges is a member of Canam Group, which has over 5,100 employees and operates 22 plants in North America, as well as engineering offices in Canada, Romania, India and the Philippines.
Job Description 
Your life at Canam Bridges As a Metrologist at Canam Bridges, you will be responsible for taking factory measurements using “Station Total” and “Laser Tracker Faro” surveying tools. Your analytical mind will allow you to use your 3D vision superpowers to complete dimensional measurements. To break your routine, you will alternate between taking factory measurements, recording data, and writing reports. Your computer knowledge will make you an expert in AutoCAD and Polyworks. That said, it is your team that will give you the most satisfaction, because at Canam Bridges, we are a solid combination of expertise and pride!
Job Description Assist Plant Manager and production staff in developing production plans, ensure production objectives are met, offer recommendations, and implement production events and programs. The Metrologist is responsible for performing such work consistent with the company’s corporate mission, values, and departmental financial objectives.
Essential Functions
<ul>
<li>Assist in the production-planning process, schedules, assignments, and&nbsp;production sequences to meet production goals.</li>
<li>Read and analyze data, production schedules, and other records and reports to determine production productivity and to evaluate current production estimates and outputs.</li>
<li>Identify direct and indirect labor issues and production problems, make recommendations, and assist management in developing a corrective action plan.</li>
<li>Compile production planning notes, sketches, prints, schedules, contract documents and specifications into a formal build plan.</li>
<li>Aid in the detailing and manipulation of models to accommodate additional views for fabrication per planning session. Assist on designing fixtures and jigs to aid fabrication.</li>
<li>Responsible for conventional and CNC machining, to include managing direct labor to accomplish coverage on equipment in support of production needs.</li>
<li>Train and assist production members in the operation of conventional and CNC machining equipment in line with formal build plans.</li>
<li>Perform other job duties as assigned by the Plant Manager.</li>
</ul>
Qualifications 
<ul>
<li>Associate’s degree (A. A.) or equivalent from two-year college or technical school and/or experience in detailing and fabrication.</li>
<li>Must be able to use logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to production or productivity problems.</li>
<li>Experience with AutoCAD, Tekla, FeatureCam, Polyworks, Station Total, Laser Tracker Faro, and other software preferred.</li>
<li>Ability to communicate information and ideas in speaking, so others will understand.</li>
<li>Analyze information and evaluate results to choose the best solution and solve problems.</li>
<li>Must be able to schedule events, programs, and activities, as well as the work of others.</li>
<li>Job requires a willingness to lead, take charge, and offer opinions and direction.</li>
</ul>
 Additional Information 
Work Environment General office and production environment. Daily exposure to computer display and shop environment.&nbsp;&nbsp;
Remuneration We offer a competitive compensation and benefits package, as well as excellent opportunities for training and advancement.
Canam&nbsp;is an Equal Opportunity/Affirmative Action employer.&nbsp;All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
If you need a reasonable accommodation for any part of the employment process, please contact us by email at <a href="mailto:lorri.boynton@canamgroupinc.com" target="_blank">lorri.boynton@canamgroupinc.com</a> and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this e-mail address.

Metrology Technician

<h3>Job Description</h3>
Job Description
Job Description
<ul>
<li>
Are you passionate about protein biochemistry and mass spectrometry? Join a cutting-edge team at the forefront of bioanalytical science. We're looking for a detail-oriented and curious scientist to support our protein mass spectrometry lab.
</li>
<li>
You'll play a key role in preparing biological samples and developing analytical methods that drive impactful research.
</li>
<li>
This is a hands-on, lab-based role ideal for someone who thrives in a collaborative environment and is eager to learn and grow.
</li>
<li>
Prepare biological samples (cells, tissues, plasma) for LC-MS analysis
</li>
<li>
Perform protein lysis, immunoprecipitation, digestion, filtration, and concentration
</li>
<li>
Design and execute experiments in collaboration with scientists
</li>
<li>
Develop and optimize analytical methods
</li>
<li>
Analyze, interpret, and document results in electronic lab notebooks
</li>
<li>
Present findings and contribute to team discussions
</li>
<li>
Maintain high standards of lab safety and data integrity
</li>
<li>
Work on meaningful science with real-world impact
</li>
<li>
Collaborate with top-tier scientists in a supportive environment
</li>
<li>
Gain exposure to innovative technologies and methodologies
</li>
<li>
Grow your skills in a dynamic, fast-paced lab setting
</li>
</ul>
Qualifications:
<ul>
<li>
BS in Chemistry, Biochemistry, or related field + 3-5 years of experience OR
</li>
<li>
MS + 1-3 years of experience
</li>
<li>
Strong experience with LC-MS sample preparation workflows
</li>
<li>
Familiarity with proteomics and immunoanalytical techniques
</li>
<li>
Exposure to Parallel Reaction Monitoring (PRM) is a plus
</li>
<li>
Comfortable operating lab equipment and following complex protocols
</li>
<li>
Excellent data organization and communication skills
</li>
<li>
Independent and self-motivated
</li>
<li>
Strong team player with collaborative mindset
</li>
<li>
Eager to learn and apply new techniques quickly
</li>
<li>
Hands-on role in protein mass spectrometry, supporting innovative research in pharmacokinetics and metabolism.
</li>
<li>
Emphasize LC-MS sample prep as the core skill-candidates with strong experience here are highly valued.
</li>
<li>
PRM and proteomics are preferred but trainable-encourage candidates with LC-MS and immunoassay backgrounds to apply.
</li>
<li>
Designed for BS/MS-level scientists-a great opportunity for those who want to stay hands-on in the lab and deepen their expertise.
</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.

LC-MS Research Associate

<h3>Job Description</h3>
Job Description
With a strategy centered on people and sustainability, Braskem is engaged in contributing to the value chain to strengthen the Circular Economy. Braskem's 9,000 team members dedicate themselves every day to improving people's lives through sustainable solutions in chemicals and plastics. With its corporate DNA rooted in innovation, Braskem offers a comprehensive portfolio of plastic resins and chemical products for diverse industries, such as food packaging, construction, manufacturing, automotive, agribusiness, health and hygiene, and more. With 40 industrial units in Brazil, the United States, Mexico, and Germany, Braskem exports its products to clients in over 70 countries.
Braskem America is an indirect wholly owned subsidiary of Braskem S.A. headquartered in Philadelphia. The company is the leading producer of polypropylene in the United States, with six production plants located in Texas, Pennsylvania, and West Virginia, an Innovation and Technology Center in Pittsburgh, and a New Renewable Innovation Center in Boston focused on leveraging groundbreaking developments in biotechnology and advanced materials. For more information, visit <a href="http://www.braskem.com/usa" target="_blank">www.braskem.com/usa</a>.
Department: Innovation &amp; Technology
Location: Renewable Innovation Center - Lexington, MA 
Travel Involved: 0-5%
Job Type: Full Time, On Site 
Description:
Braskem, a global leader in the production of bio-based materials, has recently opened a new renewable research and development facility in Lexington, MA. This new 35,000 SFT facility will bring together scientists and engineers from a variety of disciplines to ideate and develop novel technologies for the production of bio-based chemicals and materials. We are looking for an Analytical Research Associate to join our team. 
The ideal Analytical Research Associate candidate will have a background in the field of analytical chemistry, preferably in support of metabolic engineering and/or fermentation-based bioproduction processes. In this role, you will work alongside a team of Scientists and Research Associates supporting research initiatives at our Lexington, MA, location. The ideal candidate will have experience executing analytical methods to characterize and quantify small molecules. The ability to work collaboratively in a cross-functional and agile team to deliver against aggressive deadlines is essential. Expertise using techniques including GC, HPLC, and LC/MS is required. An adaptable and agile mindset that thrives with flexibility, newness, and change while upholding quality standards. Strong technical, organizational, and communication skills, and the ability and drive to maintain commitment to scientific excellence and high-quality work in a fast-paced, milestone-driven company are essential.
Required Skills, Education, and Experience:
<ul>
<li>BS or MS in analytical chemistry, chemistry, chemical engineering, biochemistry, or a related field</li>
<li>0 - 5 years of industrial experience, preferably in an analytical chemistry group at an industrial biotechnology company; relevant graduate research will be considered</li>
<li>Perform analytical testing that supports various activities in early development</li>
<li>Operate and maintain analytical instrumentation, including but not limited to GC, UPLC, and QQQ mass spectrometers</li>
<li>Review and deliver reports to multidisciplinary R&amp;D team members</li>
<li>Track assay performance: execute detail-oriented data mining, trending, and statistical evaluation to assess assay performance and data integrity</li>
<li>Analyze, summarize, and present experimental results to the manager and other team members</li>
<li>Work collaboratively with other R&amp;D team members to accomplish project goals and milestones</li>
<li>Use creative problem-solving skills to troubleshoot experimental challenges</li>
<li>Apply DOE methodology to optimize assays for minimal CV and increased reproducibility</li>
<li>Ensure accuracy of data and timely turnaround of results coming out of the Analytical Chemistry group</li>
<li>Analyze, summarize, and present technical data to the manager and other team members</li>
<li>Work collaboratively with other R&amp;D team members to accomplish project goals and milestones</li>
<li>Detail-oriented tracking and documenting of experimental results and instrument performance in electronic laboratory notebooks and company databases</li>
<li>Must be authorized to work in the United States and not need any current or future sponsorship</li>
</ul>
What we offer
At Braskem, we offer more than just a competitive pay package. Our total rewards package includes a wide range of benefits you need for every stage of your life. Our benefits include:
<ul>
<li>Medical, Dental, and Vision Benefits</li>
<li>Retirement Benefits</li>
<li>Maternity and Paternity Leave</li>
<li>Life Insurance</li>
<li>Short- and Long-Term Disability Insurance</li>
<li>Teladoc</li>
<li>A wide range of voluntary benefits like Pet Insurance, Legal and ID Theft Insurance</li>
<li>Flexible work schedules like 9/80 schedules for eligible team members</li>
</ul>
Depending on qualifications, the successful candidate may be offered a position at a more appropriate level and/or ladder.
Candidates must be currently eligible to work in the United States without the need for any type of sponsorship now or in the future. Braskem is committed to equal employment opportunity and providing reasonable accommodations to qualified candidates and employees according to applicable law. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, military and veteran status, gender identity or expression, genetic information, or any other characteristic protected by federal, state, or local law. If you require reasonable accommodation as part of the application process, please contact the Talent Acquisition team.

Analytical Research Associate

<h3>Job Description</h3>
Job Description
About the Team:
The Sensors Division specializes in the development of advanced sensor systems, with a particular focus on airborne and surface-based radar, space-based sensing, electronic warfare, and underwater acoustics. This position is within the Space Missions and Sensing (SMS) Sector of the Sensors Division. In this sector, we develop and deliver technology to advance space-based sensing, space control, and counter-sensing missions.
If you're seeking an opportunity to apply your deep technical knowledge and creativity to make a lasting impact in national security, we invite you to join us. 
The Role:
As a Principal Algorithm &amp; Signal Processing Researcher, you will develop and apply state-of-the-art algorithms and techniques for signal detection, classification, autonomous sensor decision-making, sense making, radar electronic warfare, and electronic support measures. You'll engage directly with our customers to understand and address their most critical challenges. You'll lead a team of researchers in creating innovative systems while collaborating closely with our engineering teams to demonstrate state-or-the-art system capabilities.
What you will do: 
<ul>
<li>Engage directly with customers to understand their unique requirements and national security needs, and shape our solutions to meet their objectives</li>
<li>Design and apply cutting-edge signal processing and machine learning techniques to solve complex radar and RF sensing and counter-sensing challenges </li>
<li>Collaborate with diverse teams, bringing together different perspectives to develop and deploy prototype systems that demonstrate our ability to extend the boundaries of what's possible</li>
<li>Lead and inspire multi-disciplinary teams, guiding them towards success with your technical expertise and leadership skills</li>
<li>Drive business development initiatives and support proposal writing efforts, playing a key role in shaping the future direction of our projects and organization</li>
</ul>
Who You Are: 
<ul>
<li>This position requires the ability to obtain a secret security clearance, for which U.S. citizenship is needed by U.S. Government</li>
<li>PhD, MS, or BS in Electrical Engineering, Applied Mathematics, Physics, or related technical discipline</li>
<li>8+ years of experience on EW or Radar programs, including the development of sensor system modes and advanced signal- and data-processing algorithms from mathematical/analytical derivation through testing and verification of system performance</li>
<li>2+ years experience in two or more of the following areas:</li>
<ul>
<li>RF/radar signal processing, optimization, waveform design, electronic warfare, machine learning, adaptive signal processing, AI/ML algorithm development, algorithm development, model &amp; simulation, systems engineering, test engineering, radar modelling,</li>
</ul>
<li>Experience providing technical briefs to subcontractors, senior level executives, and customers</li>
<li>Proficiency in in one or more scientific or mathematical programming languages, such as MATLAB, Python, and C/C++</li>
<li>Experienced researcher and team member who is excited to work with mission partners to leverage cutting-edge technology and research for immediate impact</li>
<li>Excellent communicator and briefer, who is comfortable communicating with both technical and non-technical audiences</li>
<li>Strong mathematical, troubleshooting, written, and verbal communication skills</li>
</ul>
Even Better:
<ul>
<li>Active Secret or TS/SCI Clearance</li>
<li>Demonstrated leadership of complex research, development, and engineering efforts   </li>
<li>Advanced degree in Electrical Engineering, Applied Mathematics, Physics, or a related technical discipline </li>
<li>Experience with:</li>
<ul>
<li>Radar and RF technologies in the defense sector, particularly for RF sensing and electronic warfare applications including electronic attack, electronic protection, cognitive EW, and advanced ESM techniques and algorithms </li>
<li>Machine learning tasks such as natural language processing, image recognition, semantic segmentation, reinforcement learning, approaches such as Bayesian, deep convolutional and graph neural network methods, and tools such as PyTorch, Ray, TensorFlow/board, and MLflow   </li>
<li>Interacting with decision-makers and customers to translate mission needs into an end-to-end solution   </li>
</ul>
<li>Ability to apply novel, innovative and interdisciplinary approaches to challenging engineering problems  </li>
</ul>
Join us and be part of a team that's making an impact at the forefront of technology and innovation.
STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us.
STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer.
STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at <a href="http://www.str.us" target="_blank">www.str.us</a> for more info.
 STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws.
If you need a reasonable accommodation for any portion of the employment process, email us at <a href="mailto:appassist@str.us" target="_blank">appassist@str.us</a> and provide your contact info.
Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

Principal Algorithm & Signal Processing Researcher

<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.
Title: Scientist -Research and Development - Drug Delivery 
Who You Are: 
We are seeking an experienced drug delivery/excipient scientist to join our team. The candidate should have experience developing novel dosage forms for the optimal delivery of small molecule drugs and/or supplements. Experience in developing technologies to improve solubility, absorption and PK are critical. Experience in oral, buccal and sublingual formulation development are a must. 
What You'll Do: 
<ul>
<li>Design formulations for solid dosage forms in nutraceutical/ natural products</li>
<li>Manage multiple development projects and develop formulations in a timely manner</li>
<li>Write protocols, master manufacturing records, and product development reports.</li>
<li>Provide support to production in process improvement and troubleshooting.</li>
<li>Stays current with recent advances and trends in the drug delivery technology and regulatory policies.</li>
<li>Other responsibilities as assigned by Senior Management.</li>
<li>Optimize emulsion formulations to achieve minimal flavor impact while maintaining excellent stability and functionality.</li>
<li>Design and optimize emulsification processes including high-pressure homogenization, sonication, and other advanced emulsification techniques</li>
<li> Scale emulsion processes from laboratory to pilot and commercial production scales.</li>
<li>Document bench scale processes and aggregate data for presentation and evaluation by R&amp;D, Production and Senior Leadership teams.</li>
</ul>
 What You'll Bring:
<ul>
<li>MS or Ph.D. degree in Pharmaceutical Sciences or chemical engineering</li>
<li>Experience with formulation equipment such as blender, fluid bed dryer, high shear granulator, tablet press and other such equipment.</li>
<li>Desire to work in a fast-paced manufacturing facility with unlimited career growth potential.</li>
<li>Experience in Pharmaceutical R&amp;D formulation or similar</li>
</ul>
Massachusetts Hiring Range$90,000—$100,000 USD
What We Offer:
<ul>
<li>Career Growth Opportunities</li>
<li>Competitive Pay and Benefits (Health, Dental Vision)</li>
<li>Generous PTO and Parental Leave</li>
<li>401(K) Retirement Plan</li>
<li>Life/AD&amp;D Insurance, Short &amp; Long-Term Disability</li>
<li>Community Involvement Initiatives</li>
<li>Employee Referral Bonuses and Product Discounts</li>
</ul>
Not all benefits listed above are available to all employees at all locations. 
Curaleaf Awards and Achievements:
<ul>
<li>2023 Ragan's Top Places to Work</li>
<li>2022 TIME100 Most Influential Companies</li>
<li>2020 Cannabis Doing Good's Good Neighbor Award</li>
<li>2020 Minorities for Medical Marijuana's Diversity &amp; Inclusion Award</li>
</ul>
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 corporate Social Responsibility is Rooted in Good. We believe in taking corporate and social responsibility very seriously, from our educational outreach to national partnerships, state-wide initiatives, and local causes. Giving back to the communities where we operate is important to us and helps to change old attitudes by showing the positive impact of cannabis in creating jobs, changing lives, and helping local communities. 
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.

Scientist -Research and Development, Drug Delivery

<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
The Sr Scientist/Technical Lead Analytical Development will be part of the Process Development group, reporting to the Director of Process Development. He/She focuses on defining and managing the execution of the analytical development strategies and activities across the program/project lifecycle supporting process development and characterization. 
The Sr Scientist owns the analytical development assay lifecycle both from a technical and planning standpoint. Responsibilities will include scientific review and oversight of assay design, development, qualification, troubleshooting, and transfer as well as product characterization. The Sr Scientist will also be responsible for ensuring oversight of the analytical project timelines, and alignment across different teams and contributors to the analytical development efforts. The Sr Scientist is also responsible for management, training, and mentorship of junior Scientists and Associates within the Analytical Development team. 
ESSENTIAL JOB FUNCTIONS
The Sr. Scientist/Technical Lead will be a contributor to the activities of the Process Development group with specific attention toward the critical activities of the team: 
<ul>
<li>Developing, qualifying and transfer of client/product-specific assays to be used for in-process, release testing, and process characterization </li>
<li>Providing analytical support to Upstream and Downstream process development team activities by ensuring consistent and timely execution of standardized platform product characterization assays, including data review, storage and trending</li>
<li>Facilitating integration of new products into Genezen analytical platforms, to ensure timely progress of transfers and timelines</li>
<li>AD team leadership including training, development and mentoring</li>
<li>Owns the development lifecycle (method development, qualification, transfer), planning and timelines for multiple projects</li>
<li>Responsible for analytical strategy and timeline definition and monitoring in line with overall project timelines and functional team input</li>
<li>Oversees the project from an analytical standpoint as core member of the project team, and has key interactions with Upstream &amp; Downstream process development, supply chain, and external consultants and vendors</li>
<li>Communicates and aligns with internal and external stakeholders' activities relevant to specific projects planning and progression</li>
<li>Prepare data overviews and reports, including interpretation of results. Proposes next steps in experimental design including rational and timelines</li>
<li>Presents project updates, progress and results to internal and external stakeholders</li>
<li>Drafts or reviews laboratory and technical documentation such as SOPs, protocols, reports, position papers and memos</li>
<li>Assist team members with their planning and coordination of activities</li>
<li>Ensure all laboratory activities are performed according to applicable procedures to ensure a safe working environment and high data quality</li>
<li>Provide improvement suggestions and enforce improvement implementation </li>
</ul>
SPECIAL JOB REQUIREMENTS
<ul>
<li>Adaptability required as work schedule may change based on business needs</li>
<li>Criminal background check required</li>
<li>Other duties as assigned</li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
MSc with 10+ years of industrial experience in a Life Sciences related field (biochemistry, molecular biology, biotechnology)
Essential
PhD with 6+ years of industrial experience in a Life Sciences related field (biochemistry, molecular biology, biotechnology)
Preferred
ON-THE-JOB EXPERIENCE

Broad knowledge of the pharmaceutical industry, including in depth operating knowledge of functions and assays relevant to viral vector therapeutic analytical within drug development processes
Essential
Demonstrated experience in project management skills and leadership experience, including setting timelines, alignment and helping others meet timelines
Essential
Prior managerial experience
Preferred
SKILLS / ABILITIES

Thorough scientific knowledge and hands-on experience with cell-based assays and bioassays, specifically in vitro potency assays
Essential
Thorough scientific knowledge and hands on experience with relevant molecular biology techniques (e.g. qPCR &amp; dPCR, DNA electrophoresis)
Essential
Thorough scientific knowledge and hands on experience with biochemical analyses (e.g. protein electrophoresis, western blotting, ELISA)
Essential
Thorough scientific knowledge in the process of assay design, assay development and trouble shooting
Essential
Experience in viral vaccines or gene therapy
Essential
PHYSICAL DEMANDS 
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
<ul>
<li>Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning</li>
<li>Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities</li>
<li>Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock</li>
<li>Occasionally exposed to extremely loud noise levels</li>
<li>Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required</li>
</ul>
Movement
<ul>
<li> Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms</li>
<li>Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 10 pounds</li>
<li>Occasionally lift and/or move up to 25 pounds</li>
</ul>
Vision 
<ul>
<li>Frequently utilize close vision and the ability to adjust focus</li>
</ul>
Communication
<ul>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

Sr. Scientist - Analytical Development

<h3>Job Description</h3>
Job Description
Xometry (NASDAQ: XMTR) powers the industries of today and tomorrow by connecting the people with big ideas to the manufacturers who can bring them to life. Xometry's digital marketplace gives manufacturers the critical resources they need to grow their business while also making it easy for buyers at Fortune 1000 companies to tap into global manufacturing capacity.
Xometry is seeking a Principal Data &amp; ML Scientist to join our Generative AI team. The ideal candidate will have a passion for advancing machine learning and generative AI capabilities, particularly for fine-tuning generative and language models, multimodal document understanding, and structured data extraction. This person will leverage their expertise in generative models and data science to develop and optimize innovative AI-driven solutions that enhance Xometry's service offerings.
Responsibilities:
<ul>
<li>Provide technical leadership to the Generative AI team, setting technical direction, defining best practices, and ensuring the team follows industry standards in AI and ML development.</li>
<li>Lead strategic planning and roadmap development for generative AI initiatives, identifying high-impact projects and aligning them with Xometry's business objectives.</li>
<li>Develop and deploy generative AI models and large language models (LLMs) for multimodal document processing, focusing on extracting structured data from technical drawings, purchasing orders, and other complex documents.</li>
<li>Lead the exploration and development of innovative text and image-based data processing solutions, including training and fine-tuning generative and language models.</li>
<li>Design and implement efficient workflows for data preparation, cleaning, and augmentation to support the training of generative AI models.</li>
<li>Utilize cloud platforms (e.g., Amazon Web Services) for large-scale data processing, model training, and deployment.</li>
<li>Collaborate with cross-functional teams, including engineering and business teams, to align generative AI solutions with business needs and drive impactful applications.</li>
<li>Mentor and guide team members on advanced machine learning techniques, model architecture design, and problem-solving strategies to elevate the team's technical capabilities.</li>
<li>Continuously experiment and iterate on model performance, tuning architectures and parameters to improve accuracy and efficiency in a fast-paced, agile environment.</li>
<li>Stay updated with the latest research in generative AI, deep learning, and multimodal data processing, incorporating best practices and advancements into model development.</li>
</ul>
Qualifications:
<ul>
<li>A bachelor's degree is required, but an advanced degree (M.S. or PhD) in computer science, machine learning, AI, or a related field is highly preferred.</li>
<li>7+ years of experience in data science and machine learning, focusing on generative models, LLMs, or computer vision.</li>
<li>Expertise in large-scale language and vision models (e.g., Transformers, GPT, VLMs).</li>
<li>Experience with multimodal data processing (e.g., combining text, image, and 3D data).</li>
<li>Proficient in Python, including key libraries such as PyTorch, TensorFlow, pandas, and numpy.</li>
<li>Strong background in probability, statistics, and optimization techniques relevant to generative modeling.</li>
<li>Familiarity with cloud computing resources and tools for model training and deployment (e.g., AWS SageMaker).</li>
<li>Familiar with software engineering principles, including version control, reproducibility, and continuous integration.</li>
<li>Experience in the manufacturing, supply chain, or similar industries is a plus.</li>
</ul>
#LI-Hybrid
Xometry is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
For US based roles: Xometry participates in E-Verify and after a job offer is accepted, will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Principal Machine Learning Data Scientist, Gen AI

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose:
Generate and analyze precise, reliable, and reproducible data in a timely manner, under the direction of a more senior scientific leader. Demonstrate experimental precision and should possess general understanding of core discipline.
Responsibilities:
<ul>
<li>Completely follow established experimental protocols and assess results with supervision.</li>
<li>Recognize and report experimental variances.</li>
<li>Apply basic scientific principles to research.</li>
<li>Learn and effectively implement new experimental protocols and/or techniques. Maintain laboratory equipment and optimize laboratory operations for efficient use of time and laboratory supplies and reagents, when appropriate.</li>
<li>Consult literature to understand scientific purpose of assignments. Impact projects predominantly through lab and/or pilot plant based activities.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree, or equivalent education.</li>
<li>Theoretical and practical knowledge to carry out job functions.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements understate or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it&nbsp;will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested,and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any otherform of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company'ssole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole andabsolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist, I

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
We are seeking a highly motivated Senior Scientist I to join the Purification Process Development group within the Operations Product Development Science &amp; Technology -Biologics organization.&nbsp; Our group is responsible for purification process development across early- and late-stage of therapeutic proteins at AbbVie Bioresearch Center in Worcester, MA.&nbsp; As one of leaders in the Purification Development group, this is a dynamic role which will drive the development and transfer of robust and effective purification processes for IND and BLA-enabling programs.&nbsp; In addition, the ideal candidate will develop and apply next generation technologies (i.e. laboratory automation / robotics, modeling, advanced data analysis) and outside-of-the-box thinking to drive efficiency of the purification lab, platforms, and strategies.&nbsp; The candidate will also coordinate and lead purification development activities within cross-functional CMC teams with a collaborative and progressive mindset. &nbsp;
This position is an onsite role in a lab-based function. To be successful candidates must enjoy and thrive in an onsite, highly collaborative lab environment with daily face-to-face cross-functional interactions between scientists.
Responsibilities
<ul>
<li>Development, optimization, scale-up, and tech transfer of purification processes for biologics candidates to support early and late-stage development &nbsp;</li>
<li>Maintain a high level of productivity and accuracy in the lab&nbsp;</li>
<li>Demonstrate creative 'out of the box' thinking to solve difficult problems and champion new technologies to achieve project goals.&nbsp;</li>
<li>Proactively seek out new tools, techniques, and strategies to implement into the overall downstream platform, specifically with respect to the use of lab automation, robotics, and the use of next gen data analytics tools (ML/AI). &nbsp;</li>
<li>Represent purification development team and actively influence development strategy on cross-functional CMC teams &nbsp;</li>
<li>Work efficiently, collaboratively, and cross-functionally toward project timelines and goals&nbsp; &nbsp;</li>
<li>Transfer processes to pilot and GMP manufacturing</li>
</ul>
<ul>
<li>Work with contract labs and carry out viral clearance studies &nbsp;</li>
</ul>
<ul>
<li>Write technical publications, reports, presentations, and regulatory filings including publishing research in peer-reviewed journals and presenting work at scientific conferences &nbsp;</li>
<li>Mentor and train junior scientists&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>Degree in Chemical Engineering, Biochemistry, Chemistry or other sciences</li>
<li>Bachelor’s degree + typically 10 or more&nbsp;years of experience OR Masters + typically 8 or more years of experience, OR a PhD&nbsp;with no experience</li>
</ul>
<ul>
<li>Must have expertise in developing standard bioprocess unit operations such as chromatography separations (resin/membrane: affinity, CEX, AEX, HIC, MM) and/or filtration operations (depth filtration, virus filtration, sterile filtration, TFF)&nbsp;</li>
</ul>
<ul>
<li>Able to independently design, execute, and interpret laboratory experiments to answer scientific questions&nbsp;</li>
</ul>
<ul>
<li>Able to independently learn, understand and execute novel/advanced scientific techniques&nbsp;</li>
</ul>
<ul>
<li>Must have excellent attention to detail and ability to keep detailed electronic lab notebook records&nbsp;&nbsp;</li>
</ul>
<ul>
<li>Proven record of authoring publications, technical reports, regulatory documents, and presentations&nbsp;</li>
</ul>
<ul>
<li>Has strong communication skills including verbal, written, and scientific data presentation&nbsp;</li>
<li>Has proficiency with Microsoft Office software, ability to learn new software applications &nbsp;</li>
</ul>
Preferred:&nbsp;
<ul>
<li>Proficient in writing methods and operating AKTA chromatographic instruments (such as AKTA Avant, AKTA Purifier, AKTA Pure, AKTA Ready or similar)&nbsp;</li>
<li>Experience with automated or robotic liquid handling systems (TECAN, Hamilton, or other) for high-throughput experimentation or sample handling and capable of driving the design of experiments using these systems.</li>
<li>Experience with analytical techniques, such as HPLC or ELISA and integration of these methods with automation tools.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

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