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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 DescriptionCompany Description 
Eurofins Scientific is a global leader in life sciences, providing comprehensive analytical testing services to ensure the safety, authenticity, and quality of products across multiple industries. From food and water to pharmaceuticals and cosmetics, our work helps make life and the environment safer, healthier, and more sustainable.
Job Description 
We are seeking a detail-oriented Analytical Lab Associate to support particulate testing of pharmaceutical drug products. This role involves performing qualified analytical methods, troubleshooting, and contributing to CMC activities in a fast-paced, collaborative environment. You will work onsite at a client facility in Boston, MA, starting January 2026.
Key Responsibilities
<ul>
<li>Perform batch and stability testing using qualified particulate analysis methods.</li>
<li>Troubleshoot and resolve testing-related issues.</li>
<li>Maintain accurate documentation in electronic laboratory notebooks (ELN).</li>
<li>Review and report analytical data; participate in audits.</li>
<li>Support assay development, qualification, and technology transfer.</li>
<li>Ensure compliance with GLP, cGMP, and EHS guidelines.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Chemistry or related field; 0–2 years of industry experience.</li>
<li>Hands-on experience with microscopy techniques (FIM, SEM, fluorescence) preferred.</li>
<li>Familiarity with particle characterization methods (e.g., Raman) and counting techniques (e.g., light obscuration).</li>
<li>Knowledge of cGMP/GLP and regulatory requirements.</li>
<li>Strong attention to detail and documentation skills.</li>
<li>Ability to thrive in a fast-paced, collaborative environment.</li>
<li>Authorized to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
Position is full-time, Monday - Friday, 8:00 am - 5:00 pm.&nbsp; Candidates currently living within a commutable distance of Cambridge, MA, are encouraged to apply.
<ul>
<li>Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Compensation is between 23.00-29.00 per hour, depending on education and experience&nbsp;</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Analytical Lab Associate - Pharmaceutical Particulates

<h3>Job Description</h3>
Job Description
Description: CBSET, Inc. is a recognized leader in preclinical biomedical research. We make it our mission to help our sponsors accelerate the development of novel and innovative pharmaceuticals, biotechnologies, and medical devices. CBSET offers extensive regulatory and scientific expertise to the Medtech and biopharma industry around the globe in order to rapidly transform early-stage concepts into novel therapies.
 
By working as an InVivo Research Technician I/II/III, you will be part of a collaborative effort with our clients to advance biomedical research through innovative, high-quality services. In addition, CBSET is proud to offer a generous benefits package, which includes health, dental and vision plans, life insurance, short-term and long-term disability, and an opportunity to participate in a 401(k) plan.
 
Please be aware that the requirements presented within this job listing are the basic qualifications required for the InVivo Research Technician position; however, the job title will be contingent upon the level of experience of the candidate in those requirements. This is also for the PM position (shift begins at noon).
 
BASIC SUMMARY: An entry-technical level with the expectations of supervised functionality, demonstrating a comfortable level of technical skills in the Veterinary Services and Technical Operations Department Vivarium.
 
ESSENTIAL DUTIES AND RESPONSIBILITIES:
<ul>
<li>Handle and restrain multiple species of animals, perform and record daily clinical observations, perform anesthetic management, pre and post-operative nursing care, perform dose administration and sample collection</li>
<li>Generate and manage data in compliance with GLP guidelines, document deviations and incidents with supervision, submit data in a timely manner</li>
<li>Perform data collection and quality control on assigned studies</li>
<li>Must have effective oral and written communication skills and work effectively as a team member</li>
<li>Perform other related duties as required</li>
</ul>
Qualifications:
<ul>
<li>A minimum of one year of experience in a regulatory pre-clinical environment with involvement in the conduct of GLP studies</li>
<li>Certification/Licensure: Driver’s license; CVT, ALAT and/or LAT preferred</li>
<li>Education: High school or GED required. Associates (AS) or Bachelor’s degree (BS) preferred; CVT preferred</li>
<li>Experience: Minimum of one year experience in a regulatory pre-clinical environment with involvement in the conduct of GLP studies</li>
<li>Certification/Licensure: Driver’s license; CVT, ALAT and/or LAT preferred. Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus. Ability to consistently lift and move at least 50 pounds.</li>
<li>PHYSICAL DEMANDS: Must be able to perform laboratory procedures, which require talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (Personal Protective Equipment) according to OSHA regulations and company standards.</li>
</ul>
Benefit Conditions:
<ul>
<li>Only full-time employees eligible</li>
</ul>
Work Remotely
<ul>
<li>No</li>
</ul>
Job Type: Full-time

InVivo Research Technician

<h3>Job Description</h3>
Job Description
Are you detail-oriented and passionate about maintaining high-quality standards in a fast-paced environment? We're looking for a fill-time Post Processing Technician I to join our team in the Processing Department. Available shifts include Monday through Friday 7:30AM - 4:00PM or Friday through Monday 7:00AM - 5:30PM. This position plays a vital role in supporting the post-processing process, ensuring compliance, and maintaining product quality from start to finish. If you're excited to work with a dedicated team in a dynamic setting, this could be the perfect opportunity for you!
As a Post Processing Technician I, you will be responsible for performing routine tasks across all processing areas, working under the guidance of the Processing Supervisor and Post Processing Technician III. Your responsibilities will include conducting green waste disposal processes, trimming batches by hand and machine, and assisting with the dry and cure processes. You'll play a role in maintaining quality control measures, ensuring batches meet product standards, and supporting inventory management by keeping accurate records. In addition, you will be expected to keep your workspaces and machinery clean, sanitized, and organized to maintain operational efficiency.
Previous experience is preferred but not required. The ideal candidate will have a keen eye for detail and the ability to focus on sensitive and complex tasks. Strong verbal and written communication skills, flexibility, and adaptability are essential to succeed in this role. You must be able to stand for extended periods, lift up to 50 lbs occasionally, and perform manual tasks requiring fine motor skills. Safety is a priority, and you will be required to maintain balance while using ladders or performing tasks such as stooping, kneeling, or reaching.
If you're ready to be part of a supportive team in an evolving environment and are excited about contributing to our post-processing process, we encourage you to apply today!

Post Processing Technician 1

<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
Wildlife Exclusion Assistant
The Wildlife Exclusion Assistant plays a crucial role in supporting the Wildlife Exclusion team in ensuring that properties are securely protected from wildlife intrusions. This position involves working closely with the Lead Technician, primarily assisting with tasks from the ground while the technician works at height. The role requires attention to detail, safety, and teamwork. This position is an excellent opportunity to start your career with Freedom Pest Control, with potential for growth and advancement within the company.
Key Responsibilities:
<ul>
<li>Support the Exclusion Technician: Assist the Lead Technician by providing tools, materials, and assistance from the ground to ensure efficient and safe operations on ladders or elevated workspaces.</li>
<li>Material Handling: Prepare, carry, and organize materials such as exclusion barriers, sealants, and other necessary tools for the day's work.</li>
<li>Site Preparation and Cleanup: Ensure the work area is prepared and maintained throughout the job, including setting up safety zones, organizing tools, and cleaning up the site after work is completed.</li>
<li>Wildlife Exclusion: Assist in the installation of exclusion materials, including inspecting potential entry points, measuring and cutting materials, and applying sealants under the direction of the Lead Technician.</li>
<li>Safety Compliance: Follow all safety protocols, including proper use of personal protective equipment (PPE), ladder safety, and maintaining a clean and organized work environment to prevent accidents.</li>
<li>Communication: Maintain clear and effective communication with the Lead Technician to ensure the smooth progression of work tasks and address any issues that arise during the job.</li>
<li>Customer Interaction: Occasionally interact with customers, providing updates on the work process and addressing any concerns in a professional manner.</li>
<li>Equipment Maintenance: Assist in the maintenance and care of all tools and equipment used in wildlife exclusion tasks, ensuring they are in good working condition.</li>
</ul>
Qualifications:
<ul>
<li>High School Diploma or GED.</li>
<li>Previous experience in a hands-on role, such as construction, maintenance, or other physically demanding jobs, is preferred.</li>
<li>Comfortable with outdoor work in various weather conditions.</li>
<li>Physical ability to lift 50 pounds and work on your feet for extended periods.</li>
<li>Strong communication skills and the ability to work effectively as part of a team.</li>
<li>Attention to detail and a commitment to safety.</li>
</ul>
Work Environment:
<ul>
<li>The role involves working outdoors and may include exposure to various weather conditions, heights, and wildlife.</li>
</ul>

Wildlife Exclusion Assistant

<h3>Job Description</h3>
Job Description
Title: Research Scientist – Animal Studies Location: Marlborough, MA (Hybrid) Contract Length: 6-12 months with possibility for extension/conversion
General Description
<ul>
<li>Experience with benchtop models using phantoms.</li>
<li>Participation in preclinical investigations with tissue collection and biologic metrics.</li>
<li>Familiar with numerical models with finite element methods.</li>
<li>Skills on data collecting, analyzing, interpreting, and communicating experimental results to the team and organization.</li>
</ul>
Responsibilities and Duties
<ul>
<li>Collaborate with the research team to develop experimental methodologies in benchtop, numerical, and preclinical methodologies.</li>
<li>Execute benchtop and preclinical trial investigations, including collection, analysis, interpretation, and distribution of research findings.</li>
<li>Capacity to integrate research outcomes into meaningful technological advances.</li>
<li>Support regulatory submissions.</li>
<li>Generation of reviews supporting technical documentation and product development phases.</li>
<li>Contribute to the generation of intellectual property for the company.</li>
<li>Interaction with third-party service research providers.</li>
<li>Compilation and analysis of research data for scientific publications and technical writing.</li>
<li>Attendance at relevant scientific conferences and meetings.</li>
</ul>
Requirements
<ul>
<li>Advanced degree in Engineering, Biomedical Engineering, or a related scientific field. A PhD is highly valued.</li>
<li>Previous participation in a multidisciplinary project including benchtop, numerical, and preclinical. Experience pulsed electric fields and electroporation applications is highly valued.</li>
<li>Basic knowledge of electricity, mechanic, human anatomy and physiology.</li>
<li>Self-driven skills for execution and education.</li>
</ul>

Research Scientist- Animal Studies

<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 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:
We invite early-career scientists to apply for the Associate Scientist II position within the Operations PDS&amp;T Biologics Scientist Development Program (SDP) at AbbVie. In this 3-year program, you’ll help advance AbbVie’s First-in-Human (FiH) biologics pipeline by generating and analyzing reliable data within two core functions of the FiH workflow, working under the guidance of senior scientific leaders. This position offers a fast-paced, hands-on environment and the opportunity to develop your skills while contributing to meaningful therapies that improve patient lives. If you are motivated to learn and make a difference in biologics development, we encourage you to join our team.
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>Interest in learning and implementing new digital or data management capabilities.</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, biological compounds, and GxP compliance.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Chemical Engineering, Biology, Chemistry, Biochemistry, Biotechnology,</li>
</ul>
or a related scientific discipline, or equivalent education
<ul>
<li>Typically, 3 or more years’ relevant experience, or Master’s degree (or equivalent education)</li>
</ul>
with no additional experience required
<ul>
<li>Sound theoretical and practical understanding necessary to perform the job functions</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience or education in enabling new digital or data management capabilities</li>
<li>Knowledge of programming languages (e.g., Python, R), artificial intelligence/machine learning (AI/ML), and/or cloud platforms (e.g., AWS, GCP)</li>
<li>Demonstrated motivation to learn, innovate, and contribute as an early-career scientist</li>
</ul>
 Additional Information 
All your information will be kept confidential according to EEO guidelines.
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>
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