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<h3>Job Description</h3>
Job Description
Grow with Welch's! 
Welch's is on a journey towards our bold ambition of being the global-leader of convenient, good for you fruit-based food and beverages. To turn this goal into a reality we need you and other exceptionally talented, agile, and innovative individuals who are eager to contribute to something extraordinary!
At Welch's, we're not just offering a job; we're inviting you to be a part of a vibrant, authentic, and inclusive culture where you not only belong, but also have the opportunity to unleash the best, most authentic version of you.

Position Summary: 
The R&amp;D Coordinator provides operational, administrative, and technical support to ensure the Research &amp; Development function runs efficiently and in alignment with business priorities. This role manages business operations, budget and contract administration, purchasing workflows, system oversight, and cross-functional communication. The coordinator serves as a central point for communication, resource planning, purchasing, and data management across R&amp;D.
Success in this role requires strong attention to detail, exceptional organizational skills, and the ability to manage high-volume data and documentation with accuracy.
The R&amp;D team is a collaborative and close-knit group that values teamwork, positivity, and continuous improvement. 
Where You'll Work: 
This role will be based out of our Waltham, MA headquarters where you will be immersed in a dynamic workplace where innovation thrives and collaboration is key. 
Our company in-office schedule is designed to maximize collaboration &amp; relationship building balanced with flexibility and well-being with 3 days in office and Thursdays/Friday being remote, flex days. 
What You'll Do:
Business Coordination &amp; Operational Support
<ul>
<li>Serve as the primary business coordinator for R&amp;D, ensuring alignment with company strategies, operational goals, and cross-functional priorities. </li>
<li>Facilitate resource planning, project tracking, financial monitoring, and cost-savings initiatives, including preparing related reports, dashboards, and documentation. </li>
<li>Maintain the Airtable program and associated dashboards, ensuring accurate data, streamlined workflows, and clear visibility into R&amp;D priorities and project status. </li>
<li>Manage purchasing workflows, including PO requisitions, invoice tracking, status follow-ups, and issue resolution with internal and external partners. </li>
<li>Support R&amp;D capital projects by setting up projects in the ERP system, managing related purchasing activities, tracking invoices, and monitoring progress through installation, asset tagging, and closure. </li>
<li>Administer contracts and vendor agreements, ensuring compliance with legal and company policies, maintaining a central repository, and coordinating renewals, amendments, and expenditures. </li>
<li>Monitor vendor performance and oversee contract lifecycle activities from initiation through renewal or closeout. </li>
<li>Support budget processes by helping to build budget forecasts, tracking expenses, monitoring spending trends, identifying deviations to plan, and preparing financial summaries, and ERP-related financial workflows. </li>
<li>Maintain organized and secure files, training logs, skill matrices, databases, and confidential records with high attention to detail and data accuracy. </li>
<li>Coordinate communication and information flow between R&amp;D and cross-functional teams to ensure timely collaboration and operational efficiency. </li>
</ul>
Specialized Systems &amp; Technical Support
<ul>
<li>Manage systems such as SharePoint, SpecNet, DevEx, Accolade, Infor, and other R&amp;D platforms by configuring data, maintaining permissions, generating dashboards, and running queries. </li>
<li>Support data entry, configuration, and validation tasks associated with future ERP system transitions, ensuring high data integrity. </li>
<li>Oversee compliance requirements related to R&amp;D permits, licenses, and regulatory documentation, tracking deadlines and preparing required submissions. </li>
<li>Provide coordination support for R&amp;D safety programs, including maintaining Safety Data Sheets (SDS), managing training schedules, supporting audits, and taking meeting notes for safety committee meetings. </li>
<li>Maintain and support document management, product lifecycle management, and enterprise resource planning systems with accurate data, user access oversight, and process troubleshooting. </li>
<li>Learn and utilize generative AI tools (e.g., ChatGPT, MS Co-pilot, etc.) to automate workflows, create summaries, and increase team efficiency.  </li>
<li>Research and propose new tools and strategies to optimize team productivity.  </li>
<li>Train R&amp;D team members on emerging tools and technologies to enhance operational processes, whether through formal training sessions or informal knowledge-sharing, depending on team needs.  </li>
<li>Other duties as assigned. </li>
</ul>
Who You Are: 
<ul>
<li> A team player with a "can-do" attitude who is proactive, curious, and eager to learn. </li>
<li>Strong capacity for work and ability to handle multiple tasks efficiently. </li>
<li>Makes decisions that positively impact the current and future state of the business. </li>
<li>Develops meaningful relationships and collaborates across departments. </li>
<li>Continuously changes the status quo and seeks ways to improve and develop.</li>
<li>A collaborative mindset that fits with the positive, supportive, and fun culture of the R&amp;D team. </li>
</ul>

What You'll Need: 
<ul>
<li> 5+ years of experience in project coordination, operations, or business management role supporting technical or senior leadership teams. </li>
<li>Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment. </li>
<li>Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). </li>
<li>Demonstrated ability to work with a high level of detail, accuracy, and consistency, especially in data-heavy workflows. </li>
<li>Excellent written and verbal communication skills with demonstrated cross-functional collaboration. </li>
<li>High level of discretion when working with sensitive, confidential, or proprietary information. </li>
</ul>
Preferred:
<ul>
<li>AS or BS degree </li>
<li>Experience supporting technical or R&amp;D teams strongly preferred. </li>
<li>Experience working in a food &amp; beverage or manufacturing environment. </li>
<li>Familiarity with financial and procurement systems (e.g., Oracle or other ERP systems). </li>
<li>Proficiency with enterprise systems (SharePoint, Product Lifecycle Management tools, or equivalent). </li>
<li>Experience with AI tools for administrative and operational efficiency. </li>
<li>Experience supporting project and contract administration, video conferencing tools (Zoom, RingCentral, Teams), and budget management.</li>
</ul>

What You'll Enjoy: 
<ul>
<li>Organization with a bold, clear purpose &amp; vision for the future</li>
<li>Inclusive Culture: Be a part of an inclusive workplace where you not only belong but also have the opportunity to be the best version of yourself</li>
<li>Passionate Community: You are encouraged to have a voice, share your opinions, and have individual impact on the success of the business</li>
<li>Hybrid Work Model: Flexible &amp; collaborative work environment to maximize well-being &amp; success</li>
<li>Paid Time Off and Holidays: Enjoy time away from the office to rest and recharge</li>
<li>Paid Volunteer Time Off: 40 hours of paid volunteer time for all non-union employees</li>
<li>Development &amp; Advancement: Access to LinkedIn Learning as well as both formal and informal opportunities to develop and grow your career</li>
<li>Compensation Package Consisting of Competitive Base Salary and Annual Incentive Plan (Bonus)</li>
<li>401K plan with Generous Company Match</li>
<li>Flexible Benefits from your first day: Choose the benefits that meet your needs and preferences
<ul>
<li>Health, Dental &amp; Vision Insurance</li>
<li>Health Savings Accounts</li>
<li>Life and accident insurance</li>
<li>Employee Assistance Programs</li>
<li>Tuition reimbursement program</li>
<li>Additional benefits available through Perks at Work</li>
<li>Paid parental (and adoption) leave – Available after 12 months of employment</li>
</ul>
</li>
</ul>
The anticipated hiring base salary range for this position is $60,000 to $70,000 annually for US-based employees. This range reflects the minimum and maximum for the position across all US locations, is based on a full-time work schedule, and is Welch's good faith estimate as of the date of this posting. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. In addition to base salary, this role is eligible for participation in a bonus plan.
#LI-Hybrid

Welch's is an Equal Employment Opportunity Employer. We are committed to the prevention of employment discrimination based on race, religion, color, sex, gender identity, national origin, age, marital status, disability and/or military or veteran status, sexual orientation or any other action covered by federal or applicable state/local laws.
Welch's offers more than just a job - it's an opportunity to grow, innovate, and make a global impact with a passionate community.

R&D Coordinator

<h3>Job Description</h3>
Job Description
Our client is seeking a Product Development Scientist to develop and optimize medical nutrition beverages and powder formulations that support patient outcomes and clinical evidence. This role combines hands‑on bench formulation, ingredient research, stability testing, and cross‑functional collaboration across R&amp;D, Clinical, Manufacturing, and Marketing.
You will play a key role in advancing the company's medical nutrition portfolio, supporting new product innovation, ingredient initiatives, and regulatory compliance.
Onsite | No Visa Sponsorship | Relocation Assistance: Limited
Responsibilities:
Formulation &amp; Product Development
<ul>
<li>Execute sensory, stability, and shelf‑life studies.</li>
<li>Develop and optimize medical nutrition beverages and powders.</li>
<li>Conduct bench‑level formulation, testing, and troubleshooting.</li>
<li>Evaluate ingredient functionality, nutrient stability, and processing impact.</li>
</ul>
Cross‑Functional Collaboration
<ul>
<li>Partner with Medical Nutrition, Marketing, Sales, and Clinical teams.</li>
<li>Support clinical evidence development for new and existing products.</li>
<li>Present scientific findings at conferences and clinician meetings.</li>
</ul>
Ingredient &amp; Vendor Management
<ul>
<li>Research new ingredients and medical nutrition opportunities.</li>
<li>Manage vendor relationships and source compliant ingredients.</li>
</ul>
Regulatory, Quality &amp; Compliance
<ul>
<li>Ensure adherence to GMP, food safety, and FDA regulations.</li>
<li>Support IP protection for formulations, processes, and ingredients.</li>
</ul>
Additional Responsibilities
<ul>
<li>Perform other duties as assigned.</li>
<li>Provide scientific support across R&amp;D and manufacturing.</li>
<li>Participate in pilot plant trials and scale‑up activities.</li>
</ul>
Qualifications/Must Haves:
<ul>
<li>Familiarity with GMPs and FDA regulations.</li>
<li>Experience conducting shelf‑life and stability studies.</li>
<li>Proven bench‑level formulation and troubleshooting experience.</li>
<li>Strong understanding of ingredient functionality and nutrient stability.</li>
<li>Bachelor's degree in Food Science, Nutrition, or related field (Masters preferred; PhD/PharmD a plus)</li>
<li>5+ years of hands‑on product development experience in food, beverage, nutrition, supplement, or nutraceutical industries.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Exposure to EU regulatory frameworks.</li>
<li>Experience with PLM systems and nutritional formulation tools.</li>
<li>Experience with aseptic processing or medical nutrition products.</li>
<li>Experience in small to mid‑sized food or medical nutrition companies.</li>
</ul>

Product Development Scientist - Medical Nutrition | Ayer, MA | Onsite

<h3>Job Description</h3>
Job Description
Biocytogen is seeking highly skilled and motivated scientists to join our antibody discovery team. This role is dedicated to optimizing therapeutic antibody binders from our RenBiologics program, which generates an extensive library of therapeutic antibodies targeting thousands of druggable genes. The successful candidate will utilize advanced antibody engineering techniques to improve binding affinity, specificity, stability, and therapeutic functionality. This work supports the development of antibodies across diverse therapeutic areas, including immuno-oncology, inflammatory and autoimmune diseases, neurology, cardiovascular conditions, and metabolic disorders.

Key Responsibilities
Target Selection and Program Design
•Select and evaluate therapeutic targets with a strong understanding of MOA, druggability, and delivery options.
•Design experimental strategies to advance candidates from Biocytogen’s RenBiologics Antibody Binder/Lead Library toward therapeutic development.
Project Management
•Drive projects by assembling resources, managing timelines, and ensuring alignment with program objectives.
Antibody Engineering and Optimization
•Engineer antibodies to improve affinity, specificity, stability, and manufacturability.
•Optimize antibodies through advanced molecular designs, such as Fc engineering or bispecific formats.
 Lead Evaluation and Development
•Evaluate lead antibodies for binding, function, and developability, ensuring readiness for preclinical development.
Collaboration and Reporting
•Work with discovery, manufacturing, and BD licensing teams to advance and out-license antibody assets.
•Maintain clear documentation and present findings to internal and external stakeholders.

Requirements
•PhD in Biochemistry, Molecular Biology, Immunology, or a related field with 2+ years of relevant experience, or MS with 5+ years of experience in antibody engineering and project management.
•Strong expertise in target biology research, including understanding MOA, druggability, and formulation requirements.
•Proven experience in antibody engineering and optimization, including affinity maturation and stability improvement.
•Demonstrated ability to independently drive projects, assemble resources, and meet critical milestones.
•Excellent collaboration and communication skills for working with cross-functional teams and presenting findings effectively.
Benefits
<ul>
<li>Medical Insurance </li>
<li>Dental Insurance </li>
<li>Vision Insurance </li>
<li>Health Reimbursement Accounts </li>
<li>Life and AD&amp;D Insurance </li>
<li>Short &amp; Long Term Disability Insurance </li>
<li>401K with Company Match</li>
<li>Paid Time Off</li>
<li>Paid Sick Days &amp; Holidays </li>
</ul>

BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one’s qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Scientist/Sr. Scientist-Preclinical Antibody Drug Development

<h3>Job Description</h3>
Established nearly two centuries ago, FM is a leading mutual insurance company whose capital, scientific research capability and engineering expertise are solely dedicated to property risk management and the resilience of its policyholder-owners. These owners, who share the belief that the majority of property loss is preventable, represent many of the world’s largest organizations, including one of every four Fortune 500 companies. They work with FM to better understand the hazards that can impact their business continuity to make cost-effective risk management decisions, combining property loss prevention with insurance protection.
&nbsp;
 
Join a world-class research team dedicated to reducing the impact of natural hazards and climate risks. FM is a market leader in commercial and industrial property insurance and loss prevention, serving over one-third of FORTUNE 1000 companies with engineering-based risk management and property insurance solutions. FM helps clients maintain business continuity through state-of-the-art engineering and research.
&nbsp;
The Structures and Geohazards Research Group at FM is seeking a creative and self-motivated Senior Research Scientist with a strong foundation in wind engineering and a specialized focus on computational wind engineering (CWE). The ideal candidate will possess deep expertise in fluid dynamics, high-performance computing, and wind tunnel testing, along with a demonstrated ability to conduct innovative, high-impact research.
&nbsp;
This role is integral to a strategic research initiative aimed at advancing the understanding of wind-related hazards and developing effective mitigation strategies. The successful candidate will contribute to cutting-edge projects that blend computational modeling with experimental validation to address real-world challenges in wind engineering.
&nbsp;
Responsibilities:
Develop computational fluid dynamics (CFD) models to simulate wind flow around buildings and infrastructure, capturing complex aerodynamic interactions. Analyze wind loading on structures using high-resolution simulations; validate results with wind tunnel experiments or field measurements. Collaborate with interdisciplinary teams to incorporate wind effects into risk models, design standards, and resilience strategies. Publish and present research in peer-reviewed journals and at scientific or industry conferences. Contribute to strategic planning and innovation in wind engineering research initiatives.
 
PhD degree. Mechanical, Civil, Aerospace Engineering or related fields.
Hands-on experience with CFD software, both open-source (e.g., OpenFOAM) and commercial (e.g., ANSYS Fluent). Proficient in programming languages such as C++, Python, R, MATLAB. Skilled in high-performance computing (HPC) and parallel computing environments. Experience with wind tunnel testing or field measurements is highly desirable. Familiarity with relevant building codes and standards is a plus. Proven track record of publishing high-quality research and effectively communicating complex technical concepts to diverse audiences.Strong problem-solving abilities, creativity, and the capacity to work independently as well as collaboratively.
 The final salary offer will vary based on geographic location, individual education, skills, and experience. The position is eligible to participate in FM's comprehensive Total Rewards program that includes an incentive plan, generous health and well-being programs, a 401(k) and pension plan, career development opportunities, tuition reimbursement, flexible work, time off allowances and much more.
&nbsp;
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.

Senior Research Scientist - Computational Wind Engineering

<h3>Job Description</h3>
Company – Our client is a prominent healthcare organization operating multiple hospitals and care centers across the northeastern United States. Known for clinical excellence and patient-centered innovation, they have been consistently ranked among the top regional healthcare systems.
 
Job Title – Clinical Laboratory Supervisor – Blood Bank
Location – Melrose, MA
Role Type – Direct Hire
 
Must Have Skills:
<ul>
<li>Bachelor’s degree in Biology, Chemistry, Clinical Laboratory Science, or Medical Technology (must meet CLIA &amp; State requirements)</li>
<li>Minimum 3 years of experience as a Technologist/Technician in Blood Bank</li>
<li>Previous supervisory or leadership experience preferred</li>
<li>ASCP and/or AMT certification a plus</li>
<li>Strong working knowledge of CLIA, CAP, and state regulatory requirements</li>
</ul>
 
<ul>
<li>Responsibilities and Job Details:</li>
<li>Supervise day-to-day operations of the Blood Bank department at a leading regional hospital</li>
<li>Oversee staffing, workflow, training, and scheduling to ensure departmental efficiency</li>
<li>Ensure quality control and regulatory compliance with CLIA, CAP, and state guidelines</li>
<li>Train and mentor team members while managing performance and development</li>
<li>Perform bench work as needed to support lab operations</li>
<li>Ensure accurate and timely reporting of laboratory test results</li>
<li>Lead and participate in process improvement and quality assurance initiatives</li>
<li>Maintain and audit documentation for compliance and quality control</li>
<li>Handle administrative tasks including payroll and personnel documentation</li>
<li>Serve as liaison with other departments and external partners as needed</li>
<li>Schedule: Monday–Friday, 8:00am–5:00pm</li>
<li>Opportunity includes a $15,000 sign-on bonus for external candidates and strong potential for career advancement within a stable and growing healthcare system</li>
</ul>

Clinical Laboratory Supervisor - Blood Bank

<h3>Job Description</h3>
Company – Our client is a nationally recognized academic medical center located in the heart of Boston. Known for clinical excellence, cutting-edge research, and advanced education, this prestigious healthcare institution consistently ranks among the top hospitals in the region and is a leader in patient-centered care.
 
Job Title – Laboratory Supervisor – Blood Bank
Location – Boston, MA
Role Type – Direct Hire
 
Must Have Skills:
<ul>
<li>Minimum 5 years of experience as a Technologist/Technician</li>
<li>Previous Senior or Lead Technologist experience preferred</li>
<li>Associate’s degree in a Chemical or Biological Science, Clinical Laboratory Science, or Medical Technology (Bachelor’s preferred)</li>
<li>ASCP or AMT certification preferred</li>
<li>Strong knowledge of CLIA, CAP, and state laboratory regulations</li>
</ul>
 
Responsibilities and Job Details:
<ul>
<li>Supervise daily operations of the Blood Bank department, ensuring accuracy and timeliness of testing and reporting</li>
<li>Oversee staffing schedules, performance, and training of lab personnel</li>
<li>Maintain compliance with all applicable regulations including CLIA, CAP, and state requirements</li>
<li>Perform bench work as needed and ensure adherence to laboratory protocols</li>
<li>Participate in continuous process improvement initiatives</li>
<li>Coordinate with leadership to uphold high standards of patient care and safety</li>
<li>Provide mentorship and leadership to laboratory technologists and technicians</li>
<li>Ensure proper documentation and reporting within the lab information system</li>
<li>Monitor inventory and order supplies as needed for uninterrupted operations</li>
<li>Ensure readiness for inspections and audits by regulatory bodies</li>
<li>Schedule: Monday–Friday, 3:00pm–11:30pm with rotating weekends</li>
</ul>

Laboratory Supervisor - Blood Bank

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
The Immunology R&amp;D organization is hiring for its early discovery team in Cambridge, MA. 
</li>
<li>
We are seeking a highly motivated contractor with a passion for learning and excellent attention to detail to join the Functional Immunology and Innovative Technologies team.
</li>
<li>
This scientist will specifically support target identification and validation efforts through various profiling methods and functional experiments in collaboration with different teams within immunology discovery.
</li>
<li>
Our team is seeking a candidate with existing academic or industry experience in molecular biology, preferably NGS technologies, and who is willing to learn and develop new techniques and learn deep analysis using different approaches.
</li>
<li>
Candidates will be expected to have experience with RNAseq library preparation workflows and experience with ligand-based assays like ELISAs, as well as routine lab techniques such as DNA/RNA extraction, nucleic acid QC, and PBMC isolation and handing.
</li>
<li>
Execute RNAseq library preparations and QC generated libraries using Tapestation/Qubit instruments.
</li>
<li>
Prepare libraries for sequencing and operate Illumina sequencers understanding output and troubleshooting where necessary.
</li>
<li>
Perform multiplexed secreted factor measurements using Luminex.
</li>
<li>
Perform functional experiments with primary human immune cells including stimulation and cell culture.
</li>
<li>
Accurately document project and sample information, protocols, and experimental details through the Electronic Lab Notebook (ELN)
</li>
<li>
Conduct experiments, troubleshoot, and optimize protocols independently and in collaboration with colleagues to deliver high-quality data in a timely fashion.
</li>
<li>
Interpret findings and communicate effectively to present scientific data, concepts, and recommendations to various internal audiences.
</li>
<li>
Interface with computational biologists and data scientists to generate and interpret RNAseq datasets.
</li>
<li>
Work in matrixed environment and support activities for different groups across the organization, which may include alignment meetings.
</li>
</ul>
Qualifications:
<ul>
<li>
Bachelor's Degree or equivalent education with typically 5 years of experience, or Master's Degree or equivalent education with typically two years of experience.
</li>
<li>
Strong background in basic molecular biology and/or genomics with proficiency in molecular biology lab techniques such as DNA/RNA extraction and nucleic acid QC, as well as familiarity with primary human cell handling and culture.
</li>
<li>
Builds strong relationships with peers and cross functionality with partners outside of the team to enable high performance.
</li>
<li>
Learns fast, grasps the "essence", and can change course quickly where indicated.
</li>
<li>
Raises the bar and is never satisfied with the status quo.
</li>
<li>
Creates a learning environment, open to suggestions and experimentation for improvement.
</li>
<li>
Embraces the ideas of others and nurtures innovation to make possibilities real.
</li>
<li>
Experience with RNAseq workflows including library preparation and QC is require
</li>
<li>
Experience handling PBMCs, primary cells, and/or tissues is required
</li>
<li>
Background in biology, immunology, molecular biology, or other related field
</li>
<li>
Experience with ligand-based assays such as ELISA, MSD or Luminex.
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Experience running end-to-end bulk RNAseq libraries and sequencing.
</li>
<li>
Experience with complex cell cultures and stimulations is preferred.
</li>
<li>
Familiarity with 10X Genomics platforms, particularly scRNAseq and/or scATACseq, is preferred.
</li>
<li>
Background in R is a plus but not required.
</li>
<li>
Background in immunology is a plus but not required.
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Scientist

<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're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics.

We are seeking a Senior Research Associate to join our DNA &amp; Strain Construction team in Boston, MA. The ideal candidate will have a proven track record designing and constructing plasmids, using different assembly strategies. They will be a key contributor to our team, working closely with other DNASC team members using the latest molecular biology and automation techniques to help advance our high throughput DNA construction pipeline, at the same pushing the limits of DNA assembly capabilities. They will also work closely with Asimov’s Synthetic Biology, High Throughput and Cell Line Development teams. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the foundation for engineering biology.

About the Role:
<ul>
<li>
Conduct PCR, Golden Gate or Gibson Assembly, plasmid purification, and sequencing prep to validate DNA constructs, both manually and in high-throughput using liquid handlers (e.g., Echo, Bravo, Hamilton STAR) following Standard Operation Procedures (SOPs)
</li>
<li>
Contribute to vector assembly design, and remediation plans.
</li>
<li>
Work with your manager to generate regulatory reports to support our customers’ needs.
</li>
<li>
Maintain accurate sample tracking and documentation in LIMS to ensure data integrity and reproducibility.
</li>
<li>
Assist with large-scale plasmid preparations (LSPs) to support internal and external projects.
</li>
<li>
Collaborate with scientists and other RAs to troubleshoot workflows, improve efficiency and develop new initiatives within the team.
</li>
<li>
Work as part of a multifunctional team, you’ll partner with synthetic biologists on the DNASC team as well as members of the Cell Line Development, Synthetic Biology and Software Development teams.
</li>
</ul>

About You:
<ul>
<li>
You have a B.S. or M.S. degree in biology, biochemistry, biological engineering, or a related field.
</li>
<li>
Deep bench experience is necessary to be successful in this role, and you will have 3+ years of biopharma experience.
</li>
<li>
You value teamwork and are motivated to contribute to the team’s goals.
</li>
<li>
Working as part of a highly integrated research team is exciting to you.
</li>
<li>
Automation experience is a plus but a desire to learn to develop automation of lab experiments is a must.
</li>
<li>
You will have independently or collaboratively designed an assembly plan to generate plasmids using either Gibson or Golden Gate.
</li>
<li>
You have experience, outside of coursework, with modern molecular biology and/or microbiological techniques such as various DNA assembly methods (Golden Gate, Gibson), PCR, colony picking, and DNA preps.
</li>
<li>
Being detail-oriented isn’t just a sound bite for you, it’s part of your DNA.
</li>
<li>
Experience with optimizing cloning protocols (PCR, Gibson, and especially Golden Gate) and basic mammalian cell culture techniques is a plus.
</li>
<li>
Experience extracting data using scripts from large databases or desire to learn is a plus.
</li>
<li>
We’re big on tools here! We’re happy to train you but if you know your way around Benchling, LIMS, Google Drive, and Excel, it’ll help you come up to speed quickly.
</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: $85K - $90K

Senior Research Associate, DNA & Strain Construction

<h3>Job Description</h3>
Job Description
Dynamis is seeking a Junior Open-Source Intelligence Analyst to support Immigration and Customs Enforcement in Williston, VT and Santa Ana, CA by performing analysis of information sources to obtain real-time and mission critical person-specific information.
Responsibilities:
<ul>
<li>Analysts will perform research and analysis on a myriad of data sources and initiate leads. </li>
<li>Screen, prioritize, and develop leads on incoming cases.</li>
<li>Enter leads into the leads management system of record.</li>
<li>Identify key targeting data (e.g., addresses, vehicles, places of employment, associates, etc.); collect and include additional intelligence of value to officer and operational safety, pattern(s) of travel, and potential criminal activity/criminal indicators.</li>
<li>Ensure data fields in the system of record are updated, accurate, and complete. Attach pertinent photographs, reports, and correspondence. Once entered, leads will be reviewed by PERC or NCATC federal staff for accuracy, quality, and completeness before disseminating them to ICE Field Offices.</li>
<li>Develop and/or enhance leads as directed by TOD staff or according to established priorities.</li>
<li>Use digital methods to conduct all source and open-source research and analysis on matters of national security in support of ongoing investigations.</li>
<li>Assess foreign and domestic-based, publicly available information to identify trends, patterns, and relationships that provide unique insights to address intelligence requirements.</li>
<li>Exploit data from specific sources and raw intelligence and compile them to validate intelligence collection requirements.</li>
<li>Identify trends, detect high-risk areas for weapons proliferation, and prioritize enforcement approaches by applying research and advanced analytics.</li>
<li>Deliver accurate, complete, and timely data to users across the organization.</li>
<li>Work with sensitive information within the guidelines of statutes, regulations, and policies governing the customer. As detailed in the Terms and Conditions, all personnel will be required to obtain at least a Public Trust High adjudication.</li>
<li>Answer and track incoming phone calls and elicit details from the caller to identify possible allegations and specific actionable information. </li>
<li>Maintain confidentiality of information.</li>
<li>Review web tips received online to identify possible allegations and specific actionable information. </li>
<li>Compare viable tips to existing information and process as necessary. </li>
<li>Analyze content of phone and web tips to determine if allegation is within ICE jurisdiction; as dictated by current procedure, policy, or instruction. </li>
<li>Perform research in sensitive, law enforcement, DHS, and open-source databases to identify reported subjects, immigration status, and criminal history. </li>
<li>Accurately document information received from a tipster and reference findings obtained from law enforcement or open-source systems. </li>
<li>Write detailed reports to document research results, identify the appropriate field office for report dissemination and upload the report into the required database.</li>
</ul>
Requirements:
<ul>
<li>U.S. Citizenship</li>
<li>Ability to obtain ICE suitability (current ICE or DHS suitability is preferred).</li>
<li>Education/Experience:
<ul>
<li>Bachelor's degree or higher and one year of experience performing primarily social media, and open-source information research, targeting, and analysis; or,</li>
<li>Associate's degree and two years of experience performing primarily social media and open-source information research, targeting, and analysis; or, </li>
<li>High school diploma or GED and three years of experience performing primarily social media and open-source information research, targeting, and analysis.</li>
</ul>
</li>
<li> Shall provide support in accordance with NCATC duty hours (i.e., Monday through Friday 7:00 am to 6:30 pm (Eastern Time) or PERC duty hours (24x7, 365 days per year). </li>
<li>Work hours are to be aligned with the NCATC's and PERC's established hours.</li>
<li>Work is deemed mission essential and will be expected to continue during government shutdowns. </li>
<li>Telework and remote work are not generally authorized. However, in extenuating circumstances, telework and remote work may be authorized on a case-by-case basis with written telework authorization by the COR in accordance with agency policies.</li>
</ul>
Preferred:
<ul>
<li>Current or recent experience providing open-source analytical support for DHS or other US Government clients</li>
<li>Watch Center or similar threat monitoring experience</li>
<li>Federal law enforcement experience</li>
</ul>

Open-Source Intelligence Analyst

<h3>Job Description</h3>
Job DescriptionenGene (NASDAQ: ENGN) is a late-stage biotechnology company mainstreaming genetic medicines through the delivery of therapeutics to mucosal tissues and other organs, whose lead product candidate, detalimogene voraplasmid, is being evaluated in an ongoing pivotal study for patients with non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ (Cis) who are unresponsive to BCG. Detalimogene voraplasmid was developed using enGene’s PROPRIETARY, Dually Derivatized Oligochitosan (DDX) platform, which enables penetration of mucosal tissues and delivery of a wide range of sizes and types of cargo, including DNA and various forms of RNA. For more information, visit enGene.com.RoleenGene Inc. is seeking curious, passionate, and motivated Senior Scientist who will play a key role in the analytical group. In collaboration with others in the team, you will be an integral part of developing an exciting new gene therapy technology. You will be responsible for overseeing the analytical aspects of technology transfer, method validation, regulatory filing and ensuring compliance with regulatory requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES
<ul>
<li>Analytical Transfer, Validation and lifecycle management:</li>
<li>Collaborate with cross-functional teams within enGene and at our CMOs; including R&amp;D, Quality Control, Quality Assurance, Regulatory affairs, Manufacturing, to ensure robustness of analytical methods used and high quality of the product delivered to the patients.</li>
<li>Identify and mitigate potential risks during technology transfer processes.</li>
<li>Develop and implement strategies for analytical method validation in compliance with regulatory guidelines (e.g., FDA, EMA).</li>
<li>Coordinate and liaise with external vendors and partners involved in the validation process.</li>
</ul>
 Regulatory Compliance:
<ul>
<li>Stay abreast of relevant regulatory requirements and guidelines pertaining to analytical methods and technology transfer.</li>
<li>Ensure that all activities adhere to cGMP, ICH, and other relevant regulatory standards.</li>
<li>Prepare and review documentation for regulatory submissions related to analytical methods and validation.</li>
</ul>
EDUCATION AND EXPERIENCE
<ul>
<li>Advanced Degree: M.Sc. (or Ph.D.) in Analytical Chemistry, Polymer Science, Biochemistry, or a related discipline, with a minimum of 8 years of relevant experience in late-phase development (e.g., PPQ, commercialization) within Pharma/Biotech industry; or B.Sc. in the same fields with at least 10 years of relevant experience.</li>
<li>Analytical Method Validation Expertise: Strong understanding of validation principles, including specificity, linearity, limits of detection and quantification, range, accuracy, precision, robustness, and stability.</li>
<li>Regulatory Documentation Experience: Proven track record in preparing documents for regulatory submissions (FDA, health Canada, EMA) such as IND, IMPD and BLA.</li>
</ul>
SKILLS
<ul>
<li>Experience with analytical methods like HPLC, GPC (SEC), LC/MS, FTIR, UV-vis, fluorescence spectroscopy, DLS, Karl Fischer titration, and gel electrophoresis (CE, AGE) are great assets.</li>
<li>Strong critical thinking, analytical and troubleshooting skills.</li>
<li>Extensive experience with cGMP and guidelines (ICH, FDA, EMA, Health Canada).</li>
<li>Experience working with nucleic acids and/or polymers preferred</li>
</ul>
Location: USA Boston Massachusetts&nbsp;Salary: The salary range for this role is $150,000-$165,000The base salary range provided represents a good faith estimate of the compensation for this position at the time of posting. Actual compensation will be determined based on a number of factors, including, but not limited to, relevant skills, experience and education.&nbsp;enGene USA Inc. 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. At enGene USA Inc., we are building a community of intelligent and passionate team members that share our Vision, Mission, and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability. 
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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