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<h3>Job Description</h3>
Job Description
Nanobiosym is an innovative nanotechnology company in Cambridge, MA, developing novel technologies to address a broad range of diseases. Nanobiosym was founded by an MIT/Harvard alum to work at the interface of physics, nanotechnology, and biomedicine. Nanobiosym was awarded the 2013 X-PRIZE- the first X-PRIZE ever awarded for healthcare.
DUTIES
<ul>
<li>Lead molecular diagnostic assay development in a hands-on manner through successful FDA submission</li>
<li>Manage and contribute to regulatory documents</li>
<li>Project management; personnel management skills preferred</li>
<li>Design assay performance specifications</li>
<li>Ensure assay development process meets milestones and timelines</li>
<li>Troubleshoot and solve technical issues</li>
<li>Maintain compliant laboratory documents and procedures</li>
<li>Pro-actively improve efficiency, quality and effectiveness of R &amp; D efforts</li>
</ul>
QUALIFICATIONS
<ul>
<li>PhD in Nucleic Acids Biochemistry, Molecular Biology, or related field</li>
<li>Minimum of 7 years of relevant industry experience and IVD assay development</li>
<li>In depth knowledge and hands on experience with qPCR, sequencing and standard molecular biology techniques</li>
<li>Demonstrated technical, managerial and leadership expertise in assay development</li>
<li>Strong understanding of FDA and global regulatory requirements</li>
<li>Prefer commercial assay experience</li>
<li>Demonstrated experience and understanding of quality systems (e.g., GLP, ISO, etc.)</li>
<li>Prefer experience working in BSL-2 laboratory facilities</li>
<li>Strong work ethic and ability to generate high quality work under tight deadlines</li>
<li>Flexibility in work schedule</li>
<li>Self-motivated, independent and a driving force of efficient execution</li>
<li>Strong organizational and project management skills</li>
<li>Excellent oral and written communication skills</li>
</ul>
 Job Posted by ApplicantPro

Senior Scientist: IVD Assay Developer

<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 
The Analytical Research &amp; Development team is seeking a talented, highly motivated candidate with experience in the characterization of peptide and oligonucleotide biomolecules.&nbsp; The successful candidate will be responsible for leading the design, development, and implementation of analytical methods for the characterization of peptides/oligonucleotides using advanced analytical techniques, with an emphasis on high order characterization.&nbsp; We are looking for diverse candidates with strong scientific and leadership experience to join the AbbVie Analytical R&amp;D team and can offer exciting and rewarding career opportunities for these candidates. The ideal candidate will have significant CMC expertise in analytical development for biomolecule therapeutics. The candidate will be responsible for assisting with the development and execution of analytical methods to support CMC and will participate in phase-appropriate characterization of material and products at all stages of the development process, as well as monitoring completion of tasks and projects.
Responsibilities:
<ul>
<li>Lead development and implementation of advanced analytical characterization methods to support complex peptide and oligonucleotide development programs.&nbsp;</li>
<li>Utilize cutting-edge structure elucidation techniques (e.g., high-resolution, tandem mass spectrometry) to characterize a wide range of modalities across AbbVie’s pipeline, including oligonucleotide, peptide, and small molecule APIs, starting materials, intermediates, and impurities.</li>
<li>Lead cross-functional teams and collaborate with multi-disciplinary experts to develop strategies to enable the structure elucidation aspects of a project to advance programs through the development pipeline.</li>
<li>Advance scientific expertise beyond ARD organization. Proactively advise and share knowledge and expert opinions with subordinates, peers, and senior management. Mentor and train colleagues and assesses current and emerging business challenges enabling functional goal achievement.</li>
<li>Ensure quality and effectiveness of key results of major project plans through sound design, early risk assessments, and implementation of fallback strategies.</li>
<li>Source and identify emerging scientific trends in the field of molecular characterization of therapeutics from internal and external sources and assess relevance. Integrate trends into functional short-term objectives. Advance cross discipline technology and direction within area of discipline.</li>
<li>Apply imagination and innovation by creating, inventing, and implementing new or better approaches, alternatives and breakthrough ideas across disciplines.</li>
<li>Make significant contributions to project team and deliver results in a team-oriented setting and will work across scientific disciplines to drive programs through critical milestones.</li>
<li>Generate new scientific proposals and lead those efforts. Anticipate and critically evaluate scientific or regulatory advances and respond with appropriate new strategies.</li>
</ul>
Qualifications 
<ul>
<li>PhD (with 10+ years’ experience) in scientific discipline (e.g., Analytical Chemistry, Biochemistry, Chemical Biology or related field) with previous laboratory experience.</li>
<li>Deep understanding of peptide and/or oligonucleotide characterization, including higher order structure, chiral identification, and comparability assessments by mass spectrometry and other biophysical techniques (e.g. optical spectroscopy, structure, and binding).&nbsp; Experience in biomolecule analysis and interpretation by NMR spectroscopy a plus.</li>
<li>Practical experience and strong knowledge of LC separations (e.g., IP-RP LC, SEC), capillary electrophoresis, and other separation techniques as applied to peptide/oligonucleotide analysis.</li>
<li>Must possess demonstrated experience in peptide/oligonucleotide chemistry and biochemistry, particularly in the high order characterization activities &nbsp;related to drug development process and formulation characterization.</li>
<li>Experiences with the project leadership in the development of peptides and traditional small molecule modalities.</li>
<li>Proven ability to innovate with a history of new or improved product release.</li>
<li>High-quality written and oral communication skills and ability to interact effectively with interdisciplinary scientists and engineers.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;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>

Senior Principal Research Scientist, Analytical Chemistry

<h3>Job Description</h3>
Job DescriptionDescription:
At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively and completely eliminate the root causes of autoimmune and allergic diseases, and to achieve deep, durable responses while preserving essential immunity. We are looking for passionate individuals to join our mission to transform treatment paradigms across the spectrum of antibody-driven diseases.
 
We are looking for a self-motivated and intellectually curious Scientist/Senior Scientist to join our Biology/in vitro pharmacology group. The role will support pre-clinical efforts to characterize mechanism-of-action of therapeutics aimed at treating antibody-driven diseases. The ideal candidate is skilled lab-based in vitro biologist with a strong background in immunology and/or biologics drug discovery who can drive forward projects that serve multiple programs. 
 
Responsibilities:
<ul>
<li>Help drive multiple autoimmune programs to Development Candidate and IND</li>
<li>Design and execute in vitro experiments to support preclinical drug discovery including disease modeling, and mechanism-of-action studies to deeply characterize our molecules.</li>
<li>Collaborate with internal groups and lead study design for external CRO-based work, including biochemical analyses and in vivo studies</li>
<li>Independently develop and execute quantitative assays (ELISAs, cell proliferation assays, etc.) to support molecule progression to DC and IND.</li>
<li>Managing inventory and testing of patient samples that support multiple pre-clinical programs</li>
<li>Interpret, summarize and present research findings in internal scientific meetings as part of our collaborative learning culture.</li>
<li>Proactively review literature to bring newest scientific findings, ideas and technologies for discovery research</li>
</ul>
Requirements:
<ul>
<li>PhD in with 0-3 years, a Masters with 6+ years, or a Bachelors with 8+ years of post-graduate academic or industry experience in relevant scientific fields such as immunology, cell/molecular biology or signal transduction</li>
<li>Experience culturing and assaying human and mouse immune cells and cell lines using standard cell biology and molecular techniques (flow cytometry, ELISAs, Western Blot, PCR) is required.</li>
<li>Experience culturing primary human B cells is a plus, as is experience designing viral vectors to express antigen receptors (particularly BCRs) and characterizing downstream signaling. </li>
<li>Ability to work within a dynamic, matrixed environment.</li>
<li>Excellent written and verbal communication skills, as well as strong organizational and problem-solving abilities.</li>
</ul>
Merida Biosciences is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
 
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.

Scientist/Senior Scientist, Biology

<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
Director of Research and Development - Medical Device Greater Boston (0n-site role) Sorry, relocation and sponsorship are NOT provided. The Director, R&amp;D Engineering is a hands-on leader and will oversee all development and sustaining efforts including the continued evolution of the companys breakthrough aesthetic skin technology, refinement and further development of thecompany'score platform technology, and the development of commercial products from early-stage product concepts through supportingaftermarket launch. This position is responsible for partnering with commercial, regulatory, clinical, and operations, including early supply chain, design transfer from R&amp;D to Manufacturing, any in-house R&amp;D manufacturing efforts as well as project management and interfaces with external resources.
The Director, R&amp;D Engineering, is expected to lead and drive a team of professionals, across the organization, driving employee development, teamwork, and innovation.
In this role, youwill be responsible for:
<ul>
<li>Directing mechanical design, hardware, software developmentto ensure high-quality innovative products.</li>
<li>Leading engineering teamsto promote a high-performance and results-driven environment. Monitoring and leading a team of engineersto meet project timelines and ensure effective development of new products</li>
<li>Work with marketingin developing a strong product pipeline and formulating long-term strategies for new technologies.</li>
<li>Contribute toFormulateand implement a long-term strategy fornew and emerging technologies and support the identification and monitoring of new technologies.</li>
</ul>
<ul>
<li>Leads research and development activities for current product line and early innovation on future products.</li>
<li>Formulate and drives test plans and verification activities to support changes and new products.</li>
<li>Work with regulatory and clinical on new product and indication strategies.</li>
<li>Supports products on the market with sustaining engineering.</li>
<li>Accountable for meeting operational group strategic measures, developing business and strategic plans, organizational effectiveness, and vision and effectiveness</li>
<li>Strategic thinking and big picture orientation /business acumen with strong interactions with key external stakeholders including the KOL community.</li>
<li>This role requires a strong understanding of electromechanical engineering principles, experience in product development, and the ability to foster a culture of engineering excellence and accountability.</li>
</ul>
Qualifications / Requirements:
Required
<ul>
<li>Bachelor's degree in engineering</li>
<li>Medical Device experience required</li>
<li>At least 12+ years in R&amp;D and/or Engineering. 5+ year of Medical Device</li>
<li>Must have demonstrated track record in a leadership position with device experience.</li>
<li>Expert at achieving strong results in a matrix environment by leading through influence and deep collaboration across the enterprise.</li>
<li>Excellent communication and influencing skills and ability to build and maintain relationships at all levels in the organization and with external customers and regulatory agencies.</li>
<li>Meaningful experience in strong execution of product launches and measurable track record of creating value through new innovations.</li>
</ul>
Preferred
<ul>
<li>Advanced degree preferred</li>
<li>Preferred Area of Study: Electrical / Mechanical / Biomedical Engineering</li>
<li>Class II / Class III Medical Devices experience</li>
</ul>
Our Client offers a comprehensive and competitive benefit packaging including health, dental and vision care, long and short term disability and a dependent care account. In keeping with it's philosophy of providing a healthy work/life balance, the company provides 3 weeks PTO (to start), 12 holidays and 5 sick days. Additionally, a generous matching 401K plan is available. Come join the excitement and get your career looking and feeling great! Apply today Feel free to DM me at <a href="mailto:jjohnson@incendia.com" target="_blank">jjohnson@incendia.com</a> - subject line Director of Engineering #LI-JJ1 #ZR Company DescriptionA Winner of Inavero’s Diamond Award 2016-2021 Best of Staffing® Client and Talent Awards for providing superior service to our clients and job seekers and an Inc. 500 honoree three consecutive years from 2007-2009, Incendia provides recruiting and staffing services to companies that have resource or hiring needs. Incendia Partners, the most progressive provider of recruiting and staffing services is fueled by a single purpose: finding the solution to your staffing needs. With over 20 years of recruiting experience, we use our talent to find the talent you need. Our simple, straightforward process cuts through the clutter, arming you with the right facts for maximum efficiency. We help you fill more positions faster, all while never sacrificing the personal touch that sets us apart from the rest. Whether you’re a business looking for full-time, contract, contract-to-hire or just need hourly or project based recruiting services in Software &amp; IT, Accounting &amp; Finance, Human Resources, or just about any position you're hiring for, or you are a professional looking for your next great career opportunity, Incendia will fire on all cylinders until you meet your match. 
<h3>Company Description</h3>
A Winner of Inavero’s Diamond Award 2016-2021 Best of Staffing® Client and Talent Awards for providing superior service to our clients and job seekers and an Inc. 500 honoree three consecutive years from 2007-2009, Incendia provides recruiting and staffing services to companies that have resource or hiring needs. \r\n\r\nIncendia Partners, the most progressive provider of recruiting and staffing services is fueled by a single purpose: finding the solution to your staffing needs. \r\n\r\nWith over 20 years of recruiting experience, we use our talent to find the talent you need. Our simple, straightforward process cuts through the clutter, arming you with the right facts for maximum efficiency. We help you fill more positions faster, all while never sacrificing the personal touch that sets us apart from the rest. Whether you’re a business looking for full-time, contract, contract-to-hire or just need hourly or project based recruiting services in Software &amp; IT, Accounting &amp; Finance, Human Resources, or just about any position you're hiring for, or you are a professional looking for your next great career opportunity, Incendia will fire on all cylinders until you meet your match.

Director of Research and Development

<h3>Job Description</h3>
Job Description
Company Overview 
1910 Genetics is a Series A stage biotechnology company that is pioneering a novel Input-Transform-Output (ITO™) platform as the first ever horizontal AI infrastructure for drug discovery. 
In a crowded space with hundreds of AI drug discovery companies, 1910's ITO™ platform is differentiated by: 
<ul>
<li>Modality agnostic drug discovery: our platform is capable of designing both small molecule and large molecule therapeutics across all disease areas, with an initial focus on neuroscience, oncology, and autoimmune diseases.</li>
<li>Proprietary massive multimodal data, which overcomes the data scarcity problem that prevents frontier AI models from being utilized for drug discovery.</li>
<li>Multi-AI agent systems that include a robust collection of frontier AI/ML models, each of which works in a task-oriented manner to achieve the multi-parameter optimization problem of drug discovery and development.</li>
<li>A state-of-the-art (SOTA) fully-automated, high throughput wet laboratory in the premier Boston Seaport District for both data generation for AI model training as well as validation of the safety and efficacy of drug candidates that are outputted by our frontier AI models.</li>
<li>An unprecedented partnership with Microsoft, which positions 1910 as the only biotech/pharma company leveraging Azure Quantum Elements, a groundbreaking, AI-driven, high performance computing (HPC) cloud architecture for advanced AI.</li>
<li>Bespoke conversational AI chatbots that provide a customer friendly UI/UX to access our platform for specific drug discovery tasks.</li>
<li>Being the only biotech company helping pharma companies integrate 6 core areas of AI infrastructure.</li>
</ul>
1910 Genetics is looking for an In Vitro Pharmacology Assay Scientist to work closely with our biologists in the discovery of antibodies. An expert in biochemical characterization of biological drug molecules, the ideal candidate will have experience in antibody drug discovery and characterization of a variety of molecular types. 
Role Responsibilities 
<ul>
<li>Validate target material in functional biochemical assays prior to the start of antibody discovery. </li>
</ul>
<ul>
<li>Design, validate and execute in vitro biochemical assays for the screening of molecules from 1910 Genetics' AI-driven large molecule therapeutics platform </li>
</ul>
<ul>
<li>Develop, validate and execute assays for the biophysical characterization of antibodies in various formats and for various modalities </li>
</ul>
<ul>
<li>Work closely with 1910 scientists to refine assays to help drive delivery of program objectives </li>
</ul>
<ul>
<li>Maintain detailed records of experimental procedures and results in electronic lab notebook </li>
</ul>
<ul>
<li>Present experimental results/progress in a timely manner and contribute to scientific discussion in group meetings </li>
</ul>
<ul>
<li>Collaborate with cross-functional teams, including AI Research and Computational Chemistry to discuss project updates as well as ensure the project milestones and timelines are met </li>
</ul>
<ul>
<li>Assist laboratory operations, including maintenance of equipment, reagent tracking and monthly inspections for safety equipment </li>
</ul>
<ul>
<li>Develop and execute standard operating procedures and best practices to enhance lab efficiency and productivity </li>
</ul>
<ul>
<li>Contribute to the preparation of scientific reports, presentations, and publications. </li>
</ul>
<ul>
<li>Provide intellectual input into small molecule projects when required </li>
</ul>
<ul>
<li>Stay current with scientific literature and emerging technologies in the fields of large and small molecule research </li>
</ul>
#LI-Onsite
Qualifications 
<ul>
<li>PhD in Biology with a focus on Biochemistry, Cell Biology, In Vitro Pharmacology, Biomedical Sciences or a related field </li>
</ul>
<ul>
<li>Postdoctoral experience or relevant industry experience in drug discovery or In Vitro Pharmacology </li>
</ul>
<ul>
<li>Experience in developing, validating and implementing biology, biochemical, and cell-based assays </li>
</ul>
<ul>
<li>Familiarity with signal transduction pathways in relevant therapeutic areas such as Immunology &amp; Inflammation, neuroscience, oncology, and cardiometabolic diseases </li>
</ul>
<ul>
<li>Experience with immune cell isolation and assay development </li>
</ul>
<ul>
<li>Experience using analytical techniques/instrumentation for characterization and quantification of large molecules, including chromatographic techniques such as HIC (Hydrophobic Interaction Chromatography) and RP (Reverse Phase), SEC (Size Exclusion Chromatography), SDS-PAGE, UV-Vis, etc. </li>
</ul>
<ul>
<li>Familiarity with conjugation, purification and characterization of antibody drug conjugates </li>
</ul>
<ul>
<li>Excellent problem-solving, critical thinking, and data analysis skills </li>
</ul>
<ul>
<li>Ability to work independently and as part of a collaborative team in a fast-paced and dynamic research environment </li>
</ul>
<ul>
<li>Strong track record of research accomplishments, as evidenced by publications in scientific journals </li>
</ul>
Diversity and Inclusion (1910's Promise) 
At 1910, we believe that a diverse, equitable, and inclusive workplace furthers relevance, resilience, and longevity. We encourage people from all backgrounds, ages, abilities, and experiences to apply. 1910 is proud to be an equal-opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If, due to a disability, you need an accommodation during any part of the interview process, please let your recruiter know. While 1910 supports visa sponsorship, sponsorship opportunities may be limited to certain roles and skills. 
Benefits and Perks 
<ul>
<li>Competitive compensation package </li>
<li>Above market benefits </li>
<li>Generous vacation and parental leave </li>
<li>Super cool team building activities </li>
<li>Great colleagues </li>
</ul>

Scientist I, Antibody Assay Development (Biochemistry / Cell Biology)

<h3>Job Description</h3>
Job Description
<ul>
<li>Associates degree in a technical discipline strongly preferred or applicable technical expertise.&nbsp;&nbsp; Military Veterans encouraged to apply.</li>
<li>Knowledge of Geometric Dimensional Tolerancing (GD&amp;T), mechanical print reading and measurement best practices is required.</li>
<li>Proficiency in use of Mitutoyo CMM, Quick Vision Software and Hardware (touch Probe and Vision)</li>
<li>Proficiency in Fluke Calibration Asset Management Software, Met/Team.</li>
<li>Must be a team player able to work in a fast-paced environment with demonstrated ability to handle multiple competing tasks and demands</li>
<li>Strong communication skills; oral and written</li>
<li>Strong organization, planning and time management skills to achieve results</li>
<li>Strong personal and professional ethical values and integrity</li>
<li>Holds self-accountable to achieving goals and standards</li>
<li>Proficient in Microsoft Office programs (Outlook, Word, PowerPoint, and Excel)</li>
<li>Strong interpersonal &amp; collaboration skills to work effectively with all levels of the organization including suppliers and/or external customers</li>
</ul>

Dimensional & Metrology Lab Specialist - Urgent Hiring!!

<h3>Job Description</h3>
Job DescriptionQuality Control ChemistJoin a team where science meets purpose!
We’re looking for a detail-oriented and driven Analytical Chemist to support critical testing operations in a fast-paced pharmaceutical environment. If you're passionate about precision, thrive in a collaborative setting, and are ready to make an immediate impact, we want to hear from you.
What You’ll Do
<ul>
<li>Perform routine and advanced chemical testing using cutting-edge techniques and instruments.</li>
<li>Operate and maintain specialized lab equipment including HPLC, GC, ICP, and more.</li>
<li>Lead and support investigations to troubleshoot and resolve analytical issues.</li>
<li>Ensure strict adherence to cGMP standards, data integrity, and documentation practices.</li>
<li>Collaborate with cross-functional teams to support raw material testing and product release.</li>
</ul>
What You Bring
<ul>
<li>Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.</li>
<li>Hands-on experience in the pharmaceutical or biotechnology industry.</li>
<li>Proficiency with analytical instruments such as HPLC, GC, and ICP.</li>
<li>A strong understanding of regulatory compliance and quality standards.</li>
</ul>
Why Join Us?
<ul>
<li>Be part of a mission-driven organization focused on improving patient outcomes.</li>
<li>Work in a collaborative, innovation-focused environment.</li>
<li>Gain exposure to advanced technologies and industry-leading practices.</li>
</ul>
Pay and Benefits
The pay range for this position is $65000.00 - $80000.00/yr.
Health Vision 401 K Dental Relocation Assistant
Workplace Type
This is a fully onsite position in Fall River,MA.
Application Deadline
This position is anticipated to close on Jul 9, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<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 
Role Summary
AbbVie is building a best-in-class, AI-enabled antibody discovery engine. We need an industry proven leader to architect, deploy, and continuously improve this platform, applying state-of-the-art machine learning and protein language models to advance large molecule assets from Hit ID through IND.
<ul>
<li>Reporting structure: VP of Discovery Research Biotherapeutics.&nbsp;</li>
<li>Department: Biotherapeutics &amp; Genetic Medicine (BGM) – Discovery Research</li>
</ul>
Core Responsibilities
<ul>
<li>Provide scientific direction, resource prioritization, and career development for a cross functional computational sciences team.</li>
<li>Embed AI/ML tools—including protein LLMs, structural prediction, and generative design—into antibody discovery workflows (target assessment, hit generation, affinity maturation, developability).</li>
<li>Partner with discovery biology, structural biology, preclinical safety, developability, and enterprise AI groups to co-deliver portfolio impact.</li>
<li>Serve as matrix leader for digital transformation initiatives; track KPIs and communicate progress to executive leadership.</li>
<li>Scout emerging technologies, benchmark against academic/industry best practice, and position AbbVie as an innovation partner of choice.</li>
</ul>
Key Outcomes 
<ul>
<li>Define, socialize, and execute a multiyear AI/ML strategy for antibodies and other biotherapeutic discoveries.</li>
<li>Hire, mentor, and inspire an interdisciplinary team of computational and experimental scientists.</li>
<li>Deliver digital transformation “use cases” that shorten design–make–test cycles or improve candidate quality (e.g., ML-driven CDR diversification, developability prediction, in-silico humanization).</li>
<li>Establish data architecture that makes BGM discovery data FAIR (findable, accessible, interoperable, reusable) and ML-ready.</li>
<li>Build external research and vendor partnerships that augment internal capabilities.</li>
</ul>
Qualifications 
<ul>
<li>Ph.D. in Computational Biology, Protein Engineering, Bioinformatics, Computer Science, or related field with 8+&nbsp;years post-PhD industry experience (or M.S. with 14+, B.S. with 16+).</li>
<li>Deep domain expertise in antibody discovery and engineering (e.g., display technologies, repertoire mining, developability, CMC considerations).</li>
<li>Proven record inventing or deploying AI/ML methods (protein language models, generative models, deep learning, Bayesian optimization) to solve large molecule R&amp;D problems.</li>
<li>Demonstrated success hiring, leading, and retaining high-performing scientific teams.</li>
<li>Track record influencing cross-functional stakeholders and presenting complex ideas to scientific and executive audiences.</li>
<li>Strong publication and/or patent portfolio in computational antibody/biologics discovery.</li>
</ul>
Preferred Experience
<ul>
<li>Delivery of an antibody therapeutic into pre‑clinical development or beyond.</li>
<li>Handson experience with cloud-native ML infrastructure and modern data architectures (e.g., MLOps, DataOps).</li>
<li>Established network within academic/industry AI drug discovery community.</li>
</ul>
Location &amp; Travel
<ul>
<li>Based in Worcester,&nbsp;MA to enable close collaboration with BGM leadership; up to 20&nbsp;% travel to Abbott&nbsp;Park&nbsp;(IL), South&nbsp;San&nbsp;Francisco&nbsp;(CA), and key external partners.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>This is primarily an on-site opportunity that observes a hybrid working model. Ideal on-site location is AbbVie's ABC Worcester, MA location.&nbsp;</li>
<li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​&nbsp;Salary: $177,000 - $336,000</li>
<li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</li>
<li>This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​</li>
<li>This job is eligible to participate in our long-term incentive&nbsp;programs​</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;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>

Director II, Discovery Biotherapeutics AI/ML

<h3>Job Description</h3>
Job DescriptionSalary: $19 - $23.57/hour 
Interested in Fishery Sustainability, Management and Hands on Marine Biology Work? Become a Marine Biologist!
 
A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline. AIS is looking forMarine Biologists(At-Sea Monitors)to work at sea collecting and recording data and biological samples for the National Marine Fisheries Service (NMFS) Northeast Fisheries Science Center (NEFCS) aboard commercial fishing vessels.
 
The primary goals of Northeast federal fishery observation programs are to provide quantitative biological, vessel, and gear-selectivity information for various New England and Mid-Atlantic fisheries. The At-Sea Monitor program focuses specifically on the groundfish industry, a grouping of fish that includes many commonly consumed fish such as cod, haddock and various flounder species. Each fishery observer or monitor operates on commercial fishing vessels operating in ports throughout New England and the Mid-Atlantic.If you ever wanted to make a difference, this is how.
 
Commercial fishing dates back hundreds of years. Today commercial fishing continues to be possible due to cooperation between fishermen and fisheries management scientists like yourself. In order to facilitate that cooperation, marine biologists collect data pertaining to fishing programs, economics, catch data, and fishing efficiency. Collected data is used to document stock information which is then used to protect the environment and preserve future generations of fish/fishermen. Commit to the journey!
 
Click to Learn More about Becoming a Fisheries Observer
 
At-Sea Monitors record detailed information on the gear and fishing activity of the vessels. Monitors work on deck on vessels ranging from 20 to 100 on trips roughly ranging from 1 to 14 days collecting data on fish catch and discard and incidental takes such as marine mammals, seabirds, and marine turtles. After attending a 3-week paid training in-person training inFalmouth, MAmonitors are deployed from ports throughout New England and Mid-Atlantic states. Gear types assessed include, trawl, gillnet, longline and handline.
 
Accommodations and meal reimbursement during in person session of training are provided.Training includes instructions on sampling protocols, gear, fisheries, fish identification, marine mammal/sea turtle identification, and safety.
 
This is a challenging job, and candidates must be mentally prepared to be away from home for multiple days, and must be physically able to handle heavy lifting, working odd hours, and long days in rough seas. Observing provides an excellent career in marine biology, as observers and monitors are widely recognized as being excellent field biologists. A broad range of advancement opportunities are available to those who demonstrate appropriate capabilities. Those opportunities include, but are not limited to, project management, field supervisors, and fieldwork in other programs.
 
Compensation:Monitorsstarting pay is $19.00/hour.Dependent on enrollment in our H&amp;W benefit, biologists may also be eligible for anadditional $4.57/hourfor the first 40 hours worked on each calendar week for a total of$23.57 hour. This is a fulltime position with benefits.Annually, monitors earn between $35K - $55K a yeardependent on their availability to deploy offshore and their personal sea day accomplishments. Monitors will be paid a minimum of 12 hours for each calendar day offshore and are also eligible for additional compensable activities while on land.
 
AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits.Potential additional compensation consists of Data quality bonuses, Service awards, Fitness center reimbursement, Candidate Referral bonus.
 
Travel is reimbursedat an hourly rate along with compensation for miles accrued on a personal vehicle as well as per diem at the specified Government rate.
 
Minimum Qualifications:
<ul>
<li>High school diploma is required.</li>
<li>Experience with data entry on computers.</li>
<li>Monitor candidates must be U.S. citizens, or be legally authorized to work in the U.S.</li>
<li>Candidates must be physically able, as determined by a licensed physicians certification to perform observer duties.</li>
<li>Your own transportation is required.</li>
<li>Candidates are expected to commit to the program for at least one year.</li>
</ul>
 
Preferred Qualifications:
<ul>
<li>Bachelor's degree in biology or a related field from an accredited college or university with 30 credits of biology coursework, 6 credits of marine science is preferred.</li>
<li>At least one undergraduate course in math or statistics preferred.</li>
<li>At-sea experience</li>
<li>Coursework in Dichotomous Keys</li>
<li>Experience collecting Field Data and entering databases.</li>
</ul>
 
Locations:
<ul>
<li>Applicants must be currently living or be willing to live within 50 miles of Gloucester, Ma.</li>
</ul>
 
Contact:
If you would like to apply for one of these exciting new openings, please click the following link Careers Pageto submit the following information.
 
<ul>
<li>Resume</li>
<li>Cover Letter detailing sea and fish experience.</li>
<li>3 to 5 academic/professional references (name, email address and phone number)</li>
<li>Unofficial copies of your college (or high school if applicable) transcripts. </li>
</ul>
All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please feel free to reach out to the Talent Team or 508-990-9054.
 
An Equal Opportunity Employer
It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law.
 
Must be able to work in the U.S. VEVRAA Federal Contractor Request Priority Protected Veteran Referrals Equal Opportunity Employer

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