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<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 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 
AbbVie is seeking an experienced and highly motivated in vivo electrophysiologist to join our Circuit Biology team within Discovery Psychiatry. This pivotal role involves&nbsp;facilitating electrophysiological insights of circuit dysfunction in psychiatric disorders and treatment. This is an excellent opportunity to work at the forefront of psychiatry drug discovery research, contributing to target validation and compound profiling studies within a dynamic and collaborative team.
Responsibilities
<ul>
<li>Independently conceive, execute, and communicate original technical ideas and novel multi-disciplinary research that achieves project and area goals</li>
<li>Drive internal in vivo electrophysiology efforts by developing and optimizing recording strategies from disease-relevant circuits</li>
<li>Develop and maintain in vivo electrophysiology technology, methodology, and utility in psychiatric drug discovery</li>
<li>Generate, through lab-based activities, multi-unit electrophysiology, local field potential and/or EEG data to support projects</li>
<li>Ensure alignment of electrophysiology efforts with the broader goals of cross-functional teams</li>
<li>Present findings to internal teams and external collaborators or conferences</li>
<li>Contribute to strategic decision-making in psychiatry drug discovery</li>
<li>Provide scientific guidance and training to junior scientists and research associates</li>
<li>Serve as a lead scientist on projects and contribute scientific insights across multiple other project teams</li>
</ul>
Qualifications 
<ul>
<li>BS, MS, or PhD in neuroscience, or related field, with typically 12+ (BS), 10+ (MS), or 4+ (PhD) years of experience</li>
<li>Extensive experience in unanesthetized, in vivo multi-unit electrophysiology</li>
<li>Extensive experience using large-scale neural recording with single cell resolution with strong analytical skills</li>
<li>Experience with local field potentials and EEG recordings and analyses</li>
<li>Demonstrated expertise in the design and execution of hypothesis-driven studies related to synaptic and circuit function</li>
<li>Ability to process and interpret large datasets using appropriate software tools</li>
<li>Strong ability to work in cross-functional teams and effectively communicate scientific findings</li>
</ul>
Desired Qualifications
<ul>
<li>Previous industry experience within early discovery, preferably within psychiatry research</li>
<li>Expertise in AI/ML methodology for signal analysis</li>
<li>Recognized and sought out as an expert in field or discipline</li>
<li>Track record of impactful publications&nbsp;</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.​&nbsp;Salary: $106,500 - $202,500
</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 Scientist II, In Vivo Electrophysiology

<h3>Job Description</h3>
Job Descriptionjob summary: 
Step into a vital role at a state-of-the-art biopharma research facility in Worcester, MA, where innovation fuels the development of life-changing therapies. As a Research and Development Laboratory Technician, you'll be at the heart of scientific discovery-managing and processing critical biological and chemical samples that support early-stage drug development.
This is a hands-on opportunity to work alongside a collaborative team of scientists in a fast-paced lab environment. You'll leverage your biology background and attention to detail to maintain sample inventory, operate specialized lab equipment, and contribute directly to research that makes a real-world impact. If you're motivated, organized, and ready to be part of something meaningful, this role offers challenge, growth, and purpose.
 location: Worcester, Massachusetts job type: Contract salary: $30.00 - 34.23 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Coordinate and manage the shipment of materials from Company to other sites and collaborators, ensuring compliance with all applicable regulations and guidelines.</li>
<li>Prepare and review shipping documents, including bills of lading, shipping labels, and customs documentation, to ensure accuracy and completeness.</li>
<li>Collaborate with internal teams to ensure proper coordination and execution of shipments.</li>
<li>Communicate with internal and external partners, including freight forwarders and carriers, to schedule and track shipments, ensuring on-time delivery.</li>
<li>Maintain accurate records of all shipments, including tracking numbers, delivery confirmations, and any relevant documentation.</li>
<li>Monitor and manage inventory levels of shipping supplies, such as boxes, labels, and packing materials, ensuring adequate stock is maintained.</li>
<li>Identify and resolve any issues or delays in the shipping process, working closely with internal and external stakeholders to find timely solutions.</li>
<li>Stay up-to-date with relevant shipping regulations, guidelines, and industry best practices, ensuring compliance and continuous improvement.</li>
<li>Assist in the development and implementation of shipping-related policies, procedures, and standard operating protocols.</li>
<li>Provide regular reports and updates to management on shipping activities, including metrics, performance, and any potential risks or opportunities.</li>
</ul>
 qualifications: 
<ul>
<li>Proven experience as a Shipping Coordinator or similar role, preferably in a pharmaceutical or biotechnology industry.</li>
<li>Accustomed to spending extended periods of time working in a bio-hood</li>
<li>Strong knowledge of shipping regulations, including domestic and international requirements, customs procedures, and hazardous materials handling.</li>
<li>Proficient in using shipping software and systems, such as FedEx, UPS, or DHL, to schedule and track shipments.</li>
<li>Excellent organizational and time management skills, with the ability to prioritize tasks and meet deadlines in a fast-paced environment.</li>
<li>Attention to detail and accuracy, ensuring all shipping documents and records are complete and error-free.</li>
<li>Effective communication and interpersonal skills, with the ability to collaborate and build relationships with internal and external stakeholders.</li>
<li>Problem-solving and decision-making abilities, with a proactive approach to identifying and resolving shipping-related issues.</li>
<li>Proficient in using Microsoft Office Suite (Word, Excel, Outlook) and other relevant software applications.</li>
<li>Ability to lift and move heavy packages, as required. </li>
<li>Independent, take leadership, well organized, juggle or manager</li>
</ul>
 #LI-ST1? 
 skills: GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Research and Development Laboratory Technician

<h3>Job Description</h3>
Job Description
Position Summary:
The Senior Research Associate&nbsp;is a member of the Platform Group and will support laboratory research activities towards development of novel technologies enabling next generation genomic medicines. The successful candidate will have a strong understanding of the technical and equipment needs in a lab as well as significant hands-on experience with standard and cell culturing and in vitro cell biology techniques. They will work independently and as part of a collaborative team.

Key Responsibilities:
Performing laboratory assays and tasks including flow cytometry, mammalian cell culture, animal sample processing, cell isolation, plate-based reporter assays, cell killing assays, transfection, and protein binding assays.
Developing new assays or optimizing existing ones based on in-depth knowledge of laboratory techniques
Analyzing and accurately documenting assay results in an electronic lab notebook or other technical reporting formats

Basic Qualifications:
<ul>
<li>M.S. or B.S. in Biology, Biochemistry, Molecular Biology, or related field with 3-5+ years of relevant experience</li>
<li>Previous experience with immune cell isolation and flow cytometry characterization is required.</li>
<li>Strong primary and cell line culture experience, including experience executing protocols, troubleshooting assays, and carrying out literature searches for method evaluation and refinement</li>
<li>Knowledge of immunology and experience with BLI on octet instruments is a plus</li>
<li>Prior experience working with lipid nanoparticles is a plus</li>
<li>Proven ability to work independently and cross-functionally with highly skilled teams in a fast-paced, entrepreneurial, and technical environment</li>
<li>Strong organizational and problem-solving skills.</li>
<li>Motivated, curious, and comfortable working with highly technical projects and personnel</li>
<li>Excellent communication and presentation skills, capable of conveying technical information in a clear and thorough manner</li>
<li>Comfortable delivering against challenging commitments</li>
</ul>
Company DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities. 
<h3>Company Description</h3>
Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting &amp; Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Sr. Research Associate

<h3>Job Description</h3>
Job Description Description:
We are Pest-End - one of the fastest-growing, family-owned, and operated wildlife and pest management companies in New England. Our company culture is single-handedly the most essential component of our continued success. We believe that to succeed as a business, our team members must thrive as individuals. That encompasses passionate and empathetic leadership, a 'think big, act small' mentality, and providing career paths that promote growth and internal promotions. We provide you with everything needed to be successful, competent, and confident in your role with Pest-End.
Who we need
Our business and team are growing. We are currently hiring wildlife service technicians in Massachusetts, looking to begin or continue a career in professional wildlife control. Qualified candidates will have skills or experience with carpentry work.
Wildlife technicians thrive on independence and enjoy occasional detective work to solve every day to intricate wildlife problems for our residential and business customers. Due to the nature of our work, candidates must be willing to work both outdoors and indoors throughout the year. Some scenarios require our service technicians to use ladders to more efficiently and effectively complete a job. Pest-End provides ladder safety training for our team.
Job Responsibilities:
<ul>
<li>Driving company vehicle to customer locations.</li>
<li>Meeting with customers to diagnose and explain services needed.</li>
<li>Inspecting interior and exterior of customers' properties. This position requires the use of a ladders and climbing on roofs, or entering tight places like a crawl space.</li>
<li>Capturing nuisance wildlife in a safe manner.</li>
<li>Performing basic exclusion and repair work on the areas where wildlife enter the customers' home or business.</li>
<li>Obtaining state wildlife certification</li>
<li>Obtaining state pesticide licenses to assist our Intergrated Pest Management team.</li>
<li>Maintain notes and records about customers and the services they have had.</li>
<li>Keeping an open line of communication between yourself, office staff, and managers.</li>
<li>Ability to lift 40 lbs + comfortably.</li>
</ul>
What our benefits and perks look like:
<ul>
<li>Paid time off and holidays</li>
<li>401K with an employer match up to 3%</li>
<li>Monthly cell phone stipend</li>
<li>Comprehensive health, dental, and vision insurance</li>
<li>Employer funded life insurance policy</li>
<li>Paid training, and state certifications provided for non-licensed new hires</li>
<li>Company vehicle and gas card</li>
<li>Short and long term disability through Aflac</li>
<li>Company supplied uniforms</li>
</ul>
 
Requirements:
What we require:
<ul>
<li>Valid driver's license with a driving record free of major incidents</li>
<li>18 years or older</li>
<li>2+ years of carpentry experience </li>
<li>Complete a pre-employment background check and drug screening</li>
<li>High school diploma or equivalent</li>
<li>Ability to work full-time with the potential for overtime during May - September</li>
</ul>
Physical Requirements:
While performing the duties of this job, the team member is frequently required to stand, walk, sit, climb, bend, kneel and crawl within tight spaces. Specific hearing and vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. The employee may occasionally lift and/ or move up to 50 pounds. Additionally, wildlife technicians should be comfortable with ladder work and on roofs and be able to lift and maneuver up to a 40-foot ladder. 
 
Pest-End, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
 
PIadc89cdc380e-25405-37817427

Wildlife Service Technician

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
If you’re looking for a rewarding career, a place to call home, apply with us today
Job Description 
<ul>
<li>Meticulously prepare complex media at various scales to support cell culture for various iPSC differentiation workflows, ensuring timely and accurate execution of requested formulations.</li>
<li>Read, review, and execute SOPs for preparation of reagents, stock solutions, and media handling and formulation.</li>
<li>Track expiry of corresponding stock solutions and complete complex media.</li>
<li>Maintain an updated media inventory database for forecasting, tracking raw material use &amp; stock, lot usage, and overall material performance.</li>
<li>Maintain accurate and meticulous record keeping with internal ELN system, independent data analysis, and reporting of data in written and oral formats.</li>
<li>Perform work in full compliance with safety policies and technical protocols and complete all required training activities in the timeframe specified.</li>
<li>Perform complex algebraic mathematical calculations with high accuracy to determine critical parameters such as molarity, molality, and percentages.</li>
<li>Precisely calculate volumes of solution components based on intricate mathematical formulas, ensuring exact proportions for experimental and manufacturing processes.</li>
<li>Troubleshoot media preparation challenges and deviations when necessary.</li>
<li>Collaborate with process development scientists to support high throughput optimization of media formulations for scale-up, reproducibility, and cost-efficiency.</li>
<li>Operate automation platforms (e.g., liquid handlers, automated dispensers, robotic mixing systems) to support streamlined media preparation, increasing throughput, reproducibility, and data traceability.</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>B.S. and/or M.S. in biological or biochemical sciences (or a related field). B.S., 1-2 years of experience or M.S., less than 1 year of experience.</li>
<li>Demonstrated proficiency in aseptic technique and reagent, stock solution, and complex cell culture media preparations.</li>
<li>Advanced skills in algebraic calculations: molarity, percentages, solution component volumes.</li>
<li>Unwavering commitment to safety protocols and procedures</li>
<li>Proven capacity to ensure work product quality and understand the impact on downstream processes.</li>
<li>Work within a team-oriented lab environment and work within cross-functional project teams.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Preferred Qualifications:
<ul>
<li>Exposure to automated systems (e.g., liquid handlers, automated dispensers, robotic mixing systems).</li>
<li>Track record of working in or supporting high-throughput or high-volume laboratory environments. &nbsp;</li>
</ul>
 Additional Information 
What to Expect in the Hiring Process:&nbsp;
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>60 Minute Onsite Meeting</li>
</ul>
Additional Details:&nbsp;
Position is Full Time, Monday-Friday, 8am-5pm with occasional weekends (once every 1-2 months) to support cell culture.Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Media Preparation Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Biologist Location: Boston, MA 02210 Duration: 6 Months+ Shift: 8 hours a day Monday - Friday Payrate: $50- $52.75/ hr. on W2 Job Description:(3-5 years) Responsibilities: • Execute NGS library preparation (e.g., bulk RNA, scRNA, snRNA sequencing), quantification, and sequencing workflows to support the DOCTA team. • Internalize and develop new NGS workflows to support evolving needs. • Develop and adhere to standard operating procedures for workflows to ensure consistent production of high-quality data. • Work in the sequencing space cross-functionally, with the ability to manage multiple requests and queues. • Deliver NGS data with clear expectations of timelines to multiple teams and promptly update stakeholders of run completion. • Effectively manage inventory of DNA, RNA, libraries, and sequencing reagents. • Perform additional related tasks (i.e., RNA extraction, qPCR/ddPCR) as needed to help the team meet goals and deliverables. • Maintain detailed documentation of NGS run performance and scientific work in an electronic notebook. • Participate in assessment of sample prep and sequencing workflows at other sites (Indianapolis and/or contract research organizations) to enable flex capacity when demand is high (no travel required). Qualification/ Requirements: • B.S. and/or M.S. in biological or biochemical sciences (or a related field) with 3-5 years of laboratory research experience. • Molecular biology mastery of nucleic acid extraction and purification, quantification, NGS library preparation/QC, and qPCR. • Strong background in NGS technologies and their applications, including quantification, sequencing, and data QC (preferably Illumina). Direct experience with RNA-seq (bulk) and amplicon-seq. • Experience with single-cell and single-nuclei RNA-seq applications. Additional Skills/Preferences: • Familiarity with CRISPR-based gene editing and high-throughput screening is a plus. • Experience with automation is a plus (Mantis, Integra systems, Liquid Handlers, SPTLabtech Firefly, Tecan, etc). • Strong organizational, time management, and communication skills. • Experience with documentation in electronic notebook software. #sczr2

Biologist

<h3>Job Description</h3>
Job DescriptionMaterials Scientist - Aerospace - Technical Ceramics- Relocation available! This Jobot Job is hosted by: Matt Swaneveld Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $100,000 - $150,000 per year 
A bit about us:
 We are a leader in manufacturing advanced materials and are known for our custom designed technical solutions. Due to growth, we are looking for a Materials Scientist to assist in our well structured engineering department. As a Materials Scientist, you will be responsible for developing and testing new materials, analyzing and improving existing materials, and ensuring that all materials meet our high standards of quality and performance. This is a challenging and exciting role that requires a deep understanding of ceramics, materials, raw material testing, and scientific principles. If you have a background in technical ceramics and are looking to take the next step in your career, please read on! 
Why join us?
 
<ul>
<li> We are an industry leader with an assortment of versatile advanced material products</li>
<li> Stable company with well over 50+ years behind us</li>
<li> Great starting salary </li>
<li> Comprehensive benefits package including health/dental/wellness/and more</li>
<li> 401K+ employee match </li>
<li> Relocation assistance package if needed</li>
</ul>
 
Job Details
 Qualifications: 
<ul>
<li> Bachelor's degree in Materials Science, Ceramics, or a related field (Master's / PhD preferred) </li>
<li> Industry experience with Aerospace/Defense/ITAR/Medical</li>
<li> 9+ years of experience in ceramics, materials, or a related field</li>
<li> Potential to obtain a government security clearance</li>
<li> Strong knowledge of scientific principles and research methods</li>
<li> Experience with raw material testing and analysis</li>
<li> Excellent problem-solving skills and attention to detail</li>
<li> Strong communication and collaboration skills</li>
<li> Ability to work independently and as part of a team</li>
<li> Experience with advanced scientific equipment and techniques</li>
<li> Ability to write technical reports and present findings to management and other stakeholders</li>
</ul>
 Responsibilities: 
<ul>
<li> Conduct research and development activities to create new materials that meet our specific needs and requirements</li>
<li> Analyze and improve existing materials to enhance their performance, durability, and reliability</li>
<li> Perform raw material testing to ensure that all materials meet our quality standards</li>
<li> Collaborate with other scientists and engineers to develop new products and improve existing ones</li>
<li> Use advanced scientific equipment and techniques to analyze and test materials</li>
<li> Keep up-to-date with the latest developments in materials science and technology</li>
<li> Write technical reports and present findings to management and other stakeholders</li>
</ul>
 If you are a skilled and experienced Materials Scientist with a passion for innovation and a commitment to quality, we want to hear from you. This is an exciting and rewarding opportunity to work in a dynamic and fast-paced environment, where you will have the opportunity to make a real impact on the manufacturing industry. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.Company DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

Senior Materials Scientist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
We are seeking a highly motivated Senior Scientist I to join our Analytical Development team in the Product Development Science and Technology, Biologics Development Launch division. Our team is responsible for the development, qualification, and execution of analytical methods to provide product and process understanding for biological entities from discovery through commercial stages.
The successful candidate will be a part of the Biomolecular Interaction Group which is mainly focused on method development and implementation of various immunoassays to monitor process impurities and to assess potency of AbbVie’s Biologics to support product and process development for early-phase, late-phase, and commercial programs.&nbsp; Some of the techniques/methods utilized in the group include 1) ELISAs to monitor and detect process related impurities; 2) surface plasmon resonance using Biacore for assessment of antigen binding and binding of antibody Fc receptors; and 3) qPCR to measure levels of residual DNA and mycoplasma. The role will &nbsp;involves managing all analytical aspects of biologics products on the market, overseeing commercial methods throughout their lifecycle - from method transfer, performance monitoring, troubleshooting, to method enhancement. The individual will also play a key role in establishing commercial product specifications, stability programs, and regulatory filings. Collaboration with other analytical teams, process development, global QC, and manufacturing science and technology groups is a crucial part of this role to meet business objectives and program milestones.
Responsibilities:
<ul>
<li>Partner with Analytical Development groups to achieve commercial method readiness using traditional and advanced analytical techniques, including but not limited to ELISA, bioassays, spectrophotometric and compendial methods.</li>
<li>Participate in cross-functional, multi-site, global meetings / projects and oversee commercial analytical method transfer between sites, product/process investigations, method performance monitoring and troubleshooting.</li>
<li>Establish scientifically sound, analytical lifecycle strategies, including methods, stability, specification and change management that meet Health Authority best practices and expectations.</li>
<li>Participate in the preparation and review of technical documents to ensure global compliance - including validation protocols and reports, reference standard qualification reports and analytical test procedures.</li>
<li>Author regulatory submissions, support regulatory inspections and provide scientifically sound responses to agency deficiency letters.</li>
<li>Conduct periodic review of methods and work with program leads to design, execute remediation experiments, and implement changes to new or existing commercial methods when necessary.</li>
</ul>
Qualifications 
<ul>
<li>BS or equivalent education in Biology, Biochemistry, Engineering or related discipline and 8+ years of experience in the biopharmaceutical industry; MS and 6+ years experience; PhD and 3+ years experience.</li>
<li>Industry experience in method development, qualification, validation, and method transfer in support of development and/or commercialization of biological products. &nbsp;</li>
<li>Methods including but not limited to ELISA, western blot, qPCR, ddPCR, SPR and automation</li>
<li>Ability to lead and manage projects/teams of significant scope and complexity, while meeting all deliverables and timelines.</li>
<li>Ability to think critically and demonstrate troubleshooting and problem-solving skills.</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.​&nbsp;Salary: $106,500 - $202,500
</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 Scientist, II- Analytical Development ( On-site-Worcester, MA)

<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 Biologics Discovery Sciences group at AbbVie is seeking a highly skilled and self-motivated scientist to join a dynamic team supporting Discovery Biotherapeutics. This position will impact projects through engineering, production, and characterization of multispecific biopharmaceutical products. The ideal candidate should have extensive experience with biologics and multispecifics production platforms, analytical characterization (e.g., SEC, MS), and a proven track record implementing multispecific engineering and production strategies to advance early- and late-stage discovery programs. The ideal candidate will also have people and project management experience. The applicant should be an enthusiastic, creative scientist who will make tangible contributions to the continuous improvement and innovation within the organization.
Key Responsibilities:
<ul>
<li>Responsible for design, engineering and production of multispecific biologics to support all Abbvie therapeutic areas</li>
<li>Evaluate and integrate state-of-the-art technology to improve therapeutic production platforms, and demonstrate creative “out-of-the-box” thinking to solve difficult problems</li>
<li>Supervise 1-2 scientists, evaluate team performance, and is accountable for the effective performance of team</li>
<li>Serve as a Multispecifics Engineering representative for cross-functional teams, and contribute scientific insights into multiple projects across various therapeutic areas; recognized expert in multispecifics design and production</li>
<li>Serve as the Biologics lead on projects to coordinate activities and transitions from hit generation through candidate nomination</li>
<li>Identify and solve technical problems independently, conceive and implement innovative process research ideas</li>
<li>Ensure consistency and quality of technical reports</li>
<li>Provide project update, analysis and advice to cross-functional teams and senior management</li>
<li>Present original work internally across departments and at internal and external scientific conferences; may author or co-author peer-reviewed scientific papers or patents</li>
</ul>
Qualifications 
Qualifications:
<ul>
<li>PhD, MS, or BS degree in Biochemistry, Biochemical engineering or related disciplines with typically 4+ (PhD), 10+ (BS) or 12+ years of experience</li>
<li>Extensive experience in multispecific biologics engineering and knowledge of biologic pipeline progression from exploratory through candidate nomination</li>
<li>Extensive experience with protein, biologics, fragments, and multi-specifics design, expression and purification</li>
<li>Experience managing direct reports and providing performance evaluations and development opportunities</li>
<li>Program management experience preferred</li>
<li>Experience with CRO coordination</li>
<li>Ability to explore and develop new approaches to further advance innovative purification and screening technologies for multispecifics</li>
<li>Sound scientific understanding of current state of protein expression/separation/analytical technologies</li>
<li>Experience with in vitro analytical techniques for protein characterization (e.g. SEC, MS, DSF); experience with developability screening for multispecifics preferred</li>
<li>Strong molecular biology skills (e.g. molecular cloning)</li>
<li>Experience with sequence analysis tools (Vector NTI, Geneious, Genedata)</li>
<li>Excellent organizational skills and the ability to manage multiple projects simultaneously</li>
<li>Team player with the ability to operate in a fast-paced multi-disciplinary environment</li>
<li>Adapt to rapid changes in project priorities and timelines</li>
<li>Recognized in the scientific community through a sustained record of peer-reviewed publications and patents preferred</li>
<li>Candidate must be a goal-oriented team player with excellent verbal and written communication skills and strong can-do attitude</li>
</ul>
Key AbbVie Competencies:
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable high performance.</li>
<li>Learns fast, grasps the “essence” and can change the 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, nurtures innovation and manages innovation to reality.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​
​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​ Salary: $106,500 - $202,500
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive programs.&nbsp;​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

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