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<h3>Job Description</h3>
Job Description
Scientist III (Bioassay) for Pharmaron (Boston) Lab Services LLC to work at our Woburn, MA loc. Develop, troubleshoot, + optimize new assays based on client needs. 
Write Validation Protocol + SOP. Develop plate maps for validation. Determine parameters for validation + acceptance criteria. Perf sci + tech review of validation data + reports. 
Responsible for overall conduct of GxP projects, including sci + regulatory aspects. 
In collaboration w/ Project management, serve as a point contact for client communication. 
Notify QAU + Sponsor of any deviations that occur during validation, + participate in documenting + investigating deviation including participating in root cause investigations. 
In collaboration w/ QA, confirm assay meets regulatory req standards, + approve Validation report + Sample analysis report. 
Review audit reports, respond to audit findings, + ensure timely completion of any corrective + preventive actions. 
Author + review Protocols, Reports, Deviations, + Audit responses. 
Train Scientists on techniques + assays, + provide tech assistance to assigned research staff. 
Oversee the work of up to three junior scientists. 
Perf RUO + GxP assays independently. 
Perf sample analysis following established SOPs under RUO/GLP/cGMP conditions. 
Perf QC function to review data + reports to ensure accuracy of laboratory-related processes. 
Provide high quality documentation of all lab related activities, including assay batch record + sample inventory. 
Maintain regular communication w/ scientists, PIs, + other project staff as well as external clients. 
Adhere to all lab standards as defined in each written SOP. 
May undergo background checks incl drug screening. 
Wage: $87,589 to $100,000. 
Must have Bach in Biology, Biochem, Biomedical Engineering or rel sci field, 3 yrs rel exp working in a laboratory following GLP and cGMP regulations, and the following skills (3 yrs exp): 
cell-based neutralizing Abs (Nab), Potency assays, ELISpot, or Flow Cytometry development and validation; and Microsoft Office, including Word, Excel, and PowerPoint. 
In the alternative, must have Master's in Biology, Biochem, Biomedical Engineering or rel sci field, 1 yr rel exp working in a laboratory following GLP and cGMP regulations, and the following skills (1 yr exp): cell-based neutralizing Abs (Nab), Potency assays, ELISpot, or Flow Cytometry development and validation; and Microsoft Office, including Word, Excel, and PowerPoint. 
In the alternative, must have PhD in Biology, Biochem, Biomedical Engineering or rel sci field. 
Apply at <a href="https://www.pharmaron.com/careers/job-openings/" target="_blank">https://www.pharmaron.com/careers/job-openings/</a> click US Job Openings, ref job Scientist III (Bioassay).

Scientist III (Bioassay)

<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

Marine Biologist (ASM) - Gloucester, Ma

<h3>Job Description</h3>
Job Description
Who We Are: 
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview: 
Join our dynamic Chemical Process Research &amp; Development team as a Senior Scientist. In this role, you will be instrumental in advancing the synthesis of active pharmaceutical ingredients (APIs) and intermediates by championing and implementing cutting-edge manufacturing technologies. Your primary focus will be on leveraging your expertise in flow chemistry, Process Analytical Technologies (PAT), lab automation, and predictive modeling to design, develop, and optimize innovative, robust, and scalable chemical processes.
Core Responsibilities: 
<ul>
<li>Spearhead the design, development, and optimization of flow chemistry processes for API and intermediate synthesis.</li>
<li>Implement and utilize Process Analytical Technologies (PAT) for real-time reaction monitoring, data acquisition, kinetic understanding, and process control.</li>
<li>Employ lab automation systems and automated workstations to streamline experimental workflows, enable high-throughput screening, and enhance data quality.</li>
<li>Develop and apply kinetic, mechanistic, and process models to deepen understanding, guide experimental design, and accelerate the optimization of continuous and batch processes.</li>
<li>Drive the adoption and scale-up of innovative continuous manufacturing solutions from laboratory to pilot plant.</li>
<li>Collaborate effectively with cross-functional teams, including analytical chemists, engineers, and manufacturing personnel, providing technical leadership in your areas of expertise.</li>
<li>Ensure meticulous documentation of experiments, results, technical reports, and contributions to intellectual property.</li>
</ul>
Qualifications:
Required
<ul>
<li>PhD in Organic Chemistry, Chemical Engineering, or a related scientific discipline; or an MS/BS degree with significant equivalent industrial experience.</li>
<li>5+ years of hands-on experience in chemical process development within the pharmaceutical or fine chemical industry.</li>
<li>Demonstrated expertise in designing, executing, and optimizing flow chemistry processes.</li>
<li>In-depth, practical experience with Process Analytical Technologies (PAT) (e.g., FTIR, Raman, online UPLC/HPLC, FBRM) for in-situ reaction monitoring and control.</li>
<li>Proficiency in lab automation tools, automated reactor systems (e.g., Mettler Toledo, Syrris, Vapourtec), and associated control software.</li>
<li>Experience with chemical process modeling and simulation software (e.g., Dynochem™, Aspen, MATLAB, gPROMS) and its application to reaction kinetics, process understanding, or optimization.</li>
<li>Deep understanding of organic reaction mechanisms, reaction kinetics, thermodynamics, and transport phenomena as they apply to continuous processing.</li>
<li>Excellent problem-solving skills, critical thinking abilities, and a proactive approach to innovation.</li>
<li>Strong written and verbal communication skills, with the ability to present complex technical information clearly.</li>
<li>Proven ability to work independently and collaboratively in a fast-paced team environment.</li>
</ul>
 Preferred
<ul>
<li>Experience with the development and scale-up of API manufacturing processes under GMP guidelines.</li>
<li>Familiarity with Design of Experiments (DoE) principles and statistical analysis software (e.g., JMP).</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
</ul>
<ul>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
</ul>
<ul>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
</ul>
<ul>
<li>Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
If you are a veteran, first responder, or in the process of transitioning from service member to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team.
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: <a href="mailto:pharm.hr@veranova.com" target="_blank">pharm.hr@veranova.com</a> (US) or <a href="mailto:UKHR@veranova.com" target="_blank">UKHR@veranova.com</a> (UK).
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Lead Scientist - Chemical Process Technologies

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
Eurofins PSS is seeking a highly experienced and motivated scientist to support analytical method development, validation, and GMP sample testing. This role also includes team leadership responsibilities, overseeing a group of Eurofins PSS employees at a client site.
Technical Duties:
<ul>
<li>Perform complex GMP assays (PCR, ELISA, NGS, cell-based assays)</li>
<li>Lead method transfer, qualification, and validation for bioassays</li>
<li>Author/review SOPs and technical reports</li>
<li>Collaborate with cross-functional teams on method development and investigations</li>
<li>Analyze and trend assay data for consistency and compliance</li>
</ul>
Leadership Duties:
<ul>
<li>Supervise and support a team of on-site Eurofins PSS employees</li>
<li>Assist with hiring, onboarding, and training</li>
<li>Provide mentorship and performance feedback</li>
<li>Ensure lab operations meet quality and efficiency standards</li>
<li>Foster a collaborative and positive team environment</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree with 3–8 years or Master’s degree with 2–5 years of relevant experience</li>
<li>Strong background in GMP method validation and sample testing</li>
<li>Experience with method transfer into GMP labs</li>
<li>Knowledge of FDA/EMA regulatory expectations</li>
<li>Excellent communication and problem-solving skills</li>
<li>Supervisory experience preferred</li>
<li>Potency assay and LIMS experience a plus</li>
<li>Must be authorized to work in the U.S. without restriction or sponsorship</li>
</ul>
 Additional Information 
The position is full-time and permanent,&nbsp;Monday-Friday, 8 am-5 pm,&nbsp;with overtime as needed.&nbsp;Candidates living near or in&nbsp;Cambridge, MA,&nbsp;are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>Comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and 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 a 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.

Analytical Method Development Scientist & Team Lead - GMP Environment

<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 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 Description
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer, and commercial leader in ePaper technology. The Billerica Research &amp; Development team is thriving and growing as we help develop products that are changing how people access information every day. We are seeking qualified candidates who are self-driven, looking to advance their career and become a high-impact player on a team.
Based on technology from MIT’s Media Lab, E Ink has transformed and defined the eReader market. Its Electrophoretic Display products make it the worldwide leader for ePaper. The Company’s corporate philosophy aims to deliver revolutionary products, user experiences and environmental benefits through advanced technology development.
Our diversity of people, backgrounds, experiences, thoughts and perspectives is fostered to create an inclusive work environment.
Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that fosters a strong employee engagement, teamwork, safety and wellness.
We offer a competitive/generous benefits package that fits the needs of our employees. It includes health, dental, vision, wellness programs, employee discounts, 401k matches, ongoing development, advancement opportunities and more. This position is also eligible for our bonus program. (see E Ink │ Our Company)
About the position:
As a member of E Ink’s Process Development Team, the Senior Chemical Process Systems Engineer will be entrusted with fulfilling our mission of bringing smart displays to the world. This role is responsible for creating, improving, and maintaining pilot-scale systems that enable commercial-scale production of E Ink’s unique electrophoretic materials – including pigments, colloidal dispersions, microcapsules, and other additives.
We’re looking for someone who can help us build what we need, but also someone who can figure out what we should be building in the first place. This candidate will have experience designing and building specialized equipment and will be excited to drive equipment-based innovation across the organization!
Responsibilities
<ul>
<li>Design new process systems. Create PFDs, evaluate alternative technologies, generate P&amp;IDs, perform engineering calculations, draft fabrication drawings, work with outside vendors to select and customize process equipment, select components, and size lines</li>
<li>Lead the installation of new process systems in collaboration with both internal and external teams</li>
<li>Act as a companywide technical resource on process equipment such as reactor vessel design, pumps, mixers, temperature control systems, and sensors</li>
<li>Evaluate, select, and communicate with all relevant third-party vendors (piping, controls, etc.) required for the design and installation of new process equipment</li>
<li>Perform hands-on assembly, modification, commissioning, and troubleshooting of new and existing pilot-scale chemical process systems</li>
<li>Collaborate cross-functionally to coordinate capabilities within Development and Research departments, communicate support needs to Facilities department, and ensure responsiveness to EHS requirements</li>
</ul>
Qualifications
<ul>
<li>BS or MS in Chemical or Mechanical Engineering or equivalent work experience</li>
<li>7+ years of industrial process systems engineering experience</li>
<li>Ability to read P&amp;IDs, process flow diagrams, and fabrication drawings</li>
<li>Experience sizing and selecting chemical fluid lines, pumps, valves, and instrumentation</li>
<li>Basic electrical knowledge to read wiring diagrams and troubleshoot low voltage circuitry</li>
<li>Working knowledge of process automation (P&amp;ID controllers, instrumentation, transmitters, VFDs, PLCs)</li>
<li>Experience troubleshooting processes and equipment</li>
<li>Strong mechanical aptitude and hands-on attitude</li>
<li>Clear and effective communication skills</li>
<li>Ability to function effectively as a member of cross-functional, cross-disciplinary, and inter-corporate teams</li>
<li>Effective prioritization and time management to meet project goals / milestones</li>
</ul>
Preferred skills
<ul>
<li>Experience designing pressure vessels that comply with ASME BPVC</li>
<li>Experience commissioning new process equipment</li>
<li>Experience with mixer design</li>
<li>AutoCad proficiency</li>
<li>LabVIEW proficiency</li>
<li>Working knowledge of industrial codes (NFPA, NEC, ASME)</li>
<li>Basic SolidWorks and 3D printing skills</li>
<li>Experience operating machining equipment such as drill presses and lathes</li>
<li>Basic project management skills such as creating budgets, timelines, and updates on multiple small projects</li>
<li>Familiarity with Six Sigma / statistical analysis methods</li>
<li>Knowledge of typical fabrication methods</li>
</ul>
Benefits
<ul>
<li>Competitive total compensation package</li>
<li>Medical, dental and vision on 1st day</li>
<li>Company 401K match</li>
<li>20 PTO days</li>
<li>Generous sick leave policy</li>
<li>Casual day to day work environment</li>
<li>Hybrid/flexible work environment (for some positions)</li>
</ul>
E ink is committed to a diverse and inclusive workforce. E Ink is an equal opportunity employer and does not discriminate on the basis of race, ethnicity, gender, identity, sexual orientation, veteran’s status, disability, age, or on any basis prohibited by federal and state law.

Senior Chemical Process Systems Engineer 1100S-AD

<h3>Job Description</h3>
Job Description
Job Title:&nbsp;Dimensional &amp; Metrology Lab Specialist
Location: Attleboro, MA
Pay Range: $28/hr - $40/hr
JOB DESCRIPTION In this position the selected candidate will provide measurement and inspection services to engineering, manufacturing, quality, and process engineering teams.&nbsp;&nbsp;The individual will interpret mechanical prints, develop inspection programs utilizing CMM software, collect data, develop data reports, prioritize scheduling of work and offer consultation support with respect to GD&amp;T and mechanical print interpretations.&nbsp;&nbsp;In addition to dimensional inspection related activities, the selected candidate will also support calibration activities for the organization.&nbsp;&nbsp;Calibration activities include retrieval of items due for calibration, calibration of various items such as thread rings, thread plugs, calipers, balances, force gauges etc. in accordance with documented procedures as well as recording these activities for quality purposes. Job Details: ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Dimensional&nbsp;Inspection activities include: o&nbsp;&nbsp;&nbsp;Mechanical print reading and GD&amp;T interpretation o&nbsp;&nbsp;&nbsp;CMM program development o&nbsp;&nbsp;&nbsp;3D Laser scanning o&nbsp;&nbsp;&nbsp;Hand tool measurement o&nbsp;&nbsp;&nbsp;Data collection and reporting ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Calibration&nbsp;activities include: o&nbsp;&nbsp;&nbsp;Collection of items due for calibration at scheduled intervals o&nbsp;&nbsp;&nbsp;Data collection and documentation of As Found / As Left results o&nbsp;&nbsp;&nbsp;Updating records within calibration lab management system for tracking purposes &nbsp;Job Requirements: ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Associates degree in a technical discipline strongly preferred or applicable technical expertise.&nbsp;&nbsp; Military Veterans encouraged to apply. ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Knowledge of Geometric Dimensional Tolerancing (GD&amp;T), mechanical print reading and measurement best practices is required. ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proficiency in use of Mitutoyo CMM, Quick Vision Software and Hardware (touch Probe and Vision) ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proficiency in Fluke Calibration Asset Management Software, Met/Team. ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Must be a team player able to work in a fast-paced environment with demonstrated ability to handle multiple competing tasks and demands ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong communication skills; oral and written ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong organization, planning and time management skills to achieve results ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong personal and professional ethical values and integrity ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Holds self-accountable to achieving goals and standards ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proficient in Microsoft Office programs (Outlook, Word, PowerPoint, and Excel) ·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong interpersonal &amp; collaboration skills to work effectively with all levels of the organization including suppliers and/or external customers This position requires eligibility to obtain authorization under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR). Non-US Persons, as defined in the ITAR and EAR, may not be eligible to obtain authorization. &nbsp;
If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

About ManpowerGroup, Parent Company of:Manpower, Experis, Talent Solutions, and Jefferson Wells
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands –&nbsp;Manpower, Experis, Talent Solutions, and Jefferson Wells&nbsp;– creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.

Dimensional & Metrology Lab Specialist - 1

<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 DescriptionSalary: $121,073-$146,643+DOE 
Orum Therapeutics is seeking a highly motivated and accomplished scientist to lead the Bioanalytical and PK/PD function. The successful candidate will have extensive experience in bioanalytical and PK/PD method development and validation, quantitative and qualitative sample analysis, and data interpretation with a particular focus on small molecules and biologics. In this role, you will oversee technical monitoring throughout the bioanalytical method development, validation, and sample analysis processes, whether performed in-house or through external vendors. You will be responsible for managing method transfers between CROs, reviewing validation reports, and ensuring adherence to GLP/GCP regulations. Additionally, you will be accountable for analyzing pharmacokinetic (PK) data and generating PK/PD predictions to support the progression of our projects.
Principal Duties and Responsibilities
<ul>
<li>Oversee all bioanalytical needs, whether in-house or through external vendors, to support DMPK and PK/PD studies.</li>
</ul>
<ul>
<li>Advise on analytical methods for measuring and quantifying small molecule transformations. Manage metabolism, drug-drug interaction (DDI), and transporter studies at CROs.</li>
</ul>
<ul>
<li>Conduct site visits, inspections, and SOP reviews to ensure compliance with regulatory standards and internal protocols.</li>
</ul>
<ul>
<li>Review and approve validation reports, experimental bioanalytical documentation, and archive relevant study documents in consultation with the clinical team.</li>
</ul>
<ul>
<li>Integrate drug metabolism and pharmacokinetics (DMPK) predictions into bioanalytical workflows to support early-phase drug development and optimization. </li>
</ul>
<ul>
<li>Utilize modeling and simulation tools for human PK/PD predictions, enabling dose projection or safety evaluation. </li>
</ul>
<ul>
<li>Collaborate with and support other disciplines across the R&amp;D organization and support regulatory document preparation as needed. </li>
</ul>
<ul>
<li>Maintain up-to-date knowledge of relevant scientific literature, regulatory guidance, and best practices.</li>
</ul>
Skills, Abilities &amp; Competencies
<ul>
<li>Extensive experience with pharmacokinetic and biodistribution studies of antibody-drug conjugates and relevant analytical methods including LC-MS/MS for small molecule quantitation and MSD for ELISA and LBA-based assays.</li>
</ul>
<ul>
<li>Proven experience in developing and validating assays for antibody-drug conjugate modalities including total antibody, total and free payload, ADA, and NAb assays for ADC clinical PK samples.</li>
</ul>
<ul>
<li>Strong expertise in non-compartmental analysis of PK data, with demonstrated experience in PK-PD modeling and simulation, population PK, and meta-analysis (preferred).</li>
</ul>
<ul>
<li>Deep understanding of ADME processes and screening strategies from feasibility to candidate nomination. </li>
</ul>
<ul>
<li>Experience with pharmacokinetic analysis software and understanding of PK and PK/PD principles for interpreting results (preferred). </li>
</ul>
<ul>
<li>Good understanding of GLP/GCP regulations and their application in bioanalytical contexts.</li>
</ul>
<ul>
<li>Demonstrated ability to work independently in a fast-paced biotech environment while thriving in a collaborative, and global multidisciplinary team setting.</li>
</ul>
<ul>
<li>Excellent oral and written communication and time-management skills, and the ability to handle multiple projects simultaneously.</li>
</ul>
<ul>
<li>Strong work ethic and ability to work independently with minimal supervision.</li>
</ul>
Education- Ph.D. or equivalent degree in Analytical chemistry or a related field with minimum 5 years' experience. Level will be commensurate with experience and accomplishments.
*U.S. citizens and those authorized to work in the U.S. (green card) are encouraged to apply. We are unable to sponsor at this time.
*Candidate must be able to pass a background investigation.
*Unable to work with 3rd party candidates or agencies.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily within the context of the representative work environment and physical demands described above. Likewise, qualifications listed are representative of the knowledge, skills, and abilities required to perform the positions essential functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
Orum Therapeutics is an Equal Opportunity Employer (EOE).

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