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<h3>Job Description</h3>
$15,000 sign on bonus (external candidates only)

Are you an experienced clinical laboratory professional looking for leadership opportunity? Are you detail oriented, process focused, and enjoy leading others?&nbsp; Are you looking for an industry leading company that offers growth and stability?&nbsp; LabCorp is seeking a Clinical Laboratory Team Leader to join our team at Tuft Medical Center in Boston, MA.&nbsp; In this position, you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives".

**Pay Range: $90,000 - $120,000 annually
All job offers will be&nbsp;based on a candidate’s skills and prior relevant experience, applicable&nbsp;degrees/certifications,&nbsp;as well as internal equity and market data.&nbsp;

Work Schedule: Monday-Friday 3:00pm-11:30pm; rotating weekends.

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.&nbsp; Casual, PRN &amp; Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.&nbsp;For more detailed information, please&nbsp;click here.&nbsp; 

Job Responsibilities
<ul>
<li>Supervise the day to day operations of the Blood Bank department</li>
<li>Ensure laboratory tests are accurately performed and results are reported in a timely manner</li>
<li>Directly supervise, train, and mentor laboratory personnel of the department</li>
<li>Monitor daily workflow in the lab and schedule adequate assay coverage</li>
<li>Responsible for ensuring all shifts in the department are properly staffed</li>
<li>Research and resolve any production errors while escalating when necessary</li>
<li>Engage in continuous process and service level improvements</li>
<li>Ensure all equipment is being properly maintained through Quality Control</li>
<li>Prepare and maintain Quality Assurance records and documents</li>
<li>Evaluate new process improvements and make appropriate recommendations</li>
<li>Meet regularly with direct reports to provide coaching and feedback for their development</li>
<li>Perform bench work as needed and maintain proficiency/competency in technical operations</li>
<li>Ensure all work is in accordance with state and Federal regulations</li>
<li>Responsible for administering and managing policies and procedures</li>
<li>Process and maintain payroll and personnel files</li>
<li>Perform administrative duties as needed</li>
</ul>

&nbsp;Requirements
<ul>
<li>Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA &amp; State) requirements – Bachelor’s degree is a plus</li>
<li>Minimum 5 years of experience as a Technologist/Technician </li>
<li>Previous Senior or Lead Technologist experience is highly preferred</li>
<li>ASCP or AMT certification is preferred</li>
<li>Strong working knowledge of CLIA, CAP and relevant state regulations</li>
<li>Understanding of laboratory operations as well as policies and procedures</li>
<li>Proficient with Laboratory Information Systems and Microsoft Office</li>
<li>Strong communication skills; both written and verbal</li>
<li>High level of attention to detail with strong organizational skills</li>
<li>Comfortability making decisions in a changing environment</li>
<li>Ability to handle the physical requirements of the position</li>
</ul>

If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!

Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.&nbsp;

We encourage all to apply
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our&nbsp;accessibility site&nbsp;or contact us at&nbsp;Labcorp Accessibility. For&nbsp;more information about how we collect and store your personal data, please see our&nbsp;Privacy Statement.

Laboratory Supervisor - Blood Bank

<h3>Job Description</h3>
Date Posted:
2025-11-11
Country:
United States of America
Location:
MA102: Andover MA 362 Lowell Plymouth 362 Lowell Street Plymouth, Andover, MA, 01810 USA
Position Role Type:
Onsite
U.S. Citizen, U.S. Person, or Immigration Status Requirements: 
U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract.
Security Clearance: 
DoD Clearance: Secret

At Raytheon, the foundation of everything we do is rooted in our values and a higher calling – to help our nation and allies defend freedoms and deter aggression.&nbsp; We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today’s mission and stay ahead of tomorrow’s threat.&nbsp; Our team solves tough, meaningful problems that create a safer, more secure world.&nbsp;

Job Summary:
An opportunity exists in the Advanced Microelectronics Solutions (AMS) Department, a part of Raytheon, for a 2nd Shift Metrology Process Support Engineer. AMS develops, designs, and manufactures compound semiconductor devices, millimeter/microwave integrated circuits, focal plane arrays, and modules for defense and commercial applications.&nbsp;

The individual in this role will serve as a process engineer within the Metrology Workcenter, which will focus primarily on supporting the production line through measurement techniques such as CDSEM and overlay. The ideal candidate will have experience in both electron and optical microscopy and a general understanding of measurement systems analysis.&nbsp; They would also demonstrate the ability to analyze data and clearly communicate results with process and development engineers. Further, they would have experience leading or contributing to process improvement projects.&nbsp; The candidate will support the operational goals of the facility through the collection of reliable data to support the other process areas.

The candidate should have a general understanding of the overall techniques involved in semiconductor wafer fabrication and integration, with some experience of analog device processing.&nbsp; Experience with statistical analysis software such as JMP, Minitab, R, etc. is preferred.

This position is 100% onsite and will be based in Andover, MA.

What You Will Do:
<ul>
<li>Supporting the production line through custom job writes, lot disposition, and data validation.</li>
<li>Collaborating with Engineering, Operations, and Quality to troubleshoot efforts with production processes</li>
<li>Working with the Metrology lead engineer to drive efforts to improve measurement and data quality.</li>
<li>Supporting capital qualification efforts.</li>
</ul>

Qualifications You Must Have:
<ul>
<li>Typically, a Bachelor’s in Science, Technology, Engineering, or Mathematics (STEM) and 5+ years of prior work experience OR a STEM Master's and 2+ years of prior work experience related to semiconductor metrology techniques such as automated optical inspection, CDSEM, overlay, reflectometry, ellipsometry, or others.</li>
<li>Experience troubleshooting production process equipment.</li>
<li>The ability to obtain and maintain a U.S. government issued security clearance is required. U.S. citizenship is required, as only U.S. citizens are eligible for a security clearance.</li>
</ul>

Qualifications We Prefer:
<ul>
<li>Master’s in Science, Technology, Engineering, or Mathematics (STEM).</li>
<li>Experience supporting process improvement projects</li>
<li>Experience working with SQL databases</li>
<li>Experience with statistical analysis software (JMP, Minitab, R, SPSS, MATLAB, etc)</li>
<li>Experience with compound semiconductor devices.</li>
<li>Experience in statistical process control (SPC) and/or advanced process control (APC)</li>
<li>Strong communication skills and the ability to clearly present data and analyses</li>
</ul>

What We Offer:
Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Trust, Respect, Accountability, Collaboration, and Innovation.


As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend&nbsp;select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote.

The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate’s work experience, location, education/training, and key skills.


Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.

Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company’s performance.

This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.

RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window.

RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans’ Readjustment Assistance Act.

Privacy Policy and Terms:
Click on this link to read the Policy and Terms

2nd Shift Metrology Process Support Engineer

<h3>Job Description</h3>
UII America, Inc., a subsidiary company of Shanghai United Imaging Intelligence Healthcare Co. Ltd. (UII), is building an organization of highly-motivated, talented and skillful AI experts and software developers to strengthen our R&amp;D power and address the need of our innovative products in the USA market. United Imaging Intelligence (UII) is committed to providing AI solutions for medical devices, imaging, and diagnosis – to helping clients better understand and embrace AI. United Imaging Intelligence is led by two world-renown leaders in the AI industry. Together, they will lead UII in focusing on “empowerment” and “win-win.” UII empowers doctors and equipment in order for doctors and hospitals to win, for research institutions to win, and for third-party companies to win. UII America, Inc. is building a world-class research and development team in Boston, MA.
 
We have immediate openings for LLM Research Interns with the following qualification requirements:
[ Responsibilities ]
<ul>
<li>Research and develop automated evaluation pipelines for Large Language Models (LLMs) in the medical domain, integrating clinical logic and bioinformatic standards;</li>
<li>Implement and optimize evaluation frameworks using LLM/Agent-as-a-judge techniques and reward models to assess complex clinical reasoning capabilities;</li>
<li>Conduct deep-dive analysis on model performance from both technical (NLP) and clinical perspectives, identifying failure modes and providing actionable insights for model alignment;</li>
<li>Extend and improve the company's existing algorithms and evaluation libraries;</li>
<li>Work closely with colleagues and management to develop company assets in NLP/LLM and Conversational AI;</li>
<li>Be ambitious to lead the changes in future Healthcare with innovations.</li>
</ul>
[ Qualifications ]
<ul>
<li>Currently pursuing a PhD or Master’s degree in Computer Science (AI/ML), Bioinformatics, Medical Informatics, Computational Biology, or a related quantitative/medical field;</li>
<li>Strong interest in the intersection of AI and Healthcare, with the ability to bridge technical model evaluation and clinical domain knowledge;</li>
<li>Strong programming skills with Python and familiarity with deep learning frameworks such as PyTorch;</li>
<li>Understanding of the LLM life cycle, including data preparation and reinforcement learning (RLHF/RLAIF);</li>
<li>Proven track record of publications in top-tier conferences and journals (e.g., NeurIPS, ICML, ACL, EMNLP, etc.) is a plus;</li>
<li>Passion for applying AI to make a positive impact in the healthcare domain;</li>
<li>Ability to develop practical solutions to challenging problems;</li>
<li>Strong writing, communication, and cross-discipline collaboration skills</li>
</ul>

Research Intern, LLM

<h3>Job Description</h3>
Are you an experienced Biochemist - High-Throughput Screening with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Biochemist - High-Throughput Screening to work at their company in Rahway, NJ.
 
Primary Responsibilities/Accountabilities: The Chemical Biotechnologies Group at the client is seeking an experienced researcher to support our high-throughput capabilities.
<ul>
<li>The mission of the group is to invent, develop, and implement biomolecules and biocatalytic processes to advance the client’s pipeline and our impact on the scientific community.</li>
<li>This position in our biochemistry team is responsible for lysing E. coli cell pellets to liberate enzyme in solution or generate enzyme from in vitro transcription translation (ivTT) mix, setting up reactions using this solution as a catalyst solution, quenching reactions and prep them for HPLC analysis, running the HPLC, and analyzing the data generated in support of our protein directed evolution workflow.</li>
<li>The candidate will perform high throughput workflows with 96 or 384 well formats using various automation instruments.</li>
<li>The candidate will have hands-on, extensive experience with instrumentation essential for monitoring substrates and products profiles for reactions, especially Agilent UPLC systems.</li>
<li>In this position, the candidate will have the opportunity to work with a diverse group of team members to effectively coordinate efforts and operate multiple projects.</li>
<li>The candidate ensures activities of assignments are executed such that project deliverables and timelines are met.</li>
<li>The candidate is responsible for good housekeeping and performing work in a safe manner in the work area by applicable safety equipment and personnel protective equipment (PPE).</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor's degree in Molecular Biology, Synthetic Biology, Bioengineering, Biochemistry or related field with +5 years’ of experience, or MS with +2 years of experience, or PhD.</li>
<li>Experienced in high-throughput screening and automated liquid handling (Biomek or Tecan liquid handling systems) and various analytical methods (HPLC, LC-MS, spectrophotometry, gel electrophoresis, FPLC).</li>
<li>Proficient in preparing chemical and biochemical reactions</li>
<li>Experience with protein handling and biochemical, biophysical, and/or phenotypic protein characterization techniques (e.g., activity assays, SDS-PAGE, UV-Vis spectrophotometry).</li>
<li>Understanding of experimental design and data analysis principles</li>
<li>Strong organizational skills and attention to detail</li>
<li>Excellent teamwork and multitasking</li>
<li>Good documentation of experimental reports</li>
<li>Software Skills: MS office (Word/Excel)</li>
</ul>
 
Preferred:
<ul>
<li>Experience with one or more of the following: next-generation sequencing, directed evolution, protein expression or microfluidics</li>
<li>Experience in protein characterization and purification</li>
<li>Experience in protein expression platforms (yeast, bacillus, mammalian) is a plus</li>
<li>Experience with data analysis using Python, R, Excel, or similar tools</li>
<li>Industry experience is preferred.</li>
</ul>

Biochemist - High-Throughput Screening

<h3>Job Description</h3>
Job DescriptionDescriptionUnder general supervision, responsible for the synthesis of chemicals through various routine manufacturing procedures including the operation of high-pressure reactors. Responsible to work safely with process equipment and hazardous chemicals. Key Responsibilities·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to execute tasks on the manufacturing floor through various routine manufacturing procedures including the operation of high-pressure reactors.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to operate safely process equipment and work with hazardous chemicals.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for assembling, configuring and leak testing high-pressure reactors.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for maintaining in good operational condition production equipment, including high-pressure reactors, process piping and process valves.·&nbsp; Responsibleformaintainingacleanandorderlyworkareawhileobservingstringentsafety requirements.&nbsp;·&nbsp; &nbsp; &nbsp; &nbsp;Responsible for recording and maintaining accurate production, quality and safety records.·&nbsp; &nbsp; &nbsp; &nbsp;Responsible to follow and sustain company`s policies, internal procedures, systems and programs.·&nbsp; &nbsp; &nbsp; &nbsp;May perform computer-based tasks as necessary such as working with Excel and Word software. May perform other facilities duties of a similar complexity as requested, including support of building maintenance, support issues troubleshooting, housekeeping activities, assist Lab activities, and assisting with company`s environmental and safety programs. Minimum Qualifications·&nbsp; &nbsp; &nbsp; &nbsp;Mechanical aptitude and the ability to work with hand tools.·&nbsp; &nbsp; &nbsp; &nbsp;Passing&nbsp; medical evaluation for, and the wearing of a respirator while working is required.&nbsp;&nbsp;Educational Requirements: ·&nbsp; &nbsp; &nbsp; &nbsp;High school diploma or equivalent required ·&nbsp; &nbsp; &nbsp; &nbsp;Previous experience on checmical manufacturing floor or handling chemicals is a plus.&nbsp; Benefits
<ul>
<li>Medical, Dental, Vision - effective day one of employment.</li>
<li>401(k) with company match with immediate vesting - effective first of the month, following date of hire.
<ul>
<li>First 3% is matched dollar-for-dollar.&nbsp;</li>
<li>Second 3% is matched at 70 cents on the dollar.&nbsp;</li>
</ul>
</li>
<li>3 Weeks' Vacation.</li>
<li>12 Paid Holidays.</li>
<li>Basic Life, AD&amp;D, STD, and LTD provided at no cost to employee.</li>
</ul>

Chemical Facilities Technician I

<h3>Job Description</h3>
Job Description
Job Title: Associate Scientist
Location: Andover, MA 01810
Duration: 12 months of Contract (with possible extension)
Shift Available: 8:00am to 5:00pm (Monday – Friday)
Pay rate - $27.00/hr.
&nbsp;
Job Description
Core Responsibilities
<ul>
<li>Perform real-time batch record review during manufacturing.</li>
<li>Conduct GMP compliance walkthroughs in production suites.</li>
<li>Collaborate with operators and multiple teams to ensure compliance.</li>
<li>Support QA activities on the floor, not just desk-based review.</li>
</ul>
&nbsp;
Must-Haves
Education: Bachelor’s degree in a science field (Biology or Chemistry preferred, but flexible).
&nbsp;
Experience:
<ul>
<li>0–2 years acceptable (entry-level).</li>
<li>Prior experience with batch record review is a strong plus.</li>
<li>GMP experience is critical (must have).</li>
<li>Ability to work collaboratively with diverse teams and personalities.</li>
<li>Strong communication skills and adherence to company values.</li>
</ul>
&nbsp;
Nice-to-Haves
<ul>
<li>Previous QA experience in a manufacturing environment.</li>
<li>Familiarity with pharmaceutical or biotech operations.</li>
</ul>
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Associate Scientist

<h3>Job Description</h3>
Job Description
Overview:
The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation.
 
Responsibilities:
<ul>
<li>Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs</li>
<li>Support weekend lab operations and maintain training records</li>
<li>Assist in lab equipment and inventory maintenance, including reagent and sample prep</li>
<li>Review data timely and qualify as a data reviewer</li>
<li>Perform operational assignments (raw material processes, environmental monitoring, in-process testing)</li>
<li>Contribute to updating controlled documents (SOPs, work instructions, test methods)</li>
</ul>
 
Qualifications:
&nbsp;
<ul>
<li>B.S. in chemistry, biology, biochemistry, or related field</li>
<li>4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent</li>
<li>Experience in method transfer/implementation; understanding of method lifecycle management preferred</li>
<li>Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred</li>
</ul>
Company DescriptionR&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities. 
<h3>Company Description</h3>
R&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics.

We are seeking a Scientist I/II, Viral Vector Process Development to join our team in Boston, MA and help push the boundaries of gene therapy process development. This role is for a technical expert who will conduct lentiviral (LV Edge) and adeno-associated viral (AAV Edge) vector-based process engineering for gene therapies, design complex experimental approaches to improve our workflows and systems, and coordinate project efforts. While primarily focused on viral vector process engineering, there is a high degree of cross-functionality within the Process Development group that will also include working on biologics processes (CHO Edge).

The successful candidate will work closely with Asimov’s Synthetic Biology and Cell Line Development teams, as well as interfacing with external partners. This role reports to the Head of Process Development and is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering.

About the Role:
<ul>
<li>
Be involved in projects that include media/feed optimization, bioreactor process development, process scale-up and characterization at Ambr15, Ambr250, and benchtop scale, along with analytical assay development focused primarily on LV/AAV, with overlap into biologics.
</li>
<li>
Work together with the Commercial team to technology transfer developed upstream processes to external partners.
</li>
<li>
Create and optimize throughput and robustness of workflows for cell line characterization (transient/stable), small scale screening assays, and product quality assessment.
</li>
<li>
Collaborate with our internal process modeling team to test hypotheses for developing robust predictive models using DOE approaches, machine learning algorithms, and multi-omics analysis.
</li>
<li>
Author, review, and approve process development reports and technology transfer protocols.
</li>
<li>
Support clarifications, downstream processing/purification, and product quality assessment with analytical tools.
</li>
<li>
Represent the process development team on cross-functional projects, making decisions for process development activities and effectively communicating results, progress and plans.
</li>
</ul>

About You:
<ul>
<li>
You have a Bachelors in Biological Engineering, Chemical Engineering, Cell Biology, Molecular Biology, or a related field with 6-8 years of hands-on industry experience performing viral vector process development in support of gene therapies; alternatively, a MS with 3-4 years or PhD with 0-2 years of this type of experience.
</li>
<li>
You’re a creative problem solver and get excited about the opportunity to drive the creation of industry-disruptive technology.
</li>
<li>
HEK293-based viral vector process development is squarely in your wheelhouse. Additional CHO-based experience is not required but preferable.
</li>
<li>
You have experience with Ambr15, Ambr250, and/or benchtop scale viral vector bioreactor processes. Analytical development and downstream purification experience is also highly preferable.
</li>
<li>
Being detail-oriented isn’t just a sound bite for you, it’s part of your DNA. Keeping track of a bunch of moving parts is easy for you because you’re highly organized. It’s not your first time following a standardized workflow or pipeline.
</li>
<li>
Experience in the technology transfer of manufacturing processes and CMC filing in the pharmaceutical industry is desirable.
</li>
<li>
You are an expert in spreadsheets such as Google Sheets or Excel and ideally Spotfire, Google Apps Script (JavaScript) and/or BigQuery to facilitate data management and analysis.
</li>
<li>
Experienced with using DOE software to develop robust experiments. Familiarity with implementing algorithm-based design approaches is a plus.
</li>
</ul>
 We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.
Compensation Range: $120K - $130K

Scientist, Viral Vector Process Development

<h3>Job Description</h3>
Job Description
Mitsubishi Electric Research Laboratories (MERL) invites qualified candidates to apply for the position of Research Scientist in the Multiphysical Systems Group. Current areas of interest include physics-based modeling and numerical simulation of thermofluid and mechatronic systems, control system design and development, nonlinear state estimation, and applications of machine learning. Successful candidates will be expected to perform original, relevant research in the areas of nonlinear state estimation and system inversion for complex multiphysical systems.
The Multiphysical Systems Group at MERL conducts fundamental, academically-oriented research in model-based design and analysis of complex multiphysical systems, emphasizing thermofluid, electrical power, and mechatronic applications. Using state-of-the-art languages, we construct system-level dynamic models and use them to design new estimation and control algorithms, analyze dynamic behaviors, optimize product performance, and prototype new products and services that are enabled by these tools and methods. Current research interests include data-driven optimization and estimation for large-scale, nonlinear system models, development of next-generation tools for scientific computing, and design and analysis of robust nonlinear control and model predictive control. Specific areas of interest include state and parameter estimation for physics-based models comprised of hybrid (discrete and continuous state) nonlinear differential algebraic equations, particle filtering and ensemble estimation methods, variational methods for data assimilation and model inversion, and other cutting-edge estimation technologies. The successful candidate will bring an independent research agenda and a track record commensurate with experience and be capable of working within interdisciplinary R&amp;D teams.
Responsibilities for this position include:
<ul>
<li>Conducting innovative and relevant research on modelling, estimation and control for multiphysical systems</li>
<li>Developing and advancing a research agenda impacting the scientific community and company technology</li>
<li>Publishing results in leading technical journals and conferences, and drafting patent applications </li>
<li>Partnering with business units, corporate R&amp;D, and academic groups in the execution of R&amp;D projects</li>
<li>Transferring results and technology to Mitsubishi Electric corporate research laboratories</li>
</ul>
Qualifications for this position are:
<ul>
<li>A Ph.D. or equivalent from an internationally recognized institution in mechanical engineering, chemical engineering, electrical engineering, applied mathematics, or other related fields, with a focus on estimation, control theory, and/or data assimilation</li>
<li>Extensive experience with physics-based modeling, simulation, and dynamic analysis of multiphysical systems</li>
<li>Expertise in thermofluid systems is preferred, but background in mechatronic or other systems will also be considered</li>
<li>Strong programming skills, in at least some of Julia, Modelica, C/C++, Python, and Matlab</li>
<li>A strong publication record in leading conferences and journals, consistent with experience</li>
<li>A record for independently proposing and executing research programs with academic impact</li>
<li>Strong teamwork, communication (oral and written), teaching, and listening skills</li>
</ul>
The pay range for this position at the commencement of employment is expected to be between $135,000 and $170,000 per year. Actual base pay will depend on a variety of individualized factors, including job-related knowledge, skills, and experience.
In addition to base salary, the total compensation package will include an annual performance-based bonus and a comprehensive benefits program encompassing medical, dental, and vision coverage; a generous 401(k) match; commuting and home office stipends and various paid time off programs (including vacation, sick time, personal and parental leave). Specific details regarding participation in these programs will be provided upon an offer of employment.
Employment is considered “at-will,” and the Company reserves the right to modify base salary or any other compensation program at any time, including for reasons related to individual performance, departmental or Company performance, and market conditions.
PRINCIPALS ONLY. No phone calls please.
Mitsubishi Electric Research Laboratories, Inc. is an Equal Opportunity Employer.
Mitsubishi Electric Research Labs, Inc. "MERL" provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, MERL complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. 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.
MERL expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of MERL's employees to perform their job duties may result in discipline up to and including discharge.
Working at MERL requires full authorization to work in the U.S and access to technology, software and other information that is subject to governmental access control restrictions, due to export controls. Employment is conditioned on continued full authorization to work in the U.S and the availability of government authorization for the release of these items, which might include without limitation, obtaining an export license or other documentation. MERL may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to MERL facilities and information systems, as MERL deems appropriate, to ensure practical compliance with applicable employment law and government access control restrictions.

Staff - Research Scientist - Multiphysical Systems

<h3>Job Description</h3>
Job DescriptionInnovative Chemical Products Group (ICP Group) is a leading formulator and manufacturer of specialty coatings, adhesives, and sealants serving the construction and industrial end markets. ICP Group is comprised of leading brands known for innovation, quality, and performance. Founded in 2015 and supported by a lean corporate team, ICP Group has scaled rapidly through organic and acquisition growth into one of the largest coatings, adhesives, and sealants companies in North America. ICP Group is headquartered in Andover, MA and has manufacturing and distribution sites throughout North America, Latin America, UK, Europe and the Asia Pacific region. ICP Group is seeking an experienced R&amp;D Director to lead our research and development efforts at our Andover, MA facility. This individual will oversee a team of chemists and technicians in developing and optimizing innovative coating technologies, ensuring alignment with strategic business goals and market demands. The scope of products supported by this position can range from Architectural paints and stains to sport surface products, intumescent coatings, cleaning and disinfecting products and others based on company need.&nbsp; In this role you will be responsible for the following: Leadership &amp; Strategy:
<ul>
<li>Lead and mentor a team of scientists and technicians engaged in formulation, testing, and scale-up of innovative products for the Specialty Coatings business</li>
<li>Define R&amp;D priorities and manage project pipelines to support innovation and continuous improvement initiatives.</li>
<li>Collaborate with senior management to align R&amp;D objectives with business strategy.</li>
</ul>
&nbsp;Product Development &amp; Innovation:
<ul>
<li>Direct the research and formulation of new products across a range of applications, including architectural paints, sport surfaces, intumescent coatings, and specialty products.</li>
<li>Oversee modification and enhancement of existing products to improve performance, sustainability, or cost-effectiveness.</li>
<li>Evaluate raw materials, benchmark competitive products, and drive material innovation.</li>
</ul>
Technical Oversight:
<ul>
<li>Ensure adherence to performance testing standards, QC procedures, and scale-up protocols.</li>
<li>Collaborate with manufacturing, quality, and regulatory teams to ensure seamless product transfer from lab to production.</li>
<li>Serve as the technical expert for assigned product lines and provide support for customer inquiries, complaints, and product certifications.</li>
</ul>
Cross-functional Collaboration:
<ul>
<li>Work closely with Business Unit leadership, project management, operations, and commercial teams to drive project execution and timely product launches.</li>
<li>Partner with customers, suppliers and external research organizations to evaluate new technologies and raw materials.</li>
<li>Communicate technical findings and recommendations effectively across the organization.</li>
</ul>
 Requirements:
<ul>
<li>Bachelor’s degree in Chemistry, Chemical Engineering, or a related field (Master’s or Ph.D. preferred).</li>
<li>8+ years of experience in research and development, including at least 3 years in a leadership or management role.</li>
<li>Strong background in surface coatings chemistry, with expertise in film formation, polymer chemistry, and coating performance testing preferred</li>
<li>Demonstrated ability to manage multiple projects and lead cross-functional teams.</li>
<li>Excellent organizational, communication, and presentation skills.</li>
<li>Self-motivated, results-driven, and innovative thinker with a passion for leading teams and driving organizational growth.</li>
</ul>
 ICP Group is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Applicants will receive fair and impartial consideration without regard to race, sex, color, national origin, age, disability, veteran status, genetic data, or religion or other legally protected status. &nbsp;
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