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<h3>Job Description</h3>
Job Description
Job Title: Associate Scientist, Cell Therapy
Location: 100% on-site in Cambridge
&nbsp;
Remote Flexibility: No; 100% Onsite
&nbsp;
Contract Term: 6 months to start; 40 hours/week (potential to extend)
Experience required:
<ul>
<li>Background in immunology – especially in NK cell, TCR-T and CAR-T cell biology</li>
<li>This role will be a lot of time in the lab performing experiments towards building a donor section criteria for our Allogenic CAR-T call program.</li>
</ul>
&nbsp;
As an Immunologist, you will join our Cell Therapy group, where we leverage top-notch CRISPR technology to fully unleash the power of cell-based therapy for autoimmune and Immuno-Oncology indications. Your main responsibilities will include:&nbsp;
<ul>
<li>Designing, implementing, and troubleshooting experiments, both independently and in collaboration with colleagues, to reach desired goals&nbsp;</li>
</ul>
<ul>
<li>Establishing and performing in vitro/in vivo assays to support NK cell, TCR-T and CAR-T related projects&nbsp;</li>
</ul>
<ul>
<li>Using technical and literature knowledge to analyze and interpret results. Communicate research and development findings with internal and external teams/partners in a clear and concise manner&nbsp;</li>
</ul>
&nbsp;
&nbsp;
About You&nbsp;
Are you an Immunologist with a strong interest in genomic editing and cell therapy? Our ideal candidate will have a M.S. in Immunology, cell biology or related field with a solid background in immunology, especially in NK cell, TCR-T and CAR-T cell biology. If you are a team player looking to work with a highly motivated and energetic team, we encourage you to apply
&nbsp;
<ul>
<li>Team spirit and can-do attitude are must-to-have in an individual who thrives and enjoys working in a collaborative environment</li>
</ul>
<ul>
<li>Ability to isolate immune cells from leukopak using magnetic based isolation methods, in vitro culture of primary T cells and perform in vitro assays, T cell killing assay, and cytokine profiling assay by ELISA or MSD is a must.</li>
<li>Ability to perform multi-color FACS profiling assay,&nbsp; cell proliferation assay, Incucyte based assays, and mixed lymphocyte reaction (MLR) assay is required.&nbsp;Experience with cell metabolic assays using instruments like Agilent Seahorse Analyzers is a plus.&nbsp;</li>
</ul>
<ul>
<li>Experience with CRISPR gene editing and lentiviral transduction / AAV insertion in primary T cells and primary NK cells&nbsp;</li>
</ul>
<ul>
<li>Experience with Electronic Lab Notebook (ELN) to record detailed protocols and data in a timely manner.&nbsp;&nbsp;</li>
</ul>
<ul>
<li>Publication of original scientific work in peer-reviewed journal(s) is a plus&nbsp;</li>
</ul>
&nbsp;
Meet your future team:&nbsp;
&nbsp;
The Cell Therapy team are a group of bright, fun and team-first individuals. Eager to move cool projects forward, we are motivated at the opportunity to make an impact for patients. The breadth of exposure to cutting edge gene therapy development will provide you with exposure to the full spectrum of gene and cell-based therapies, starting from CRISPR guides to patients who we try our best to support. Your future hiring manager is the Senior Scientist, Cell Therapy. The team is currently working mostly onsite in a wet-lab environment. Therefore, we hope you are currently local to Cambridge MA, or open to relocating. While much of the day-to-day operations require wet-lab work, our team is focused on building not just technical expertise but fostering an environment for growth of scientists interested in a career in therapeutic biotechnology. If you join our team, you can expect to join fast, fun, exciting and collaborative environment. We look forward to fostering your skills, learning from your experiences, and building a larger team together.&nbsp;&nbsp;
The team is currently working mostly onsite in a wet-lab environment. Therefore, we hope you are currently local to Cambridge MA, or open to relocating. While much of the day-to-day operations require wet-lab work, our team is focused on building not just technical expertise but fostering an environment for growth of scientists interested in a career in therapeutic biotechnology. If you join our team, you can expect to join fast, fun, exciting and collaborative environment. We look forward to fostering your skills, learning from your experiences, and building a larger team together.
&nbsp;
&nbsp;
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.

Associate Scientist, Cell Therapy

<h3>Job Description</h3>
Job Description
Our client is seeking an individual to work closely with the RNA Chemistry Team responsible for synthetic oligonucleotides. This individual will be involved in a complete production process for the identification, implementation &amp; fulfillment of synthesis, purification and reaction scheme analytical characterization and method development of oligonucleotides.
&nbsp;RESPONSIBILITIES:
<ul>
<li>Hands-on position in an oligonucleotide chemistry lab inclusive of operating, maintaining &amp; calibrating synthesis platforms and other scientific equipment.</li>
<li>Handling automated oligo synthesizer (Expedite, Dr.Oligo, Mermaid, Akta OP-100, etc) using solid-phase.</li>
<li>Knowledge of oligonucleotide purification techniques (using Akta system) and Unicorn software.</li>
<li>Synthetic oligonucleotide method and process development participation.</li>
<li>Demonstrate basic lab competency in preparing reagents and buffers &amp; handling chemicals.</li>
<li>Follow operating procedures and process improvement documents.</li>
<li>Documentation of results and data analysis</li>
<li>Ensure safety and product quality are paramount throughout the laboratory environment.</li>
<li>Capable of repetitive tasks and performing other duties as assigned.</li>
<li>Perform general lab-operation activities.</li>
</ul>
QUALIFICATIONS:
<ul>
<li>B.S. or B.A. equivalent in Organic Chemistry, Biochemistry or related field with 2+ yrs general laboratory experience or M.S. in Organic Chemistry, Biochemistry</li>
<li>Basic computer skills including MS Office Suite.</li>
<li>More experienced candidates with oligonucleotide chemistry experience will be strongly considered.</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.

Research Associate, RNA Oligonucleotide Chemistry

<h3>Job Description</h3>
Job Title: Senior Team Leader Statistics
Location: Morristown, NJ Cambridge, MA
&nbsp;
About the Job
&nbsp;
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&amp;D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

Our Evidence Generation and Decision Science (EGDS) group at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven decision making through cutting-edge quantitative science and deliver unparalleled integrated evidence that drives innovation and scientific breakthroughs.

Join our EGDS Biostatistics I&amp;I team as Senior Team Leader Statistics, Biostatistics (Senior Director) and you’ll provide statistical leadership, guidance, and strategic input for clinical studies in large or multiple complexed projects. You’ll manage a team of biostatisticians and will have opportunities to develop innovative statistical solutions to support critical trial decision-making and advance treatment across all phases of drug development. EGDS will support your growth through people development and inclusive career opportunities that value diversity of thought and abilities, cultivating future leaders to shape the next generation of clinical science.

About Sanofi: We’re an R&amp;D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main Responsibilities:

<ul>
<li>
Oversee statistical and scientific contribution to clinical development plans, studies and submissions activities (when applicable), and provide strategic statistical leadership for responsible projects.
</li>
<li>
Manage a team of biostatisticians. Define team members priorities, performance review and development areas. Mentor junior project team members and nurture a culture of productive teamwork, quality, operational efficiency, and innovation.
</li>
<li>
Plan, monitor and manage project activities, timelines, processes, and resources to ensure operational excellence and align practices in compliant with Sanofi SOPs and Biostatistics standards.
</li>
<li>
Develop productive collaboration with other functions in the aligned project team, with other statistics project leaders, and in communicating with senior leadership.
</li>
<li>
Lead or play an influential role in EGDS development initiatives and key cross-functional activities; represent statistics in challenging regulatory meetings, key scientific or technology working groups.
</li>
</ul>
&nbsp;
About You&nbsp;

<ul>
<li>
PhD/MS in statistics or related discipline with at least 10 years of pharmaceutical experience in clinical development, including experience with Biotech, Pharma, Clinical Research Organizations (CROs), health authorities and academic clinical research centers.
</li>
<li>
Excellent knowledge and understanding of clinical development and advanced statistical concepts and techniques.
</li>
<li>
Proven successful experience in clinical development or post-marketing activities such as submissions, interactions with regulatory agencies or other external stakeholders.
</li>
<li>
Demonstrated and recognized expertise in operational or statistical or managerial aspects
</li>
<li>
Demonstrated leadership and excellent interpersonal/communication, project and people management skills.
</li>
<li>
Exhibited expertise to represent organizations in cross-company activities (e.g. consortiums or professional associations).
</li>
</ul>

Why Choose Us?

<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

#GD-SA&nbsp; #LI-SA &nbsp;&nbsp;&nbsp; #LI-Onsite
#vhd &nbsp;&nbsp;
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Senior Team Leader Statistics

<h3>Job Description</h3>
Job Title: Development Scientific Director (DSD)
Location: Cambridge, MA,

About the Job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.&nbsp;

The&nbsp;Development Scientific Director (DSD)&nbsp;role in the Neurology Clinical Development department provides clinical scientific leadership for Alzheimer’s disease clinical trials. The DSD contributes to the &nbsp;protocol development, study feasibility and risk assessment, regulatory submissions, protocol training, scientific review of data, and cross-functional collaboration to ensure scientific integrity and operational excellence. This role requires a scientifically and operationally focused, organized, and emotionally intelligent professional with strong analytical, communication, and leadership skills.
&nbsp;
At Sanofi we chase the miracles of science. Sanofi believes that the more we understand about disease pathogenesis in the human nervous system, the greater the chance we can produce life-changing therapies. Sanofi has a large internal research team including the Genomic Medicine Unit (GMU), which are committed to building the future pipeline in various neurological and ophthalmological diseases.&nbsp;Over the next five years, the Neurology &amp; Ophthalmology Development (NOD) group plans to regularly test in the clinic potentially disease-modifying treatments for Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculopathy (CIDP), Alzheimer’s disease, Parkinson’s disease, Amyotrophic Lateral Sclerosis (ALS), as well as other CNS diseases, with therapeutic modalities encompassing Small Molecules, Biologics, and Gene Therapy.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
&nbsp;
Main Responsibilities:
&nbsp;
Clinical Study Leadership
<ul>
<li>
Provide scientific expertise for study protocols, data interpretation, and clinical study reports.
</li>
<li>
Ensure scientific relevance and quality of clinical data throughout study execution.
</li>
<li>
Support feasibility assessments, risk management, and validation of clinical data.
</li>
<li>
Participate in internal governance and regulatory meetings.
</li>
</ul>

Cross-Functional Collaboration
<ul>
<li>
Serve as the scientific reference for study teams, investigators, and internal stakeholders.
</li>
<li>
Collaborate with Global Project Heads, Clinical Research Director, Safety Officer and Pharmacovigilance, Translational Medicine, Regulatory Affairs, Biostatistics, Clinical Study Units, Medical Affairs, and CROs to optimize study design and execution.
</li>
</ul>

Study Document Development
<ul>
<li>
Author, review, and validate study-related documents including trial protocols, informed consent forms, case report forms, risk management plans, training materials, clinical study reports, and publications.
</li>
<li>
Develop materials for and organize investigator meetings, steering committees, and independent data monitoring committees.
</li>
<li>
Contribute to regulatory submissions and respond to health authority queries.
</li>
</ul>

Scientific Expertise &amp; Strategy
<ul>
<li>
Maintain deep knowledge of Alzheimer’s disease pathophysiology, biomarkers, disease staging, clinical management, and drug development.
</li>
<li>
Contribute to biomarker strategy and mechanism-of-action understanding.
</li>
<li>
Support clinical development plans and integrated development strategies.
</li>
<li>
Provide scientific input for in-licensing evaluations and strategic initiatives as needed.
</li>
</ul>

Operational Oversight
<ul>
<li>
Define study timelines, budgets, and risk mitigation plans in collaboration with clinical operations and project management.
</li>
<li>
Ensure harmonization of study documents and alignment across projects.
</li>
<li>
Escalate and resolve study-level issues, sharing lessons learned across teams
</li>
</ul>

QUALIFICATIONS
<ul>
<li>
Advanced degree (PhD, PharmD, or equivalent in Life/Health Sciences); MPH or Master’s with extensive drug development experience may be considered.
</li>
<li>
Minimum 5 years of clinical development experience in academic, biopharma, or CRO.
</li>
<li>
Strong scientific and clinical development expertise, especially in neurology. Clinical research and drug development expertise in Alzheimer’s disease is highly desired.
</li>
<li>
Excellent communication, teaching, and cross-functional collaboration skills.
</li>
<li>
Fluent in English (spoken and written).
</li>
<li>
Experience working in a matrixed environment with global teams.
</li>
</ul>

Why Choose Us?
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

#GD-SA&nbsp; #LI-SA &nbsp;&nbsp;&nbsp; #LI-Onsite
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Development Scientific Director, Neurology (Early Development)

<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>
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.

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