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<h3>Job Description</h3>
Job Description
Senior Chemical Process Engineer Tewksbury, MA Direct Hire |
Summary
We are seeking a Senior Chemical Process Engineer with experience in process development, design, and construction of industrial facilities. This role will lead engineering efforts for complex process-facility projects, including new plant design, facility upgrades, and rehabilitation of high-hazard environments. The Senior Engineer will work closely with clients, vendors, contractors, and internal teams to deliver projects successfully.
Qualifications
<ul>
<li>B.S. in Chemical Engineering (minimum)</li>
<li>10+ years’ experience in chemical process engineering</li>
<li>Experience in process development, design, and construction</li>
<li>Ability to manage multiple projects and shifting priorities</li>
<li>Strong time management and leadership skills</li>
<li>Comfortable supervising junior engineers and collaborating with multidisciplinary teams</li>
<li>Background in chemical processing or related industries</li>
<li>Capital project management experience is a plus</li>
</ul>
Responsibilities
<ul>
<li>Lead and support engineering design for process-facility projects</li>
<li>Supervise and mentor engineering team members</li>
<li>Develop material &amp; energy balances and process flow diagrams (PFDs)</li>
<li>Prepare piping &amp; instrumentation diagrams (P&amp;IDs)</li>
<li>Size, specify, and procure equipment</li>
<li>Provide equipment and piping layout design support</li>
<li>Perform process and utility calculations</li>
<li>Support construction activities and process startups</li>
<li>Coordinate closely with vendors and clients to ensure requirements are met</li>
</ul>
Preferred Experience
<ul>
<li>Project management of capital projects</li>
<li>Construction support and startup/commissioning</li>
</ul>
Company DescriptionWhy Join · Collaborative, experienced engineering team. · Competitive salary &amp; full benefits. · Opportunity to deliver impactful next-generation products. 
<h3>Company Description</h3>
Why Join\r\n· Collaborative, experienced engineering team.\r\n· Competitive salary &amp; full benefits.\r\n· Opportunity to deliver impactful next-generation products.

Senior Chemical Process Engineer

<h3>Job Description</h3>
Job Description
Mitsubishi Electric Research Laboratories (MERL) is seeking a self-motivated senior Ph.D. candidate in Computer Science or Electrical Engineering for a 3–month internship focused on developing and applying multi-modal large language models (LLMs) with application in anomaly detection, time sequence analysis, and predictive maintenance, etc. The ideal candidate will have a strong background in machine learning and signal processing, with a proven publication record in top conferences and journals. Experience in fine-tuning LLM foundation models is preferred. The intern will collaborate with MERL researchers to design and develop LLM-based frameworks for analyzing multi-modal sensor data, prepare technical reports, and contribute to manuscripts for scientific publications. The start date is flexible. 
Required Specific Experience 
<ul>
<li>Experience with LLMs. </li>
<li>Multi-modal time sequence data analysis</li>
<li>Ph.D Candidate </li>
</ul>
The pay range for this internship position will be 6-8K per month.
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. 
In addition to base pay, interns receive a relocation stipend, covered travel to and from MERL, and a monthly Charlie Card for local commuting. Interns are invited to participate in weekly social gatherings and professional development opportunities, including research talks by both internal and external speakers. Interns who meet the 90-day waiting period are also eligible for health insurance coverage. MERL provides immigration support for qualified candidates as needed. 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.

Internship - Fine-tuning Large language models

<h3>Job Description</h3>
Job Description
MERL is looking for research interns to conduct research into building and training novel architectures for small (~1 billion parameters) vision + language models. Interesting research directions include (a) diffusion and flow matching-based architectures, (b) architectures for improved visual reasoning, and (c) reducing confabulation using information-theoretic principles. Prior experience with machine learning/computer vision/natural language processing research, and proficiency in building and experimenting with machine learning models using a framework like PyTorch are required. Candidates well into their PhD program with publications in top-tier machine learning, natural language processing or computer vision venues, ideally connected to building generative models, are strongly preferred. Candidates are also expected to collaborate with MERL researchers for preparing manuscripts for scientific publications based on the results obtained during the internship. Duration of the internship is 3 months with a flexible start date.
Required Specific Experience 
<ul>
<li>Research experience with recent vision and text generative models, demonstrated through publications</li>
<li>Deep understanding of neural network architectures</li>
<li>Proficiency in machine learning frameworks like PyTorch</li>
</ul>
The pay range for this internship position will be 6-8K per month.
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. 
In addition to base pay, interns receive a relocation stipend, covered travel to and from MERL, and a monthly Charlie Card for local commuting. Interns are invited to participate in weekly social gatherings and professional development opportunities, including research talks by both internal and external speakers. Interns who meet the 90-day waiting period are also eligible for health insurance coverage. MERL provides immigration support for qualified candidates as needed. 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.

Internship - Training Compact Vision + Language Models

<h3>Job Description</h3>
Job DescriptionSalary: 
The Opportunity
The Sr. Scientist, Preclinical Development is responsible for activities related to transitioning drug development candidates into early development with a focus on the execution of preclinical studies to support health authority submissions (i.e. IND, CTA). The Sr. Scientist will collaborate with Research teams positioning their pipeline programs to make the Research to Development transition through candidate screening, hit to lead, and final candidate nomination. The Sr. Scientist will work side by side with their research team colleagues to ensure a smooth transition of lead candidates into early clinical development. This includes obtaining a deep understanding of the target biology and the drugs mechanism of action to facilitate the design and management of non-regulated pharmacokinetic and pharmacodynamic studies in relevant species. The Sr. Scientist will collaborate with the Research team to document all preclinical PK/PD study findings and contribute to the pharmacology sections of regulatory submissions.
Visterra is seeking a flexible candidate with a broad-based knowledge of immunology and biologics drug development. The primary focuses will be in vivo pharmacology, defining pharmacodynamic endpoints, establishment of pharmacokinetic/pharmacodynamic relationships and identification of key efficacy thresholds, as well as immunogenicity assessments and mechanistic studies addressing mechanism of action and safety. This individual is responsible for design, technical oversight, and documentation for preclinical programs. The individual will actively participate in program teams, as well as collaborate effectively across functions. The successful candidate shall demonstrate a proven track record in development and have experience with biologics and understanding of INDs and FDA/EMA guidelines. This individual will be highly analytical, goal-oriented, and timeline sensitive while maintaining high quality standards.
This is an onsite position in Waltham, MA.
Responsibilities 
<ul>
<li>Oversee external contractors and internal staff to leverage appropriate preclinical in-vitro and in-vivo models and procedures to support development programs.</li>
<li>Oversee and conduct preclinical efficacy and mechanism of action studies.</li>
<li>Prepare and review reports and packages for regulatory submissions.</li>
<li>Identify translation biomarkers for pharmacology endpoints and oversee technology transfer if applicable for assay method development and validation to support regulated studies.</li>
<li>Review and analyze preclinical study data to support late-stage research and development activities.</li>
<li>Present data at cross functional team meetings, summarize data in reports to support IND filings.</li>
<li>Organize reports (pharmacology, pharmacokinetics, toxicology) from research and preclinical groups and track statuses to support timely regulatory filings</li>
<li>Assist in collecting and summarizing data from reports into regulatory documents (from briefing books for early regulatory interactions through to IND modules and Investigators Brochures)</li>
<li>Oversee method development at CROs to support pharmacodynamic assessments</li>
<li>Establish and maintain high-quality systems for outsourcing, managing and reporting data from preclinical studies that meet both regulatory guidelines and industrys best practices.</li>
<li>Effectively present data to mixed audiences both internally and to external partners.</li>
<li>Demonstrates a strong ability to effectively communicate in a cross-functional team setting.</li>
<li>Proven ability to meet deliverables and timelines.</li>
</ul>
<ul>
<li>Maintains a contemporary knowledge of current industry and regulatory trends, standards and methodologies.</li>
<li>Performs other duties as required.</li>
</ul>
Requirements 
<ul>
<li>A minimum of five years of working experience in academia or the biotech industry, including strong track record of hands-on experience in R&amp;D.</li>
<li>S. or Ph.D. in Immunology, Biology or related field of study is preferable. Candidates with a Bachelor of Science degree with significant research experience are also encouraged to apply.</li>
<li>Working experiences with biologics drug discovery and development is highly desirable.</li>
<li>Familiarity with antibody pharmacokinetics and WinNonlin software a plus</li>
<li>Knowledge of regulatory requirements, including GLP, GCP, ICH and other applicable guidelines for Nonclinical development in support of regulatory submissions.</li>
<li>Experience in outsourcing and managing CROs for assay development and preclinical studies.</li>
<li>Ability to think critically, synthesize and extract simple principles from complex datasets, communicate effectively across broad spectrum of audience both internal and external, excellent written skills.</li>
</ul>
Benefits
We provide comprehensive benefits and resources to support your work, life, and balance.
<ul>
<li>A 401(k) retirement plan with a 10% dollar-for-dollar match.</li>
<li>Medical, dental and vision benefits, with Visterra contributing 85% to the monthly premium.</li>
<li>A rich mental &amp; behavioral wellness program.</li>
<li>Short- and long-term disability programs.</li>
<li>Group and voluntary life insurance.</li>
<li>Pre-tax flexible spending and commuter accounts.</li>
<li>17 days of personal time, discretionary sick time, and 11 holidays per calendar year. Personal time accrual grows to 22 days after 3 years, with an additional one-time grants of 5 days every 5 years.</li>
<li>Twelve weeks of paid parental leave for birth or adoption.</li>
<li>A broad fitness reimbursement program.</li>
<li>Tuition and student loan reimbursement.</li>
<li>A variety of employee discounts.</li>
</ul>
 
About Us
Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney diseases and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs.
Visterra is a wholly-owned subsidiary of Otsuka America, Inc., which is a U.S. holding company and a wholly owned subsidiary of Otsuka Pharmaceutical Co., Ltd. of Japan. Visterra has approximately 125 employees and is located in Waltham, Massachusetts.
Visterra provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Sr. Scientist, Preclinical Development

<h3>Job Description</h3>
Baranov lab at the Harvard Medical School / Massachusetts Eye and Ear is looking for a Research Fellow in Single-cell and Spatial Transcriptomics to support the development of cell therapies for neurodegenerative diseases, including Glaucoma, Neurofibromatosis, Alzheimer’s, and Leber’s Hereditary Optic Neuropathy.
 
 
We are a diverse team, particularly interested in the functional integration of stem cell-derived organoids and neurons and the role that the retinal, brain, and optic nerve microenvironment plays in this process. Our multidisciplinary group combines experience in cell therapy, transplantation, stem cell differentiation, retinal development, retinal cell biology, retinal electrophysiology, small and large animal models of disease, bioinformatics, and single-cell and spatial advanced transcriptomics analysis. The lab is supported by grants from the BrightFocus Foundation, Gilbert Family Foundation, Massachusetts Lions, and NIH/NEI Audacious Goal Initiative. Being at the forefront gives us unique access to the experts in the field and multi-omics datasets.
 
 
The Harvard Medical School, Schepens Eye Research Institute and Massachusetts Eye and Ear provide an outstanding environment and visa support for research and career development. We have state-of-the-art facilities for benchwork and functional animal studies, access to on-site workstation / cloud computing for heavy computations and image processing. The mentoring program is supported by NIH T32 Training Grant. We are affiliated with the Harvard Stem Cell Institute which brings together talented scientists from different fields, and fosters networking and collaborations. My lab alumni work in industry, clinical settings, and academia.
 
We are seeking a highly motivated computational scientist with a strong background in single-cell or/and spatial transcriptomics to join our interdisciplinary research team. The successful candidate will lead computational analysis pipelines for single-cell and spatial omics datasets and atlases and contribute to biological discovery projects focused on neural and glial biology, development, and disease.
 
Key Responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Design, iteratively update, implement, and maintain analysis pipelines for single-cell RNA-seq, single-nucleus RNA-seq, and spatial transcriptomics datasets
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Process raw sequencing data (10x Genomics Cell Ranger, STAR, Velocyto, etc.) and perform downstream analysis (QC, clustering, integration, differential expression, trajectory analysis, cell-cell communication, gene regulatory networks)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Build large-scale atlases that include multiple species/tissues/conditions (1-10M cells)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Develop scalable workflows for multi-dataset integration (scVI), metadata management, batch correction, and reproducible data processing
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Perform advanced computational analyses including machine learning, pseudotime inference, RNA velocity, pathway analysis, and ligand-receptor modeling
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Collaborate closely with wet-lab biologists to interpret results and refine experimental hypotheses
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Help maintain code repositories, documentation, and data-management standards
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Prepare figures and data summaries for publications, grant applications, and presentations
 
Minimum Qualifications
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;MS or PhD in Computational Biology, Bioinformatics, Computer Science, Systems Biology, Neuroscience, or related field (or equivalent research experience)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Demonstrated experience analyzing single-cell omics data using established pipelines
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proficiency with R and/or Python for bioinformatics workflows (Seurat, Scanpy, scVI, scVelo, CellChat, etc.)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Familiarity with Linux environments, version control (Git)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong understanding of transcriptomics, genomics, and basic molecular biology concepts
 
Preferred Skills
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with spatial omics (e.g., Visium, MERFISH, CosMx, MIBI)
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Knowledge of machine-learning methods for high-dimensional biological data and large-scale atlas integration
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Prior experience in neuroscience, computational, or developmental biology
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability to communicate results clearly to both computational and experimental audiences

Computational Biology

<h3>Job Description</h3>
Job Description
Location: Cambridge, MA
*This role will require regular presence at our client sites in Cambridge, MA*
**This role is not eligible for relocation assistance**
The Zifo Lab Automation Analyst provides technical laboratory automation services, including multivendor instrument, information technology and validation/compliance services when applicable. The individual will work as part of Zifo’s Lab Automation team to implement customer needs and address gaps to propose solutions for the desired automated state. He or she will work with business users and managers of customers in conjunction with the internal Zifo support teams.  
Requirements
<ul>
<li>Provides technical support of customer laboratory environments </li>
<li>Ensure that common automation equipment is properly maintained and in good working order. This includes stand-alone liquid handlers (Hamilton, Echo, Tecan, etc), plate readers (SpectraMax, Envision, Neo2, etc) plate washers/dispensers, as well as several fully integrated robotic systems. </li>
<li>Install, operate, maintain, QC, troubleshoot problems, create methods/scripts, and train users on instruments is required. </li>
<li>Configured in-lab settings for automation software (eg: Cellario, Green Button Go) as required to train robotic equipment. </li>
<li>Perform unit test scripts for in-Lab automation equipment to validate the remote programmed software. </li>
<li>Able to build and operate debugging scripts and perform simple parallel development in the production environment. </li>
<li>Modify existing systems, instruments, methods and software to meet evolving needs. </li>
<li>Work collaboratively with discovery, engineering and expression groups at the local sites to optimize research efficiencies through implementation of automation process improvements and novel technologies </li>
<li>Ensures adherence to client’s corporate policies through periodic reporting and compliance programs </li>
<li>Document procedures, policies, troubleshooting and best practices </li>
<li>Perform system preventative maintenances based on client’s schedule, if applicable </li>
</ul>
Required Skills: 
<ul>
<li>Knowledge of laboratory safety practices as defined by the company and/or customer’s site safety code </li>
<li>Experience in the operation, maintenance, troubleshooting and scripting for liquid handlers, dispensers, plate washers, plate readers, Octet, etc. required. </li>
<li>Programming experience using Python, Java, C# or VB.NET </li>
<li>Experience with scheduling, operation, training and troubleshooting of fully integrated robotic systems </li>
<li>Expertise with Hi-Res BioSolutions’ Cellario or Biosero’s Green Button Go scheduling software is a plus. </li>
<li>Experience with Titian Mosaic is a plus </li>
<li>Exemplary interpersonal skills including the ability to work with other automation engineers and non-automation scientists. </li>
<li>Excellent organizational skills, as exemplified by an aptitude for clear record-keeping and data analysis, and the ability to prioritize work across multiple projects. </li>
<li>Excellent customer service skills complemented by an ability to listen to and interpret client requests </li>
<li>Ability to troubleshoot complex instrument and technology issues </li>
<li>Strong oral and written communication skills </li>
<li>Ability to identify, track and complete tasks for multiple projects </li>
</ul>
About you: 
<ul>
<li>Independent, self-motivated &amp; results driven individual </li>
<li>Willingness &amp; ability to acquire quickly new technical skills &amp; business principles </li>
<li>Ability for Critical Thinking and Logical Reasoning  </li>
<li>Good understanding of pharmaceutical research and drug Discovery &amp; development processes and biologics workflows (preferred, not required) </li>
</ul>
Required Education/Experience:
<ul>
<li>Bachelor of Science in computer science, life science or equivalent industry experience </li>
<li>2+ years of relevant technical experience including (but not limited to); biotech/pharmaceutical company or an automation provider. </li>
<li>Experience with scientific instrumentation (preferred) </li>
</ul>
Benefits
About Zifo:
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&amp;D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Lab Automation Analyst

<h3>Job Description</h3>
Job DescriptionAbout UsDeep Genomics is at the forefront of integrating artificial intelligence and complex biology to transform drug discovery. Our proprietary machine learning platform decodes the complexity of RNA biology to identify novel drug targets, mechanisms and therapeutics inaccessible through traditional methods. With expertise spanning machine learning, bioinformatics, data science, genetics, chemistry and drug development, our multidisciplinary team in Toronto and Cambridge, MA is revolutionizing how medicines are created. About the RoleThe Principal Research Associate/ Research Scientist will join our in vivo Pharmacology team within the Platform Biology group and will be a key player in driving our cutting-edge AI RNA therapeutics discovery platform. In this role, you will be responsible for helping lead in vivo therapeutic efficacy testing efforts of novel RNA therapeutics in various animal models. You will also support target validation, therapeutic lead optimization and drug profiling through the implementation and execution of novel molecular assays to advance our internal therapeutics portfolio. The ideal candidate will have a strong molecular biology background with expertise in processing tissue samples as well as experience with rodent models. Relevant knowledge of RNA modalities such as ADAR, ASO, mRNA and/or siRNAs is also highly beneficial. The successful candidate should demonstrate initiative and be able to thrive in a dynamic work environment with cross-functional teams working together to achieve company goals. Title is commensurate with prior experience.&nbsp; This position is onsite at our Cambridge, MA site.Key Responsibilities
<ul>
<li>Perform standard molecular biology techniques in a consistent and reproducible manner (e.g. PCR, qPCR, ddPCR, ELISA, Western blot, Jess/Leo capillary-based Western blot, etc.).</li>
<li>Support the development of novel molecular, cellular and functional assays on animal samples for our internal therapeutic pipeline.</li>
<li>Plan and execute in vivo rodent studies to enable drug discoveryCollaborate with a cross-functional team in a dynamic, matrixed environment to achieve shared company deadlines.</li>
<li>Clearly document experiments, standard operating procedures (SOPs) and data in an electronic lab notebook (ELN).</li>
<li>Communicate and present experimental design and findings with colleagues and project teams</li>
</ul>
Basic Qualifications
<ul>
<li>Degree in Pharmacology, Biology, Molecular Biology, Genetics, Biochemistry or a related field with a BS and 6-8+ years of relevant experience, a MS and 4-6+ years of relevant experience, or a PhD and 0-2+ years of relevant pharmaceutical or biotechnology experience.</li>
<li>Strong understanding of molecular biology and tissue sample processing for RNA and protein readouts as well as a familiarity with Next-Generation Sequencing techniques (NGS).</li>
<li>Experience with rodents, running animal studies, and in vivo study design is highly desirable.</li>
<li>Experienced in design,&nbsp; execution and analysis of molecular assays.</li>
<li>Excellent communication, organizational skills and a willingness to learn.</li>
<li>Ability to work independently and manage priorities in a fast-paced technical environment</li>
</ul>
Preferred Qualifications
<ul>
<li>Hands-on experience using liquid handlers is preferred (ex. Beckman Echo, Agilent Bravo and Hamilton STAR/STAR V.).</li>
<li>Past experience with RNA editing and/or RNA oligonucleotides.</li>
<li>Knowledge of histology and immunohistochemical assays and quantification is a bonus.</li>
<li>Demonstrated experience working in cross-functional teams.</li>
<li>Experience working in an advanced data and computing environment.</li>
</ul>
What we offer
<ul>
<li>A collaborative and innovative environment at the frontier of computational biology, machine learning, and drug discovery.&nbsp;</li>
<li>Highly competitive compensation, including meaningful stock ownership.</li>
<li>Comprehensive benefits - including health, vision, and dental coverage for employees and families, employee and family assistance program.&nbsp;</li>
<li>Flexible work environment - including flexible hours, extended long weekends, holiday shutdown, unlimited personal days.</li>
<li>Maternity and parental leave top-up coverage, as well as new parent paid time off.&nbsp;</li>
<li>Focus on learning and growth for all employees - learning and development budget &amp; lunch and learns.</li>
<li>Facilities located in the heart of Toronto - the epicenter of machine learning and AI research and development, and in Kendall Square, Cambridge, Mass. - a global center of biotechnology and life sciences.</li>
</ul>
Deep Genomics welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process. Deep Genomics thanks all applicants, however only those selected for an interview will be contacted.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Principal Research Associate/Research Scientist, in vivo Pharmacology

<h3>Job Description</h3>
Job Description
Description
The client is seeking a motivated full time contract Biostatistician. This is a hybrid position (requires minimum of 1 day/ week in the office in Watertown, MA). In this role, you will be supporting all statistical activities across multiple studies at the biotech including study monitoring, reporting, simulation studies and generating real word evidence. The position reports to the Head of Biometrics.
Responsibilities
• Perform simulations, modeling, and validation of datasets, tables, listings, and figures to ensure accuracy and compliance.
• Independently perform statistical analyses as per the analysis plan. Collaborate with study teams to ensure the delivery of high-quality outputs according to the timelines. Identify and anticipate issues arising in the study design, conduct and propose scientifically sound approaches. 
• Develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.
• Work collaboratively with multifunctional study teams.
Additional Skills &amp; Qualifications
• Minimum Ph.D. in Statistics or related field
• Strong proficiency in R and Python 
• Extensive experience in simulation, various data visualization, and analytics
• Previous internship or work experience at a biotech or CRO is a plus 
• Excellent communication skills, strong organizational skills, and ability to work independently in a fast-paced setting.
Job Type &amp; Location
This is a Contract position based out of Watertown, MA.
Pay and Benefits
The pay range for this position is $45.00 - $55.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a hybrid position in Watertown,MA.
Application Deadline
This position is anticipated to close on Nov 14, 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.

Biostatistician

<h3>Job Description</h3>
Job Description
Job Description
We are seeking a Chemical / Process Engineer to join our team. The ideal candidate will develop, maintain, and optimize our chemical finishing processes while ensuring safety, quality, and compliance with industry standards. This role is hands-on and requires close collaboration with production, quality, and environmental health &amp; safety teams.
Responsibilities
<ul>
<li>
Develop, implement, and improve electroplating, anodizing, conversion coating, and passivation processes.
</li>
<li>
Monitor and control chemical bath conditions, ensuring consistent performance and compliance with specifications.
</li>
<li>
Troubleshoot and resolve process issues related to adhesion, corrosion resistance, and finish quality.
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Support audits and maintain compliance with NADCAP, ISO, AS9100D, and customer specifications.
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Drive process improvements using Lean, Six Sigma, and data-driven problem solving.
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Ensure compliance with environmental, health, and safety regulations for chemical handling and waste treatment.
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Document standard operating procedures, work instructions, and process records.
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Collaborate with cross-functional teams to meet production, quality, and cost goals.
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</ul>
Qualifications
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Bachelor’s degree in Chemical Engineering, Materials Science, Chemistry, or a related field.
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3+ years of experience in chemical or surface finishing processes (electroplating, anodizing, coatings, etc.).
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Strong understanding of process control, bath chemistry, and troubleshooting.
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Familiarity with NADCAP, ISO, and AS9100 requirements preferred.
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Knowledge of safety practices for handling hazardous chemicals.
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Excellent problem-solving, analytical, and communication skills.
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Ability to work hands-on in a production environment.
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</ul>
Preferred Certifications (Not Required)
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Lean Six Sigma (Green Belt or higher).
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Certified Quality Engineer (CQE).
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OSHA / HAZWOPER or other EHS-related training.
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Professional Engineer (PE) license is a plus.
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</ul>
Benefits
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Competitive salary with performance-based incentives.
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Health, dental, and vision insurance.
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Retirement plan with company match.
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Paid time off and holidays.
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Opportunities for career growth and professional development.
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</ul>
Company DescriptionCentral Metal Finishing (CENMET) is a NADCAP- and AS9100D-certified leader in precision metal finishing, providing electroplating, anodizing, coating, and passivation services for aerospace, defense, automotive, and industrial customers. We are committed to quality, safety, and innovation in every project we deliver. 
<h3>Company Description</h3>
Central Metal Finishing (CENMET) is a NADCAP- and AS9100D-certified leader in precision metal finishing, providing electroplating, anodizing, coating, and passivation services for aerospace, defense, automotive, and industrial customers. We are committed to quality, safety, and innovation in every project we deliver.

Chemical Process Engineer

<h3>Job Description</h3>
Established nearly two centuries ago, FM is a leading mutual insurance company whose capital, scientific research capability and engineering expertise are solely dedicated to property risk management and the resilience of its policyholder-owners. These owners, who share the belief that the majority of property loss is preventable, represent many of the world’s largest organizations, including one of every four Fortune 500 companies. They work with FM to better understand the hazards that can impact their business continuity to make cost-effective risk management decisions, combining property loss prevention with insurance protection.
 
The purpose of this position is to develop new scientific knowledge, technologies and engineering solutions to problems in material flammability, fire dynamics and Lithium-ion battery safety research, which can be used for the prevention or control of industrial property loss.&nbsp;&nbsp;&nbsp;
The principal responsibilities are to carry out research projects in the areas of flammability, fire spread, and heat transfer in fires from solid combustible as well as Lithium-ion batteries. Key areas of research include understanding of fire behavior at the medium and large scales via bench-scale experiments and theoretical models on material flammability and flame heat transfer. Projects can also involve advanced flame diagnostic of buoyant turbulent sooty flames and wall fires. The experimental and theoretical studies will be closely integrated with Computational Fluid Dynamic (CFD) model development and validation within the work group.&nbsp;
The position is responsible for all aspects of project management including project proposals, execution, and reporting.
 
The position requires a PhD in Mechanical, Chemical Engineering, Fire Protection Engineering, or related fields with a strong fundamental background in combustion, fluid mechanics, heat transfer, material science and applied mathematics.&nbsp; Extensive experience in experimental methods in thermal fluids, material flammability, heat transfer, combustion/fire, and an understanding of associated numerical methods are required. Research experience with advanced laser diagnostics in flame, experimental measurement in turbulent flame, heat transfer and failure analysis of battery is desirable. Also needed are excellent written and verbal communication skills, as well as demonstrated expertise in developing solutions to challenging technical problems.
The final salary offer will vary based on geographic location, individual education, skills, and experience. The position is eligible to participate in FM's comprehensive Total Rewards program that includes an incentive plan, generous health and well-being programs, a 401(k) and pension plan, career development opportunities, tuition reimbursement, flexible work, time off allowances and much more.
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.
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