field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionCompany Description 
About Mote Therapeutics
Are you a scientific leader with a passion for advancing RNA therapeutics and the drive to make a difference in the world? Do you want to be a part of a dynamic and innovative team at the forefront of RNA medicines? If so, join our new RNA Venture and be a part of the revolution in RNA therapeutics!
Backed by Fapon Biotech, an international leader in in vitro diagnostics, biologics, and precision medicines, Mote Therapeutics is an innovative Lexington-based biotechnology startup building the RNA medicines of tomorrow. Led by a pioneer in the field of RNA therapeutics and supported by Fapon’s Greater Boston R&amp;D Center of Excellence, we’re pulling together a team of talented scientists, leaders, and operations specialists to solve some of the major barriers to success that RNA therapeutics face.
About Fapon Biotech
Founded in 2001 and headquartered in Guangdong, China, Fapon Group is mainly engaged in product R&amp;D and services of in vitro diagnostics (IVD), biological therapies, and precision diagnostics and treatments. With our core value of "foresee and prepare for what the future demands", Fapon has historically focused on three major businesses: raw material solutions, IVD ecosystem platform service, and intelligent digital diagnosis and treatment. Fapon’s recent expansion into therapeutics was recently marked by success with the receipt of IND approval from the FDA for a differentiated CD47 antibody drug, the first in a rapidly expanding therapeutics effort.
With a global footprint, Fapon has established major production and sales (R&amp;D) bases in Beijing, Shenzhen, Shanghai, the United States, Germany, India and other locations throughout the world, forming a global R&amp;D, production, marketing, and service network with products being widely sold in 61 countries and regions.
You can learn more about us by visiting <a href="https://en.faponbiotech.com" target="_blank">https://en.faponbiotech.com</a>
An equal-opportunity employer, Fapon welcomes and encourages diversity in our workforce.
Job Description 
We are seeking a scientific contributor to develop validated analytical assays for LNP and drug product characterization. This role will be responsible for designing, developing and validating analytical assays for a targeted LNP drug product to support the platform and pipeline development. The candidate would have the opportunity to work in a collaboration-oriented role in which they would coordinate with other teams and provide analytical support to the discovery and PD teams. The ideal candidate is a sciences major with strong exposure to analytical techniques and who is excited by the idea of being a core participant in building an early startup and guiding the scientific vision of the company. They would be engaged in science and driven by our mission to create therapies that help people in ways that are currently impossible.
<ul>
<li>Designing, developing and validating analytical assays for LNP and targeted LNP drug product characterization</li>
<li>Develop assays for LNPs including lipid raw material QC, composition assessment, Lipid/cargo profiling and LNP/tLNP characterization using HPLC (SEC, Reverse Phase), fluorescence-based methods and other analytical techniques</li>
<li>Work with cross-functional groups including LNP discovery, PD and CMC team to support needs of analytical method development, characterization, and transfer</li>
<li>Perform CRO outreach including experimental planning, work coordination and data interpretation for as analytical SME</li>
<li>Support technology transfer to Industry Partners</li>
<li>Foster collaborative relationships across the team and company and engage in a positive and exciting work environment</li>
<li>Contribute to hiring, training, and collaborating with scientists (as needed)</li>
<li>Author technical documents, including SOPs for analytical methods, maintain diligent records and demonstrate proficiency in scientific communication</li>
<li>Support high-quality documentations to support regulatory filings</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>BS/MS in life sciences, pharmaceutical sciences, or related field, preferably with 7/5 years of relevant experience. The title will be commensurate with experience.</li>
<li>Hands on experience developing analytical methods for complex biological therapeutics</li>
<li>Prior experience in developing analytical methods for LNP characterization is a must and will be key for this role</li>
<li>Knowledge of ICH/USP guidelines</li>
<li>Experience in analytical methods with HPLC (IPRP, SEC, IEx), UV-vis, colorimetric and fluorescence-based</li>
<li>Must be eligible to work in the United States</li>
</ul>
&nbsp; Preferred Qualifications:
<ul>
<li>Experience in developing validated analytical assays</li>
<li>Experience in advanced analytical methods for LNP characterization such as LC-MS, MALS, SEC-MALS etc</li>
<li>Strong communication skills and ability to present complex technical topics to diverse audiences with varying technical depth.</li>
<li>Strong collaborative instinct with good time and resource management skills to match the fast-paced start-up work culture.</li>
<li>Able to collaborate on and execute multiple parallel studies</li>
</ul>
 Additional Information 
What We Offer:
At our RNA Venture, we aim to outmatch the typical benefits you might see in an early startup. We offer:
<ul>
<li>Financial security through competitive compensation, incentives, and retirement plan</li>
<li>Health care and well-being programs including competitive medical, dental, vision &amp; medical benefits</li>
<li>Generous paid time off including vacation, sick time, holidays, and winter shutdown</li>
<li>401(k) retirement savings with a generous company match</li>
<li>Commuter benefits</li>
<li>Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more</li>
<li>We continue to optimize our benefits &amp; wellness programs as we grow our organization to make sure they meet our diverse workforce needs</li>
<li>The stability of a startup backed by a company with a record of strong financial performance year over year</li>
</ul>

Senior/Principal Research Associate (LNP Analytics)

<h3>Job Description</h3>
Job Description
About General Fluidics General Fluidics is a clinical diagnostics startup developing the Axess™ platform, a breakthrough point-of-care system that delivers laboratory-grade performance across clinical chemistry, hematology, and immunoassays from a single blood sample. By integrating three “gold standard” analytical technologies into one compact instrument, we are transforming how clinicians access and act on diagnostic data. Learn more at generalfluidics.com.
The Role We are seeking a highly motivated Senior Research Associate to join our R&amp;D team and help expand our menu of diagnostic assays for veterinary and human health applications. This is an R&amp;D-focused laboratory role—ideal for a scientist who thrives on experimental design, assay development, and hands-on instrumentation work. You will design, troubleshoot, and interpret experiments where answers are unknown, not simply execute QC protocols.
Reporting to the VP of Assay Development, you will work closely with engineers and scientists to optimize assay and instrument performance, generate data for analytical validation, and accelerate our path to regulatory clearance and product launch. This role is best suited for a junior scientist with prior industry experience and&nbsp;self-starter who can work independently under mentorship, with the drive to solve problems in a fast-paced, startup environment.
Key Responsibilities
<ul>
<li>
Design, develop, and validate clinical chemistry, hematology, and immunoassays on the Axess™ point-of-care instrument.
</li>
<li>
Independently plan and execute experiments to optimize assay and instrument performance, collaborating closely with engineers on system integration.
</li>
<li>
Perform data analysis and statistical evaluation to guide assay development and regulatory submissions.
</li>
<li>
Author experimental protocols, R&amp;D reports, and supporting documentation.
</li>
<li>
Support quality assurance through calibration, control protocols, and proficiency testing.
</li>
<li>
Work safely with human and animal blood specimens in compliance with biosafety regulations.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s, Master’s, or PhD in biotechnology, biomedical engineering, chemistry, physics, or related field.
</li>
<li>
3-6 years of prior industry R&amp;D experience (not academic lab or QC/manufacturing)&nbsp;
</li>
<li>
Experience designing and interpreting experiments, analyzing data, and troubleshooting unexpected results.
</li>
<li>
Hands-on laboratory skills: pipetting, assay development, reagent preparation, use of biosafety cabinets.
</li>
<li>
Familiarity with clinical instrumentation (e.g., flow cytometry, hematology analyzers, clinical chemistry, immunoassays) strongly preferred.
</li>
<li>
Exposure to diagnostic assay development, validation, or instrumentation is a plus.
</li>
<li>
Comfortable in a dynamic startup environment: onsite presence, ownership mentality, willingness to push projects forward outside a strict 9–5.
</li>
<li>
Excellent communication skills, with the ability to clearly present scientific concepts and data.
</li>
</ul>
Who You Are
<ul>
<li>
Curious, creative, and excited to tackle open-ended scientific questions.
</li>
<li>
Thrives on independence but values mentorship and collaboration.
</li>
<li>
Driven by the opportunity to help build a transformative diagnostic platform from the ground up.
</li>
</ul>
Company DescriptionGeneral Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus. 
<h3>Company Description</h3>
General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus.

Senior Research Associate

<h3>Job Description</h3>
Job DescriptionSalary: 
The Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute that is addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. Our research strategy uses molecular and genomic technologies to address questions related to Oceans and Human Health in two divisions (1) Marine Biomedical Discovery and (2) Healthy Oceans and Fisheries. GMGI is looking for a highly motivated Research Associate who will play an important role in contributing to our eDNA Service Lab within the Healthy Oceans and Fisheries Division.
 
The ideal candidate will have strong experience in molecular biology/ecology applied to fisheries and knowledge of common molecular laboratory techniques and data analysis. The candidate must be capable of working independently to design experiments, generate high quality data, and analyze results for a variety of projects directed by GMGI research staff. Experience with eDNA is highly desirable. This position is an extraordinary opportunity for an ambitious and entrepreneurial person who is interested in helping to contribute to a world-class research institute.
 
Responsibilities
 Design and execute experiments using molecular biology/genomics techniques
 Perform DNA/RNA isolations and quantification, PCR, qPCR, RT-qPCR, ddPCR
 Prepare libraries and run Illumina next-generation sequencing
 Conduct eDNA metabarcoding and species presence/absence assays
 Apply knowledge of experimental design, bioinformatics, and statistics to analyze results
 Participate in field collections for eDNA samples, including tissue dissection and processing
 Organize, process, and archive field and lab samples following established protocols
 Prepare client-facing reports and scientific communications (presentations, manuscripts, etc)
 Communication with clients via email and meetings to provide updates, answer questions, and ensure project success.
 
Qualifications
 Bachelors or Masters degree in biology, molecular biology, marine biology, or related discipline
 Hands-on experience with molecular biology techniques including qPCR, RT-qPCR, and Next-Generation Sequencing
 Experience working with genomics instruments and laboratory automation tools
 Demonstrated ability to plan and carry out experiments independently
 Familiarity with the command line interface, Linux, and R; hands-on experience in analyzing metabarcoding data
 Strong scientific writing and documentation skills
 Excellent verbal communication skills and comfort working in a team setting and with clients
 Commitment to scientific integrity and rigorous data quality standards; willingness to troubleshoot
 Adaptability and initiative in a fast-paced, start-up and research-driven environment
 Enthusiasm and commitment to GMGIs mission for science and education
 Self-starting, independent, creative thinker with strong problem-solving skills
 
This position will report to the eDNA Service Platform Manager.
Salary commensurate with experience.
 
It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes:
 Health and Dental Insurance
 Medical and Dependent Flex Spending Accounts
 Long Term Disability
 Life Insurance
 Paid Time Off
 403(b) Retirement Plan
 12 Paid Holidays
 
Applicants must be authorized to work in the US.
 
About GMGI
Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to address critical challenges facing our oceans, human health and the environment through innovative scientific research and education GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics.
GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need.
 
In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization, and in building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: <a href="http://www.gmgi.org" target="_blank">www.gmgi.org</a>

Research Associate I - eDNA Service

<h3>Job Description</h3>
Job DescriptionContract Research Associate – Virology (contract 3-4 months) &nbsp;Why Work for Us?At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. We are a high performing team, showing up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.Our Science: Advancing Cancer ImmunotherapiesCandel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: <a href="http://www.candeltx.com" target="_blank">www.candeltx.com</a>Position Summary:We are seeking a highly motivated and collaborative Research Associate with a strong foundation in virology to support the development of next-generation HSV-1 viral immunotherapy candidates. This individual will contribute to the enLIGHTEN™ Discovery Platform through hands-on experimental work, including viral vector testing, mammalian cell culture, and virology-specific assays. The ideal candidate will bring a passion for innovation and a desire to work in a fast-paced, cross-functional research environment.Key Responsibilities:
<ul>
<li>Support the design, production, and testing of novel HSV-based viral vectors.</li>
<li>Conduct classical virology techniques such as virus production, purification (e.g., ultracentrifugation), and titering.</li>
<li>Execute virology-specific assays including plaque assays, TCID50, viral titration, and viral genome quantification using qPCR.</li>
<li>Contribute to viral vector engineering and optimization of workflows.</li>
<li>Maintain mammalian cell culture operations, including cryopreservation, routine culture, and cell banking.</li>
<li>Perform in vitro to evaluate viral vector transduction and biological activity.</li>
<li>Document experiments in electronic laboratory notebooks, analyze data, and prepare reports for internal review.</li>
<li>Contribute to a scientific culture that values creativity, rigor, and innovation.</li>
</ul>
Qualifications:Education:
<ul>
<li>MS in Virology, Biotechnology, or related field with 1–3 years of industry experience, or</li>
<li>BS with 3–5 years of relevant experience.</li>
</ul>
Experience and Skills:
<ul>
<li>Hands-on experience with virus production, purification, and quantification techniques (e.g., plaque assays, TCID50, qPCR) required.</li>
<li>Solid foundation in mammalian cell culture and aseptic technique.</li>
<li>Familiarity with viral vector design and characterization, particularly HSV-based systems.</li>
<li>Strong analytical and organizational skills with attention to detail.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficiency in Microsoft Office, GraphPad Prism, and SnapGene (preferred).</li>
</ul>
&nbsp;Work Environment:This is a lab-based position in Needham, Massachusetts. &nbsp;
Powered by JazzHR
dtiN9KRel3

Contract Research Associate - Virology

<h3>Job Description</h3>
Job DescriptionDescription:
JOB OVERVIEW
 
Ethos Laboratories, Massachusetts facility, is CLIA-certified clinical diagnostic testing facility. The Supervisor Core Lab is primarily responsible for the day-to-day operation of the Core Lab. They will ensure that all patient sample accessioning, preparation, toxicological analysis using EIA and LC-MS/MS instrumentation, and report releasing occurs according to established SOPs. In addition, they will primarily operate and maintain LC-MS/MS instrumentation and ensure that data analysis and report certification meets established turnaround time (TAT) requirements.
 
ESSENTIAL FUNCTIONS
<ul>
<li>Supervise Clinical Laboratory Technician(s) and all testing processes including accessioning, sample preparation, screening, and confirmatory toxicological testing at Core Lab</li>
<li>Guide the day-to-day workflow of the lab and the Clinical Laboratory Technician(s)</li>
<li>Prepare, run, and analyze urine specimens on LC-MS/MS instrumentation</li>
<li>Maintain, troubleshoot, and operate LC-MS/MS instrumentation</li>
<li>Interpret, analyze, and release patient toxicological reports using EIA and LC-MS/MS instrumentation</li>
<li>Prepare solutions for LC – requiring candidate to perform calculations related to basic chemistry, such as molarity, buffers, dilutions, etc.; also requires appropriate documentation of solutions prepared, opened, and filled </li>
<li>Wash used reagent bottles/glasses/graduated cylinders </li>
<li>Update MS for changes in methods, test menus, or changes in testing consumables, such as columns, solvents, etc. – requiring tracking maintenance repairs and monitoring use of consumables to stay within budgets </li>
<li>Execute the successful tuning and calibration of LC-MS/MS systems, identify system errors, troubleshoot tuning/calibration errors, and work in close contact with Laboratory Director to correct instrumentation errors </li>
<li>Prepare daily work lists for all methods and all matrices, ensuring accuracy of methods and most efficient use of instrument time </li>
<li>Work on selected projects as determined by the Laboratory Director, and meet all established deadlines and project goals </li>
<li>Review and certify patient reports following established protocols – specifically for urine testing – utilizing and reporting point of care testing, EIA screening, and LC-MS/MS confirmation testing results </li>
<li>Answer incoming phone calls from customers, including questions regarding basic toxicology, basic drug metabolism, assistance with report issues, and sending reports </li>
<li>Coordinate with Newport lab for data analysis and/or certifying reports support when necessary</li>
<li>Complete internal and external rerun requests</li>
<li>Review calibration and quality control data for each batch of patient samples </li>
<li>Utilize established protocols to confirm retention time, precursor and product ions, and qualifier ions are within established ranges for peak qualification and note any discrepancies </li>
<li>Identify patient samples requiring reinjections or re-extractions following established protocols </li>
<li>Assist in proficiency testing, monitoring of daily controls, and be responsible for operating within the established quality controls parameters; including the recognition of invalid data and bringing all errors to the supervisor’s attention </li>
<li>Adhere to CAP/CLIA compliance standards </li>
<li>Participate in developing new testing opportunities and method development as needed </li>
<li>Prepare quality controls and calibrators from certified standard materials</li>
<li>Prepare reports of technological findings by collecting, analyzing, and summarizing information. Participates in Proficiency Testing of unknown samples according to Laboratory’s policy for testing survey samples.</li>
<li>Maintain safe and clean working environment by complying with procedures, rules, and regulations.</li>
<li>Protect patients and employees by adhering to infection-control and hazardous waste policies and protocols; follows patient identification procedures.</li>
<li>Adhere to HIPPA and PPE Policies, and Office Rules (Maintains patient confidentiality, and protects the clinic by keeping private information confidential.)</li>
<li>Create staff schedules, organizes workloads and assigns duties to staff, including securing sufficient coverage</li>
<li>Participate in hiring, evaluation and training of new employees</li>
<li>Monitor TAT for Core Lab tests and KPIs for Core Lab employees</li>
<li>Participate in CAP preparation, inspections and compliance</li>
<li>Orient new employees</li>
<li>Participate and perform employee competencies</li>
<li>Additional duties as assigned</li>
</ul>
 
Requirements:
PROFESSIONAL REQUIREMENTS
<ul>
<li>Regular and prompt attendance </li>
<li>An advanced understanding of drug metabolism, toxicology, forensic testing, P450 enzymes, or testing principles specifically related to urine and oral fluid metabolism </li>
<li>An advanced understanding of LC-MS/MS systems and data interpretation </li>
<li>Proficient in operating complex laboratory instrumentation and computers with scientific software </li>
<li>Ability to participate in method development, validation or research with Technical Supervision preferred </li>
<li>Able and willing to follow established protocols employing acceptable forensic standards of analysis and the use of judgment in searching for solutions or new applications within one’s own experience </li>
<li>Must be able to work with limited supervision where the work assignments are subject to established procedures, practices, precedents, methods, techniques, standards, and/or well-defined policies </li>
<li>Must be able to achieve superior results when work is reviewed in terms of quality, volume, timeliness, and adherence to established methods, standards and policies </li>
<li>Participate in ongoing training and continuing education courses related to drug metabolism, toxicology, and LC-MS/MS systems </li>
<li>Must be able to supervise a team, communicate to all team members, and organize day-to-day responsibilities</li>
<li>Must be able and willing to wear personal protective equipment (PPE) when required </li>
<li>Proficient with Microsoft Office applications</li>
<li>Ability to multitask in a fast-paced environment, organize and prioritize work as needed</li>
<li>Can recognize problems with instrumentation and samples that could impact results</li>
<li>Communicates effectively with both internal and external customers</li>
<li>High level of attention to detail</li>
</ul>
EDUCATION AND EXPERIENCE REQUIREMENTS
<ul>
<li>Master’s Degree in Life Science, Pharmacology, Toxicology, Biology, Physics, or similar analytical science field with 1 year of related experience, or Bachelor of Science with 2-3 years of relevant experience</li>
<li>At least 1 year of supervisory experience required</li>
<li>Preference for candidates with familiarity of LC-MS/MS instrumentation</li>
<li>Preference for candidates with familiarity with Agilent MS and LC systems – specifically MassHunter Acquisition and Quantitation Programs</li>
<li>Previous experience with laboratory information systems preferred; familiarity with Windows software applications a plus</li>
</ul>
KNOWLEDGE, SKILLS AND ABILITIES
<ul>
<li>Ability to communicate effectively, orally and in writing</li>
<li>Demonstrated leadership ability</li>
<li>Ability to coordinate laboratory functions and represent the toxicology laboratory professionally</li>
<li>Excellent time management, scheduling, documentation, and organizational skills</li>
<li>Demonstrated troubleshooting abilities</li>
<li>Must be flexible, innovative, and self-motivated</li>
<li>Ability to function independently and in a team environment</li>
</ul>
PHYSICAL REQUIREMENTS
<ul>
<li>Work is performed in a laboratory environment and exposes the incumbent to normal laboratory hazards and chemicals, including biohazard materials</li>
<li>Work in varying degrees of temperature (heated or air conditioned)</li>
<li>Position requires sitting, walking, reaching, bending, stooping, and handling objects with hands and/or fingers, talking and/or hearing, and seeing</li>
</ul>
DIRECT REPORTS
<ul>
<li>Clinical Laboratory Technician</li>
</ul>

Supervisor Core Lab

<h3>Job Description</h3>
Job Description
Part Time Shift: Every other Saturday and Sunday 7:00am-3:30pm Hourly Pay Range: $25.00-$30.00 (Based on experience)
POSITION SUMMARY 
Performs lab testing and associated activities within the Microbiology section, including Serology, Virology and Parasitology.
Essential Position Duties 
<ul>
<li>Reviews the daily specimen management report.</li>
<li>Troubleshoots and maintains the LIS and instruments interface and software.</li>
<li>Performs Clostidium difficile assays.</li>
<li>Resolves client problems as needed.</li>
<li>Performs and records all quality assurances systems required to maintain precision and accuracy, including proficiency testing.</li>
<li>Performs other tasks and procedures in Microbiology as required which are commensurate with education, training and experience.</li>
<li>Assists in maintaining adequate inventory of supplies.</li>
<li>Record lot numbers and ensures compliance with State requirements for documentation of lot numbers with quality control and specimen records.</li>
<li>Performs all clerical functions associated with the department.</li>
<li>Reads bacterial and viral cultures. Performs biochemical identification procedures as necessary and record MIC results. </li>
<li>Follows all safety protocols as outlines in safety manual.</li>
<li>Identifies and pursues self improvement needs.</li>
<li>Seeks coaching/mentoring when appropriate.</li>
<li>Performs other duties as assigned</li>
</ul>
Compliance Responsibilities 
<ul>
<li>Participates in required orientation, Compliance and HIPAA training programs.</li>
<li>Cooperates with monitoring and audit functions and investigations.</li>
<li>Participates, as requested, in process improvement responsibilities.</li>
</ul>
POSITION QUALIFICATIONS 
Core Competencies/Skill Sets 
<ul>
<li>Excellent verbal and written communication skills.</li>
<li>Detail oriented and organizational skills.</li>
<li>Exercises accuracy and precision in completion of prescribed tasks and treatments.</li>
</ul>
Professional Experience/Educational Requirements 
<ul>
<li>Bachelor’s degree or MT (ASCP or equivalent preferred); Associates degree with MLT</li>
<li>Minimum of one (1) year experience in the area of Microbiology.</li>
<li>Some computer experience required.</li>
</ul>
Certification/Licensure
<ul>
<li>Must qualify as a clinical laboratory technologist under CLIA regulations.</li>
</ul>
Benefits:
TridentCare offers a competitive wage and robust benefit package to full time employees. Part time employees are eligible for many of the same below, pro-rated. Benefits include:
<ul>
<li>Two weeks of vacation time</li>
<li>Health Insurance after 30 days!</li>
<li>Sick time</li>
<li>8 paid holidays</li>
<li>Same day pay available</li>
<li>Medical insurance allowance, giving you the freedom to customize your plan to fit your needs</li>
<li>Dental insurance</li>
<li>Vision insurance</li>
<li>Disability insurance</li>
<li>Company paid life insurance</li>
<li>401(k)</li>
</ul>
#MBX

Microbiologist/ MLT, Microbiologist

<h3>Job Description</h3>
Job DescriptionTitle: Research Model Husbandry Job Location: Wilmington, MA Job Duration: 6 Months- Temp to Permanent Shift: Work shift – Monday to Friday – Std Pay: $20- $21.25/Hour on W2 Position Summary: Essential duties and responsibilities:
<ul>
<li>Has substantial understanding and knowledge to perform husbandry tasks, including supplying food, bedding, water and environmental enrichment.</li>
<li>Proficient at maintaining rat and mouse colonies, including setting up matings, weaning and sexing of offspring, genetic sampling of animals, processing samples and other technical tasks as required.</li>
<li>Proficient at handling rodents (mice and rats), including restraining of animals for collection of fecal pellets, ear/tail sampling as well as tagging animals for identification.</li>
<li>Has substantial understanding and knowledge to observe animals for any abnormalities or common health issues.</li>
<li>Has substantial understanding and knowledge to identify and select specific animals for customer shipments, genotyping, health monitoring, matings, transfers or other various tasks as needed.</li>
<li>Learn, understand, and comply with all Standard Operating Procedures (SOPs). Able to complete new processes/tasks with minimal instruction. Strictly follow all animal welfare standards and biosecurity procedures necessary to maintain isolator integrity and animal health status, including the proper sterilization and entry of supplies/animals into isolators.</li>
<li>Workload contains complex projects and requires judgement in resolving issues and/or in making recommendations. Be detailed-oriented and enter accurate data entry into Internet Colony Management (ICM).</li>
<li>Ensure compliance with all local, state and federal laws governing the use of research animals. Ability to collaborate with others to train and mentor on knowledge and skills learned.</li>
<li>Ability to self-organize, plan and execute daily tasks.</li>
<li>Perform general housekeeping and adhere to EHS, safety, and ergonomic procedures. Has substantial understanding of using general computer skills and ability to quickly learn and master required computer programs, databases and other applications (i.e. ICM and Microsoft Office)</li>
<li>Engage in studies, special projects, efficiency improvements, engagement opportunities, etc.</li>
<li>Identify issues and recommend potential solutions to management.</li>
<li>Able to effectively apply and incorporate client DNA into day-to-day work.</li>
<li>Perform all other related duties as assigned.</li>
</ul>
 Minimum Qualifications:
<ul>
<li>To qualify for this role, candidates must possess one of the following combinations of educations/experience:</li>
<li>Bachelor’s Degree (B.A./B.S.) plus a minimum of 0-1 years of related experience.</li>
<li>Associate’s Degree (A.A./A.S.) plus a minimum of 1-2 years of related experience.</li>
<li>High School diploma or GED plus a minimum of 2-4 years related experience.</li>
</ul>
 In addition:
<ul>
<li>Competent with using a tablet computer for data entry and communication (emails, IM’s, etc)</li>
<li>The ability to develop knowledge of, respect for, and skills to engage with those of other cultures or backgrounds is required.</li>
<li>The ability to communicate clearly and effectively is required.</li>
<li>Must possess a high level of initiative and ability to work with minimal supervision</li>
<li>Proficient in computers (IE: MS Office Suite)</li>
</ul>
 Preferred Qualification: • AAALAS certification at the ALATG. #sczr2

Research Model Husbandry

<h3>Job Description</h3>
Summary:
Under the general direction of the Laboratory Managers and Medical Director, is responsible for staff orientation, training, and competency assessment, and daily supervision of work activities of personnel.
 
Does this position require Patient Care? No
 
Essential Functions:
-Provides daily supervision of technical, clerical, and service employees.
-Plans, organizes, delineates, and schedules duties and responsibilities of Laboratory staff in conjunction with the Laboratory Managers. 
-Assists other technologists as needed with technical problems and interpretation of results. 
-Determines the priority of work at the laboratory, assuring the timely completion of work. 
-Is responsible for ordering and maintaining an appropriate level of inventory and laboratory supplies. 
-Maintains manuals on all Standard Operating Procedures and required records and reports. 
-Responsible for ensuring staff adhere to all safety policies and procedures. 
-Responsible for orientation, training, and competency assessments, assuring staff:
1. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results.
2. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient samples.
3. Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed.
4. Follow the laboratory's established corrective action policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.
5. Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical consultant, technical supervisor, clinical consultant or director; and
6. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications.
 
Education:
Bachelor's Degree Medical Technology required or Bachelor's Degree Laboratory Sciences required and Other Certificate/Diploma Clinical Laboratory Sciences required.
 
Can this role accept experience in lieu of a degree?
No
 
Licenses and Credentials:
Medical Technologist (ASCP) [MLT, MT, MLA, Histologists] - American Society for Clinical Pathology Board of Certification (ASCP-BOC) required.
 
Experience:
Lab experience 3-5 years required and Supervisory experience 1-2 years preferred.
 
Knowledge, Skills and Abilities:
- The knowledge, both practical and theoretical, of tests and procedures necessary to review findings and advise and direct subordinates in action.
- Demonstrates advanced level of analytical skills and judgment.
- Must have a relatively high level of analytical ability to work with complex instrumentation, resolve technical equipment problems, relate test results to normal and pathological states, and interpret quality control data.
- Must have understanding of computer technology and its application to analytical procedures and quality control.
- Must have a comprehensive understanding of laboratory equipment and its operation, maintenance and repair, and analytic techniques.
- Must have the ability to work independently, evaluate situations and act appropriately.
- Detailed knowledge of applicable federal, state and accreditation requirements.
- Ability to multitask in a fast-paced environment.
- Advanced computer skills.
- Comprehensive understanding of test principles, equipment operation and computer system operations.
- Make appropriate decisions, develop and complete follow-up actions in conjunction with lab leadership.
- Must be able to perform as a senior team member, providing direction and guidance to less experienced technologists.
- Must have the ability to pay careful attention to detail and to adhere to written protocols, including communication to lab leadership when issues are identified.
- Must be able to perform as a team member.
- Excellent interpersonal skills.
- Ability to interact professionally and effectively with numerous staff, including physicians, hospital personnel, employees, and patients.

Supervisor, Clinical Laboratory

<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.
</li>
<li>
Support audits and maintain compliance with NADCAP, ISO, AS9100D, and customer specifications.
</li>
<li>
Drive process improvements using Lean, Six Sigma, and data-driven problem solving.
</li>
<li>
Ensure compliance with environmental, health, and safety regulations for chemical handling and waste treatment.
</li>
<li>
Document standard operating procedures, work instructions, and process records.
</li>
<li>
Collaborate with cross-functional teams to meet production, quality, and cost goals.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s degree in Chemical Engineering, Materials Science, Chemistry, or a related field.
</li>
<li>
3+ years of experience in chemical or surface finishing processes (electroplating, anodizing, coatings, etc.).
</li>
<li>
Strong understanding of process control, bath chemistry, and troubleshooting.
</li>
<li>
Familiarity with NADCAP, ISO, and AS9100 requirements preferred.
</li>
<li>
Knowledge of safety practices for handling hazardous chemicals.
</li>
<li>
Excellent problem-solving, analytical, and communication skills.
</li>
<li>
Ability to work hands-on in a production environment.
</li>
</ul>
Preferred Certifications (Not Required)
<ul>
<li>
Lean Six Sigma (Green Belt or higher).
</li>
<li>
Certified Quality Engineer (CQE).
</li>
<li>
OSHA / HAZWOPER or other EHS-related training.
</li>
<li>
Professional Engineer (PE) license is a plus.
</li>
</ul>
Benefits
<ul>
<li>
Competitive salary with performance-based incentives.
</li>
<li>
Health, dental, and vision insurance.
</li>
<li>
Retirement plan with company match.
</li>
<li>
Paid time off and holidays.
</li>
<li>
Opportunities for career growth and professional development.
</li>
</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>
Job Description
Description:
<ul>
<li>
The Associate QC Scientist performs laboratory testing within a fast paced GMP environment in support of one or more of the following areas; raw materials, in-process product, final Bulk product, stability, and/or validation. 
</li>
<li>
Analyzes test data and evaluates results. 
</li>
<li>
Writes procedures with guidance. 
</li>
<li>
Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties.
</li>
<li>
Assists in trending data to support assay performance. 
</li>
<li>
Assists in writing lab Investigation reports.
</li>
<li>
Performs test methods as written to support product/material release.
</li>
<li>
Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.
</li>
<li>
Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.
</li>
<li>
Will perform a multitude of laboratory techniques for which they are trained.
</li>
<li>
Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.
</li>
<li>
Revises procedures as necessary and provides support for department.
</li>
<li>
Helps maintain trend reports, which support departmental performance.
</li>
<li>
Support investigations
</li>
<li>
Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.
</li>
</ul>
Qualifications
<ul>
<li>
BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.
</li>
<li>
3 + years of related work experience
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

584 Science Jobs