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<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;
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dtiN9KRel3

Contract Research Associate - Virology

<h3>Job Description</h3>
Job Description
Nanopath is a well-funded Series A-stage company working to develop a first-in-class in vitro diagnostics platform to revolutionize the way we diagnose disease. Nanopath works to disrupt existing lengthy molecular testing methodologies by bringing them closer to the patient. We aim to improve the lives of patients, starting with women, using our purpose-built tool that provides actionable information within a single office visit.
The company is headquartered at The Engine, the premier tough technology incubator in the Kendall Square ecosystem. As a company, we are committed to health equity and the design of solutions for underserved populations and low-resource settings. Corporate sustainability – both environmental and social - is at the forefront of our decision making.
About the Role
<ul>
<li>Support and manage a variety of assay development tasks. We are happy to tailor key responsibilities to the candidate ranging from molecular biology, cell culture, biomanufacturing, and bioinformatics. </li>
<li>Participate in critical team discussions, meetings, and presentations. Our co-ops are given critical and important projects!</li>
<li>Work directly with our tight-knit team of scientists and engineers to drive our product forward.</li>
<li>Learn more about cutting edge biophysics and interdisciplinary medtech development.</li>
</ul>
Qualifications:
<ul>
<li>Ability to commit to 15+ weeks of full-time and onsite work in Cambridge, MA</li>
<li>Sophomore or above with demonstrated experience through past internships or research projects</li>
<li>Excellent communication and presentation skills, highly organized with demonstrated curiosity, scientific rigor and creative problem-solving</li>
<li>Proactive self-starter with eagerness to adapt to a fast-paced, dynamic startup environment</li>
<li>Passion for technology translation and willingness to shape Nanopath's future</li>
<li>Current enrollment in a relevant academic program - we are open to undergraduate and graduate degree opportunities</li>
</ul>
This is a full-time onsite role in Cambridge, MA starting in early January, lasting no less than 5 months.
Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Nanopath we are dedicated to building a diverse and inclusive workplace, so if you're excited about this role but your past experience doesn't align perfectly with every point in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles!
Nanopath Inc. is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Nanopath does not accept unsolicited resumes from recruiters or agencies and we will not be responsible for any fees related to resumes that are unsolicited. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Nanopath, and Nanopath will not owe any referral or other fees with respect thereto.

Research Associate Co-op (January '26 Start)

<h3>Job Description</h3>
Job Description&nbsp;Work closely with Scientists to evaluate antibodies, proteins, small molecules, and drugs by in vitro cell-based assays including cytotoxicity assays, flow cytometry, functional assays, and molecular biology assays, including ELISA, WB, ect.&nbsp; Job will involve maintaining cell lines, setting up and developing in vitro assays, working closely with in vivo team to supply cells and then receive ex vivo samples and analyzing assays with harvested blood serum/tissue, and maintaining a lab notebook.&nbsp; &nbsp;
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YmFHsmtNfV

Research Associate I/II/III

<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.

Chemist

<h3>Job Description</h3>
Job Description
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer, and commercial leader in ePaper technology. The Billerica Research &amp; Development team is thriving and growing as we help develop products that are changing how people access information every day. We are seeking qualified candidates who are self-driven, looking to advance their career and become a high-impact player on a team.
Based on technology from MIT’s Media Lab, E Ink has transformed and defined the eReader market. Its Electrophoretic Display products make it the worldwide leader for ePaper. The Company’s corporate philosophy aims to deliver revolutionary products, user experiences and environmental benefits through advanced technology development.
Our diversity of people, backgrounds, experiences, thoughts and perspectives is fostered to create an inclusive work environment. Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that fosters a strong employee engagement, teamwork, safety and wellness.
We offer a competitive/generous benefits package that fits the needs of our employees. It includes health, dental, vision, wellness programs, employee discounts, 401k matches, ongoing development, advancement opportunities and more. This position is also eligible for our bonus program. (see E Ink │ Our Company)
About the position:
The Chemical Engineer will perform hands-on laboratory and pilot-scale operations to support the synthesis, processing, and finishing of organic pigments. This role involves preparing and operating chemical equipment, performing wet chemistry reactions, monitoring process parameters, and conducting quality control tests to ensure materials meet specifications.
Key Responsibilities
<ul>
<li>Carry out chemical reactions of organic synthesis of organic pigments and dyes, etc.</li>
<li>Operate wet chemistry equipment such as reactors, filtration units, washing stations, and dryers</li>
<li>Carry out pigment finishing process steps (flushing, drying, grinding, surface treatment)</li>
<li>Take in-process samples and perform analytical tests (pH, solids content, particle size, color strength, shade, etc.)</li>
<li>Record all process parameters and observations accurately in batch records</li>
<li>Work closely with R&amp;D scientists and engineers to scale up reactions from lab to pilot plant</li>
<li>Support process optimization and troubleshooting efforts</li>
<li>Work with senior technical staff to conduct laboratory experiments in the area of pigment surface modification and ink formulations</li>
<li>Perform electrical and electro-optical measurements for new color displays</li>
</ul>
Qualifications
<ul>
<li>Bachelor or associate’s degree in Chemistry, Chemical Engineering, Material Engineering, Polymer Engineering or a related field; or equivalent hands-on industrial experience</li>
<li>1–3 years in chemical manufacturing, preferably with pigments, dyes, or fine chemicals</li>
<li>Experience with wet chemistry techniques (organic and polymer synthesis, media milling, precipitation, filtration, washing, drying)</li>
</ul>
Skills &amp; Competencies:
<ul>
<li>Strong understanding of basic chemistry principles and chemical safety</li>
<li>Ability to follow detailed batch instructions and standard operating procedures (SOPs)</li>
<li>Hands-on experience with laboratory and pilot-scale chemical equipment</li>
<li>Good record-keeping, observation, and problem-solving skills</li>
</ul>
 Benefits:
<ul>
<li>Competitive total compensation package</li>
<li>Medical, dental and vision on 1st day</li>
<li>Company 401K match</li>
<li>20 PTO days</li>
<li>Generous sick leave policy</li>
<li>Casual day to day work environment</li>
<li>Hybrid/flexible work environment (for some positions)</li>
</ul>
E Ink is committed to a diverse and inclusive workforce. E Ink is an equal opportunity employer and does not discriminate on the basis of race, ethnicity, gender, identity, sexual orientation, veteran’s status, disability, age, or on any basis prohibited by federal and state law.

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