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field_job_employment_type

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<h3>Job Description</h3>
Job Description
SCOPE OF WORK: To conduct tutoring sessions and math workshops and coordinate the operations and services provided in the Math Lab in the Academic Center for Excellence (ACE). This position reports to the Vice President of Student Success (VPSS) at NHTI, Concord’s Community College.
ACCOUNTABILITIES: 
<ul>
<li>Tutors students individually or in small groups in the Math Lab;</li>
<li>Conducts workshops for math skill building;</li>
<li>Directs and supervises tutors, including peer and professional tutors;</li>
<li>Coordinates and supervises the daily operations of the Math Lab, under the guidance of the VPSS;</li>
<li>Maintains the Math Lab sign in kiosk and database;</li>
<li>Collaborates with Math faculty;</li>
<li>Assists other Academic Center for Excellence staff with upholding high standards of student success;</li>
<li>Ensures compliance with the overall mission of the Academic Center for Excellence;</li>
<li>Complies with all college, system, state and federal rules and regulations;</li>
<li>Other duties as assigned.</li>
</ul>
MINIMUM QUALIFICATIONS:
Education: Bachelor's degree from a recognized college or university with major study in mathematics, physics, engineering, education, or a related field. 
Experience: Two years' experience as a teacher, academic advisor, academic program coordinator/manager, student services/support advisor, or related academic or student services experience. 
License/Certification: Possession of a valid Driver’s License or access to statewide transportation. 
DESIRED QUALIFICATIONS: Advanced knowledge of foundational and most upper-level Math courses (Finite Mathematics, Statistics, Calculus, Trigonometry).
RECOMMENDED WORK TRAITS: Knowledge of teaching methods and materials, problems and subject matter as relates to course of instruction. Knowledge of program and academic standards. Ability to maintain comprehensive records of the progress and development of the individual student. 
General knowledge of student success models within higher education. Ability to detect and define problem areas and causes and to create and develop effective solutions, including the exercise of sound judgment in evaluating situations, planning action, making decisions and setting priorities. Ability to work independently to develop new or alternative approaches to meet changing and variable conditions. Ability to communicate effectively orally and in writing. Ability to establish and maintain effective working relationships with students and college personnel. Must be willing to maintain appearance appropriate to assigned duties and responsibilities as determined by the college appointing authority.
DISCLAIMER STATEMENT: This class specification is descriptive of general duties and is not intended to list every specific function of this class title.
Notice of Non-Discrimination: The Community College System of New Hampshire is an equal opportunity employer. The Community College System of NH does not discriminate on the basis on race, creed, color, religion, national or ethnic origin, age, sex, sexual orientation, gender identity and expression, physical or mental disability, genetic information, or law enforcement, or military, veteran, or marital status.

Academic Support Coordinator - Math Lab

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and BA Sciences. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes products to determine chemical and physical properties.</li>
<li>Will perform work under partial supervision and will provide over site to projects and assist other Chemists as needed.</li>
<li>Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks.</li>
<li>Performs data generation, analysis and more complicated problem solving with a minimal rework.</li>
<li>Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.</li>
<li>Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualification include a Bachelors degree in Chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required.
 
SHIFT
Wed-Sat 1st

MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Chemist II

<h3>Job Description</h3>
Job DescriptionDescription:
As a Research Assistant reporting to the Project Director, you will play a pivotal role in the Center for AIDS Research Network of Integrated Systems (CNICS). This dynamic project is a leader in HIV disease management research, capturing a wealth of data that informs clinical decisions and management strategies in HIV care. CNICS stands out for its capacity to provide peer-reviewed, open access to evolving clinical research platforms, collecting validated outcomes, longitudinal resistance data, detailed Patient Reported Outcomes (PROs), and biological specimens.
Your key responsibilities will include recruiting study participants for CNICS, obtaining informed consent, and processing, storing, shipping, and maintaining blood specimens. You will also be responsible for the administration of PRO surveys. Collaborating closely with patients, providers, and our research team, you will contribute significantly to the successful implementation and conduct of CNICS and its sub-studies, both within Fenway Community Health / The Fenway Institute and in partnership with external co-investigators.
This role demands a high level of attention to detail, organizational + communication skills, and a commitment to ethical research practices. If you are passionate about leveraging large-scale data sets to advance the field of HIV disease management and patient care, this position offers an excellent opportunity for growth and impact.
 
Essential Functions
 
Study Participation and Protocol Adherence Responsibilities
<ul>
<li>Participant Outreach: Proactively contact potentially eligible study participants, employing effective communication strategies to engage them in the research process.</li>
<li>Conduct Research Activities: Conduct research interviews, surveys, and study visits, demonstrating a keen attention to detail and unwavering adherence to specific research protocols.</li>
<li>Survey Administration: Administer participant surveys, ensuring the accuracy and reliability of data collection processes.</li>
<li>Specimen Handling and Management: Process, store, and maintain blood specimens according to established protocols and safety guidelines. Ensure specimens are properly labeled and stored to preserve their quality for analysis.</li>
<li>Shipping and Documentation: Coordinate the shipment of specimens to collaborators, adhering to safety and transport regulations. Maintain detailed documentation of specimen handling, storage, and shipping to ensure traceability and compliance with research standards.</li>
<li>Confidentiality and Ethics: Maintain strict confidentiality and uphold the highest standards of ethical accountability in all interactions with study participants, fostering a trustworthy research environment.</li>
<li>Study Design Assistance: Collaborate in the study design and protocol development process, taking into account funders' guidelines and federal HIPAA requirements to ensure compliance and relevance.</li>
<li>Communication of Results: Efficiently relay lab results and other pertinent information to primary care providers as authorized by participants, ensuring all communication aligns with department policy and participant consent.</li>
</ul>
Data Management and Analysis Responsibilities
<ul>
<li>Data Entry and Quality Assurance: Assist in the data entry process and rigorously check the quality of data. Proactively identify and resolve inconsistencies in data and data collection methods, and design effective systems and structures for file management.</li>
<li>Statistical Analysis: Routinely generate descriptive statistics, forecast future trends in follow-up, retention, and compliance, and conduct additional data analyses as required, adhering to the highest standards of precision.</li>
<li>Supervise Data Quality: Oversee the integrity and quality of data, ensuring accuracy and reliability.</li>
<li>Confidentiality and Record Maintenance: Maintain strictly confidential records of interested candidates and study participants, ensuring data security and privacy.</li>
<li>Demographic Data Management: Ensure that demographic information on research clients is not only complete but also regularly updated to reflect current data.</li>
<li>Foster Open Communication: Actively promote open communication and discussion among team members about any changes in protocol procedures and other information crucial to the department's and study's goals and objectives.</li>
<li>Standard Operating Procedures: Develop and regularly update standard operating procedures, aligning them with study protocols and laboratory safety regulations.</li>
<li>· Site Visit Coordination: Efficiently coordinate site visits with study monitors or collaborators, ensuring availability during these visits, and organize responses to site visit reports.</li>
<li>· Interagency Collaboration: Maintain necessary contact with external agencies involved in the study, such as laboratories, data centers, and contractors, facilitating smooth collaboration.</li>
<li>· Coordination with Stakeholders: Work closely with funders and other project staff to ensure that project data collection is on track and aligned with the study protocol and established timelines.</li>
</ul>
Communication and Collaboration
<ul>
<li>Relationship Management: Establish and maintain relationships with medical providers, collaborating with them to identify and recruit eligible patients for research studies. Act as a liaison between the research department and healthcare professionals to facilitate participant recruitment.</li>
<li>Protocol Development: Engage in the development and revision of research protocols and questionnaire formats, providing insights and suggestions to enhance the research process.</li>
<li>Project Communication: Regularly communicate initiatives, progress, and updates to the Project Director and Principal Investigator, ensuring transparency and alignment on the status of projects.</li>
<li>Regulatory Compliance: Assist with all Institutional Review Board (IRB) submissions concerning protocol changes and annual reviews. Prepare and submit these documents to the IRB with the approval and assistance of the site Principal Investigator or research scientist, ensuring adherence to ethical and regulatory standards.</li>
<li>Meeting Participation: Attend all regularly scheduled research meetings, trainings, forums, and pertinent Fenway Community Health staff meetings, ensuring active and meaningful participation.</li>
</ul>
Agency Participatory Expectations
<ul>
<li>Policy Adherence: Consistently adhere to all agency and departmental policies and procedures, demonstrating a commitment to organizational standards and ethical practices.</li>
<li>Quality Improvement Participation: Actively participate in quality assessment and improvement activities as requested, contributing to the continuous enhancement of research processes and outcomes.</li>
<li>Confidentiality Compliance: Uphold the highest principles of patient and client confidentiality, ensuring the trust and privacy of all individuals involved in the research.</li>
<li>Safety Vigilance: Strictly adhere to established safety policies, procedures, and precautions. Proactively identify potential or actual unsafe situations in the research environment and take prompt measures to rectify them, ensuring a safe and secure working environment.</li>
<li>Professional Development: Attend all required meetings, in-services, and professional trainings, demonstrating a commitment to ongoing learning and professional growth.</li>
<li>Competence Maintenance: Maintain the professional competence necessary to perform job responsibilities, ensuring the highest standards of research conduct and expertise.</li>
<li>Committee Participation: Serve on agency committees and participate in professional organizations when requested, demonstrating a willingness to engage in broader organizational and professional initiatives.</li>
</ul>
Perform Related Duties as Assigned
Requirements:
<ul>
<li>Educational Background: Bachelor's degree in a related field (e.g., public health, psychology, social sciences) or equivalent experience.</li>
<li>Research Skills: Experience with research concepts and techniques, including qualitative interviewing and basic quantitative analytical skills.</li>
<li>Communication Skills: Excellent written and verbal communication and interpersonal skills.</li>
<li>Administrative and Detail-Oriented Skills: Demonstrated strong administrative skills and a strong attention to detail.</li>
<li>Computer Proficiency: Strong computer skills and familiarity with data entry, management, and analysis.</li>
<li>Teamwork and Autonomy: Ability to function autonomously in a collaborative interdisciplinary team involving research, medical, and behavioral health care.</li>
<li>Diversity and Inclusivity: Ability to work harmoniously with diverse groups of individuals.</li>
</ul>
Preferred Skills:
<ul>
<li>Human Subjects Experience: One to two years’ experience working with human subjects.</li>
<li>Relevant Work Experience: Work experience in a biological or health science-related field.</li>
<li>HIV Knowledge: Familiarity with working with HIV-infected or at-risk individuals.</li>
<li>Clinical Research Background: Clinical research experience.</li>
<li>EMR/EHR Proficiency: Experience with Electronic Medical Records (EMRs) or Electronic Health Records (EHRs).</li>
<li>Cultural Experience: Experience working in an ethnically, culturally, and racially diverse environment.</li>
<li>Language Skills: Proficiency in Spanish, Haitian Creole, Brazilian Portuguese, and/or Arabic</li>
</ul>
Working Conditions and Physical Effort
Physical Demands:
<ul>
<li>Extended Computer Use: Ability to work at a computer station for prolonged periods, which is essential for managing and analyzing data, conducting literature reviews, and maintaining communication.</li>
<li>Keyboarding Proficiency: Frequent keyboarding required for data entry, report writing, and correspondence, emphasizing the need for comfort and efficiency in typing tasks.</li>
<li>Participant Interaction: Capability to conduct physical assessments and interviews with research participants, requiring physical mobility, manual dexterity, and interpersonal skills.</li>
</ul>
Working Environment:
<ul>
<li>Office Setting: Primarily based in an office environment, conducive to focused research work and data management.</li>
<li>Laboratory Interaction: Occasional visits to laboratory settings for specimen handling and understanding laboratory processes, adhering to safety protocols.</li>
<li>Fieldwork Flexibility: Potential for fieldwork involving participant recruitment and data collection, requiring adaptability and resilience.</li>
</ul>
Supervisory Responsibility
<ul>
<li>None</li>
</ul>
 
 This is a union position in a Fenway Health bargaining unit represented by 1199 SEIU United Healthcare Workers East 
 
We offer competitive salaries, and for those who qualify, an excellent benefits package; including comprehensive medical and dental insurance plans, and a retirement plan with employer match. We also provide 11 paid holidays, paid vacation, and more.LGBTQIA+ identified persons, Black, Indigenous, and other people of color (BIPOC), and individuals from other historically underrepresented communities are strongly encouraged to apply.

Research Assistant, Data Team

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
This opportunity provides analytical support to internal process development groups.
</li>
<li>
The position will work with a number of different analytical techniques that will include UPLC, HPLC, GC, and CE.
</li>
<li>
If applicable, analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method qualification and method transfer.
</li>
<li>
Analyzes early-stage lab samples, pilot plant samples, production samples, in process samples and CRO samples.
</li>
</ul>
Qualifications:
<ul>
<li>
BSc with at least 5+ years relevant experience
</li>
<li>
MSc with at least 2+ years relevant experience
</li>
<li>
Possesses extensive knowledge of various laboratory instruments like U/HPLC, GC, and CE.
</li>
<li>
Someone to jump right in, hands on exp.
</li>
<li>
Pharma preferred, Mix of academic and industry is good too
</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.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionWho We Are
TetraScience is the Scientific Data and AI Cloud company. We are catalyzing the Scientific AI revolution by designing and industrializing AI-native scientific data sets, which we bring to life in a growing suite of next gen lab data management solutions, scientific use cases, and AI-enabled outcomes. 
TetraScience is the category leader in this vital new market, generating more revenue than all other companies in the aggregate. In the last year alone, the world’s dominant players in compute, cloud, data, and AI infrastructure have converged on TetraScience as the de facto standard, entering into co-innovation and go-to-market partnerships: Latest News and Announcements | TetraScience Newsroom: 
In connection with your candidacy, you will be asked to carefully review the Tetra Way letter, authored directly by Patrick Grady, our co-founder and CEO. This letter is designed to assist you in better understanding whether TetraScience is the right fit for you from a values and ethos perspective. 
It is impossible to overstate the importance of this document and you are encouraged to take it literally and reflect on whether you are aligned with our unique approach to company and team building. If you join us, you will be expected to embody its contents each day. 
Who You Are
You are a strategic, analytically minded professional with a passion for bridging scientific insights and cutting-edge technology. You thrive in environments where you can collaborate with scientists, product managers, and engineers to transform complex scientific data into actionable outcomes.
With deep domain knowledge in drug discovery/preclinical development, CMC, or Quality, you are skilled at uncovering innovative use cases that drive AI and machine learning applications. Your ability to engage with scientists and business leaders alike makes you a key player in maximizing the value of scientific data.
You will need to be a high clock speed and forward-thinking individual with a passion for developing requirements for complex solutions targeted to R&amp;D and Quality personas inside of Life Sciences. 
You will need to be a high clock-speed, forward-thinking individual with a passion for developing requirements for complex solutions targeted to R&amp;D and Quality personas inside Life Sciences. You embody extreme ownership and have a demonstrated history of deriving maximum value from data through enrichment, analysis, and integration with AI and machine learning applications.
You should also be energized by regularly working onsite with customers. You thrive in dynamic, high-impact, face-to-face collaborative environments where you can build deep relationships and drive scientific transformation firsthand.
Requirements
What You Have Done
<ul>
<li>PhD with 15+ years of industry experience in life sciences, preferably across pharma, biotech, or health tech, with deep domain expertise in discovery, preclinical, CMC, and/or Quality.</li>
<li>Extensive hands-on experience or direct oversight in one or more of the following areas: high throughput screening, preclinical toxicology, materials engineering, analytical development, drug substance (DS) synthesis and manufacturing.</li>
<li>Delivered requirements for AI/ML-driven solutions in operational or productized environments that improved efficiency, reduced cost, and enhanced data utilization.</li>
<li>Extensive hands-on experience with scientific data workflows and lab automation; exposure to FAIR principles and modern data architecture is a plus.</li>
<li>Strong coding or scripting background (e.g., Python, Nextflow, AWS, SDKs) and familiarity with scientific tools, databases, and ontologies is preferred.</li>
<li>Exceptional communication and storytelling ability to engage technical and executive stakeholders.</li>
<li>Prior experience in customer-facing, consulting, or commercial-scientific interface roles.</li>
</ul>
What You Will Do
<ul>
<li>You will be a critical team member in a unique partnership to industrialize Scientific AI. As such, you will engage directly with customers onsite up to 4-5 days per week in the Boston Region</li>
<li>Customer Data Exploration: Investigate diverse customer datasets, identifying enrichment and AI-readiness opportunities.</li>
<li>Scientific Use Case Development: Collaborate with customers to define, iterate, and implement innovative scientific AI/ML use cases.</li>
<li>Stakeholder Engagement: Conduct onsite interviews and workshops to deeply understand customer challenges and data landscapes.</li>
<li>Data Analysis and Enrichment: Perform exploratory data analysis and define transformation workflows that enable scientific AI.</li>
<li>Workflow Documentation: Develop visual documentation including workflow diagrams, ERDs, and ontology definitions.</li>
<li>AI Model Evaluation: Provide practical scientific input on model output, with suggestions to improve real-world performance.</li>
<li>Customer Enablement: Deliver onsite demonstrations, conduct working sessions, and act as a trusted advisor in AI adoption.</li>
<li>Strategic Insight: Propose new directions, experiments, or platforms that can amplify scientific discovery and development.</li>
</ul>
Benefits
<ul>
<li>100% employer-paid benefits for all eligible employees and immediate family members</li>
<li>Unlimited paid time off (PTO)</li>
<li>401K</li>
<li>Remote working opportunities, when not at customer sites </li>
<li>Company paid Life Insurance, LTD/STD</li>
<li>A culture of continuous improvement where you can grow your career and get coaching</li>
</ul>

Scientific Business Analyst, Scientific AI- Boston

<h3>Job Description</h3>
Job Description
Job Description:
<ul>
<li>
We are seeking a highly motivated purification scientist to be a part of the Protein Sciences group (Biotherapeutics and Genetic Medicine department) who will contribute to Biologics research projects.
</li>
<li>
This scientist will work independently as well as part of teams to purify proteins in support of drug discovery.
</li>
<li>
The successful candidate will demonstrate scientific excellence, a strong work ethic, and dedication to team/project goals.
</li>
<li>
Develop protocols to purify proteins using AC, IEX, and SEC chromatography.
</li>
<li>
Work with AKTA FPLC systems to purify proteins.
</li>
<li>
Maintain a high level of productivity in the lab.
</li>
<li>
Effectively coordinate with colleagues and research teams.
</li>
<li>
Contribute to experimental design and process optimization.
</li>
<li>
Read and apply relevant scientific literature to improving protocols.
</li>
<li>
Effectively communicate research progress through oral presentations and written documentation.
</li>
<li>
Keep accurate, detailed, and timely records of laboratory work.
</li>
</ul>
Qualifications:
<ul>
<li>
BS and 3-5 years of relevant experience; MS and 2+ years of relevant experience or a recent PhD.
</li>
<li>
Strong laboratory skills, effective documentation skills and the ability to present data clearly are necessary.
</li>
<li>
Candidates should have experience in purification of proteins from E. coli, insect, and human cell culture systems.
</li>
<li>
Experience with high throughput purification a plus.
</li>
<li>
Experience with protein analysis: SDS-PAGE, western blot, and analytic SEC.
</li>
<li>
Experience in expression construct design and structural work is beneficial.
</li>
<li>
Experience in research and development of protein therapeutics is a plus.
</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.

Biologist

<h3>Job Description</h3>
Job Descriptionjob summary: 
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena.
Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!
#LI-AS1
 location: Andover, Massachusetts job type: Contract salary: $29.60 - 36.75 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
A position is available for a bioanalytical scientist to join a protein mass spectrometry laboratory lab in Pharmacokinetics Dynamics and Metabolism department.
The lab based role will focus on small scale preparation of biological samples such as cells, tissues or plasma for subsequent mass spectrometry measurement. This includes lysis, protein immunoprecipitation using beads and antibodies, protein digestions, filtration, pre-concentrations of proteins and peptide digests.
The successful candidate is detail-oriented and, following training, can operate independently. This position requires demonstrated experience in successfully executing complex bioanalytical procedures. Expertise in immunoanalytical workflows and in protein biochemistry, or proteomics techniques is a plus. We are looking for a scientist passionate about learning and quickly applying new skills to project needs.
<ul>
<li>Preparation of samples for mass spectrometry analysis</li>
<li>Design of experiments in collaboration with colleagues</li>
<li>Conduct analytical experiments and method development as needed</li>
<li>Identify and exploit new scientific concepts</li>
<li>Interpretation and documentation of experimental results</li>
<li>Communication of experimental results to team members</li>
<li>Maintaining high quality record in electronic lab notebook</li>
</ul>
 qualifications: 
Required:
<ul>
<li>BS/MS degree in chemistry, biological sciences, biochemistry or related fields (NON-PhD); BS + 3 years exp, MS + 1 year exp</li>
<li>LC-MS biological sample preparation involving a multi-step process to isolate, purify, and concentrate the analytes of interest for the LCMS analysis</li>
<li>Operation of laboratory equipment</li>
<li>Strong data organization, analysis, and communication skills</li>
</ul>
#LI-AL1
 skills: MS-WORD, MS-EXCEL, Chemistry 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

LC-MS Research Associate

<h3>Job Description</h3>
Job Description
Job Description:
<ul>
<li>
We are seeking a highly motivated contract scientist to join the Molecular Assessment and Profiling group in BioMedicine Design.
</li>
<li>
Will work with a talented team of scientists to develop innovative protein biotherapeutics to bring curative treatments to patients.
</li>
<li>
Will perform critical biophysical/analytical assays using a suite of established methods.
</li>
</ul>
Qualifications:
<ul>
<li>
BA/BS biochemistry major with 0-2 years with biochemistry research experience
</li>
<li>
Able to clearly communicate experiment results; experienced with using Microsoft PowerPoint and Excel for data presenting and reporting.
</li>
<li>
Familiar with protein bioanalytical characterization concepts including but not limited to aSEC (aggregation), iCE (charge profile), CGE (fragmentation) and DSC (thermal stability)
</li>
<li>
Fast learner, detail oriented and highly organized; ability to complete experiments with limited supervision after fully trained
</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.

Bench Scientist

<h3>Job Description</h3>
Job Description
Job Description:
<ul>
<li>
We are currently seeking a highly motivated and passionate scientist specializing in cellular immunology and biology to join our team in the Immunology Discovery department based in Cambridge, MA.
</li>
<li>
The candidate will focus on establishing novel therapeutic modalities using multiple in vitro assays, including primary immune cell and fibroblast cell culture, immunology assays, and basic biology and biochemical skills.
</li>
<li>
The scientist will be responsible for the execution and analysis of the data.
</li>
<li>
This position offers a unique opportunity for a talented scientist to work in a dynamic, innovative, and multi-disciplinary environment to develop their career at the interface of basic research and cutting-edge early drug discovery.
</li>
</ul>
Qualifications and Requirements:
<ul>
<li>
Must have a bachelor's degree in Biological Science or a related field with 3-5 years of experience in a biotech or pharmaceutical setup.
</li>
<li>
A Master's degree with 1-3 years of industrial experience or a Ph.D. is preferred.
</li>
<li>
Extensive hands-on experience in immunology, especially with multi-color flow cytometry (BD Canto II / Fortessa / LSR II), and independently analyzing data using analytical software such as FlowJo is required.
</li>
<li>
Motivated to execute well-thought-out and well-planned in vitro experiments using the tool reagents generated.
</li>
<li>
Basic cell biology and biochemical skills, including tissue culture, transfection, and cell line generation.
</li>
<li>
mRNA LNP candidate screening and assay experience is preferable.
</li>
<li>
Biology and biochemical assays, qPCR, RT-PCR, Western Blotting will be a nice to have.
</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.

Scientist

<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:
E Ink is the world leader in ePaper display technology. At the Billerica Innovation Center, we invent new materials for the development of next generation E Ink products. But we can’t improve product performance without evaluating the materials that go into them – that is where individuals like you come in. Reporting to the Senior Program Manager of the Analytical Chemistry Group, the Analytical Scientist will be a member of the Chemistry team responsible for carrying out and developing qualitative and quantitative analytical methods to measure critical component properties required to ensure the quality, performance, and reliability of our existing and future display products throughout their lifecycles.
Job Responsibilities
<ul>
<li>Support characterization of ePaper materials using a combination of techniques to include but not limited to GC-MS. LC-MS and NMR.</li>
<li>Be the analytical leader in root cause investigations to determine defects/failure mechanisms in ePaper coatings and laminates.</li>
<li>Develop and validate new quantitative analytical methods as needed to support product launch deadlines. Write SOP’s to support documentation of new procedures.</li>
<li>Be the owner responsible for maintenance and upkeep of assigned laboratory instrumentation.</li>
<li>Manage sample workflow of assigned test requests through the lab’s submission software.</li>
</ul>
Skill Requirements
<ul>
<li>B.S. in Science, Engineering or equivalent with minimum of 10 years chemical laboratory experience or M.S. in Science, Engineering with minimum of 4 years lab experience</li>
<li>In depth knowledge of and experience with quantitative gas chromatography-mass spectroscopy using a variety of sample introduction techniques (liquid injection, headspace, pyrolysis)</li>
<li>In depth knowledge of quantitative 1H and 13C NMR. Experience using Mnova NMR data processing software</li>
<li>Experience using Excel, Powerpoint and JMP to process and present data</li>
<li>Excellent organizational and communication skills, a strong sense of urgency and a performance metrics-driven style</li>
<li>Good analytical skills and attention to detail in a fast-paced environment</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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