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<h3>Job Description</h3>
Job Description
Production Technician II – Air Separation Unit (ASU)
 
Location:&nbsp;Armorel, AR 72310 Schedule: Swing Shift | 12-Hour Shifts (7AM–7PM Central) Duration: 18-Month Contract | Onsite Position Estimated Start Date: ASAP
Note: Some ASU experience is required
Work Environment
<ul>
<li>Primary work areas: Control room and outdoor plant environment</li>
<li>PPE required: Hard hat, safety glasses, steel-toe boots</li>
<li>Chemicals handled: Oxygen, Nitrogen, Argon</li>
<li>Safety Sensitive Position: Yes</li>
<li>Heights: Up to 300 ft</li>
<li>Lifting: Up to 60 lbs</li>
<li>Driving: None</li>
<li>OSHA compliance and PPE adherence required</li>
</ul>
General Summary
The Production Technician II is responsible for the safe operation, maintenance, and optimization of Airgas Merchant Gas production facilities. This includes maintaining plant production efficiency, ensuring regulatory compliance, and upholding safety standards.
The role operates both independently and collaboratively, performing outside/truck loading, board operations, compressor start-up/shutdown, and Air Separation Unit (ASU) system monitoring.
Essential Duties &amp; Responsibilities
Operational Duties
<ul>
<li>Perform outside/truck loading, basic board operations, compressor start-up/shutdown.</li>
<li>Conduct warm plant start-ups for ASU/NLU/LCO2/HPN systems and routine VSA start-ups.</li>
<li>Execute minor maintenance, manage local spare parts, issue Safe Work Permits, and lead Lockout/Tagout (LOTO) and pre-job briefings.</li>
<li>Apply process safety programs, support root cause analysis, and document incidents in Intelex.</li>
<li>Ensure contractor/vendor training compliance and maintain proper documentation.</li>
<li>Adhere to all local/federal regulations including FDA, OSHA, EPA, DOT, and cGMP.</li>
</ul>
Communication &amp; Collaboration
<ul>
<li>Coordinate with national and local product scheduling teams to ensure on-time delivery and complete accurate reports/documentation.</li>
<li>Communicate effectively with site management, contractors, and customers regarding production activities.</li>
</ul>
Safety &amp; Regulatory Compliance
<ul>
<li>Model and promote a strong safety culture; complete Airgas Safety Pledge and required HSES training.</li>
<li>Participate in MOC, PSSR, and QIR processes.</li>
</ul>
Minimum Qualifications
Education
<ul>
<li>Associate degree or equivalent technical training (required)</li>
<li>Bachelor’s degree (preferred)</li>
</ul>
Experience
<ul>
<li>1+ year of related ASU operations experience</li>
</ul>
Knowledge, Skills &amp; Abilities
<ul>
<li>Proficient in HMI screens/control stations</li>
<li>Familiar with work order systems and SAP or Lucene Image Retrieval (LIRE)</li>
<li>Ability to implement Emergency Action Plans</li>
<li>Can operate plant systems in steady state and emergency conditions</li>
<li>Understands interlock schedules, P&amp;IDs, and plant schematics</li>
<li>Strong English communication (written and verbal, 12th grade level minimum)</li>
<li>Mechanically inclined with strong troubleshooting ability</li>
</ul>
Physical Demands
<ul>
<li>Ability to lift up to 60 lbs</li>
<li>Work rotating shifts and be on call as required</li>
<li>Must wear PPE including respirator protection as needed</li>
<li>Willingness to travel for training or temporary site support</li>
</ul>
Work Environment
<ul>
<li>Combination of control room and outdoor conditions</li>
<li>Moderate overnight travel may be required</li>
<li>Reliable transportation required</li>
<li>Frequent regional site visits with varying layouts and accessibility</li>
</ul>
Company Description***PLEASE ATTACH RESUME*** ***PLEASE ATTACH RESUME*** ***PLEASE ATTACH RESUME*** ***PLEASE ATTACH RESUME*** ***PLEASE ATTACH RESUME*** ***PLEASE ATTACH RESUME*** 
<h3>Company Description</h3>
***PLEASE ATTACH RESUME*** ***PLEASE ATTACH RESUME***\r\n***PLEASE ATTACH RESUME*** ***PLEASE ATTACH RESUME***\r\n***PLEASE ATTACH RESUME*** ***PLEASE ATTACH RESUME***

Chemical Production Technician

<h3>Job Description</h3>
Job Description
Greater Lynn Senior Services, Inc has a great opportunity for a hands-on experience that would be ideal for a Math, Business, Economics, Healthcare Administration or Social Work major!
Summary
This internship will assist the CEO and Senior Leaders in data collection and analysis focused on the Strategic Planning efforts. In addition, this internship will provide administrative support and research for the Lynn Non-Profit Leadership Group as requested.
Qualifications
<ul>
<li>College level aptitude in data collection and analysis</li>
<li>Professional demeanor with the ability to handle confidential information and documents with discretion and according to GLSS policy and HIPAA guidelines</li>
<li>Must be proficient in the use of Microsoft Word, Excel and Outlook</li>
<li>Ability to meet established deadlines and demonstrate excellent time management and efficiency</li>
<li>Excellent interpersonal skills with the ability to ask questions to obtain detailed and complete information</li>
<li>Ability to work both independently and as part of a team</li>
<li>Well-developed listening skills</li>
</ul>
Responsibilities
<ul>
<li>Assist strategic planning work groups with date gathering and administrative support as requested</li>
<li>Assist with community based needs surveys for strategic planning work groups</li>
<li>Assist CEO with research and support for Lynn Non-Profit Leadership initiatives</li>
<li>Research and identify funding mechanisms to support innovation capacities across strategic planning work groups</li>
</ul>
Hours: 20 hours per week - Starting January 2026
*GLSS is an affirmative action and equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including gender identity, sexual orientation, and pregnancy), national origin, age (40 or older), disability or genetic information.*
*GLSS will provide reasonable accommodations to applicants with disabilities upon request*

Unpaid Research and Analytics Intern

<h3>Job Description</h3>
Job Description
Position Purpose:
We are seeking an analytical chemist with broad experience in analytical chemisty including expertise in spectroscopy, solid-state characterization techniques, chromatography and mass spectrometry. This role will focus on supporting material characterization of energetic and related materials, and other novel materials of interest.
 Essential Duties and Reponsibilities:
<ul>
<li>Develop and apply spectroscopy methods (e.g. Raman, FTIR, UV-Vis, fluorescence) for characterization of energetic materials and novel compounds.</li>
<li>Develop and apply chromatographic and mass spectrometry methods (e.g. GC-MS, LC-MS, HRMS) for characterization of energetic materials and novel compounds.</li>
<li>Perform thermal and crystallographic analyses (e.g. DSC, TGA) to evaluate material stability, polymorphism, and structure–property relationships.</li>
<li>Collaborate with synthesis teams to identify and quantify trace impurities arising from benchtop chemical reaction experiments.</li>
<li> Develop and validate analytical methods to detect unknown and known impurities at trace levels.</li>
<li>Integrate spectroscopy data with chromatographic and mass spectrometric results for comprehensive material profiling.</li>
<li> Contribute to expanding organizational capability into broader materials science (e.g., polymers, co-crystals, composites).</li>
<li>Perform routine maintenance and troubleshooting for a variety of analytical instrumentation.</li>
<li>Maintain rigorous safety practices appropriate for handling energetic and hazardous materials.</li>
</ul>
Required Knowledge, Skills &amp; Abilities:
<ul>
<li>Demonstrated expertise in spectroscopy techniques (Raman, FTIR, UV-Vis).</li>
<li>Demonstrated expertise in chromatographic and mass spectrometry techniques (GC-MS, LC-MS, HRMS).</li>
<li>Experience with thermal analysis and crystallographic methods (emphasis on DSC/TGA).</li>
<li>Familiarity with energetic materials, explosives, or hazardous chemical handling is highly desirable.</li>
<li>Strong collaborative skills; ability to communicate across technical teams.</li>
<li>Track record of method development and problem-solving in analytical chemistry.</li>
<li>Advanced skills in maintenance of analytical chemistry equipment including spectroscopy and mass spectrometry instruments is desired. </li>
</ul>
 Education/Experience:
<ul>
<li>Ph.D. in Chemistry, Materials Science, or related field; or</li>
<li>MS in Chemistry, Materials Science, or related field with 2+ years relevant experience.</li>
<li>BS in Chemistry, Materials Science, or related field with 5+ years relevant experience.</li>
</ul>
 Certificates &amp; Licenses:
 None required
 Clearance:
This position requires that the candidate be willing and able to complete a successful background screening for a security clearance. Candidates with an active security clearance will receive preference.
 Supervisory Responsibilities:
 None required.
 Working Conditions/Equipment:
 This is a full-time, fully on-site position. This position primarily operates during standard business hours, with occasional needs for extended workdays or weekend work to meet project timelines. A significant portion of this role (approximately 75%) involves hands-on laboratory work. You should be comfortable spending extended periods of time conducting experiments and working at a computer. The role may also require occasional domestic travel for conferences, trade shows, or research-related meetings. The ability to lift and carry light loads (under 25 lbs) without assistance is necessary. 
 Powered by ExactHire:186047

Analytical Chemist

<h3>Job Description</h3>
Nightingale Nurses - Allied is seeking a travel Physicist for a travel job in Atlanta, Georgia.
Job Description &amp; Requirements
<ul>
<li>Specialty: Physicist</li>
<li>Discipline: Allied Health Professional</li>
<li>Start Date: 12/01/2025</li>
<li>Duration: 13 weeks</li>
<li>40 hours per week</li>
<li>Shift: 8 hours, days, nights, flexible</li>
<li>Employment Type: Travel</li>
</ul>

Travel Physicist

<h3>Job Description</h3>
Design a career and build your future... Because it matters!
 
GIS Specialist 
McMillen Inc. is looking for a GIS Specialist with 10+ years of professional experience to lead geospatial workflows for hydropower, watershed, and environmental projects. This position offers the opportunity to apply advanced GIS and data management skills across disciplines including hydrology, geomorphology, and ecology. The successful candidate will oversee spatial data integration, analysis, and visualization to support complex modeling, regulatory, and design projects. This role requires a balance of technical expertise, project management ability, and a passion for transforming geospatial data into actionable insights that inform sustainable water-resource and infrastructure solutions.
 
Responsibilities:
<ul>
<li> Lead GIS workflows supporting hydropower relicensing, dam removal, watershed modeling, hydraulic analysis, and environmental compliance projects.</li>
<li> Manage, process, and QA/QC large spatial datasets (LiDAR, topobathymetric surveys, DEMs, orthophotos, UAV-SfM) for use across engineering, geomorphic, and ecological disciplines.</li>
<li> Build geodatabases and automated geoprocessing workflows (ModelBuilder, Python, SQL) to ensure efficient, reproducible analyses and defensible regulatory documentation (FERC, NEPA/CEQA, ESA).</li>
<li> Conduct hydrologic and terrain analyses—watershed delineation, change detection, floodplain mapping, sediment characterization, and habitat suitability modeling.</li>
<li> Prepare and translate inputs and outputs for 1D/2D hydraulic, sediment transport, and habitat models, ensuring spatial consistency and model-ready datasets.</li>
<li> Develop basemaps, dashboards, and story maps to communicate modeling results and monitoring data to clients, regulators, tribes, and the public.</li>
<li> Produce high-quality cartographic and visualization products for technical reports, permitting, and stakeholder engagement.</li>
<li> Maintain metadata, QA/QC, and data management standards to support transparency, repeatability, and defensible technical deliverables.</li>
<li> Collaborate closely with engineers, geomorphologists, hydrologists, and biologists to integrate GIS analyses into design, modeling, and decision-making.</li>
<li> Mentor junior staff in geospatial methods, database management, and quality assurance practices.</li>
<li> Serve as GIS lead in proposal development, project planning, and data-management strategy for multi-disciplinary teams.</li>
</ul>
 
Qualifications:
<ul>
<li> Minimum of 10 years of experience applying GIS and spatial analysis in support of engineering, hydrology, or environmental science projects.</li>
<li> Bachelor’s degree in Geography, GIS, Environmental Science, or related field required; Master’s degree or graduate GIS certificate preferred.</li>
<li> Advanced proficiency in ArcGIS Pro or QGIS for terrain analysis, cartography, and spatial data management.</li>
<li> Proven ability to manage, process, and QA/QC large geospatial datasets (LiDAR, DEMs, topobathymetric surveys, orthophotos, UAV-SfM).</li>
<li> Strong understanding of hydrologic, geomorphic, and environmental datasets, and their application in watershed, habitat, and infrastructure studies.</li>
<li> Demonstrated experience building and maintaining geodatabases and automated workflows using ModelBuilder, Python, or SQL.</li>
<li> Familiarity with 1D/2D hydraulic, sediment transport, or habitat modeling and preparation of model-ready spatial inputs and outputs.</li>
<li> Skilled in developing high-quality cartographic and visualization products for technical reports, permitting, and stakeholder communication.</li>
<li> Excellent data management, documentation, and metadata practices ensuring transparency and reproducibility.</li>
<li> Experience mentoring junior GIS staff and contributing to proposal development and project planning.</li>
<li> Strong written and verbal communication skills, with the ability to collaborate across disciplines and convey technical concepts to varied audiences.</li>
</ul>
 
Compensation Package:
<ul>
<li>Pay Range: $47 hr. – $76 hr. (DOE) </li>
<li>Benefits: McMillen provides a full Benefits Program consisting of Medical, Dental, Vision, Life, Disability, FSA, EAP, 401(k) and match, 9 Paid Holidays, generous PTO, opportunity for Stock Ownership and Wellness Reimbursement.</li>
</ul>
 
Company Bio: McMillen, Inc. designs and builds solutions that shape the future of water resources. As an employee-owned firm, we take pride in every project because we know our work truly matters. Our people thrive on solving complex challenges, pushing boundaries, and refining their craft. We don’t look for the complacent or the comfortable. We seek problem solvers, innovators, and experts who are always striving to be better. We support continuous learning, cutting-edge technology, and a balanced work-life environment so our employees can build careers they’re proud of.
We are focused in the dams, energy, fisheries, natural resources, and infrastructure markets. With staff across the United States, Canada, Europe, and beyond, we bring global best practices to our clients. Our people integrate engineering, environmental, and construction expertise to deliver practical, results-driven outcomes. From concept to completion, projects are guided through feasibility studies, permitting, design, construction, and commissioning, ensuring technical precision and real-world functionality.
 
EEO: McMillen, Inc. is an EEO/Affirmative Action Employer and will make all employment related decisions without race, color, religion, sex, national origin, disability or protected veteran status.
Visa sponsorship, including renewal during employment, will not be provided for this position.
 
No recruiters, please.

GIS Specialist

<h3>Job Description</h3>
Senior Scientist – Assay Development &amp; Quality Control
&nbsp;Location: Pittsburgh, PA |&nbsp; Full Time | Reports to Director of Life Science
 
BioForge’s mission is to accelerate innovations and breakthroughs in both the development and manufacturing of precision medicines to speed their delivery, use, and impact.
 
A fundamental shift is occurring in how medicines and therapeutics are delivered to people.&nbsp; Treatments are increasingly moving from an era of chemicals and drugs towards gene and cell therapies for multiple and diverse conditions such as cancer, blindness and degenerative neural diseases. Furthermore, precision biologic medicines – by their very nature – need manufacturing solutions capable of rapid, efficient and cost-effective switching between therapy productions without switching production tools or processes. How do we deliver a billion therapies, a hundred, ten thousand, or a hundred thousand at a time?
 
Such a shift requires fundamentally new approaches and innovations in the manufacturing of such gene and cell therapies. These approaches will bring to bear new and emerging technologies such as artificial intelligence/machine learning, continuous-flow fluidic processing, in-line sensing and control and closed-system automated design to develop next-generation manufacturing tools. With innovation comes the need for quality—demanding robust QC and QA tools that ensure standards are upheld throughout the R&amp;D pipeline.
 
We are seeking a Senior Scientist with expertise in analytical method development, assay design, and quality control. This role is central to developing, optimizing, and executing assays that characterize critical quality attributes (CQAs) across a range of biologic platforms. The ideal candidate has a deep command of assay technologies and is equally comfortable executing validated protocols and developing novel methods from scratch.
 
About the Role
 
You will work as a key member of our R&amp;D team, leading the development and execution of both routine and innovative assay platforms to support the characterization of complex biologics. This role offers the opportunity to shape and implement critical quality control strategies, contribute to cross-functional platform development, and design custom analytical workflows that support scalable, high-quality biomanufacturing. It is ideal for a technically advanced scientist passionate about continued assay development, building quality systems, and enabling the future of biologics through analytical science.
 
Responsibilities:
 
<ul>
<li>Design, develop, and optimize analytical assays to support quality control and product characterization</li>
<li>Independently lead method development efforts across biochemical, molecular, and cell-based techniques</li>
<li>Evaluate and measure product quality attributes and create CoAs</li>
<li>Create standard operating procedures (SOPs) and qualification reports</li>
<li>Perform assay qualification and validation in alignment with regulatory expectations (e.g., precision, accuracy, linearity, specificity)</li>
<li>Collaborate with R&amp;D, manufacturing, and regulatory teams to ensure analytical strategies meet program goals</li>
<li>Investigate assay failures, troubleshoot technical issues, and drive continuous improvement</li>
<li>Maintain rigorous documentation and ensure compliance with internal and external quality standards</li>
</ul>
 
Qualifications:
 
<ul>
<li>PhD or MS in Biology, Biochemistry, Bioengineering, Analytical Chemistry, or related field&nbsp;</li>
<li>5-8 years of laboratory experience in a QC, assay development, or analytical environment</li>
<li>Proven hands-on expertise with multiple assay formats, such as:</li>
<li>HPLC/RP/SEC/IE</li>
<li>Spectroscopy (UV-Vis, fluorescence, absorbance)</li>
<li>Electrophoresis (gel, capillary)</li>
<li>PCR/ddPCR/qPCR</li>
<li>ELISA or immunoassays</li>
<li>Cell-based assays</li>
<li>Chromatography or particle sizing</li>
<li>Microscopy</li>
<li>Demonstrated ability to develop and qualify custom assays</li>
<li>Strong documentation and technical writing skills</li>
<li>Experience working in regulated environments (GMP, GLP, ISO)</li>
</ul>
Desirable:
<ul>
<li>Strong interpersonal skills and the ability to work as part of a team</li>
<li>Familiarity with statistical tools for method validation (e.g., DOE, regression, precision studies)</li>
<li>Experience transferring methods between teams or to external partners</li>
<li>Strong project ownership and ability to work independently in a fast-paced setting</li>
<li>Strong interpersonal skills and the ability to work as part of a team for company wide goals</li>
</ul>
 
What You’ll Gain:
<ul>
<li>A collaborative, forward-thinking environment with cutting-edge projects</li>
<li>Hands-on access to state-of-the-art analytical tools</li>
<li>Competitive compensation and benefits</li>
</ul>
 
How to Apply
 
To apply, please apply through Linkedin or submit the following materials to <a href="mailto:info@pittbioforge.org" target="_blank">info@pittbioforge.org</a> with the subject line: “QC”
<ol>
<li>Resume/CV</li>
<li>Brief statement of interest (1–2 paragraphs) outlining your relevant experience</li>
</ol>
 
Application Deadline: December 15, 2025
Start Date: January 2026

Senior Scientist - Assay Development & Quality Control

<h3>Job Description</h3>
Yoh presents an excellent long-term&nbsp;Internal Laboratory Testing Coordinator&nbsp;opportunity with a trusted, long-term client located in Waltham, MA. Scientist/Sr. Research Associate -ESI&nbsp;Multiplex assays/Flow Cytometry Scientist/Sr. Research Associate The Yoh resource is expected to apply expertise across several areas in support of Sanofi Vaccines R&amp;D Global Immunology function developing innovative vaccine solutions for infectious diseases. Key Responsibilities:
<ul>
<li>Design and execute complex immunological experiments to evaluate vaccine candidates</li>
<li>Analyze immune responses using state-of-the-art techniques including multiparameter flow cytometry, ligand-binding, and cell-based assays</li>
<li>Support optimization of the automation of protocols and testing of the samples in automated immune assays as needed</li>
<li>Develop novel immunological assays to support vaccine development programs</li>
<li>Generate, analyze, visualize, and interpret scientific data sets, record experimental procedures and raw and analyzed data in electronic laboratory notebook</li>
<li>Author technical reports, SOPs, and contribute to regulatory submissions as required</li>
<li>Prepare and present findings to internal stakeholders</li>
<li>Provide technical guidance to junior team members as required</li>
<li>Collaborate within immunology and cross-functional teams across R&amp;D</li>
<li>Comply with the company HSE policies and minimize risk to self, others, and the environment, consistent with the community and industry standards.</li>
</ul>
Required Responsibilities:
<ul>
<li>Expertise in cellular and molecular immunology techniques</li>
<li>Proven experience with:</li>
<li>Spectral flow cytometry or flow cytometry with primary mammalian cells</li>
<li>Primary cells isolation and culture</li>
<li>Immunological assays development and implementation (ligand binding, multiplex (Luminex, MSD), cell-based)</li>
<li>Data visualization and analysis</li>
<li>Strong analytical and problem-solving skills</li>
<li>Excellent documentation and record-keeping abilities</li>
<li>Proficiency in standard laboratory software and data analysis tools</li>
<li>Strong written and verbal communication skills</li>
</ul>
Preferred Responsibilities:
<ul>
<li>Experience with vaccine development or infectious disease research</li>
<li>Working knowledge of Good Research Practices (GRP) and electronic note booking</li>
<li>Proficiency in advanced data analysis tools (FlowJo, OMIQ, GraphPad Prism, &amp; other)</li>
<li>Experience with automated/semi-automated platforms/ liquid handlers</li>
</ul>
Education Experience:
<ul>
<li>Data Review</li>
<li>Training</li>
<li>Scheduling</li>
<li>GDP</li>
<li>GRP, compliance requirements for clinical trial samples</li>
<li>Master's degree in Immunology, Microbiology, or related field with 2+ years of relevant industry or academia experience</li>
<li>Bachelor's degree with 4+ years of relevant experience</li>
<li>Experience in pharmaceutical or biotechnology industry preferred. </li>
</ul>
 Estimated Min Rate: $31.50 Estimated Max Rate: $45.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: 
<ul>
<li>Medical, Prescription, Dental &amp; Vision Benefits (for employees working 20+ hours per week)</li>
<li>Health Savings Account (HSA) (for employees working 20+ hours per week)</li>
<li>Life &amp; Disability Insurance (for employees working 20+ hours per week)</li>
<li>MetLife Voluntary Benefits</li>
<li>Employee Assistance Program (EAP)</li>
<li>401K Retirement Savings Plan</li>
<li>Direct Deposit &amp; weekly epayroll</li>
<li>Referral Bonus Programs</li>
<li>Certification and training opportunities </li>
</ul>
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day &amp; Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit <a href="https://www.yoh.com/applicants-with-disabilities" target="_blank">https://www.yoh.com/applicants-with-disabilities</a> to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:&nbsp;<a href="https://www.yoh.com/privacy-notice" target="_blank">https://www.yoh.com/privacy-notice</a>

Scientist/Sr. Research Associate-ESI Multiplex assays/Flow Cytometry

<h3>Job Description</h3>
Cytotech OR Cytotechnologist Opening at a full service clinical and anatomic pathology laboratory located in Maine! This laboratory services physicians, hospitals, laboratories and clinics throughout New England and the United States!
This CAP and CLIA certified laboratory is looking to hire a permanent and full time Cytotechnologist on day shift (with some flexibility). The Cytotech will be responsible for screening both gynecological and non-gynecological specimens.
Requirements:
ASCP Certification as a Cytotechnologist (CT) Bachelor's Degree
Preferred Experience:
SurePath and ThinPrep experience Hospital based experience
This facility is offering a highly competitive compensation package including comprehensive benefits including (but not limited to) educational opportunities, 401K retirement plan, wellness program, medical, dental, life and disability insurance.
Interested in learning more? Apply below or contact Andrea at <a href="mailto:andrea@ka-recruiting.com" target="_blank">andrea@ka-recruiting.com</a> or call/text 617-746-2745.
(Reference Code: ACC 236211430)

Cytotech OR Cytology Technologist in Maine

<h3>Job Description</h3>
Title: Bioanalytical Senior Scientist
Location: Rahway, NJ
Duration: 12+ months(Extendable)
Pay Range: $45 -$53 per hour on W2.
 
 
NOTES: Must be able to travel between Rahway, NJ site and West Point, PA site as needed. Travel up to 50% may be required.
 
 
 
Qualifications:
Minimum Educational Requirement:
• Ph.D. degree in chemistry, biochemistry or related scientific discipline with 3 years of industrial experience, or Master of Science degree in chemistry, biochemistry or related scientific discipline with at least 7 years of industrial experience, preferably in a bioanalytical laboratory.
 
Required Experience and Skills:
• Experience in developing, validating and implementing ligand binding assays under GLP.
• Possess excellent written and verbal communication skills.
• Experience in Watson or other LIMS systems.
• Proficiency with Microsoft Office products.
 
Preferred Experience and Skills:
• Highly motivated individual with the aspiration to learn and develop himself/herself.
• Experience in LC-MS/MS assay.
 
Responsibilities:
Seeking a motivated individual to work as a senior bioanalytical bench scientist within its Good Laboratory Practices (GLP) bioanalytical laboratory. This is a bioanalytical senior scientist position with primary duties in performing laboratory work, preparing reports, and interacting with internal and external partners.
This position is a part of the Bioanalytical group, Global Preclinical Development, based in Rahway, New Jersey. Main responsibilities include:
• Independently developing, optimizing and troubleshooting LBA methods to support projects with method quality and efficiency in mind; writing bioanalytical methods; assumption of project responsibility in delegated bioanalytical aspects.
• Proficiently and independently implementing ligand binding assays (LBA) for the analysis of biological samples in a GLP environment, with duties inclusive of, but not limited to, sample preparation, setting up instruments, processing, and interpreting data; solving issues encountered during method implementation independently.
• Establishing LBA capability within the team including equipment purchasing, setting up lab and LBA workflow.
• Ensuring that all documentations are in real time, accurate and compliant with current GLP and departmental guidelines.
• Preparing reports (sample analysis and validation) independently; Assembling all documents for regulatory submissions; Compliance with and maintenance of required training for company and departmental SOPs, safety-related guidance and other guidelines as relevant/applicable.
• Adherence to short term goals, objectives and timelines agreed upon with management, via working independently (e.g., with little to no management oversite in this regard).
• Interaction with partners in other functional lines, such as Drug Safety and Metabolism, Quality Assurance, and program management.
• Any relevant/applicable additional BA assignments as directed by management.
• Ability to multi-task and be a team player.

Bioanalytical Senior Scientist

<h3>Job Description</h3>
Job Description
Position Purpose:
The primary purpose of this position is to perform chemistry tasks at the Transportation Security Laboratory (TSL).
Essential Duties and Responsibilities:
<ul>
<li>Collects and analyzes data using gas chromatography (GC), liquid chromatography with mass spectrometry detection (LCMS), and ion chromatography (IC).</li>
<li>Performs troubleshooting, maintenance, and method development on GC, LCMS, and IC instrumentation.</li>
<li>Performs wet chemistry (dilutions, extractions, etc.).</li>
<li>Collects and analyzes data using explosive trace detection (ETD) systems.</li>
<li>Performs microscopy measurements using stereomicroscope or polarized light microscope.</li>
<li>Composes and reviews technical reports and standard operating procedures.</li>
<li>Composes, reviews, and executes test plans.</li>
<li>Synthesizes homemade explosives.</li>
<li>Performs literature reviews.</li>
<li>Safely handles explosive and other hazardous materials.</li>
<li>Sources materials and submits purchase requests.</li>
<li>Other duties as assigned.</li>
</ul>
Required Knowledge, Skills &amp; Abilities:
<ul>
<li>Positive attitude.</li>
<li>Good working knowledge of trace analytical instrumentation (GC, LCMS, and IC).</li>
<li>Good interpersonal, verbal, and written communication skills.</li>
<li>Good listening skills.</li>
<li>Good working skills of software and tools necessary for job functions including Microsoft Office suite.</li>
<li>Previous experience handling energetic material.</li>
<li>Previous experience with ETD systems.</li>
</ul>
Education/Experience: 
Incumbent professional should have a minimum of a bachelor's degree in chemistry.
Certificates and Licenses: 
None

Clearance: 
The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position.
Supervisory Responsibilities: 
The incumbent professional has little to no supervisory responsibilities.
Working Conditions/ Equipment: 
The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%.
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor.
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