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<h3>Job Description</h3>
Job DescriptionDescription:
RETTEW is searching for a highly experienced Survey and/or GIS Team Lead to oversee and guide the project managers, surveyors, and GIS personnel in our Region 1 SVGIS Team. Our Survey/GIS group consists of both survey office and field personnel and GIS professionals. The right candidate will skillfully develop, mentor, grow, and retain a team of talented employees while collaborating closely with Practice Leadership.
 
Responsibilities:
- Collaborate with RETTEW leadership and team members across various markets, regions, and geographies to guide the success of RETTEW’s Survey/GIS team. Manage and oversee all project and team activities within the region, including project planning, budgeting, scheduling, and execution.
- Maintain and develop a high-performing, growth-focused team of Project Managers, Surveyors, and GIS personnel through the attraction, recruitment, and retention of staff within the Region.
- Actively engage in client relationships through effective communication, customer service, and responsiveness to client needs with responsibility for project and service delivery.
- Identify business development opportunities, primarily in the region, build relationships with prospective clients, and pursue new projects and contracts.
- Identify and pursue opportunities with other Team Leads, Business Development leads, Regional Directors, and Vice Presidents for sustainable company growth.
- Create and leverage relationships across RETTEW’s practices and geographies to ensure service delivery and development of innovative solutions to client needs. Collaborate with other Managers and Leadership team members to support company-wide initiatives and goals.
- Develop and implement strategic plans, including annual goals and objectives for revenue growth, client satisfaction, and employee engagement. Establish a yearly regional operating budget and monitor the financial performance.
- Retain existing clients and expand business through cross-selling services.
- Lead regularly scheduled team, resourcing, and marketing meetings.
- Function as Project Manager on high-profile, key, or complex projects
- Evaluate potential projects, clients, and contracts to assess and manage risk.
- Ensure compliance with all regulatory requirements and company policies/procedures.
 
Requirements:
- 10+ years of progressively established experience in the Survey, GIS, or engineering industry with an emphasis on staff, project, client, contract, and quality management.
- B.S. Degree in Survey, GIS or related Engineering preferred, MS or advanced business degree a plus, preferred.
- Registration or Certification in relevant field preferred
- Ability to travel to one of RETTEW’s Region 1 PA office locations (Lancaster, Allentown, or Berwin, PA).
- Strong leadership and management skills with the ability to motivate and inspire a large, diverse, multi-located team to achieve results.
- Proven track record of success in project management, business development, and client relations.
- Strong technical knowledge of Survey and/or GIS market needs.
- Established network is a plus.
- Excellent communication, interpersonal, and client service skills
 
RETTEW is an equal-opportunity employer. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected status. All employment decisions are based on qualifications, merit, and business needs.
 
Join us and be part of a dynamic team that is dedicated to making a positive impact on the communities we serve. For more about us, visit our website at <a href="http://www.rettew.com" target="_blank">www.rettew.com</a> or visit our pages on LinkedIn, Glassdoor, or Indeed. #ZR #LI-Hybrid
 
 
 
 
Requirements:
Requirements listed above.

Team Lead - Survey/GIS Team

<h3>Job Description</h3>
Chemist
Work Location: Wilson, NC -Onsite
Length of Assignment: 6 months (possibility to extend to 12 months)
Standard Hrs.: 06:00 AM to 06:30 PM/ 07:00 AM to 05:30 PM
Per Week: Monday-Thursday 10hr shifts.
 
Job Summary
Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. 
 
Primary Responsibilities
<ul>
<li>Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory.</li>
<li>Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures.</li>
<li>Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.</li>
<li>Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting.</li>
<li>Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency.</li>
<li>Aid other group members as required.</li>
<li>Ensure that equipment and working areas are maintained with good safety and housekeeping practices.</li>
<li>Re-stock chemicals and consumables used in analysis.</li>
<li>Performs other related assignments and duties as required and assigned.</li>
</ul>
Education and Experience Requirements
<ul>
<li>The incumbent must have a BA or BS degree in Chemistry or closely related science.Minimum of 1-year relevant experience preferred. </li>
</ul>
 
Necessary Knowledge, Skills, and Abilities
<ul>
<li>Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy – UV/Vis, NIR, IR, or AA/AE).</li>
<li>Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position.</li>
</ul>
 
Physical and Environmental
<ul>
<li>Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment:Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting. </li>
<li>Lift and maneuver equipment and materials weighing up to 20 pounds.</li>
<li>Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums.</li>
<li>Use small hand and power tools to perform incidental maintenance.</li>
<li>Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces.</li>
<li>Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required.</li>
</ul>

Chemist

<h3>Job Description</h3>
Job Details:

Global Pharmaceutical Company
Microbiologist
Long Term, on going Contract (No end date)
Pay up to $29/hr
Skillman, NJ, will be moving to Summit, NJ toward the end of 2025/ early 2026
 
Experience with product testing, raw material testing, and/or USP testing is a huge plus! 
USP testing includes checking for Toxicity, Enzymatic Activity, Sterility, Bioburden, endotoxin, Western Blot etc. 
 
Experience working in a consumer product company is a huge plus!
Microbiologist 
Individual should able to –
<ol>
<li>Understanding of safety, cGMPs and documentation for a Microbiology Laboratory</li>
<li>Understanding of general Microbiology laboratory procedures and Skillman campus procedures as related to routing sample management and testing, e.g. Fusion</li>
<li>Understanding of Product / Process Microbiology including: </li>
<li>Test Method Suitability and Validation</li>
<li>Microbial Limits</li>
<li>Water Activity</li>
<li>Microorganism Identification</li>
<li>Preservative Effectiveness (AET)</li>
<li>Water Testing</li>
<li>Growth Promotion</li>
<li>Media Preparation</li>
<li>Equipment Cleaning &amp; Lab Cleaning</li>
<li>Take on new assignments under direct supervision as required</li>
</ol>

Microbiologist (microbiology, USP Testing, product testing, etc.)

<h3>Job Description</h3>
Geotechnical Superintendent
Colfax, NC 27235
Direct Hire/FT
Salary 85k/ yr - 110k/ yr
Geotechnical experience (soil nails, shotcrete, micro piles, drilling)
 
Job Description:
A superintendent will be in charge of the drilling operations (solid stem, casing, down-the-hole hammer operations, hollow bar, and hollow stem auger drilling techniques, among others). The superintendent will run, set up, and operate drilling rigs and related equipment to drill holes for geotechnical construction projects along with managing designated drillers who also perform these tasks. This will include mobilization to the site and setting up and running of all aspects of a project. You must have experience in this field, to be able to perform this job, *please apply only if you have two years or more of experience in geotechnical construction.
Key Responsibilities:
This is a hands-on position you will be responsible for on-site project supervision including management of field labor, equipment, materials, safety, and production. Other duties will include: studying plans and specifications for construction, managing skilled craft workers and laborers, procurement of tools and materials, conferring with all levels of staff from laborers to engineering personnel to resolve issues and improve construction methods, preparing detailed progress reports, logs, and inspection reports.
TRAVEL: Frequent day travel and overnight travel required.
ESSENTIAL JOB FUNCTIONS:
Ability to lift drill steel and materials weighing up to 80 lbs maintenance and repairs to drill rig (as required)
Load and unload trucks
Help move drilling rigs and equipment from site to site
Set up of construction new site
Managing on-site personnel
REQUIREMENTS:
Minimum of two years experience as a Superintendent in Geotechnical Construction!
Mechanical skills preferred
Strong leadership and communication skills
Class A CDL license is a plus!
Must pass company background checks including drug screen
Must have an excellent driving record within company standards
--
Vilayath Khan
<a href="mailto:Vilayath.khan@panzersolutions.com" target="_blank">Vilayath.khan@panzersolutions.com</a>

Geotechnical Engineer

<h3>Job Description</h3>
Ready to drive sustainable dairy innovation with a 140-year industry leader? Join a cutting-edge R&amp;D team developing next-generation sanitizers and disinfectants that help feed the world safely.
 
About Our Client Our client is an established global leader in dairy technology with operations in 100+ markets, known for their innovative, collaborative, and safety-first culture. Their Kansas City facility serves as a $1M renovated R&amp;D headquarters, recently expanded to become a global innovation hub combining advanced chemistry with robotic automation.
 
The Impact You'll Make As Chemist I, you'll support product development from concept to commercialization, working on formulations that directly impact dairy farm safety and efficiency worldwide. You'll be part of a specialized team where 78% hold advanced degrees, working with state-of-the-art analytical equipment including HPLC, GC-MS, and advanced spectroscopy systems.
 
Key Responsibilities
<ul>
<li>Conduct formulation work for new dairy sanitizers and disinfectants, contributing to patent-protected innovations</li>
<li>Perform routine physical and chemical stability testing using advanced analytical techniques (HPLC, UV-VIS, titration methods)</li>
<li>Test and evaluate new raw materials for antimicrobial efficacy and regulatory compliance</li>
<li>Independently execute laboratory techniques including wet chemistry, analytical method development, and pilot batch production</li>
<li>Prepare detailed technical reports and present project progress to cross-functional teams</li>
<li>Maintain laboratory notebooks and follow GMP compliance protocols for FDA/EPA regulated products</li>
<li>Collaborate with senior chemists on scale-up procedures and commercial manufacturing support</li>
</ul>
 
Required Qualifications
<ul>
<li>BS in Chemistry, Biochemistry, or related field</li>
<li>0-3 years of analytical chemistry experience (internships and academic research count)</li>
<li>Competency in chemical analysis techniques and laboratory instrumentation</li>
</ul>
 
Preferred Qualifications
<ul>
<li>Exposure to HPLC, UV-VIS spectrophotometry, or chromatography methods</li>
<li>Experience with dairy, food science, or pharmaceutical applications</li>
<li>Knowledge of GMP, FDA, or EPA regulatory requirements</li>
<li>Academic or internship experience with formulation chemistry or product development</li>
</ul>
 
What We Offer Market-competitive salary plus comprehensive benefits from Day 1, including 401k matching up to 6%, Blue Cross Blue Shield coverage, and HSA seeding. Enjoy flexible work arrangements, paid vacation plus 1-week Christmas shutdown, and direct exposure to cutting-edge dairy chemistry innovations. Clear advancement pathway from analytical roles to formulation science and product development leadership.
 
Why This Opportunity Stands Out Join a specialized dairy chemistry team where your work directly impacts sustainable food production for 9 billion people. Access to advanced R&amp;D facilities, international collaboration opportunities, and mentorship from PhD-level scientists. Be part of integrating 140 years of innovation heritage with modern chemistry solutions.
 
Ready to Launch Your Chemistry Career? Apply via LinkedIn and Pave Talent will contact qualified candidates within 48 hours. Confidential search - your application is fully private. Start your journey in specialized dairy chemistry innovation today!

Chemist I - Dairy Innovation & Product Development (Kansas City)

<h3>Job Description</h3>
CEM Corporation is a leading global provider of solutions for critical laboratory application in analytical laboratory, chemical synthesis, biotechnology, environmental testing, and food processing markets. As a worldwide leader in laboratory instrumentation and chemical solutions, the company was founded in 1978 and has nearly 200 patents and over 10 R&amp;D 100 awards for its microwave-based products. CEM's headquarters is located in Matthews, NC and operates subsidiaries in the United Kingdom, France, Germany, Ireland, Italy, Japan, and Singapore.
 
CEM Corporation (Matthews, NC) is seeking a highly motivated and technically proficient Applications Scientist to join our Life Science division. In this customer-facing role, you will provide expert, proactive applications support for our MultiPep and Prodigy instrumentation platforms, which are used in peptide synthesis and purification. You will play a key role in ensuring the successful onboarding, training, and ongoing support of customers throughout the U.S. and Canada. 
To succeed in this role, you must maintain strong technical expertise and hands-on proficiency with CEM’s peptide instrumentation, including the ability to independently operate, train users, and troubleshoot systems. Exceptional communication skills and a proactive approach are essential to delivering a high standard of customer satisfaction. 
In addition to direct customer support, you will contribute to product development efforts through software and performance testing, create technical support documentation, and represent CEM at industry trade shows as needed. 
 
Responsibilities:
Applications Scientist Responsibilities Include but not limited to:
Customer Applications Support (MultiPep line, Prodigy) 
<ul>
<li>Provide direct, high-level applications to customers using the MultiPep and Prodigy product lines</li>
<li>Respond to inquires via phone and peptide support email</li>
<li>Partner closely with Life Science Inside Service Specialists to resolve customer issues promptly and thoroughly</li>
<li>Conduct applications training for customers, CEM personnel, and dealers as needed</li>
<li>Deliver clear, proactive communication to ensure excellent customer satisfaction</li>
</ul>
Sales &amp; Marketing Support
<ul>
<li>Supply product information, documentation, and part numbers to customers, sales staff, and representatives</li>
<li>Participate in industry conferences and trade shows to provide technical expertise and support booth activities</li>
</ul>
Product Development Support 
<ul>
<li>Perform software and instrument performance testing as needed</li>
<li>Assist in the creation of technical documentation and training materials for new and existing products</li>
</ul>
 
Qualifications:
<ul>
<li>Required: BA/BS in Chemistry, Biochemistry, or a related field scientific field </li>
<li>Strong understanding of peptide synthesis and purification workflows </li>
<li>Hands-on experience with analytical instrumentation (preferably peptide synthesizers such as MultiPep or Prodigy)</li>
<li>Excellent communication, organizational, and interpersonal skills</li>
<li>Ability and willingness to travel up to 25% across the US and Canada</li>
<li>Must be based on-site at CEM Corporation’s headquarters (this is not a remote position) </li>
</ul>
 
CEM Corporation is an equal opportunity employer, including veterans and individuals with disabilities.

Application Scientist

<h3>Job Description</h3>
Plant Microbiologist
Contract till December 2025
Onsite in Sanford, ME
 
Core Responsibilities: 
<ul>
<li>Perform microbiological testing of water and environmental monitoring samples.</li>
<li>Manage samples, chain of custody, test requests, data review, and release for microbiological samples sent for testing.</li>
<li>Assist with product and equipment validations.</li>
<li>Assist in the maintenance of lab equipment and calibrations.</li>
<li>Complete failure investigations and accurately document Out of Specification results.</li>
<li>Review microbiology documentation.</li>
</ul>
 
Education and Experience: 
<ul>
<li>Bachelor of Science degree in Microbiology, Biology, or a related major.</li>
<li>Minimum of three years’ experience in a GMP laboratory environment (Personal Care, Pharmaceutical, Food, Environmental).</li>
<li>Experience should include working in a manufacturing environment both in a lab and with exposure to plant floor micro control programs.</li>
<li>Familiarity with and ability to execute GMP-compliant failure investigations, CAPA, deviations, and change documentation.</li>
</ul>
 
Competencies: 
<ul>
<li>Solid understanding and practical experience with Good Laboratory Practices (GLPs), including general microbiological laboratory practices, instrumentation (autoclaves, gram staining, water purification systems, etc.), failure investigations of nonconforming products, and general computer skills (Google Suite, MS Word, MS Excel, SPC, SAP, email).</li>
<li>High energy level with a focus on results.</li>
<li>Excellent communication skills—both speaking and writing—to keep team members informed, maintaining lab notebooks and testing documentation.</li>
<li>Proven knowledge of microbiology, validations, cGMP, and instrumentation.</li>
<li>Ability to work independently with initiative, set priorities, and manage multiple tasks within deadlines.</li>
</ul>

Microbiologist

<h3>Job Description</h3>
Overview
 
We are seeking a Microbiologist to support the Naval Health Research Center (NHRC), Operational Infectious Diseases (OID) Directorate. OID conducts ongoing, laboratory-based surveillance of US military populations in unique environments to quantify and study the etiology of infectious illnesses. Test specimens are collected from ongoing surveillance programs and from special investigations of febrile illnesses and pneumonia among military personnel or civilians (recruits, forces afloat, deployed forces, outbreaks of concern, and border populations). In addition to the utilization of portable, rapid assay technologies to identify pathogens in the field, test specimens and limited epidemiologic data, when approved by the Institutional Review Board (IRB), are provided to the NHRC laboratory where diagnostics and, in some instances, in-depth pathogen characterization is conducted. Results are provided to sponsors, the Armed Forces Health Surveillance Center, local investigators and collaborators, and, when applicable, county health units to guide proper responses that ultimately affect both the readiness of US forces and the safety of public health.
 
CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today’s most effective, evidence-based best practices. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.
 
Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad.
 
Responsibilities
Pathogen Research &amp; Characterization
<ul>
<li>Develops laboratory workflows and optimizes assays to perform surveillance of target pathogens, particularly for wastewater.</li>
<li>Utilizes molecular biology techniques, including concentration/extraction, quantitative PCR, and sequencing, to identify and characterize microbial genomes of pathogens.</li>
<li>Works with a multi-functional team to ensure project deliverables are met.</li>
<li>Oversees technology transfer of completed assays to the operational laboratory surveillance team, including documentation of standard operating procedures, validation/verification planning, and end-user training.</li>
</ul>
 
Laboratory Management &amp; Quality Control
<ul>
<li>Ensures compliance with biosafety and biosecurity standards, especially when handling high-containment or potentially hazardous pathogens.</li>
<li>Implements quality control measures to ensure the accuracy and reliability of experimental data and laboratory procedures.</li>
</ul>
 
Collaboration &amp; Research Support
<ul>
<li>Collaborates with multidisciplinary research teams, including laboratory operations, immunologists, epidemiologists, and clinicians, to support infectious disease studies within the OID Directorate.</li>
<li>Contributes to the design and implementation of research projects by providing microbiological expertise and ensuring proper experimental design and execution.</li>
<li>Participates in field studies and operational research to monitor pathogen spread, assess environmental factors, and collect samples for microbiological analysis.</li>
</ul>
 
Data Analysis &amp; Reporting
<ul>
<li>Analyzes and interprets microbiological data using advanced statistical and bioinformatics tools.</li>
<li>Prepares scientific reports, manuscripts, and presentations for publication in peer-reviewed journals and presentations at scientific conferences.</li>
<li>Contributes to grant writing and funding proposals by providing scientific insights, research plans, and data analysis frameworks.</li>
</ul>
 
Qualifications
<ul>
<li>PhD in Microbiology, Molecular Biology, or a related field.</li>
<li>1+ years of relevant experience in assay development and optimization, with a focus on infectious diseases.</li>
<li>Proficiency in microbiological techniques, including microbial culture, pathogen isolation, molecular diagnostics (PCR, sequencing), and antimicrobial resistance testing.</li>
<li>Strong understanding of assay development/optimization and data analysis.</li>
<li>Experience with data analysis software, bioinformatics tools, and laboratory information management systems (LIMS).</li>
<li>Strong problem-solving skills, attention to detail, and the ability to work independently and in collaboration with multidisciplinary teams.</li>
<li>Excellent communication skills for presenting complex scientific data to diverse audiences.</li>
<li>US Citizenship and the ability to obtain and maintain a T3/Secret Clearance.</li>
</ul>
 
Please submit your resume online at <a href="http://www.CAMRIS.com" target="_blank">www.CAMRIS.com</a>. CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, political affiliation, marital status, military status, or any other characteristic protected by any applicable federal, state, or local law.
 
CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&amp;D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability.
 
Employment is contingent upon successful completion of a secret-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.

<h3>Job Description</h3>
Come join Pajarito Powder and help us change the world. Pajarito Powder is a world leader in the development and commercialization of advanced electrocatalysts for fuel cells and electrolyzers. We manufacture advanced catalysts for hydrogen fuel cells and electrolyzers across PEM, AEM and Alkaline chemistries. Pajarito Powder is poised for rapid growth and needs an R&amp;D Scientist. This is an ideal position for someone seeking a fast-paced challenge. Our manufacturing and R&amp;D team is world class, and the business group is exceptionally experienced. We provide a competitive salary, health, dental, vision and life insurance, paid time off, a collaborative environment, and full vesting of options after four years. 
 
Principle Tasks
 • Prepare compounds, solutions and reagents to synthesize and develop advanced materials per supervisors’ guidance and scientific principles. 
• Determine and evaluate the relationships of chemical and physical properties, composition, structures and reactions of advanced materials using characterization and catalyst performance techniques 
• Develop, improve and customize equipment, products, formulas, analytical methods and processes per supervisors’ guidance and scientific principles 
• Consult with engineers and scientists on analysis, interpretation and development of tests • Induce chemical reactions with light, energy, heat and chemicals 
• Document findings and procedures in notebooks, technical papers, and reports, preparing or following specifications and characterization and evaluation standards
• Clean and maintain laboratory instruments and equipment, making sure that all the technology is working correctly: if it isn’t, troubleshoot the issue or problem. 
• Conduct quality control tests to ensure no compounds or equipment are contaminated or are working consistently 
• Order laboratory supplies, equipment, and chemicals as needed to maintain inventory and develop catalysts and processes. 
• Follow safety protocols, perform safety evaluations on developmental procedures, contribute to safety efforts with peers. 
• Be familiar with scientific literature to expand technical and scientific knowledge to further R&amp;D operations. 
 
Knowledge, Skills, and Abilities
• Proficiency and skill with Microsoft Office Suite and company computer systems
• Able to work with accuracy and detail oriented 
• Able to communicate clearly and effectively, both verbally and in writing 
• Able to interact positively and work effectively with others 
• Able to independently gather data, compile information, and prepare reports 
• Able to take initiative in performing job and seek increased responsibilities 
• Able to multi-task and problem solve with strong analytical skills 
• Able to organize time, energy, and resources effectively to achieve goals (i.e., organizational skills) • Ability to seek different and novel ways to create efficiencies when working on problems, challenges and issues 
• Able to perform tasks and duties without constant supervision 
• Prioritizes and ensures safety of oneself and others 
 
Edu/ Training/ exp required 
• Bachelor's or master's degree in chemistry, chemical engineering, or similar degree from an accredited university/school. 
• Must possess technical skills and abilities that are generally expected from degreed engineers or chemists 
• 1 to 3 years of research experience in a chemistry lab 
• Basic understanding of catalysts and electrochemistry 
• Basic understanding of Chemical Safety 
• Use of Microsoft Word, Excel, PowerPoint and Outlook to plan, analyze, and report on projects, experimental data, and logs. 
• Experience recording and reporting on progress of work and communicating with team and supervisors effectively. 
Additional Information/Requirements 
Must be willing to relocate to and work onsite in Albuquerque, NM. For full consideration, applicants must submit a comprehensive resume that addresses the key requirements of the position. Pajarito Powder 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, or protected veteran status and will not be discriminated against on the basis of disability. 
Work Authorization Pajarito Powder will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas such as E, F-1(including those with OPT or CPT), H-1, H-2, L-1, B, J or TN, or who need sponsorship for work authorization now or in the future, are not eligible for hire.

Research And Development Scientist

<h3>Job Description</h3>
Job Description
<ul>
<li>We are hiring immediately for full time CLEANROOM TECHNICIAN positions.</li>
<li>Location: Westchester Medical Center - 100 Woods Road, Valhalla, NY 10595 Note: online applications accepted only.</li>
<li>Schedule: Full time schedule. Days may vary, 7:00 am - 3:00 pm or 3:00 pm - 11:00 pm. Must be able to work every other weekend/holiday. More details upon interview. </li>
<li>Requirement: Perform reprocessing activities within Sterile Processing and Equipment Distribution.</li>
<li>Pay Rate: $18.00 per hour.</li>
</ul>
Make a difference in the lives of people, your community, and yourself. Join a culture of opportunity with Crothall Healthcare. Our careers are filled with purpose and empower you to transform healthcare experiences. Take a look for yourself at the Power of Clean!
 Crothall Healthcare is a Compass One Company that provides specialized, high-quality, innovative, and responsive support services exclusively to the healthcare industry. Crothall is the market share leader in Environmental Services (EVS), and serves many of the top 100 Hospitals throughout its over 2,000 healthcare service teams in 47 states. Crothall has been recognized as one of Modern Healthcare's Best Places to Work and Best Places to Work in Pennsylvania in 2020 for the 8th straight time and Beckers Top 150 Places to Work in 2019 for the 4th time. A division of Compass Group USA, Crothall has more than 26,000 team members. Its EVS division is CIMS and CIMS-GB certified by the ISSA since 2009, and its HTS division is ISO 13485 certified since 2019. Our core services include: Environmental Services, Patient Transportation, Facilities Management, Healthcare Technology Solutions, Laundry and Linen Services, Ambulatory, and Sterile Processing. 
Job Summary
Summary: Maintains a sterile environment in the clean room, by garbing, cleaning the room, and behaving according to clean room procedures that align with the facilities practices or guidelines. 
Essential Duties and Responsibilities: 
<ul>
<li>Practices efficient use of cleaning techniques, solutions preparation, equipment and tool operation.</li>
<li>Performs all decontamination cleaning and project assignments within area of responsibility or as directed by supervisor with high level of consistency, accuracy and reliability. This also includes executing cleanroom cleaning SOP’s.</li>
<li>Maintains documentation on all activities and frequent (often daily) quality control testing and verifies the efficiency of the work performed.</li>
<li>Monitor and maintain the stock of cleanroom garments and cleaning materials when applicable.</li>
<li>Monitor and manage contamination sources within the cleanroom environment including materials and personnel.</li>
<li>Performs other duties as assigned</li>
</ul>
Qualifications: 
<ul>
<li>High School Diploma, GED preferred or equivalent combination of education and experience</li>
<li>1-2 years housekeeping or cleaning service experience preferred </li>
<li>Strong verbal and written communication skills.</li>
<li>Ability to read and comprehend Standard Operating Procedure Documents (SOPs)</li>
</ul>
Work Environment: 
<ul>
<li>Exposure to chemicals on a constant basis requiring special clothing and/or safety equipment. </li>
</ul>
BENEFITS FOR OUR TEAM MEMBERS
<ul>
<li>Full-time and part-time positions are offered the following benefits: Retirement Plan, Associate Shopping Program, Health and Wellness Programs, Discount Marketplace, Identify Theft Protection, Pet Insurance, and other voluntary benefits including Critical Illness Insurance, Accident Insurance, Hospital Indemnity Insurance, Legal Services, and Choice Auto and Home Program</li>
</ul>
<ul>
<li>Full-time positions also offer the following benefits to associates: Medical, Dental, Vision, Life Insurance/AD, Disability Insurance, Commuter Benefits, Employee Assistance Program, Flexible Spending Accounts (FSAs)</li>
</ul>
Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws. For positions in Washington State, Maryland, or to be performed Remotely, click here for paid time off benefits information.
Crothall is a member of Compass Group. Compass Group is an equal opportunity employer. At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law. 
Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without a reasonable accommodation. Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While this is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity. 
Applications are accepted on an ongoing basis. 
Crothall maintains a drug-free workplace. 
"We will consider for employment all qualified applicants, including those with a criminal history (including relevant driving history), in a manner consistent with all applicable federal, state, and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, and the New York Fair Chance Act."

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