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<h3>Job Description</h3>
Job DescriptionDescription:
Reporting to the CEO &amp; VP Global R&amp;D
Join our leadership team and shape the future of technical innovation in the foundry and chemical solutions industry.
About the Role
We’re seeking a visionary and hands-on Director of R&amp;D to lead innovation at the intersection of chemistry, manufacturing, and customer success. This role isn’t just about technical depth—it’s about commercial impact, global collaboration, and accelerating the pace of new product development in a highly competitive and evolving industry.
 
As a key member of the Leadership Team, you will set the direction of our technical roadmap, oversee a high-performing team of chemists, and collaborate across continents to bring breakthrough products to market. This is your opportunity to shape the future of our business and our industry.
 
What You’ll Do
<ul>
<li>Drive strategic and technical leadership across new product development, manufacturing support, and innovation pipeline.</li>
<li>Partner with Sales, Marketing, Operations, and Global Innovation Teams to align technical strategy with commercial growth.</li>
<li>Represent our technical vision with external stakeholders, key customers, and industry organizations.</li>
<li>Lead and develop a dynamic R&amp;D team while instilling a culture of innovation, accountability, and scientific rigor.</li>
<li>Translate customer pain points into breakthrough solutions—and bring them to market with discipline and speed.</li>
<li>Bridge the gap between local innovation and global collaboration, reporting into both the CEO and our parent company’s VP of Global R&amp;D in Germany.</li>
</ul>
Requirements:
What We’re Looking For
<ul>
<li>Master’s or Ph.D. in Organic or Polymer Chemistry (Ph.D. preferred).</li>
<li>10+ years in R&amp;D within the chemical or manufacturing industry, with a proven track record of successful product launches.</li>
<li>5+ years of technical team leadership, including project ownership and mentoring.</li>
<li>Strong commercial and cross-functional orientation—you speak both “lab” and “market.”</li>
<li>Familiarity with tools like ERP, CRM, Excel, and Minitab, and curiosity around data analytics and AI in R&amp;D.</li>
<li>A communicator, strategist, and builder of culture. You’re not just a scientist—you’re a change leader.</li>
</ul>
Why Join Us
<ul>
<li>Be part of a high-visibility leadership team reporting directly to the CEO.</li>
<li>Collaborate with global R&amp;D counterparts and gain exposure to international innovation strategies.</li>
<li>Work at the forefront of chemistry and manufacturing excellence with a company known for its technical integrity and market leadership.</li>
<li>We offer a competitive compensation and benefits package (bonus, 401k, 409A, profit sharing, PTO, health)</li>
</ul>
#LI-AM1

Research & Development Director

<h3>Job Description</h3>
Sr Analytical R&amp;D Chemist – Method Development &amp; Implementation
Kannapolis, NC
Full-Time, Permanent 
Summary:
As a Senior Analytical R&amp;D Chemist - Method Development &amp; Implementation, you will play a crucial role in developing cutting-edge testing methods that provide accurate nutritional profiles for food products. This position is essential in supporting our mission to revolutionize food data and improve consumer health.
Responsibilities:
<ul>
<li>Development of new methods including verification and validation procedures to enhance testing capabilities. </li>
<li>Conduct analytical testing of food, beverage and/or supplement samples using various techniques including gas chromatography, liquid chromatography and spectroscopy.</li>
<li>Ensure compliance with FDA regulations, CGMP, and GLP standards in all laboratory practices.</li>
<li>Complete hand off of onboarded methods including training and method transfers.</li>
<li>Perform quality control checks on laboratory equipment and test results to ensure accuracy.</li>
<li>Maintain detailed records of experiments and results within laboratory information management systems. </li>
<li>Generate, maintain and meet project plans and deadlines for internal and external method expansion.</li>
<li>Collaborate with cross-functional teams to support product development initiatives.</li>
</ul>
 
Requirements:
<ul>
<li>Doctorate degree in Chemistry (preferred) or related field. </li>
<li>5+ years experience in direct method development and implementation in a related industry (food and/or supplement preferred). </li>
<li>Analytical instrumentation experience with a strong understanding of equipment maintenance and troubleshooting. </li>
<li>Strong understanding of food, beverage and supplement regulations and quality assurance practices.</li>
<li>Proficiency in wet chemistry techniques and various auxiliary equipment. </li>
<li>Proficiency in report generation and scientific writing. </li>
<li>Excellent attention to detail with strong organizational skills.</li>
</ul>

Senior Analytical Chemist

<h3>Job Description</h3>
Open to: General Public
Work Week: NL (35-hour) Work Week
Salary: (P25) $77,143.55 - $113,263.75
Opening Date: 9/2/2025
Closing Date: 9/23/2025
Existing Vacancies: 2
 
Program/Location
Department of Environmental Protection
Office of the Chief of Staff
Division of Science and Research
Office of Quality Assurance
428 East State Street
Trenton, NJ 08625
 
Scope of Eligibility
Open to applicants who meet the requirements below.
 
Description
Under the limited supervision of a Research Scientist 1 or other supervisory official in a State department, institution, or agency, implements and carries out chemical research projects designed by higher-level scientific staff, primarily in a laboratory setting and may include related field and/or office work; does other related duties as required.
 
Specific to the Position
Activities include duties related to the administration of the NJDEP Laboratory Certification Program and the administration of the NJDEP Quality Assurance Program. The responsibilities will include, but are not limited to, conducting on-site audits of labs analyzing samples for drinking water, wastewater, solid/hazardous waste, and air. Areas of analytical capability may include inorganic/organic chemistry, radiochemistry, asbestos or microbiology. Assures the analytical methodology is consistent with test procedures established by national organizations, and data generated by the methodology is accurate and acceptable for use by the environmental community. Leads projects to evaluate and define the technical standards needed for the operation of scientific instrumentation used for the analyses of environmental samples. Makes qualitative evaluations related to the generation, collection, review and use of analytical data. Could require approximately 25-30% of work time traveling.
 
Preferred Skill Set
Strong knowledge of environmental testing methodologies and quality assurance/quality control procedures used in the analyses of drinking water, wastewater, and solid/hazardous waste, and experience performing analytical techniques. An understanding of state and federal regulations and requirements. Ability to multi-task, and write clear, technically sound, accurate and factual reports to evaluate a laboratory's compliance with State and Federal regulations.
 
Requirements
EDUCATION: Graduation from an accredited college or university with a Master of Science degree in chemistry or other appropriate physical or environmental science discipline.
 
EXPERIENCE: Two (2) years of experience in chemical analysis or research.
NOTE: A Doctorate in a physical, chemical, or environmental science discipline may be substituted for the experience indicated above.
 
OR
 
EDUCATION: Graduation from an accredited college or university with a Bachelor of Science degree in chemistry or other appropriate physical or environmental science discipline.
 
EXPERIENCE: Three (3) years of experience in chemical analysis or research; one (1) year of which must be in the operation of the gas chromatography mass spectrometer, gas chromatograph, high performance liquid chromatograph, fourier transform mass spectrometer, inductively coupled plasma spectrometer, atomic absorption spectrometer, x-ray defractor, transmission electron microscope, or updated replacement thereof.
 
License
Appointees will be required to possess a driver's license valid in New Jersey only if the operation of a vehicle rather than employee mobility, is necessary to perform the essential duties of the position.
 
SAME Applicants
If you are applying under the NJ SAME program, your supporting documents (Schedule A or B letter) must be submitted along with your resume by the closing date indicated above. For more information on the SAME program, please visit SAME Program, email <a href="mailto:SAME@csc.nj.gov" target="_blank">SAME@csc.nj.gov</a>, or call CSC at (609) 292-4144 and select Option #3.
 
Veteran's Preference
To qualify for New Jersey Veteran's Preference/status, you must establish Veteran's Preference through the Department of Military and Veteran's Affairs. Please submit proof of your Veteran's Preference along with your resume as indicated. For more information, please visit <a href="https://www.nj.gov/military/veterans/services/civil-service-preference/" target="_blank">https://www.nj.gov/military/veterans/services/civil-service-preference/</a>
 
Employee Benefits
As a New Jersey State Department, NJDEP offers a comprehensive benefits package that includes:
<ul>
<li>Paid Benefit Leave</li>
<li>Holiday Pay</li>
<li>Alternative Workweek Program*</li>
<li>Telework*</li>
<li>Pension</li>
<li>Deferred Compensation</li>
<li>Health Benefits (medical, prescription drug, dental &amp; vision care) and Life Insurance</li>
<li>Flexible and Health Spending Accounts (FSA/HSA)</li>
<li>Commuter Tax Savings Program</li>
<li>Public Service Loan Forgiveness (PSLF)</li>
<li>Tuition Reimbursement*</li>
</ul>
 
*Pursuant to the State/Department's policy, procedures, and/or guidelines.
 
Residency
All persons newly hired on or after September 1, 2011, have one year from the date of employment to establish, and then maintain principal residence in the State of New Jersey subject to the provisions of N.J.S.A. 52:14-7 (L.2011, Chapter 70), also known as the “New Jersey First Act”.
 
Authorization to Work
Selected candidates must be authorized to work in the United States per the Department of Homeland Security, United States Citizenship, and Immigration Services regulations. NOTE: The State of New Jersey does not provide sponsorship for citizenship to the United States.
 
Equal Opportunity Employment
The State of New Jersey seeks to increase the richness and diversity of its workforce, and in doing so, become the employer of choice for all people seeking to work in State Government. To evaluate the effectiveness of our efforts to attract and employ a diverse workforce, applicants are asked to voluntarily answer a few brief questions on the NJ Affirmative Action Information Form. All information is considered confidential and will be filed separately with the agency's affirmative action officer. This information will not be part of your application for employment and will not be considered in any hiring decision.
 
DEP Notices of Vacancy have a 4:00 p.m. deadline on the closing date. When filing for these opportunities, please be sure to have your letter of interest and credentials sent electronically before 4 p.m. on the closing date.
 
The New Jersey Department of Environmental Protection is an Equal Opportunity Employer and is committed to inclusive hiring and a diverse workforce. We strongly encourage people from all backgrounds to apply. Accommodations under ADA will be provided upon request.

Research Scientist 3

<h3>Job Description</h3>
Job DescriptionChemists are responsible for conducting a variety of analytical tests on cannabis samples, interpreting results, and ensuring the accuracy, reliability, and compliance of testing procedures in an ISO 17025 accredited testing laboratory. • Perform routine laboratory tests on cannabis samples, including potency analysis, pesticide screening, residual solvent analysis, microbial testing, and heavy metal analysis. • Follow standard operating procedures (SOPs) and test methods to ensure consistency, accuracy, and compliance with ISO 17025 standards and regulatory requirements. • Prepare reagents, standards, and samples for analysis, following established protocols and safety guidelines. • Operate and maintain laboratory equipment and instruments, troubleshoot technical issues, and perform routine maintenance and calibration procedures. • Document test results, observations, and deviations accurately and promptly in laboratory notebooks and electronic systems. • Assist with data analysis, quality control checks, and method validation studies as needed. • Collaborate with team members to troubleshoot problems, optimize processes, and improve laboratory efficiency. • Adhere to health and safety protocols, including the proper handling, storage, and disposal of hazardous materials. Requirements• Bachelor's degree in chemistry, biochemistry, or a related field. • Prior laboratory experience or coursework in analytical chemistry is preferred but not required. • Strong attention to detail, organizational skills, and ability to follow instructions. • Excellent communication and teamwork skills. • Ability to work independently and collaboratively in a fast-paced environment. • Proficiency in Microsoft Office Suite and Laboratory Information Management Systems (LIMS). BenefitsHealth Insurance Stipend Phone Stipend PTO 401k with 6% match

Chemist

<h3>Job Description</h3>
Chief Scientific Officer - Confidential Client (Biotechnology, Boston, MA) 
About the Company Our client is a cutting-edge biotechnology company dedicated to developing next-generation gene editing and gene therapy solutions for serious diseases. With a proprietary platform and strong financial backing, they are advancing multiple programs in CNS and neuromuscular disorders with the mission of delivering functional cures.
The Role The Chief Scientific Officer will serve as the scientific and strategic leader, driving discovery, translational, and preclinical efforts across the company's therapeutic portfolio. This executive will play a pivotal role in shaping the company's scientific vision and advancing novel programs toward clinical development.
Key Responsibilities
<ul>
<li>
Provide overall scientific and R&amp;D leadership across CNS and neuromuscular disease programs.
</li>
<li>
Lead teams spanning discovery, translational biology, and preclinical development.
</li>
<li>
Develop and execute strategies to progress gene editing/gene therapy programs from target validation to IND/CTA.
</li>
<li>
Partner with executive leadership, investors, and external collaborators to align R&amp;D with corporate strategy.
</li>
<li>
Stay at the forefront of advances in CNS, neuromuscular, and gene editing/therapy fields to maintain the company's leadership position.
</li>
</ul>
Qualifications
<ul>
<li>
PhD or MD/PhD in neuroscience, genetics, molecular biology, or related discipline.
</li>
<li>
10+ years of leadership experience in biotechnology or pharmaceutical R&amp;D.
</li>
<li>
Deep expertise in CNS or neuromuscular disorders and gene editing/therapy modalities (AAV, LNP, base or prime editing, etc.).
</li>
<li>
Demonstrated track record progressing programs through IND/CTA and into early clinical development.
</li>
<li>
Strong leadership, communication, and collaborative skills with the ability to inspire teams and engage stakeholders.
</li>
</ul>
Why Join? This is a rare opportunity to lead the scientific direction of a company at the forefront of gene editing, backed by a proprietary platform and committed to transforming patient outcomes in areas of urgent need.

Chief Scientific Officer - Gene Editing

<h3>Job Description</h3>
Chemical Operator
Berlin CT
Direct-Hire
3rd shift hours: 11 pm – 7 am
 
Position Summary
The Chemical Operator is responsible for the safe operation of equipment in a manufacturing facility, material handling, quality control, accurate recordkeeping, and maintaining housekeeping standards while following company policies and safety procedures.
 
Essential Functions
<ul>
<li>Operate and monitor plant systems (feeds, temperatures, pressures)</li>
<li>Follow procedures and instructions from Leads and Managers.</li>
<li>Sample, test, and record process streams per quality requirements.</li>
<li>Accurately weigh and add raw materials; monitor inventory.</li>
<li>Load finished products into bulk tankers, totes, and drums.</li>
<li>Assist with maintenance preparations.</li>
<li>Maintain housekeeping and Good Manufacturing Practices.</li>
<li>Support compliance with OSHA, EPA, PSM, and safety policies.</li>
<li>Input data into ERP system and complete logs/forms.</li>
<li>Provide improvement suggestions to management.</li>
<li>Participate in EHS and training programs.</li>
<li>Must be willing to work overtime, nights, and weekends.</li>
<li>Other duties as assigned.</li>
</ul>
 
Skills &amp; Qualifications
<ul>
<li>High school diploma required; community college certificate preferred.</li>
<li>0-5 years of chemical or manufacturing experience (certificate in Chemical Plant Technician training may substitute).</li>
<li>Basic Microsoft Office 365 skills.</li>
<li>Knowledge of hazardous materials handling, OSHA/EPA compliance, and emergency response training.</li>
<li>Strong mechanical aptitude and troubleshooting skills.</li>
<li>Ability to work effectively in teams and interact with all plant levels.</li>
<li>Full professional English proficiency (written &amp; verbal).</li>
<li>Flexible schedule availability.</li>
</ul>

Chemical Operator

<h3>Job Description</h3>
Job DescriptionDescription:
SeamonWhiteside is looking for a talented and motivated individual to join our growing Innovations team as a Geographic Information Systems Developer in our Mount Pleasant, South Carolina office. 
 
This position will focus on the design, drafting and implementation of various GIS tools tp help aid our internal teams as well as our clients. The successful candidate will be able to work closely with civil engineers, landscape architects, surveyors and water resources personnel to better understand their needs within this software and make data more accessible for our clients. 
 
About Us
Since the company’s beginning in 1985, we’ve blended the disciplines of civil engineering and landscape architecture from concept to completion to create places of legacy and inspiration for our clients, community, and family. There is a big difference in how engineers and landscape architects visualize a project. At SW+ we approach every plan from both points of view, working together to create a successfully integrated venture. In our world, that’s a good thing.
 
With the goal of being the best design firm in the region, the SW+ leadership team continues to attract the brightest talent, each with a unique expertise. SW+’s water resources team expands our diverse portfolio at a variety of scales in both the public and private sectors including utilities infrastructure design, water/wastewater and stormwater management, flood studies, , and resiliency planning.
 
With over 200+ employees, and offices in Mount Pleasant, Greenville, Summerville, and Spartanburg, SC as well as Charlotte and Raleigh, NC, SW+ inspires employees to stand behind its tagline, of designing innovative spaces that enrich lives and leave a legacy for future generations. 
 
Company culture is at the core of who we are. SW+ offers a mentorship program and other professional growth opportunities. In addition, company sponsored events, such as golf tournaments, sports teams, and happy hours, along with philanthropic endeavors provide opportunities throughout the year to lift morale and strengthen bonds between coworkers.
Requirements:
 Essential Job Functions
<ul>
<li>Work within the Technology &amp; Innovation team to design, develop, and maintain custom GIS tools that enhance internal civil engineering and landscape architecture workflows.</li>
<li>Provide technical GIS support, training, and innovation to GIS users across the company.</li>
<li>Collaborate with the Water Resources Department on client-facing GIS projects, including hydrologic, hydraulic, and environmental analysis.</li>
<li>Use ArcGIS Pro and the broader ArcGIS suite to perform advanced spatial analysis, data management, and visualization.</li>
<li>Build and deploy custom GIS applications and web maps tailored to both internal and client needs.</li>
<li>Integrate GIS solutions with other engineering and landscape architecture tools and processes.</li>
<li>Plan and conduct drone/UAS flights for data collection, and process and integrate drone imagery into GIS workflows.</li>
<li>Stay current with GIS technology trends and recommend new tools or approaches to enhance our services.</li>
</ul>
 
Minimum Requirements
 
Education: Bachelor’s degree in Geography, GIS, Environmental Science, or a related field.
Experience: Minimum of 3 years of professional experience in a GIS-based role, preferably in a civil engineering or environmental context.
<ul>
<li>Advanced proficiency with ArcGIS Pro and the ArcGIS Online suite (Survey123, Experience Builder, Map Viewer, Dashboards, etc.).</li>
<li>Strong experience in spatial analysis, geoprocessing, and data visualization using ArcGIS tools.</li>
<li>Experience building custom GIS applications and familiarity with geospatial database management.</li>
</ul>
Desired Skills
<ul>
<li>Experience with drone/UAS operations, including flight planning, data collection, and imagery processing for GIS use.</li>
<li>FAA Part 107 Remote Pilot Certification or willingness to obtain.</li>
<li>Experience with water resources modeling and analysis (HEC-RAS, SWMM, etc.).</li>
<li>Knowledge of CAD/GIS integration.</li>
<li>Spatial programming experience, including Python, SQL, Arcade, JavaScript, etc.</li>
</ul>
Other Skills/Abilities 
<ul>
<li>Excellent written, verbal, and graphic communication skills</li>
<li>Strong organizational and project management skills</li>
<li>Positive attitude and strong work ethic</li>
<li>Excellent problem solving and critical thinking skills </li>
<li>Excellent interpersonal skills - ability to effectively interact with individuals at all levels </li>
<li>Ability to be both creative and analytical</li>
<li>Positive, solution-oriented attitude</li>
<li>Detail-oriented and accurate</li>
<li>Ability to work in a team environment</li>
</ul>
 
Working Environment/Physical Demands
Working Environment
<ul>
<li>General office environment: Works generally at a desk in a well-lit, air-conditioned cubicle/office, with moderate noise levels. </li>
<li>Periods of stress may occur.</li>
</ul>
Physical Demands
<ul>
<li>Extended periods of sitting and using a computer for typing and data entry.</li>
<li>Some walking and standing relative to interaction with other personnel.</li>
<li>Regular use of the phone for conducting interviews and communication with candidates.</li>
</ul>

GIS Developer

<h3>Job Description</h3>
DescriptionA Brief Overview
A Medical Physicist within the Department of Radiation Oncology is responsible for calibrating and maintaining radiation therapy equipment and conducting quality assurance tests to ensure accurate and safe dose delivery. The Medical Physicist collaborates with radiation oncologists, dosimetrists, and radiation therapists to develop and optimize individualized treatment plans using advanced techniques such as volumetric-modulated radiation therapy (VMAT), image-guided radiation therapy (IGRT), and adaptive radiotherapy. The Medical Physicist performs rigorous quality assurance procedures to verify equipment performance and treatment accuracy, ensuring radiation safety and compliance with guidelines from the Ohio Department of Health (ODH). Additionally, the role involves contributing to clinical research, developing innovative treatment protocols, and providing education and training to medical residents, physics residents, dosimetrists, and radiation oncology students.
What You Will Do
<ul>
<li>Quality Assurance (QA): Performs routine QA checks on radiation therapy equipment, such as linear accelerators and brachytherapy sources, to ensure accurate dose delivery. </li>
<li>Equipment Calibration: Calibrates radiation therapy machines to maintain consistent and precise treatment.</li>
<li>Collaborates with radiation oncologists, dosimetrists, and radiation therapists to design effective treatment strategies.</li>
<li>Verifies the accuracy of treatment delivery through patient-specific QA processes.</li>
<li>Ensures the safety of patients and staff by monitoring radiation levels and implementing safety protocols.</li>
<li>Develops and implements advanced radiation therapy techniques, such as intensity-modulated radiation therapy (IMRT), stereotactic body radiotherapy (SBRT), and adaptive radiotherapy.</li>
<li>Educates and trains residents, radiation therapists, dosimetrists, and other healthcare professionals in medical physics principles and practices.</li>
<li>Provides ongoing education and support to clinical staff on the safe and effective use of radiation.</li>
<li>Ensures compliance with regulations and standards set by agencies such as the Nuclear Regulatory Commission (NRC), Food and Drug Administration (FDA), and local health departments such as Ohio Department of Health (ODH). </li>
<li>Participates in departmental and institutional committees and meetings, as required. </li>
</ul>
Additional Responsibilities
<ul>
<li>Performs other duties as assigned.</li>
<li>Complies with all policies and standards.</li>
<li>For specific duties and responsibilities, refer to documentation provided by the department during orientation.</li>
<li>Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.</li>
</ul>
QualificationsEducation
<ul>
<li>Master's Degree M.Sc. in Medical Physics in the physical or related sciences. (Required) </li>
</ul>
Work Experience
<ul>
<li>2+ years clinical experience in radiation oncology physics. (Required) </li>
</ul>
Knowledge, Skills, &amp; Abilities
<ul>
<li> Radiation Therapy: Knowledge of treatment planning, dose calculation, and delivery methods such as IMRT, SBRT, and brachytherapy. (Required proficiency) </li>
<li> Equipment Calibration and Maintenance: Ability to calibrate and maintain medical equipment to ensure accurate and safe operation. (Required proficiency) </li>
<li> Quality Assurance (QA): Conducting regular QA tests to ensure equipment and procedures meet established standards and safety regulations. (Required proficiency) </li>
<li> Medical Imaging: Knowledge of various imaging modalities like X-ray, CT, MRI, and PET, including image analysis and interpretation for radiation therapy purposes. Ability to perform image fusion. (Required proficiency) </li>
<li> Software Proficiency: Familiarity with specialized software for treatment planning (e.g., RayStation, Eclipse), image processing (e.g., MIM), second check software (e.g. RadCalc, Mobius, MU Check), and data analysis. (Required proficiency) </li>
<li> Clinical Protocols: Developing and implementing clinical protocols and procedures to optimize patient care. (Required proficiency) </li>
<li> Procedures: Ability to develop and write policies and procedures, in collaboration with Radiation Oncology team members. (Required proficiency) </li>
<li> Capable of working independently and as a team in a clinical environment. (Required proficiency) </li>
<li> Attention to detail, adaptability, analytical thinking, and teamwork. (Required proficiency) </li>
</ul>
Licenses and Certifications
<ul>
<li> American Board of Radiology - Therapy Physics (Required) </li>
<li> ABR Board Certified - Therapy (Required) </li>
</ul>
Physical Demands
<ul>
<li>Standing Occasionally </li>
<li>Walking Occasionally </li>
<li>Sitting Constantly </li>
<li>Lifting Rarely 20 lbs </li>
<li>Carrying Rarely 20 lbs </li>
<li>Pushing Rarely 20 lbs </li>
<li>Pulling Rarely 20 lbs </li>
<li>Climbing Rarely 20 lbs </li>
<li>Balancing Rarely </li>
<li>Stooping Rarely </li>
<li>Kneeling Rarely </li>
<li>Crouching Rarely </li>
<li>Crawling Rarely </li>
<li>Reaching Rarely </li>
<li>Handling Occasionally </li>
<li>Grasping Occasionally </li>
<li>Feeling Rarely </li>
<li>Talking Constantly </li>
<li>Hearing Constantly </li>
<li>Repetitive Motions Frequently </li>
<li>Eye/Hand/Foot Coordination Frequently </li>
</ul>
Travel Requirements
<ul>
<li>20% Travel within main campus and network locations, joint ventures, and affiliates. </li>
</ul>

Physicist- Proton Therapy

<h3>Job Description</h3>
I'm hiring for a Micro/Molecular Laboratory Supervisor in Rhode Island!
The Supervisor will direct and control the operations of the Microbiology and the Molecular laboratory including overseeing testing, instrumentation maintenance, staff training, competency assessment, proficiency evaluation, performance management and documentation; develop, engage, recognize and support technical and non-technical staff; manage department and individual performance by providing feedback and coaching to staff members; maintain departmental operating policies and procedures to include departmental programs, quality control, quality assurance and safety; review completion of patient test results, quality control results and tracks productivity; take corrective action to resolve issues involving test results, quality, instrumentation, compliance and employee performance; and provide technical training to staff.
Location: Near Barrington, RI Type: Full-time and permanent Shift: Days Requirements: College degree; ASCP cert; at least 4 years prior experience Pay: Discussed during interview Benefits: 401k; health, dental, and life insurance; PTO, etc.
Offering My clients are offering a competitive compensation and benefits package (PTO, health insurance, etc.), with potential for sign-on bonus and/or relocation assistance! There are many opportunities for growth with this company.
To apply, email your resume to <a href="mailto:leah@ka-recruiting.com" target="_blank">leah@ka-recruiting.com</a>/call or text 617-746-2751! You can also schedule a time to chat here - <a href="https://calendly.com/leahkarecruiting/10min" target="_blank">https://calendly.com/leahkarecruiting/10min</a> .
REF#LM7590
Microbiology/Molecular Lab Supervisor, Microbiology/Molecular Supervisor, Micro/Molecular Supervisor, Lab Supervisor, Laboratory Supervisor, Microbiology, Molecular
Rhode Island, Barrington, East Providence, Providence, Rumford, Pawtucket, Central Falls, Riverside, Cranston

Microbiology/Molecular Laboratory Supervisor in Rhode Island

<h3>Job Description</h3>
Job Description Summary Measure with CMM. Vison and CT scanning equipment for key quality characteristics as directed of various plastic and steel components. Prepare graphs, charts, and reports of collected data. Assist engineering in product design verifications, process qualifications and validations. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Job Summary Measure key quality characteristics as directed of various plastic and steel components. Prepare graphs, charts, and reports of collected data. Assist engineering in product design verifications, process qualifications and validations. Responsibilities 
<ul>\n
<li>Perform measurements with calipers, digital micrometers, gage pins, drop depth gages, optical comparator etc.</li>
\n
<li>Perform measurements on the Coordinate Measurement Machines (CMMs) Vision and CT Scanning for both contact and non-contact, using pre-established routines and fixtures.</li>
\n
<li>Read and interpret the basics of the engineering drawings such as dimensions, diameters, datum structure and definitions of such datum's.</li>
\n
<li>Understand and apply the tolerances of such features.</li>
\n
<li>Perform simple data analysis using Minitab.</li>
\n
<li>Ensure accuracy and traceability of measured data.</li>
\n
<li>Perform Measurement System Analysis (MSA) studies.</li>
\n
<li>Comply with all local, state, federal, and BD safety regulations, policies, and procedures. Comply with all local BD quality policies, procedures, and practices through consistent application of sound quality assurance principles.</li>
\n
<li>Other duties as assigned.</li>
\n</ul>
\n Requirements 
<ul>\n
<li>Basic math skills.</li>
\n
<li>Work with minimal direction.</li>
\n
<li>Knowledge in MS Excel and MS Word preferred</li>
\n</ul>
\n Experience using mechanical inspection and measuring equipment required. 
<ul>\n
<li>Understand simple mechanical concepts.</li>
\n
<li>Follow written and verbal instructions.</li>
\n
<li>Prioritize daily duties.</li>
\n
<li>Good communication skills, both written and verbal.</li>
\n
<li>Detailed oriented and good decision making skills.</li>
\n</ul>
\n At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit <a href="https://bd.com/careers" target="_blank">https://bd.com/careers</a> Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. #earlycareer Required Skills 2D Drawings, CMM Programming, Coordinate Measuring Machine (CMM) Operation, Coordinate Measuring Machines, Coordinate Measuring Machines (CMM) Inspection Optional Skills Primary Work Location USA UT - Sandy Additional Locations Work Shift US BD 2nd Shift 230pm-11pm (United States of America)

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