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<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>
Job Description
 OBJECTIVE: The Senior Scientist will work with a team to oversee all aspects of the protocol, experimental data, unforeseen problems, test systems and any specific regulations that must be followed. This will include interacting with clients, performing business development, acting as the study director and may prepare and oversees budgets. In addition the Sr. Scientist will play a critical role in advancing our research programs through scientific expertise, technical proficiency and collaborative problem-solving. QUALIFICATIONS AND SKILLS:
<ul>
<li>Ph.D. Cell Biology, Molecular Biology, Pharmacology, Immunology or related field with a 8+ years of relevant experience, or M.S with 15+ years of experience.</li>
<li>Proven expertise in 3D organoid culture techniques, including patient-derived organoids and microphysiological systems</li>
<li>Strong background in developing and executing high-throughput in vitro assays.</li>
<li>Proficiency in data analysis software and electronic lab notebooks.</li>
</ul>
<ul>
<li>Excellent problem-solving skills and the ability to work independently and collaboratively in a fast-paced environment.</li>
<li>Strong written and verbal communication skills for presenting data and authoring technical reports.</li>
<li>Demonstrated ability to work collaboratively with interdisciplinary teams.</li>
<li>Commitment to staying current with emerging technologies and methodologies in assay development and screening.</li>
<li>Proven experience in designing, optimizing, and executing high-throughput screening assays for lead molecule discovery and early-stage drug development.</li>
<li>Experience with automated liquid handling systems and high-content imaging platforms.</li>
<li>Familiarity with regulatory requirements for preclinical assay validation.</li>
<li>Statistical Design of Experiments (DoE): Knowledge of experimental design principles to optimize assay conditions and ensure robustness.</li>
<li>Regulatory Compliance: Understanding of GLP practices and experience in preparing documentation for regulatory.</li>
<li>Experience in a CRO or industry-based research setting.</li>
</ul>
KEY RESPONSIBILITIES:
<ul>
<li>Design, develop, and validate complex vitro assays, including 3D organoid models, to evaluate drug efficacy and toxicity.</li>
<li>Collaborate cross-functionally with internal teams to integrate in vitro findings into broader preclinical studies and ensure timely delivery of projects, maintain quality standards and meeting tight deadlines.</li>
<li>Engage directly with sponsors to understand their specific needs, providing tailored assay solutions and ensuring high levels of client satisfaction.</li>
<li>Manage multiple projects simultaneously and adapt to evolving priorities in a fast- paced environment.</li>
<li>Implement high-throughput screening (HTS) methodologies to facilitate large-scale compound testing, as applicable.</li>
<li>Lead the expansion and optimization of in vitro assay offerings in alignment with evolving market demands and sponsor requirements.</li>
<li>Stay abreast of industry trends and technological advancements to inform strategic decisions and maintain a competitive edge in assay development services.</li>
<li>Maintain accurate and detailed experimental records and contribute to technical reports and publications.</li>
</ul>

Senior Scientist

<h3>Job Description</h3>
Contract Details
<ul>
<li>Location: On-site.</li>
<li>Work Hours: Monday–Friday, typically 8:00 AM–5:00 PM or 9:00 AM–5:00 PM (40 hours/week).</li>
<li>Contract Duration: 1-year contract, reviewed annually for potential extension or termination based on performance.</li>
<li>Start Date: 1st week of December.</li>
</ul>
 
Core Technical Responsibilities
<ul>
<li>Molecular Biology Focus: Role centers around molecular biology and extensive cell culture work.</li>
<li>Techniques and Tasks:</li>
<li>Perform regular cell culture, including media changes.</li>
<li>Preserve cells in liquid nitrogen / -80°C freezer and perform cell recovery.</li>
<li>Execute Western Blot and RT-qPCR (Real-Time Quantitative Polymerase Chain Reaction).</li>
<li>Operate RT-qPCR equipment (preferred).</li>
<li>Primary cell isolation from tissues (preferred).</li>
</ul>
 
Qualifications
Education:
<ul>
<li>Master’s degree preferred (ideal for fresh graduates).</li>
<li>Bachelor’s degree acceptable only if the candidate has substantial, verifiable hands-on lab experience.</li>
<li>Theoretical knowledge alone is insufficient.</li>
</ul>
 
Experience:
<ul>
<li>Must demonstrate genuine, verifiable proficiency in molecular biology techniques (cell culture, Western blot, RT-qPCR).</li>
<li>Prior industry background (academia vs. private sector) is irrelevant if the technical skill set is proven.</li>
<li>Preference for motivated, young professionals eager to learn challenging new concepts.</li>
</ul>
 
Cultural and Retention Expectations
<ul>
<li>Loyalty and Knowledge Protection:</li>
<li>Must demonstrate commitment to confidentiality and intent to stay local.</li>
</ul>
 
Mentorship and Growth:
<ul>
<li>The role includes mentorship, providing advanced skill-building opportunities.</li>
<li>High-performing candidates may be considered for conversion to full-time employment.</li>
</ul>

Research Assistant

<h3>Job Description</h3>
Job Description
Come join our family! Microbac Laboratories is an essential business offering competitive pay and benefits including medical, dental, vision, life insurance, disability, generous paid time off including vacation, holidays and flex-time, a wellness program, referral bonus, tuition reimbursement and more! 
Whether you are just starting your career in science or looking to further it, Microbac will put you on the path of an exciting career with room to grow. Quality, safety, giving back to our communities, diversity and inclusion, customer success and employee wellbeing are part of our core culture. We are looking for motivated individuals to join our family as a Microbiology Supervisor.
ABOUT MICROBAC
Microbac Laboratories, Inc. is a premier commercial laboratory testing firm that partners with clients worldwide, offering laboratory solutions to the life science, food and nutrition, and environmental industries and serves our clients with the utmost expertise and respect for their market requirements, constraints and challenges. We embody a company-wide commitment to exceptional customer experience, which has been refined over nearly 50 years of trusted, analytical and measurement experience.
Through our network of laboratories, offices, and field services, we have the flexibility to meet the unique requirements for each client, project and scope.
As a privately held third-party testing company, Microbac operates with a commitment to safety, quality and compliance. Our diverse work portfolio includes broad accreditation offerings and tested insights across the environmental, food and nutrition and life science markets.
JOB SUMMARY
We are currently seeking a full-time Supervisor, Environmental-Microbiology, working in an accredited commercial laboratory, is responsible for conducting standard chemical and/or biological tests and analyzing results to determine composition, reactions, and chemical and/or physical properties of a variety of sample types. The position may also review processes and perform data review to ensure alignment with established SOPs and accuracy. Limited exercise of judgement and detailed work procedures required for more complex methods and procedures.
ESSENTIAL FUNCTIONS:
<ul>
<li>Thorough technical knowledge of environmental microbiology instrumentation and test methods.</li>
<li>Strong understanding of SDWA regulations and TNI standards.</li>
<li>Ability to conduct analysis and read, interpret, and report technical data.</li>
<li>Advanced understanding of principles, terminology, practices, techniques and instrumentation commonly used in an environmental laboratory. </li>
<li>Excellent computer literacy.</li>
<li>Excellent analytical problem-solving abilities.</li>
<li>Leadership ability is a strong plus.</li>
<li>Ability to prioritize time and activities to meet the demands of the overall workload.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Following established SOP’s and adhering to state, federal and other accrediting body requirements, prepare and process samples, and collect information about the composition of substances to support the analytical testing needs of clients, for such purposes as quantitative analysis, and product development </li>
<li>Prepare necessary standards, solutions, reagents, media, and samples for sample analyses</li>
<li>Utilize specialized laboratory equipment and instrumentation to process and analyze samples</li>
<li>Perform equipment and instrumentation set up</li>
<li>Accurately record observations and data and basic interpretation of data</li>
<li>Maintain the integrity of procedures and record professional activity for peer review</li>
<li>Monitor and address sample backlog issues</li>
<li>Maintain accurate, up to date logs, notebooks and equipment records</li>
<li>Perform necessary laboratory administrative functions such as filing paperwork, photocopying, reviewing of data, and entering data into computerized LIMS</li>
<li>Comply with and promote Safety, and Quality programs</li>
<li>Perform peer review and work with the QA team to maintain up to date SOPs</li>
<li>Perform advance level sample analysis</li>
<li>Troubleshoot laboratory instrumentation issues</li>
<li>Investigate and address inconsistencies with data output</li>
<li>May be involved in test method development with guidance</li>
<li>Accurately record observations and data, and interpret results</li>
<li>Maintain the integrity of procedures</li>
<li>Create data reports; Review data and reports for accuracy; perform peer reviews</li>
<li>Other duties as assigned</li>
</ul>
MINIMUM REQUIREMENTS:
<ul>
<li>Bachelor’s degree from a four-year accredited institution in a related in a related field of applied science; plus, five or more years of related experience; or six plus years of related laboratory experience with no degree.</li>
</ul>
WORKING CONDITIONS AND PHYSICAL REQUIREMENTS:
The physical demands and working conditions described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Physical Requirements: 
<ul>
<li>While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel objects, tools; talk or hear. The employee is occasionally required to stand, walk, and sit.</li>
<li>The employee must regularly lift and/or move up to 25 pounds. Specific vision abilities required by this job include color vision and depth perception.</li>
</ul>
Working Conditions: 
<ul>
<li>While performing the duties of this job, the employee will be in a general office environment.</li>
<li>The noise level in the work environment is usually moderate.</li>
<li>This job may require travel less than 20%</li>
</ul>
As a privately held third-party testing company, Microbac operates with a commitment to safety, quality, and compliance. Our diverse work portfolio includes broad accreditation offerings and tested insights across the environmental, food and life science markets.
OTHER:
This job description is not an exhaustive list of all duties an employee may be required to perform. Microbac reserves the right to revise the job description at any time. 
Employment is at-will. Microbac, promotes a drug-free, alcohol-free workplace. Applicants considered for hire must pass a drug test before beginning work. Refusal to submit to testing will result in disqualification of further employment consideration.
Microbac is an Equal Opportunity Employer – We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. All qualified applicants will receive consideration for employment.

Microbiology Supervisor

<h3>Job Description</h3>
Position Highlights:&nbsp;
<ul>
<li>Opportunity to manage a microbiology laboratory within an established healthcare organization!</li>
<li>Oversight of Supervisors and Technicians/Technologists.</li>
<li>Responsible for staff hiring, orientation, competency and ongoing training. Also, providing performance feedback to staff.&nbsp;</li>
<li>Managing day to day operations of the microbiology laboratory including ensuring laboratory compliance, develops and implementing policies and procedures.&nbsp;</li>
<li>Offering highly competitive compensation package AND Sign On Bonus!&nbsp;</li>
<li>Comprehensive benefits package including (but not limited to): health,&nbsp;dental, vision and prescription&nbsp;drug coverage; supplemental health protection plans; 401K retirement plan and stock purchase option; educational benefits and more!&nbsp;</li>
</ul>
Requirements:
<ul>
<li>Bachelor's Degree in Microbiology&nbsp;or Medical Laboratory Science (or equivalent). Masters Preferred.&nbsp;</li>
<li>MLS/MT, SM or M&nbsp;ASCP&nbsp;Certification (or equivalent)</li>
<li>At least 3 years of experience in a microbiology leadership position.&nbsp;</li>
</ul>
Location Highlights:&nbsp;
<ul>
<li>
One of the most affordable US Cities, with affordable housing and low cost rentals!
</li>
<li>
Come live in the "Heart of the Midwest" with easy access to other major cities and travel destinations.&nbsp;
</li>
<li>
Kansas City offers some of the top family friendly neighborhoods in the US!&nbsp;
</li>
</ul>
Interested in learning more? Contact Andrea at <a href="mailto:andrea@ka-recruitng.com" target="_blank">andrea@ka-recruitng.com</a>&nbsp;or call/text 617-746-2745!&nbsp;
ACC 254111050

Microbiology Manager OR Micro Laboratory Manager Opening Outside of Kansas City

<h3>Job Description</h3>
Required Details:
Required Cert: ABR
 
Required:
HDR
SRS
SBRT
TBI
IORT
 
Required: Standard radiation cases w/ higher volume of breast and prostate. Others include Lung, breast, hepatobiliary, brain, multiple myeloma, sarcomas, etc.
 
Performs the duties of quality assurance, calibration, repair, and if necessary, communication with outside vendors in relation to repairs of radiation therapy equipment. Communicates and collaborates with the appropriate radiation oncology team about equipment status and develops a mutual plan of action when equipment downtime is known and/or anticipated. Performs any other duties that may be deemed necessary for the optimal performance of the Department of Physics. Radiation therapy treatments are performed on a daily basis, as such principal functions including, but not limited to, calibration, quality assurance, etc. are to be done after normal business hours.

Medical Physicist

<h3>Job Description</h3>
Analytical Services Chemist III
Job Summary:
This position is primarily responsible for the laboratory testing of raw materials, packaging materials, in-process, release and stability samples for developmental and pre-commercial drug products, including the evaluation of new raw materials, new packaging materials, reference standard qualifications, method transfers, and develop and validate methods within the framework of cGMP compliance guidelines.
Responsibilities:
<ul>
<li>Perform routine and non-routine physical and chemical tests and assays on raw materials, API’s, in-process, finished products, experimental batches and associated stability studies</li>
<li>Testing performed to include basic and complex lab equipment and procedures, such as pH, Loss on Drying, Residue on Ignition, Water Content by Karl Fischer, Assay/Impurities by HPLC, Dissolution, Residual Solvents by GC, and wet chemistry techniques such as titrations and sample derivatizations</li>
<li>Conduct analytical research and develop analytical methods to test pharmaceutical products for conformance to established specifications with some supervision.</li>
<li>Develop and validate analytical test methods for assay, dissolution, preservatives in drug products according to ICH/FDA/USP requirements with minimal to no supervision.</li>
<li>Develop and validate test methods for residual solvents and impurities/degradation products in drug substances/excipients/drug products according to ICH/FDA/USP requirements under some supervision</li>
<li>Develop and validate analytical Cleaning Validation methods and perform testing of cleaning validation samples and generate analytical report with minimum supervision.</li>
<li>Multi-task by working on several simultaneous projects. Develop project timelines.</li>
<li>Document all laboratory testing and maintain accurate and legible notebooks and records</li>
<li>Perform peer review on other analysts’ data.</li>
<li>Provide regular update progress reports of projects</li>
<li>Comply with all relevant regulatory requirements</li>
<li>At all times strive to maintain the self-esteem of individual team members and the professionalism of the group as a whole</li>
<li>Perform laboratory troubleshooting, propose solutions and implement</li>
<li>Other projects and duties as required or assigned</li>
<li>Provide technical input for purchase of new/updated laboratory instruments and software systems</li>
<li>Train other laboratory chemists on analytical instrumentation and methods.</li>
<li>Mentor/Train team members on new/revised skills and testing procedures</li>
</ul>
Education/Qualifications:
<ul>
<li>BS Degree in Chemistry or related field and 4 – 8 years of pharmaceutical product analysis experience in a cGMP-regulated lab environment</li>
<li>Masters Degree preferred</li>
<li>Experience working in the pharmaceutical industry and/or analytical laboratory</li>
<li>Knowledge of cGMP, USP/NF, and FDA guidelines and regulations</li>
<li>Expertise in analytical methods and lab instrumentation (e.g. HPLC, GC, dissolution, wet chemistry)</li>
<li>Demonstrated ability to perform method development and validation in accordance with ICH regulations with minimal supervision</li>
<li>Excellent oral and written communication skills</li>
<li>Strong organization, time management, leadership and troubleshooting skills</li>
<li>Demonstrated ability to work as part of a cross-functional team</li>
<li>Basic knowledge in Microsoft Word and Excel</li>
<li>Experience with software associated with a Laboratory Information Management System (LIMS) and a Chromatography Data System (CDS)</li>
<li>Work mainly performed in lab</li>
<li>Travel &lt; 5%</li>
</ul>

Analytical Services Chemist III

<h3>Job Description</h3>
Description
We are seeking an enthusiastic Associate Synthetic Chemist to support the discovery of small molecules for next-generation 3D printing resins. You will work hands-on in the lab, executing syntheses of novel molecules, characterizing products, and exploring photochemical and photophysical structure–property relationships. This role is ideal for highly motivated early-career chemists who love synthesis and are excited to accelerate innovation through fast, iterative chemistry. You will be closely mentored by experienced synthetic chemists and will collaborate with analytical scientists and engineers developing our printing systems.
Responsibilities
<ul>
<li>Design, execute, and troubleshoot small molecule synthetic routes, with a focus on divergent or modular approaches to rapidly generate lead candidates.</li>
<li>Purify products using chromatography and crystallization techniques.</li>
<li>Characterize compounds via UPLC, NMR, UV/Vis and IR spectroscopy, and mass spectrometry.</li>
<li>Work with cross-functional teammates to explore photochemical and photophysical structure–property relationships that drive 3D printing performance.</li>
<li>Maintain excellent electronic lab notebook documentation.</li>
<li>Contribute to management of chemical databases (e.g., commercial, proprietary, and virtual compound libraries).</li>
</ul>
Minimum Qualifications
<ul>
<li>Bachelor’s degree in Chemistry or a closely related field with equivalent advanced chemistry coursework.</li>
<li>≥2 years of intensive organic synthesis laboratory experience (academic research and/or industrial roles).</li>
<li>Experience with synthetic planning with chemical databases (e.g., SciFinder, Reaxys). </li>
<li>Excellent command of synthetic and physical organic chemistry fundamentals.</li>
<li>Experience with air-sensitive techniques (e.g., Schlenk line), purification (chromatography/crystallization), and data interpretation (NMR / LC-MS).</li>
<li>Evidence of strong documentation and organizational skills, attention to detail, and the ability to manage multiple workflows efficiently.</li>
<li>Evidence of strong collaboration and teamwork talents/skills.</li>
<li>Ability to thrive in a fast-paced, collaborative R&amp;D environment.</li>
</ul>
Preferred Qualifications
<ul>
<li>Command of the basics of photochemistry.</li>
<li>Experience with heterocyclic and/or extended aromatic systems, especially those relevant to organic (opto)electronics.</li>
</ul>
Benefits
<ul>
<li>We offer competitive compensation packages in our VC-backed startup.</li>
<li>Benefits include a full suite of offerings covering medical, dental, vision and 401k plan. </li>
<li>Beautiful setting looking out over a river and seaport; outdoor seating and picnic areas.</li>
<li>Highly collaborative work environment.</li>
</ul>
Additional Information
<ul>
<li>Travel: Occasional travel may be required from time to time</li>
<li>Location: Boston, Massachusetts</li>
</ul>
We value diversity in our company and are an Equal Opportunity Employer.

Associate Synthetic Chemist

<h3>Job Description</h3>
Open to: General Public
Work Week: NL (35-hour) Work Week
Salary: (P21) $64,340.11 - $94,061.71 10/31/2025
Opening Date: 10/31/2025
Closing Date: 11/21/2025
Existing Vacancies: 1
 
Program/Location:
Department of Environmental Protection
Community Investment &amp; Economic Revitalization
Green Acres
401 East State Street
Trenton, NJ 08625
 
Scope of Eligibility:
Open to applicants who meet the requirements below
 
Description:
Under supervision of a higher level Geographic Information System (GIS) Specialist or other supervisory official, performs professional GIS work relating to the geographic analysis of environmental parameters and or/other factors, image processing, interpretation, and application of remote sensing data; performs geographic data digitizing; operates all computer hardware and software associated with the Geographic Information System; does related duties.
 
Specific to the Position:
The Green Acres Program is seeking a detail-oriented and motivated GIS Specialist to support the mapping and analysis of open space and parkland across New Jersey. This role is critical to maintaining and enhancing geospatial data layers that inform land acquisition, conservation planning, and public access initiatives. Key responsibilities include maintaining and updating GIS data layers such as the Open Space Preserved Recreation Inventory (OSPRI) and Conservation Easements; mapping newly acquired properties using CAD files, surveys, and parcel data; assisting in the development and maintenance of internal and public-facing GIS applications (e.g., NJDEP GeoHub); supporting land acquisition reviews by producing maps and spatial analyses for streams, wetlands, and tidelands; and collaborating with program staff to provide mapping support for grant applications, encroachment issues, and property boundary research. Qualifications include proficiency in ArcGIS Pro, ArcGIS Online, and related geospatial tools; experience working with land records, surveys, and environmental datasets; strong analytical, organizational, and communication skills; and experience with CAD-to-GIS workflows and web mapping applications. Familiarity with New Jersey land use and conservation programs is a plus.
 
Preferred Skill Set:
Preference will be given to applicants who are experienced in ArcGIS Pro, ArcGIS Online, and related geospatial tools; experience working with land records, surveys, and environmental datasets; strong analytical, organizational, and communication skills; and experience with CAD-to-GIS workflows and web mapping applications. Familiarity with New Jersey land use and conservation programs is a plus.
 
Requirements:
NOTE: Applicants must meet one of the following or a combination of both experience and education. Thirty (30) semester hour credits are equal to one (1) year of relevant experience.
 
Six (6) years of professional experience with geographic information systems, including computer graphics and computer hardware digitizing procedures.
 
OR
 
Possession of a Bachelor's degree from an accredited college or university; and two (2) years of the above-mentioned professional experience.
 
OR
 
Possession of a Master's degree in Geography or Environmental Science including or supplemented by the additional credits indicated below; and one (1) year of the above-mentioned professional experience.
 
OR
 
Possession of a specific Bachelor's degree in Geography, Environmental Science or related field with twelve (12) semester hours in computer mapping/GIS which shall have included spatial programming and digital image processing; and one (1) year of the above-mentioned professional experience.
 
NOTE: "Professional experience" refers to work that is creative, analytical, evaluative, and interpretive; requires a range and depth of specialized knowledge of the profession's principles, concepts, theories, and practices; and is performed with the authority to act according to one's own judgment and make accurate and informed decisions.
 
NOTE: All U.S. degrees and transcripts must be from an accredited college or university. All foreign degrees and transcripts must be evaluated for accreditation by a recognized evaluation service by the closing date of this posting. Failure to provide documentation may result in ineligibility.
 
License
Appointee 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.
 
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>
 
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 Civil Service Commission at (609) 292-4144 and select Option #3.
 
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”.
 
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.
 
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.
 
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.
 
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.

Geographic Information Systems Specialist 3

<h3>Job Description</h3>
PURPOSE
Primary role is to perform chemical analysis of pharmaceutical products and routine laboratory operations in a cGMP environment.
 
Reports to the Quality Control Manager. Internal relationships include Manufacturing, Research &amp; Development, Analytical Development and Quality Assurance.
 
DUTIES AND RESPONSIBILITIES
Analytical Testing &amp; Review
<ul>
<li>Conduct and review routine and non-routine analysis of raw materials, in-process materials, APIs, and finished products in compliance with SOPs, cGMPs, and cGLPs.</li>
<li>Perform testing using HPLC, GC, GC-MS, ICP-MS, FTIR, UV-Vis, and wet chemistry methods.</li>
<li>Participate in method validation and method transfer activities.</li>
</ul>
 
Equipment &amp; Instrumentation
<ul>
<li>Calibrate, maintain, and troubleshoot laboratory equipment to ensure operational readiness.</li>
<li>Proactively prevent production delays through scheduled maintenance.</li>
<li>Maintain expert knowledge of instrument components and functionality.</li>
</ul>
 
Documentation &amp; Compliance
<ul>
<li>Compile and interpret data, document test procedures, and prepare reports.</li>
<li>Administer quality control systems in compliance with FDA guidelines.</li>
<li>Write and revise Standard Operating Procedures (SOPs).</li>
<li>Investigate and document Deviations and Out of Specification (OOS) events. Provide guidance on CAPAs related to adverse quality events where applicable. </li>
<li>Ensure thorough cGMP/cGLP documentation and maintenance of quality records.</li>
</ul>
 
Leadership &amp; Team Development
<ul>
<li>Provide clear direction, coaching, and mentoring to team members to enhance skills and performance.</li>
<li>Foster a culture of accountability, integrity, and continuous improvement.</li>
<li>Demonstrate strong decision-making skills in prioritizing work under changing deadlines.</li>
<li>Lead by example in quality, safety, and compliance standards.</li>
<li>Encourage cross-functional collaboration to resolve technical challenges.</li>
<li>Take ownership of special analytical projects, including authoring protocols and reports.</li>
</ul>
 
QUALIFICATIONS
<ul>
<li>Bachelor’s degree (B.S.) in Chemistry or a closely related scientific discipline with a minimum of five (5) years of experience in FDA-regulated laboratories, or Master’s degree (M.S.) in Chemistry or a closely related scientific discipline with a minimum of three (3) years of experience in an FDA-regulated laboratory environment.</li>
<li>Strong background in principles of separation using analytical instrumentation such as HPLC and GC in a GMP environment.</li>
<li>Expert knowledge of ICH and FDA guidelines.</li>
<li>Expertise in Chromatographic Data Acquisition and LIMS Systems experience such as ChemStation (OpenLab), Chromeleon, or Empower 3.</li>
<li>Attention to details in collecting data and accurately maintaining laboratory notebooks required.</li>
<li>Drug Screen and DEA Background check required.</li>
</ul>
 
WORKING CONDITIONS/PHYSICAL REQIUREMENTS
<ul>
<li>Must be able to conduct visual inspections of incoming materials to verify appearance and printed content (e.g. product labels) meet product specifications.</li>
<li>Must accurately distinguish different colors for reporting of appearance and colorimetric tests.</li>
<li>Occasional lifting of up to 50 lbs.</li>
<li>Annual occupational medical assessment required to ensure ability to meet position requirements and based on site requirements.</li>
</ul>
 
WORKING HOURS
<ul>
<li>Monday - Friday</li>
</ul>
 
LOCATION
This position is located in Round Rock, Texas. Rock Round is located 15 miles north of Austin, TX.
 
Applicants must be legally authorized to work in the U.S. Visa sponsorship is not available at this time.
 
Positions posted for Benuvia Operations are not open to third party recruiters or agencies. Unsolicited resumes for these positions will be considered to be free referrals.

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