Senior principal scientist jobs in Jacksonville, FL - 642 jobs

Job Title: Pharmaceutical Scientist Type of Work: On-Site Schedule: Second Shift (2:00 p.m. - 11:00 p.m.) Type of Contract: Temp-to-Perm Pay Rate: Competitive - commensurate with experience and technical proficiency Department: Research & Development - Analytical & Formulation About the Opportunity A fast-growing pharmaceutical research and manufacturing organization is expanding its R&D operations in Coral Springs, FL. We are seeking motivated Scientists and Associate Scientists (Levels I & II) to support formulation and analytical development for inhalation-based drug products, including MDI, DPI, and nasal spray formulations. These are hands-on laboratory roles in a GMP-regulated environment. Successful candidates will demonstrate strong documentation skills (GDP), attention to detail, and the ability to perform and review analytical work with minimal supervision. This is an excellent opportunity to be involved in pre-formulation, formulation, analytical method development, data interpretation, troubleshooting, and continuous improvement initiatives. Key Responsibilities Perform routine and advanced analytical testing of raw materials, in-process, and finished products in compliance with GMP. Support the development of formulations (solutions, suspensions, propellant-based systems) for inhalation drug products. Operate and troubleshoot analytical instruments including HPLC, UPLC, GC, UV, and FTIR, and manage data through Empower (Waters) software. Prepare and review protocols, reports, and SOPs in alignment with quality and regulatory requirements. Ensure all documentation complies with Good Documentation Practices (GDP) and data integrity standards. Participate in method transfer, verification, and validation activities as assigned. Support investigations of OOS/OOT, deviations, and CAPA with accurate analytical input. Collaborate cross-functionally during manufacturing trials and scale-up activities. Mentor junior scientists and contribute to the team's technical development. Maintain a safe and compliant laboratory environment in accordance with EH&S and corporate policies. Qualifications PhD, MS, or BS in Analytical Chemistry, Pharmaceutics, Pharmaceutical Sciences, Biochemistry, or related discipline. Minimum 1 year of hands-on GMP laboratory experience (academic-only exposure will not be considered). Proven hands-on experience with chromatographic systems (HPLC, UPLC, GC) and analytical testing. Working knowledge of GMP/GLP, USP, ICH, and FDA regulatory expectations. Experience with Empower software for data acquisition and reporting strongly preferred. Solid understanding of GDP and deviation processes. Preferred Attributes Prior exposure to regulated audits (FDA, EMA, MHRA) is advantageous. Experience in method validation or transfer projects a plus. Strong analytical thinking, data review, and problem-solving skills. Excellent communication and teamwork abilities. High attention to detail, organization, and quality compliance. At ttg, 'We believe in making a difference One Person at a Time,' ttg OPT.

HTI is seeking a Metallurgical R&D Scientist for a brand-new facility in Augusta, GA. This is a great opportunity to work with a state-of-the-art facility and be an important contributor to the growing North American metals supply chain. What They Offer Full Medical, Dental, and Vision Benefits on Day 1 401(k) Match EAP, LTD, STD, and Life Insurance Competitive Vacation Package 12 Paid Holidays Relocation Assistance Available What You Need Bachelor's Degree in Chemical Engineering, Materials Science, Metallurgy, or a related field Minimum of 2 years of experience, ideally in R&D, materials analysis, or process engineering Recent graduates with relevant project or lab experience may be considered Strong understanding of non-ferrous metallurgy and metal extraction principles, especially copper metallurgy. Knowledge of pyrometallurgical, hydrometallurgical, and/or electrometallurgical processes Experience with: Material characterization and analysis Process troubleshooting and optimization Failure analysis and root cause investigation Familiarity with process simulation or thermodynamic modeling tools (FactSage, Thermo-Calc, HSC, etc.) is preferred but not required Experience preparing or interpreting process flow diagrams, phase diagrams, and thermodynamic calculations **Candidates must be eligible to work in the U.S. without sponsorship now AND in the FUTURE** What Your Role Will Look Like As the Metallurgical Research & Development Scientist, you will be integral to the development and enhancement of metallurgical processes, particularly in non-ferrous extractive metallurgy with a focus on copper. Collaborating with various departments, you will lead process improvement initiatives through simulation and modeling, contribute to R&D projects, and support the broader organization in achieving its production and efficiency goals. Key Responsibilities Collaborate closely with cross-functional teams, including Production, Supply Chain, and Maintenance, to develop and optimize metallurgical processes. Design and improve processes through simulation, focusing on enhancing production efficiency and effectiveness. Conduct research and development projects, such as developing new copper alloys and analyzing the impact of using different types of electronic waste. Utilize process simulation software to model and simulate metallurgical processes, implementing improvements to existing operations. Prepare detailed process flow diagrams and perform calculations related to mass balance, heat balance, and phase diagrams. Support other departments by providing expertise on chemical and material compositions and addressing process-related questions. Ensure compliance with environmental, health, and safety standards, contributing to the development of operating instructions and risk assessments. Participate in the ongoing development of R&D labs on-site, with a focus on future process improvements and innovations.

Title: Formulation Scientist - Dietary Supplement Contract Manufacturing Compensation: $60,000 - $70,000 Key Responsibilities Formulation & Bench Work Prepare bench- and pilot-scale supplement formulations (powders, blends, encapsulated products). Accurately weigh and combine ingredients, following Master Manufacturing Records (MMRs) and SOPs. Support reformulations based on ingredient changes, costs, or manufacturability. Identify and report potential issues (e.g., flow, segregation, hygroscopicity, and taste). Sampling Create and label formulation samples for internal and customer review. Maintain sample logs and organized sample libraries, ensuring all samples match approved formulas. Document all sample preparation and retain sample records. Flavoring & Sensory Support Assist in developing and optimizing flavors for powder supplements. Help evaluate sweetness, aftertaste, odor, and color, recording sensory feedback. Prepare and document flavor variations as directed. Testing & Quality Support Conduct in-house tests (e.g., flow, density, visual/sensory checks) and prepare samples for external analysis. Support uniformity and stability testing. Help manage stability and retain sample programs. cGMP & Documentation Complete all records, worksheets, and logs accurately and in a timely manner. Ensure documentation is thorough and audit-ready in compliance with FDA cGMP (21 CFR Part 111) and SOPs. Assist during audits and regulatory inspections as needed. Manufacturing Support Assist with production trials and address formulation or flavor consistency issues. Work with Quality and Procurement teams to support ingredient sourcing and approvals. Qualifications Bachelor's degree in Food Science, Chemistry, Biology, or related field (Equivalent supplement manufacturing experience considered) Experience with dietary supplements, powders, or encapsulation Exposure to flavor systems, sweeteners, or masking agents Familiarity with FDA dietary supplement cGMPs (21 CFR Part 111)

Lab Research Technician\/Researcher @ PERSOWN PERSOWN, Inc. is looking for a Research Technician to conduct lab experiments for advanced stage testing. This is a full\-time position in Jacksonville, FL working under the supervision of our principal investigator. Primary Responsibilities · Prepare reagents for testing and process samples in accordance with the laboratory's standard operating procedures (SOPs) · Work with scientists, facilities team, and vendors to improve laboratory infrastructure, organization, and processes · Follow detailed instructions about equipment operation and cleaning · Ensure safety guidelines are followed · Maintain laboratory supplies and inventory · Clean labware · Assist with quality control and quality assurance activities · Maintain laboratory equipment and instruments according to SOPs Requirements Qualifications · [Required] Basic laboratory skills · [Required] Availability to work full\-time hours at our Jacksonville, FL location · [Required] 1+ year of laboratory experience · [Highly Preferred] BS or specific training program in Biotechnology, Bioengineering, Synthetic Biology, Biological Engineering, Biomedical Engineering, Biotechnology, Chemical Engineering, or related fields. · Excellent attention to detail · Effective written and verbal communication skills · Ability to organize, multitask, and adapt to changing priorities · Drive to creatively solve problems in a fast\-paced environment. Preferred Qualifications · Entry level position, however experienced candidates may also be considered · Strongly preferred relevant coursework\/work experience: · Strong understanding of cellular, biochemical and electrochemical signals and systems. · Familiarity with data analysis\/analytics · Technical writing experience · Preferred relevant coursework\/work experience in medical devices and\/or electrochemistry ********************************* Benefits Benefit Conditions: • Waiting period may apply This Job Is: • A job for which military experienced candidates are encouraged to apply • A job for which all ages, including older job seekers, are encouraged to apply • A job for which people with disabilities are encouraged to apply COVID\-19 Precaution(s): • Remote interview process • Personal protective equipment provided or required • Social distancing guidelines in place • Virtual meetings • Sanitizing, disinfecting, or cleaning procedures in place PERSOWN, Inc. maintains a work environment free from discrimination, where employees are treated with dignity and respect. All PERSOWN employees share in the responsibility for fulfilling our commitment to equal employment opportunity. PERSOWN, Inc. does not discriminate against any employee or applicant on the basis of age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. PERSOWN, Inc. adheres to these principles in all aspects of employment, including recruitment, hiring, training, compensation, promotion, benefits, social and recreational programs, and discipline. In addition, PERSOWN, Inc.'s policy is to provide reasonable accommodation to qualified employees who have protected disabilities to the extent required by applicable laws, regulations and ordinances where a particular employee works. Upon request we will provide you with more information about such accommodations. We can't wait to hear from you! "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"698255420","FontFamily":"Verdana, Geneva, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Biotechnology"},{"field Label":"Work Experience","uitype":2,"value":"1\-3 years"},{"field Label":"Salary","uitype":1,"value":"Salary and Stock Options potential"},{"field Label":"City","uitype":1,"value":"Jacksonville"},{"field Label":"State\/Province","uitype":1,"value":"Florida"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"32254"}],"header Name":"Lab Research Scientist: BioChemist Technician","widget Id":"**********00072311","is JobBoard":"false","user Id":"**********00275003","attach Arr":[],"custom Template":"3","is CandidateLoginEnabled":true,"job Id":"**********10705013","FontSize":"12","google IndexUrl":"https:\/\/spinupcampus.zohorecruit.com\/recruit\/ViewJob.na?digest=5sGF7UvK346Q@******************************\-&embedsource=Google","location":"Jacksonville","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"bx5ab118a3887ff0448058b2830c5bff59f4e"}

The Division of Endocrinology, Diabetes & Metabolism at Nemours Children's Health, Jacksonville is seeking applications for a talented Pediatric Endocrinologist Physician Scientist to join our faculty. Our program is the premier center for the care of children and adolescents with endocrine disorders and diabetes in northeast Florida and southeast Georgia and part of Nemours Children's Health, a tertiary health care system for children and adolescents in different locales in Florida and Delaware, supported by the trust of Alfred I. Dupont. Ours is an academic division with 9 endocrine faculty, 5 APRNs, 5 Endocrine nurses, 6 certified diabetes educators as well as a team of medical and administrative assistants, and administrators that assist us in the care of our patients. As the only providers of comprehensive endocrine care in the region we have unparalleled access to all types of endocrine pathology. Our pediatric diabetes program -~1200 patients to-date - has a significant interest in advanced diabetes technology . We also have a 3-year Pediatric Endocrine fellowship program - 1 fellow per year - in collaboration with the University of Florida. Our program has had a heavy emphasis on clinical research with 25+ years track record of successful studies on the complex interactions of nutrients and hormones, specifically focusing on disorders of growth, disorders of puberty and type 1 diabetes. We have had steady funding from NIH, private foundations and industry. Our program is integrated with Wolfson Children's Hospital, our partner hospital, a state-of-the art 240 bed facility right next to our 11-story outpatient clinic on the banks of the beautiful St. John's river in Jacksonville. The hospital has a well-staffed Clinical Research Center where complex physiological and interventional studies can be carried out in children. Nemours Jacksonville is affiliated with the Mayo Clinic/Mayo Foundation which has a very large campus located in town, and our faculty has full academic appointments conferred through the Mayo system. Jacksonville is the northernmost city on Florida's east coast, located on the ocean and sprawling on the banks of the river, with a beautiful temperate climate and ample access to water. We are seeking a driven academician and innovator that can combine both clinical practice with translationally relevant clinical research. Package of support would be commensurate to the applicant's qualifications. Interested candidates can contact us directly at the emails below with a CV and letter of interest. Nelly Mauras, MD Director of Research Nemours North Florida Vice Chair of Pediatrics for Research Nemours Children's Health, Jacksonville Professor of Pediatrics Mayo Medical School ************************ Eric Sandler, MD Chairman of Pediatrics Nemours Children's Health, Jacksonville Professor of Pediatrics Mayo Medical School ************************ With a CC to: Alexis Rodgers, Physician Recruiter Nemours Children's Health **************************

Job Description Environmental Scientist III Experience Level: Mid- to Senior-Level (5+ Years) Employment Type: Full-Time About the Role The Environmental Scientist III plays a critical role in supporting environmental remediation, site assessment, and regulatory compliance projects. This position is responsible for leading environmental investigations, analyzing complex environmental data, and preparing technical and regulatory documentation to support informed decision-making. The Environmental Scientist III works collaboratively with project managers, engineers, regulatory agencies, and stakeholders to ensure compliance with federal, state, and local environmental regulations while promoting responsible environmental stewardship. Essential Duties and Responsibilities • Conduct environmental site assessments, field investigations, and sampling activities involving soil, groundwater, surface water, air, and biological media • Analyze and interpret environmental data to identify trends, assess potential environmental impacts, and evaluate regulatory compliance • Develop and implement environmental monitoring programs, corrective action plans, and mitigation strategies • Prepare technical reports, environmental impact assessments, permit applications, and regulatory submittals • Coordinate with project managers, engineers, regulators, and community stakeholders to ensure environmental compliance and project success • Provide technical guidance, mentorship, and quality control support to junior staff and interns • Stay current on applicable environmental regulations, industry standards, and scientific advancements Minimum Qualifications • Bachelor's degree in Environmental Science, Environmental Engineering, Ecology, or a closely related field • Minimum of five (5) years of professional experience in environmental science or a related discipline • Experience conducting environmental site assessments and preparing regulatory documentation • Working knowledge of federal and state environmental regulations, including but not limited to the Clean Air Act, Clean Water Act, and CERCLA • Proficiency in environmental sampling techniques and data analysis Preferred Qualifications • Master's degree in Environmental Science, Environmental Engineering, or a related field • Professional certification such as Certified Environmental Scientist (CES), Professional Geologist (PG), or similar credentials • Experience with Geographic Information Systems (GIS) and environmental modeling software • Familiarity with environmental permitting processes and stakeholder engagement • Demonstrated experience leading environmental projects or mentoring technical staff Knowledge, Skills, and Abilities • Strong analytical and problem-solving skills • Excellent technical writing and documentation abilities • Effective verbal and written communication skills • Ability to manage multiple projects and meet deadlines • Strong organizational and time management skills • Ability to work independently and collaboratively in a team environment Equal Employment Opportunity & Compliance • Bio-Tech Consulting, LLC is an Equal Opportunity Employer and does not discriminate based on race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, veteran status, or any other protected status under applicable law • Employment decisions are based on qualifications, merit, and business needs Drug-Free Workplace • Bio-Tech Consulting, LLC maintains a Drug-Free Workplace • Pre-employment drug screening, background checks, and job-related physicals are required as a condition of employment Work Authorization • Candidates must be legally authorized to work in the United States • Bio-Tech Consulting, LLC does not offer visa sponsorship or employment-based immigration support now or in the future Reasonable Accommodation • Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of the position

Jacksonville, FL Amentum is actively seeking applicants for Associate Scientist 1 Amentum Position Description: The Associate Scientist 1 shall perform, at a minimum, the following tasks and responsibilities in accordance with standard operating procedures: Must be able to obtain/maintain a DHS Suitability security clearance Handling, receipt, and processing of daily operational, Quality Assurance, verification and proficiency test samples potentially containing biological threat agents. Receiving samples may require extended walking to/from laboratory areas and up and/or down several flights of stairs. Samples may require being transferred from one area/cart/cooler to another, requiring staff to lift ~50-60 lbs. Processing samples requires more than one (1) hour, but typically not to exceed four (4) hours, of repetitive motion (e.g. twisting/cutting/pipetting/gripping) on a regular, if not daily, basis. Performing non-research biological science work utilizing microbiological and molecular techniques, which currently includes DNA extraction and real-time polymerase chain reaction (real-time PCR) to identify and characterize pathogenic bacterial and viral agents (analytical methods and technologies may change over the life of the contract). Laboratory workflow may occur in different laboratory areas (e.g., clean, high and low titer, under different conditions, such as BSL-2/BSL-3), utilizing a variety of biological safety cabinets (BSCs), and/or hoods (e.g., laminar or dead air). Laboratory work may require several PPE changes including, but not limited to, respiratory and full body protection (e.g., Tyvek suit) and gloves, for extended periods of time, not to exceed four (4) hours. Preparing reagents and samples - same as above Familiarity with Good Laboratory Practice (GLP) Decontamination of workspaces, including Biological safety cabinets, hoods/air boxes, equipment, and other items associated with processing and analysis activities. Necessitates decontamination of several rooms requiring extensive use of bleach and alcohol. For safety, proper PPE is required. Maintaining chain-of-custody (CoC) Interpretation of results - must be capable of independent analysis Data entry utilizing computerized or computer-linked systems Performing routine equipment calibration, cleaning, assembly, and maintenance in multiple lab areas Collecting, processing, and analyzing internal laboratory swipes/swabs for Quality Assurance/Quality Control (QA/QC) and contamination monitoring located across multiple lab areas Proper disposal of bio-hazardous waste. May require lifting, stooping, reaching, carrying, and/or storing biohazard waste of different sizes and/or weights up to 40 lbs. May require collecting multiple bags from BSL-2/BSL-3 areas and loading and unloading the autoclave machine when completed. For safety, proper PPE is required. Restocking and maintaining proper inventory (e.g., par levels, rotation of stock, expiration dates, etc.,) of necessary supplies. May require lifting, stooping, reaching, carrying, and/or storing consumables, supplies, and/or equipment of various sizes, shapes, and/or weights up to 70 lbs. Supporting BioWatch Program logistics in conducting and documenting annual inventory (e.g., serial numbers, disposition, PO's, packing slips, etc.) of DHS-procured durable equipment and property. May require lifting, stooping, reaching, carrying, and/or transporting equipment and/or instruments to/from different laboratory areas and/or packaging instruments for service QA/QC and acceptance testing of reagents in accordance with applicable Standard Operating Procedures (SOPs) and the Laboratory Operations Quality Assurance Program Plan (QAPP) Adhering to QA/QC requirements in accordance with the Public Health Laboratory quality management systems and the BioWatch Laboratory QAPP Maintaining documentation of records demonstrating compliance with applicable training/retraining, competencies, document reviews Analyzing routine external QA samples in accordance with the BioWatch SOP's and QA Program guidance Proper archiving, storage, and shipping of samples. May require lifting, stooping, carrying, and/or storing of sample archives of varying sizes and weights up to 40 lbs. Demonstrating ability to follow and adhere to written procedures and accepted practices in accordance with federal, state, and local regulations, safety, security and dress code policies, procedures, and guidelines, including DHS Safeguarding Sensitive but Unclassified (For Official Use Only) Information (January 2005) when visiting or working at Government facilities Preparing written and oral technical reports, answering questions, and making recommendations to the Lead Biological Scientist for inclusion in comprehensive reports Accurately performing work with confidence Demonstrating competency in various testing methodologies (e.g., multi-center studies), evaluating potential products and processes against unique environmental backgrounds, and meeting established deadlines Scheduled workdays include weekends and holidays Must be present for all hours of the workday, and be available 24/7/365 in case of emergency Position Minimum Requirements/Qualifications: Minimum of a Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences, and at least one (1) year of laboratory bench experience outside of an academic environment, utilizing PCR, aseptic techniques, and biological assays. Biological Safety Level (BSL)-3 experience is desirable. Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters.

The University of Florida College of Medicine-Jacksonville, Department of Urology, seeks a full time Assistant Scientist. The Assistant Scientist will work under the supervision of the Professor and Chair of Urology. The laboratory is focused on prostate cancer basic science research. Specifically, the laboratory is interested in cell signaling, immunology and studies involving mouse models. Responsibilities Responsible for day-to-day laboratory operations and vector construction. Coordinate with Pl in the planning of the sequence of experiments, as well as detailed experimental design at all stages. Responsible for detailed primary data analysis on each experiment, graph generation, consultations with collaborators, abstract, manuscript and presentation preparations. Attend, actively participate in laboratory meetings and departmental academic conferences. Be involved in teaching of other trainees and learners in the department. Qualifications Education: Candidates should have a PhD, MD, or MD PhD in Biological Sciences. Additional Duties: Additional duties as assigned may vary. UFJPI IS AN EQUAL OPPORTUNITY EMPLOYER AND DRUG FREE WORKPLACE

Working Title: FISHERIES & WILDLIFE BIO SCIENTIST III - 77000506 Pay Plan: Career Service 77000506 Salary: $1,730.77 biweekly + benefits Total Compensation Estimator Tool Position number - 77000506 Position Title - Biological Scientist III Rate of Pay/Salary: $1,730.77 bi-weekly + benefits Supervisor & Position number - Caity Savoia 77070560 Supervisor Contact Information: ********************** ************** Broadband Code: 19-1023-03 Class Code: 5074 Position Location: TBD within region (Office in Midway option) Region: Northwest County: Escambia to Taylor Counties Working Hours: M-F, 8 AM - 5 PM (Hours may vary with workload and may require work on weekends and non-traditional hours.) Subordinates Supervised: None Residency Requirement: within Florida, Northwest region Agency Information: The FWC envisions a Florida where fish and wildlife are abundant and thriving in healthy and connected natural landscapes with vital working lands and waterways; where natural resources are valued and safely enjoyed by all; and wherein natural systems support vibrant human communities and a strong economy. Our Mission: Managing fish and wildlife resources for their long-term well-being and the benefit of people. Every organization has an identity that is forged not only by what it does, but by how it conducts itself. The values embedded in our mission and expressed in the vision of the FWC are to make quality decisions by being dynamic, science-informed, efficient, ethical, collaborative and committed to the vitality of the state and its environment. The Division of Habitat & Species Conservation is comprised of six Sections and two offices. This position works within the Aquatic Habitat Conservation and Restoration Section of the Florida Fish and Wildlife Conservation Commission's Division of Habitat and Species Conservation. Minimum qualifications, A high school diploma and 6 years professional experience in a closely related biological field or laboratory program is required. A Bachelor of Science degree in a relevant field can substitute for four of the 6 years of required experience. Preferred Qualifications: A Bachelor of Science degree in one of the biological sciences and three years of professional biological experience. At least one year of professional wetland conservation experience and at least one year of project leader experience in conservation programs are strongly preferred. A Master of Science degree in one of the biological sciences is strongly preferred. This is a full-time employment position that is eligible for all career service state employee benefits including paid leave, health insurance, retirement benefits, tuition waivers for continuing education and numerous agency trainings for professional development. To apply: In addition to submitting an electronic State of Florida employment application and completing the qualifying questions, a resume and cover letter must be attached describing your interest in this position and relevant experience. Knowledge Skills and Abilities Required for the Position: Knowledge of coastal, estuarine and marine ecosystems; ability to identify opportunities for and conduct aquatic (marine and estuarine) habitat restoration; knowledge of terminology, principles, and techniques used in aquatic resource management or habitat restoration; knowledge of data collection methods; ability to collect, record, and analyze scientific data relating to the biological sciences; ability to plan, organize and coordinate work assignments; ability to communicate effectively verbally and in writing; ability to write technical reports; ability to pursue grant funding for restoration projects; ability to establish and maintain effective working relationships with agency staff, the public and other stakeholders; ability to work independently; ability to occasionally travel; knowledge of personal computers and related software (proficiency in the use of GPS hardware and GIS software is preferred); proficient in small boat and trailer handling Other job-related requirements for this position: The ability to spend long hours in and on the water in various weather conditions on a year-round basis. Physical stamina to perform rigorous activities in aquatic environments. The ability to effectively swim and be comfortable in the water. Licensure/registration/certification requirements: Valid state driver's license required. SCUBA open water or advanced open water certification and Boater's Safety certifications preferred. Description of Duties: This position is within the Aquatic Habitat Conservation and Restoration Section (AHCR). This position will serve as an estuarine and marine habitat enhancement/restoration project manager within the Northwest region, as part of the AHCR multidisciplinary team for aquatic habitat restoration (including marine, estuarine, and freshwater resources) and enhancement of public waterbodies and wetlands to benefit fish and wildlife. The position responsibilities span approximately from Perdido Bay through the Steinhatchee River estuaries. Coordinate with local, state, and federal agencies and stakeholder groups to identify, develop, and implement wetland and aquatic habitat restoration and enhancement projects. Pursue grant funding for identified aquatic habitat restoration and enhancement projects and with internal and external organization partners. Manage awarded grants to implement projects. Procure necessary state and federal permits, develop bid documents and contracts, and provide contract management and contractor oversight of approved aquatic habitat projects. Participate in and provide input to internal and external groups to address issues such as non-native species, resource conservation, environmental resource permitting, public outreach and imperiled species as they relate to aquatic habitat. Assist in wetland and aquatic habitat monitoring and sampling to evaluate and predict environmental response to project activities in coordination with other FWC personnel and external partners. Create and maintain databases of collected scientific data and maps of project areas using appropriate computer software, including GPS hardware and GIS programs. Prepare, publish and present project management plans and relevant project findings through internal (reports and management plans) and external (peer-reviewed publications, professional and public meeting, etc.) outlets related to aquatic habitat conservation activities including, but not limited to, restoration projects, resource monitoring and biological resource surveys. Provide oral presentations regarding FWC's aquatic habitat restoration and enhancement efforts in the Northwest region from Perdido Key through the Steinhatchee River estuary. Process or approve, as appropriate, vendor invoices for payment of goods received or services rendered. Responsible for adhering to the provisions and requirements of Section 215.422, F.S., related to State Comptroller's rules and Florida Fish and Wildlife Conservation Commission invoice processing and warrant distribution procedures. Maintain and operate all assigned vehicles, boats, and field and laboratory equipment in working condition. Work independently with limited supervision. Travel within the region, and occasionally to other regions, to complete job duties and support AHCR projects. Perform other project-related duties and tasks as directed by supervisor. Acquire and maintain FWC Scientific SCUBA and Airboat/Vessel Operation certification. The State of Florida is an Equal Opportunity Employer/Affirmative Action Employer, and does not tolerate discrimination or violence in the workplace. Candidates requiring a reasonable accommodation, as defined by the Americans with Disabilities Act, must notify the agency hiring authority and/or People First Service Center (***************. Notification to the hiring authority must be made in advance to allow sufficient time to provide the accommodation. The State of Florida supports a Drug-Free workplace. All employees are subject to reasonable suspicion drug testing in accordance with Section 112.0455, F.S., Drug-Free Workplace Act. VETERANS' PREFERENCE. Pursuant to Chapter 295, Florida Statutes, candidates eligible for Veterans' Preference will receive preference in employment for Career Service vacancies and are encouraged to apply. Certain service members may be eligible to receive waivers for postsecondary educational requirements. Candidates claiming Veterans' Preference must attach supporting documentation with each submission that includes character of service (for example, DD Form 214 Member Copy #4) along with any other documentation as required by Rule 55A-7, Florida Administrative Code. Veterans' Preference documentation requirements are available by clicking here. All documentation is due by the close of the vacancy announcement. Location:

Jacksonville, FL, USA Full-time ** **Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.** **The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.** **In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.** **In 2024, Eurofins generated total revenues of EUR 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.** **Job Description** + Perform various type of testing using chromatographic systems, HPLC, GC, IC + Execute specialized analyses and method transfer and feasibility testing + Document work as required for GMP compliance + Perform tests accurately + Troubleshoot method and instrumentation problems + Use office and instrumentation specific computer software + Produce written reports (e.g., SOP, OMC, client reports) + Develop and execute validation plans + Carry out method transfers and feasibility studies + Train technical staff **Qualifications** -Minimum Required: Bachelors, Science discipline -Chromatography Experience: BS: 4+ years; MS: 2 years -Familiarity with United States Pharmacopeia testing requirements and techniques preferred -Experience with HPLC and GC analysis, with ability to maintain and troubleshoot instruments -Ability to author reports/investigations and execute protocols with limited support -Capable of generating scientifically valid data in accordance with GMP practices -Ability to work autonomously on projects after training is completed is essential **Additional Information** Position is full-time, Monday - Friday 8:30am - 5pm. Candidates currently living within a commutable distance of Jacksonville, FL are encouraged to apply. + Excellent full time benefits including comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.**

This position will require local site visits and occasional regional site visits, up to 50% total travel. This person can be in Raleigh, NC area OR Pensacola, FL area. Are you ready to take the next step in your career? Are you an individual who takes pride in delivering exceptional work? Our Private Sector Enterprise has an immediate opening for a full-time entry-level scientist or engineer to join our Compliance and Permitting team. We are seeking a motivated, achievement-oriented individual who can help us fulfill our commitment to deliver client success on each and every project we undertake. You will work with and be mentored by nationally recognized, senior technical staff. Detailed Description: The ideal candidate will have strong technical, written, and verbal skills. We are looking for someone that is highly organized and capable of working with a diverse team of scientists and engineers on multiple tasks with competing priorities. The successful candidate will have a positive, can do attitude; will be flexible and self-motivated, creative and well-organized, and quality-oriented with attention to detail. Projects needing support include environmental compliance and permitting for private sector clients. Specific duties may include, but are not limited to the following: * Conducting Phase I and Phase II Environmental Site Assessments and report writing. * Assisting with environmental studies, permitting, and compliance reviews. * Conducting regulatory research * Technical writing of permitting documents and project delivery. * Collecting field data, auditing and documenting field activities. * Communicating environmental requirements directly to the project team and/or client. * Performing data collection and documentation related to field activities such as site investigation (soil and groundwater), and site inspections. * Performing project site visits outside the office, including commercial and industrial facilities. * Assisting with the preparation of technical memoranda and reports related to compliance and permitting. * Working independently and with teams to complete assignments with other team members in a virtual platform. * Ability and willingness to travel to support regional and national client teams. * Interacting and communicating directly with clients on behalf of Brown and Caldwell Desired Skills and Experience: * B.S. Degree in Engineering (Civil, Environmental, Chemical, Material Science) or B.S. Degree in Science (Environmental Science, Geology, Chemistry, Biology) or related field (such as Industrial Hygiene) required * 0-5 years of experience * Proficiency in Excel, Word and basic computer skills required * Basic GIS skills a plus * Permitting and compliance experience preferred with knowledge of local, state and federal environmental regulations * Strong verbal and written communication skills * Excellent organization and communication skills with extreme attention to detail * Ability to work in a team environment and manage multiple tasks * Candidate should be a self-starter, results orientated and able to work under tight deadlines * Candidate must have current driver's license and good driving record * Candidate must be willing to travel up to 25% of the time * 40-hour Hazardous Waste Operations and Emergency Response (HazWOPER) certification a plus * Willing to work occasional overtime and/or off-hours as needed * Ability to work for short periods of time in extreme temperatures including heat and cold * Ability to wear required safety equipment at sites including hard hats, steel-toed boots (or other approved toe protection), safety glasses, etc. * Ability to stand for several hours observing and documenting * Ability to operate a BC Pickup Truck to commute to jobsites and to access work areas on site * Ability to remain alert and vigilant while working around equipment and be able to walk swiftly for a short distance to clear an area where a potential hazard is identified Salary Range: The anticipated starting pay range for this position is based on the employee's primary work location and may be more or less depending upon skills, experience, and education. These ranges may be modified in the future. Location A: $58,000 - $79,000 You can view which BC location applies to you here. If you have any questions, please speak with your Recruiter. Benefits and Other Compensation: We provide a comprehensive benefits package that promotes employee health, performance, and success which includes medical, dental, vision, short and long-term disability, life insurance, an employee assistance program, paid time off and parental leave, paid holidays, 401(k) retirement savings plan with employer match, performance-based bonus eligibility, employee referral bonuses, tuition reimbursement, pet insurance and long-term care insurance. Click here to see our full list of benefits. About Brown and Caldwell Headquartered in Walnut Creek, California, Brown and Caldwell is a full-service environmental engineering and construction services firm with 52 offices and over 1,900 professionals across North America and the Pacific. For more than 75 years, we have created leading-edge environmental solutions for municipalities, private industry, and government agencies. We strive to be the company of choice-to our clients, who benefit from our passion for delivering exceptional quality, and to our employees, present and future, who share our commitment to client service, collaboration, and innovation. Join us, and you will find a home where you can do your best work, reach new levels of expertise, and enjoy exceptional development opportunities. For more information, visit ************************* This position is subject to a pre-employment background check and a pre-employment drug test. Notice to Third Party Agencies: Brown and Caldwell does not accept unsolicited resumes from recruiters or employment agencies. In the event a recruiter or agency submits a resume or candidate without a previously signed agreement and approved engagement request with Brown and Caldwell, Brown and Caldwell reserves the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency. Brown and Caldwell is proud to be an EEO/AAP Employer. Brown and Caldwell encourages protected veterans, individuals with disabilities, and applicants from all backgrounds to apply. Brown and Caldwell ensures nondiscrimination in all programs and activities in accordance with Title VI of the Civil Rights Act

Department Biology, Chair Compensation $60,000.00 Annual General Description/Primary Purpose: The Department of Biology seeks to fill a 24-month Postdoctoral Associate position in Shark Biology. This appointment is term-limited and reappointments are based on performance and funding. Position responsibilities involve participation in field and laboratory research on fish toxicology as part of a new research project funded by the Florida Institute of Oceanography's (FIO) Florida Restore Act Centers of Excellence Program (FLRACEP). The project is being conducted in collaboration with researchers from Florida State University, University of Florida, and State University of New York. The goal of this project is to examine spatial and temporal patterns of abundance, biodiversity, and toxicological responses of large deep-sea fishes with special emphasis on fish populations sampled from regions impacted by the 2010 Deepwater Horizon Oil Spill. The candidate will directly participate in two 12-day oceanographic research cruises annually (2026 and 2027), assisting in deepwater fish collection and biological sampling. Training in fish collection and biological sampling procedures will be provided by participation in UNF's fishery-independent longline survey, which is conducted on a year-round basis. The candidate will conduct laboratory tests on fish toxicology using biological samples obtained from sampling cruises. Additional responsibilities will include data management activities, oversight of undergraduate and/or graduate student research assistants, disseminating research results in presentations at professional conferences, and publishing manuscripts in peer-reviewed journals. Supervisor: This position will report to the Department Chair, Dr. Jim Gelsleichter. Working Hours: Varies Supervision Exercised: This is not a supervisory role. Required Licensure: N/A Anticipated Start Date: The position is expected to begin on January 5, 2026. Required Qualifications: Earned a doctoral degree from an acceptable accredited institution in the field of specialization or closely related discipline by the employment start date on January 5, 2026. Have demonstrated ability to carry out individual or group research at the advanced level. Have training in research procedures. Experience and specialized training necessary to develop and interpret data required for success in research projects. Preferred Qualifications and Skills: Preference will be given to candidates who possess strong skills in either marine field research or laboratory-based animal toxicological research, and who hopes to improve their training in the other field. Additional Application Materials Required: Applicants should be prepared to provide the following required documents and information: A cover letter describing professional qualifications, career goals, and specific interest in this position. Current curriculum vitae Description of research experience (1-2 pages) Unofficial transcripts Name, phone number, and email address of three professional references will be requested during the application review stage. The selected candidate will be required to submit official transcripts (and, as applicable, U.S. degree equivalency evaluations) documenting the conferral of their qualifying academic credentials by the date of hire. Additional Requirements: Applicants may be required to upload additional documents based on their responses to the Foreign Influence Review questions. Passport (all pages including blank pages) and Form DS-160 (if ever submitted. If not, upload an explanation) Application Review Date: Initial review of applications will begin on December 15, 2025. Job Posting Close Date: Open until filled. How to Apply: Applicants must submit an online application that includes all required application documents. If you have any questions about this position, please contact Dr. Jim Gelsleichter at ***************, or ************************. About the Department: The UNF Department of Biology offers baccalaureate degrees in Biomedical Sciences and in Biology with areas of concentration in Coastal and Marine Biology, Coastal Environmental Science, Ecology and Evolution, and Molecular/Cell Biology. Master's-level degrees are also offered with a focus on Coastal/Marine Biology, Ecology/Evolutionary Biology or Microbiology/Molecular Biology. Faculty in the Department have access to riverine, estuarine, and oceanic habitats, including the William C. Webb Coastal Research Station, a 1,050-acre tract of saltmarsh wetlands along the Atlantic Intracoastal Waterway less than 7 miles from the University. The university also maintains strong research ties with other agencies involved in coastal research, including the Guana Tolomato Matanzas National Estuarine Research Reserve. Departmental resources for coastal research include a fleet of towed vehicles and research vessels, a large animal necropsy facility, and a 20' x 80' greenhouse situated on the roof of the building. In recent years, UNF has transitioned to an R2 institution with an increasing focus on research while maintaining excellence in teaching. For more information about the Department visit: ******************************************** Statement(s) of Understanding This position requires a background check. In conjunction with the University's policy, this position may also require a credit check. The holder of this position is designated as a “Responsible Employee” pursuant to their role under Title IX. Therefore, the incumbent must promptly report allegations of sexual misconduct, sexual violence, and child sexual abuse by or against any student, employee, contractor, or visitor to the University's Title IX Administrator or any divisional Title IX Coordinator Pursuant to Florida Statute 1010.35, this position requires additional information from all applicants seeking research or research-related positions prior to an interview or offer of employment. Applicants MUST fully complete the Foreign Influence Review section of their application. Additional documents (e.g., passport) may be required based on form responses. Equal Opportunity The University of North Florida (UNF) is committed to providing an inclusive and welcoming environment for all who interact in our community. In building this environment, we strive to attract students, faculty and staff from a variety of cultures, backgrounds and life experiences. The University of North Florida does not commit or permit discrimination or harassment on the basis of genetic information, race, color, religion, age, sex, disability, marital status, national origin, or veteran status in any educational, employment, social, recreational program or activity that it offers. In addition, UNF will not commit or permit retaliation against an individual who reports discrimination or harassment or an individual who cooperates in an investigation of an alleged violation of university regulation. Carnegie UNF is a Carnegie Community Engaged Institution. This designation celebrates the University's collaboration with community partners from the local to the global level. It reflects UNF's mission to contribute to the public good and prepare educated, engaged citizens.

We are seeking a dedicated and detail-oriented Medical Technologist / Toxicology Analyst to join our dynamic team. In this role, you will be responsible for performing complex laboratory tests and procedures that aid in the diagnosis, treatment, and prevention of diseases. The ideal candidate will possess strong analytical skills, a solid understanding of laboratory techniques, and the ability to manage data effectively. You will work in a collaborative environment, contributing to clinical trials and research efforts while ensuring compliance with established protocols. JOB SUMMARY Toxicology Analyst with minimum of one (1) to three (3) years of experience in all areas of laboratory testing being performed. Responsible for specimen processing, performing a full range of laboratory tests and reporting laboratory findings in a non-supervisory position. Each individual performs only those high complexity tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training or experience, and technical abilities. The skills requirements for a Clinical Laboratory Scientist include: Occupational Specific Technical Skills Personal Professional Clinical Laboratory Scientists must at a minimum meet the personnel responsibilities per CLIA Sec.493.1495 Standard: Testing Personnel Responsibilities, as well as any and all State licensure/certification requirements for the position. ESSENTIAL TOXICOLOGY ANALYST DUTIES AND RESPONSIBILITIES 1. Apply the principles, theory and techniques of the practice of laboratory medicine to produce and report appropriate; a) Identify and communicate abnormal patient conditions by alerting supervisory personnel, the lab director, the provider, and/or management; reporting mandated information to the public health department or other designated officials; b) Identify the presence or quantity of drugs of abuse, therapeutic drugs and toxic substances by operating instrumentation used in toxicology chemical testing and performing manual methods for the performance of drug screens and neurotransmitter levels; c) Provide quality test results for patient diagnosis and treatment by operating general chemistry, immunochemistry, hematology, urinalysis, coagulation equipment; performing manual methods; or by operating other instrumentation as may be available in the laboratory area; 2. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results; a) Analyze and organize work by matching computer orders with specimen labeling; sorting specimens; checking labeling; logging specimens; arranging reports for delivery; keeping work surfaces clean and orderly; 3. Responsible for monitoring test analyses and specimen examinations to ensure that acceptable levels of analytic performance are maintained; a) Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed; b) Maintain quality results by running standards and controls, verifying equipment function through routine equipment maintenance and advanced trouble shooting; calibrating equipment utilizing approved testing procedures; c) Perform, interpret and record quality control data in all departments as appropriate and record corrective action(s) where appropriate; 4. Follow the laboratory's established policies and procedures whenever test systems deviate or are not within the laboratory's established acceptable levels of performance specifications; a) Capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical supervisor and lab director; b) Assure that patient test results are not reported until all corrective/remedial actions have been taken, documented and the test system is properly functioning; c) Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications; 5. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens; 6. Perform preventative and corrective maintenance on instrumentation as prescribed in procedures and/or as described by manufacturer specifications. Record corrective action where appropriate; 7. Participate in available continuing education and maintains licensure/certification as required by State law and accreditation agencies; a) Provide an analytical approach to technical resolutions by participating in staff training; answering questions of other professionals; participating in educational opportunities; and maintaining licensure and certification as required by the company, State/local laws and accrediting bodies; 8. Contribute to a safe and secure environment for co-workers and all others by following established standards and procedures; complying with legal regulations and maintaining patient confidentiality; a) Serve and protect the community by adhering to professional standards; policies and procedures; and federal, state, and local requirements; and 9. Perform other duties as assigned; a) Enhance laboratory services and the lab's reputation by accepting other duties as assigned, taking ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments and maintaining professional decorum at all times. Job Type: Full-time Benefits: Dental insurance Health insurance Life insurance Paid time off Vision insurance Experience: all areas of laboratory testing: 1 year (Required) toxicology analyst: 1 year (Required) Work Location: In person

Full-time Description JOB TITLE: Bioinformatician 2511-12755-BIO-1 Atlanta, GA, USA ASRT, Inc. provides scientific, information management, management consulting, bioinformatics, and administrative program support to the Centers for Disease Control and Prevention (CDC) and other Federal and private sector clients. The successful candidate will be a full-time employee of ASRT, Inc., and will be assigned to the National Center for Emerging Zoonotic Infectious Disease (NCEZID), Office of Advanced Molecular Detection (OAMD), CDC located at CDC Roybal Campus on Clifton Rd, Atlanta, GA, to provide services to satisfy the overall administrative and professional operational objectives for OAMD. SCOPE OF WORK The Bioinformatician II will support a unified Cloud infrastructure for data storage and analytics to allow for easy sharing of bioinformatics pipelines, laboratory and bioinformatics protocols, and related genomic sequence data. MAJOR DUTIES AND RESPONSIBILITIES Monitor the technical status and progress of work, checking on work in progress and reviewing completed work. This may include monitoring vendor and collaborator performance based on data reported on key project measures using qualitative and quantitative measures. Maintain records that provide for the proper evaluation, control, and documentation of assigned activities; prepare a variety of written correspondence, reports, and other materials as appropriate. Summarize project data for program's use (this could include creation of short briefs, presentations, dashboards, reports, charts, etc.). Support cloud implementation by working with the cloud implementation team to establish requirements and to assist with technical review of implementation and verification of work performed. Provide bioinformatics support by reviewing reports and developing standards for analysis. Review outputs from bioinformatics analysis pipelines to verify pipelines perform as expected. Work with CDC Scientific Computing Team to establish requirements, verify implementation, schedule meetings, and keep up with documentation to support the team. Assist in defining and developing statements of work for IT contracts related to cloud implementation. Perform market research related to cloud implementation. Provide technical documentation in relation to cloud implementation. Coordinate and maintain contacts and relations with as well as facilitate meetings and sessions between OAMD partners, interested external groups, and collaborating organizations Partners for knowledge-sharing, project development, and improvement. Draft and present summaries of findings to internal and external stakeholders. Confer with and represent the assigned program and division in meetings with offices within CDC, grantees, and external partners to foster collaborative working relationships to the benefit of the program. Requirements MINIMUM QUALIFICATIONS Education and Experience: Master's degree in information technology, bioinformatics, allied health, health science, or life sciences, minimum 3 years of work experience in health informatics, two years of work experience in cloud implementation, and 2 years of technical project management experience. Required: Strong quantitative skills, including proficiency in Phyton; relational database management systems; and standard Microsoft Office applications including Word, Excel, and PowerPoint. Experience with whole genomic sequencing, and genome-based typing systems. Experience performing quality control, assembly, annotation, and analysis of pathogen genome sequences. Proficiency with open source and commercially available software for bioinformatics analysis of next-generation sequencing data. Proficiency with Microsoft Word, Excel, and PowerPoint. Excellent attention to detail and the ability to efficiently organize multiple priorities. Documentation of daily work with good laboratory practice compliance. Ability to work and build coalitions with partners involved and develop strategies for effectively conveying information to partners. Skills and experience writing project reports, research protocols, and manuscripts. Ability to independently resolve conflicts. Working knowledge of CDC applications. Desirable: Experience working with a diverse interdisciplinary team. Knowledge of CDC policy, quality, and regulatory training. Language Skills: The candidate must possess excellent oral and written communication skills in English. REQUIREMENT: Must be a United States citizen or permanent resident or have authorization for employment in the United States. SALARY: Commensurate with qualifications and experience. To apply for this position: If you are viewing this position on the ASRT Career page, please click on the "Apply" button. If you are viewing this position on a site other than the ASRT Career page, you may use the "click to apply" link, or you may apply by visiting our Career page and searching for the job title and position number listed at the top of this job posting. To view all of our open positions and to apply to job openings in which you may be interested, please visit our Career page at ******************************** EEO/vets/disabled Salary Description $95,000-$105,000

Tanaq Management Services (TMS) delivers professional, scientific, and technical services and information technology (IT) solutions to federal agencies in the health, agriculture, technology, and other government services. TMS is a subsidiary of the St. George Tanaq Corporation, an Alaskan Native Corporation (ANC) committed to serving Federal customers while also giving back to the Tanaq native community and shareholders. **About the Role** We are seeking a highly motivated **Bioinformatician** to support ongoing projects within public health and the federal government. The ideal candidate will have experience analyzing biological data in the areas of phylogenetics, molecular evolution, recombination analysis, and whole genome analysis. This position will involve supporting various laboratory projects, including the development of new vaccines, the study of infectious diseases, molecular epidemiology, and surveillance. The successful candidate will have the opportunity to collaborate with various agencies and contribute to important research making a difference in the fight against disease. The Bioinformatician is responsible for R-programming and experience in Matlab applications. This role will collaborate with scientists across various disciplines to extract meaningful insights from complex datasets and contribute to ongoing research projects. This is a hybrid remote role based in Atlanta, GA. Some on-site work will be required at the client's location in Atlanta, GA; the frequency will be determined by the client's needs. **Responsibilities** + Assist in and lead projects in bioinformatics and computational biology. + Provide data analysis support for sequencing requests through the Genome Sequence Lab. + Conduct Bioinformatics Activities in support of several projects being undertaken in support of Global Polio Eradication Program. + Perform assembly & Mapping activities, including genome assembly services for all sequencing platforms in the GSL (Sanger, Roche454, Illumina, Ion Torrent, MinION, and PacBio). + Provide single platform assembly using software packages to include CLCbio, Celera Assembler, MIRA, velvet, and BWA. + Conduct Genomics analysis such as SNP/indel detection, gene structure comparisons, gene absence/presence determination, and protein sequence comparisons utilizing software packages such as kSNP, BLAST, and custom software. + Perform variant detection techniques, including Amplicon or Deep Sequencing, to determine consensus sequences. + Conduct Metagenomics techniques to identify species of microorganisms from an uncultured DNA sample utilizing BLAST/Megan, metagenefinder, QIIME, MG-RAST, and 16S databases utilizing RDP and Greengenes software packages. + Provides legacy sequencing data retrieval. + Analyze genetic sequencing data utilizing new methodologies or existing techniques that have been revised + Collaborate on genetic analysis projects and studies with internal and external partners. + Assist laboratory scientists (with varying levels of computational expertise) in the design and implementation of bioinformatics tools that support the automation of data analysis, especially for next-generation sequencing data and large data sets. + Advise senior scientists on applying a variety of bioinformatics analysis tools used to compare and categorize polio and picornavirus isolates and virus populations. + Request NGS Sequencing for Illumina MiSeq and NovaSeq; PacBio RSII and Sequel; Oxford Nanopore MiniON. + This description does not encompass all tasks; employees may perform other related duties as required. Requirements **Required Experience and Skills** + Minimum 3 years of experience in the capacity of a bioinformatician. + Experience with automation support; QMS & CLIA support; ELIMS integrations; Testing and curating new technologies, e.g., Nanopore; website development; communications and user experience + Strong experience using applications such as BLAST/Megan, metagenefinder, QIIME, MG-RAST, and 16S databases such RDP and Greengenes. + Experience with Matlab. + Experience with de novo assembly and reference mapping. + Experience with RocheAVA, CLCbio, VIP, and VarScan software packages + Experience working for the federal government or in a public health setting preferred. + Strong attention to detail. + Ability to work independently and as part of a team in a fast-paced setting. + Ability to work with a diverse interdisciplinary team. + Excellent written and verbal communication skills. + Effective organization skills. + Advanced experience with comparative genomics methods, including SNP/indel detection, gene structure comparisons, gene absence/presence determination, and protein sequence comparisons. + Ability to pass required Federal background screening, obtain and maintain government clearance. + Must be legally authorized to work in the United States without the need for employer sponsorship, now or at any time in the future Preferred Qualifications + Experience maintaining epidemiological and laboratory data using SAS, or R, REDCap, Microsoft Access, Excel, EpiInfo. + Experience developing scripts and software for data manipulation, cleaning, analysis and visualization with Python, R, BASH, and SQL. + Proficient in developing bioinformatics pipelines through workflow tools, including Snakemake or Nextflow, on Linux-based high-performance computing environments. + Ability to convert existing datasets from diverse file formats (e.g. Microsoft Excel, Access, SQL, and ASCII files) into SAS datasets. + Experience with bioinformatics associated with viral diseases at CDC. + Previous experience in federal government or public health and molecular epidemiologic research. **Education and Training** + Master's degree in Bioinformatics, Computational Biology, Computer Science, Microbiology, Biology, or closely related field, plus a minimum of 3 years of experience in the capacity of a bioinformatician. **Physical Requirements** + Prolonged periods of sitting at a desk and working on a computer. May need to lift 25 pounds occasionally. **Who We Are** Tanaq Management Services (TMS) strives to deeply understand and analyze our clients' vision, needs, and requirements so we may provide alternative solutions, empowering them to choose the best resolution. We aim to achieve excellence by delivering on our commitments to our clients, employees, and partners. **Our Commitment to Non-Discrimination** Tanaq Management Services is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to disability, status as a protected veteran or any other status protected by applicable federal, state, or local law. Tanaq complies with the Drug-free Workplace Act of 1988 and E-Verify. If you are an individual with a disability and need assistance completing any part of the application process, please email accommodation@tanaq.com to request a reasonable accommodation. This email is for accommodation requests only and cannot be used to inquire about the status of applications. **Notice on Candidate AI Usage** Tanaq is committed to ensuring a fair and competitive interview process for all candidates based on their experience, skills and education. To ensure the integrity of the interview process, the use of artificial intelligence (AI) tools to generate or assist with responses during phone, in person and virtual interviews is not allowed. However, candidates who require a reasonable accommodation that may involve AI are required to contact us prior to their interview at accommodation@tanaq.com. **To apply for this and other positions with our company, visit:** ***********************************************************************************************************************

Great Hill Solutions, LLC is part of the Seneca Nation Group (SNG) portfolio of companies. SNG is Seneca Holdings' federal government contracting business that meets mission-critical needs of federal civilian, defense, and intelligence community customers. Our portfolio comprises multiple subsidiaries that participate in the Small Business Administration 8(a) program. To learn more about SNG, visit the website and follow us on LinkedIn. Our team of talented individuals is what makes us successful. To support our team, we provide a balanced mix of benefits and programs. Your total rewards package includes competitive pay, benefits, and perks, flexible work-life balance, professional development opportunities, and performance and recognition programs. We offer a comprehensive benefits package that includes medical, dental, vision, life, and disability, voluntary benefit programs (critical illness, hospital, and accident), health savings and flexible spending accounts, and retirement 401K plan. One of our fundamental principles is to offer competitive health and welfare benefits to our team members, providing coverage and care for you and your family. Full-time employees working at least 30 hours a week on a regular basis are eligible to participate in our benefits and paid leave programs. We pride ourselves on our collaborative work environment and culture, which embraces our mission of providing financial and non-financial benefits back to the members of the Seneca Nation. Great Hill Solutions, LLC seeks a highly skilled Bioinformatician III to support the CDC. This role is critical for conducting genomic epidemiologic studies, developing bioinformatics pipelines, and analyzing next-generation sequencing data to support public health surveillance and response efforts. Duties: Develop standard operating procedures and quality documentation for sequence analysis pipelines. Provide technical assistance to integrate bioinformatics workflows with existing platforms in CORVD programs. Conduct production-level quality control and analysis on next-generation sequencing data produced locally and from outside labs. Provide technical assistance on tasks related to genomic epidemiologic studies on the evolution of viruses. Apply analytical and interpretive skills to analyze next generation sequence data from global surveillance of viruses. Provide data management and analytic support for global surveillance platforms. Construct pipelines and workflows for sequence analysis and build custom algorithms and tools for specific problems. Conduct genomic epidemiologic studies on the evolution of viruses to detect and assess the risk of new emerging variants to current vaccines. Analyze next generation sequence data using spatiotemporal, phylodynamic, and epidemiologic approaches. Use mathematical and computational approaches to understand the evolutionary and epidemiological patterns of viruses. Ensure appropriate genomic analysis methods, procedures, techniques, and quality controls are correctly conducted. Prepare reports, summaries, presentations, papers, and other documents to highlight findings and surveillance data. Contribute to abstracts, presentations, and peer-reviewed publications from related projects and studies. Basic Qualifications: MS with 10+ years' experience or PhD with 7-10+ years' experience. Desired Qualifications: Mastery of at least one general purpose, widely used scripting or programming language (e.g., Python, Perl, Rust). Working knowledge of database Structured Query Language (SQL). Familiarity with analytics languages or tools such as R or Pandas. Familiarity with pipelining tools such as Nextflow or Snakemake. Familiarity with fundamentals of nucleic acid sequence alignment and comparison. Knowledge and experience of phylogenetic analysis. Knowledge of and experience working with clinical data. Experience working with CDC staff at multiple organizational levels. Interpersonal communication: telephone, email, and business etiquette. Strong proofreading skill and attention to detail. Strong organizational skills. Experience working with CDC staff at multiple organizational levels. Work experience in the scientific field, including physician, epidemiologist, clearance reviewer, or related field (preferably in a public health setting). Equal Opportunity Statement: Seneca Holdings provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex/gender, sexual orientation, national origin, age, disability, marital status, genetic information and/or predisposing genetic characteristics, victim of domestic violence status, veteran status, or other protected class status. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leave of absence, compensation and training. The Company also prohibits retaliation against any employee who exercises his or her rights under applicable anti-discrimination laws. Notwithstanding the foregoing, the Company does give hiring preference to Seneca or Native individuals. Veterans with expertise in these areas are highly encouraged to apply.

Full-time Description JOB TITLE: Bioinformatician III 2510-CORVD-BIO-III Atlanta, GA, USA IHRC Inc. seeks a dedicated and experienced Bioinformatician III to support our clients at Centers for Disease Control and Prevention (CDC)/Coronavirus and Other Respiratory Viruses Division (CORVD). CORVD's mission is to provide the health of people by preventing illness, disability and death from respiratory viruses through public health science and practice in the United States and globally. This position is needed for accomplishing CORVD's mission. Bioinformatician III will conduct genomic epidemiologic studies, develop bioinformatics pipelines, and analyze next-generation sequencing data to support public health surveillance and response efforts. Develop standard operating procedures and quality documentation for sequence analysis pipelines. Provide technical assistance to integrate bioinformatics workflows with existing platforms in CORVD programs. Conduct production-level quality control and analysis on next-generation sequencing data produced locally and from outside labs. Provide technical assistance on tasks related to genomic epidemiologic studies on the evolution of viruses. Apply analytical and interpretive skills to analyze next generation sequence data from global surveillance of viruses. Provide data management and analytic support for global surveillance platforms. Construct pipelines and workflows for sequence analysis and build custom algorithms and tools for specific problems. Conduct genomic epidemiologic studies on the evolution of viruses to detect and assess the risk of new emerging variants to current vaccines. Analyze next generation sequence data using spatiotemporal, phylodynamic, and epidemiologic approaches. Use mathematical and computational approaches to understand the evolutionary and epidemiological patterns of viruses. Ensure appropriate genomic analysis methods, procedures, techniques, and quality controls are correctly conducted. Prepare reports, summaries, presentations, papers, and other documents to highlight findings and surveillance data. Contribute to abstracts, presentations, and peer-reviewed publications from related projects and studies. Provide leadership and oversight to the bioinformatics team if needed. Requirements MS with 10+ years' experience or PhD with 7-10+ years' experience. Desired Qualifications Mastery of at least one general purpose, widely used scripting or programming language (e.g., Python, Perl, Rust). Working knowledge of database Structured Query Language (SQL). Familiarity with analytics languages or tools such as R or Pandas. Familiarity with pipelining tools such as Nextflow or Snakemake. Familiarity with fundamentals of nucleic acid sequence alignment and comparison. Knowledge and experience of phylogenetic analysis. Knowledge of and experience working with clinical data. Experience working with CDC staff at multiple organizational levels. Interpersonal communication: telephone, email, and business etiquette. Strong proofreading skill and attention to detail. Strong organizational skills. Experience working with CDC staff at multiple organizational levels. Work experience in the scientific field, including physician, epidemiologist, clearance reviewer, or related field (preferably in a public health setting) Language Skills: The candidate must possess excellent oral and written communication skills in English REQUIREMENT: Must be United States citizen or permanent resident or have authorization for employment in the United States To apply for this position: If you are viewing this position on the IHRC Career Center, please click on the "Apply Now" button. If you are viewing this position on a site other than the IHRC Career Center, you may use the “click to apply” link, or you may apply by visiting our Career Center and searching for the position number listed at the top of this position description. To view all of our open positions, and to apply to those positions in which you may be interested, please visit our Career Center, which can also be reached by visiting ******************** and clicking on the “View Opportunities” link. EEO/Vets/Disabled

Full-time Description Tanaq Management Services (TMS) delivers professional, scientific, and technical services and information technology (IT) solutions to federal agencies in the health, agriculture, technology, and other government services. TMS is a subsidiary of the St. George Tanaq Corporation, an Alaskan Native Corporation (ANC) committed to serving Federal customers while also giving back to the Tanaq native community and shareholders. About the Role We are seeking a highly motivated Bioinformatician to support ongoing projects within public health and the federal government. The ideal candidate will have experience analyzing biological data in the areas of phylogenetics, molecular evolution, recombination analysis, and whole genome analysis. This position will involve supporting various laboratory projects, including the development of new vaccines, the study of infectious diseases, molecular epidemiology, and surveillance. The successful candidate will have the opportunity to collaborate with various agencies and contribute to important research making a difference in the fight against disease. The Bioinformatician is responsible for R-programming and experience in Matlab applications. This role will collaborate with scientists across various disciplines to extract meaningful insights from complex datasets and contribute to ongoing research projects. This is a hybrid remote role based in Atlanta, GA. Some on-site work will be required at the client's location in Atlanta, GA; the frequency will be determined by the client's needs. Responsibilities Assist in and lead projects in bioinformatics and computational biology. Provide data analysis support for sequencing requests through the Genome Sequence Lab. Conduct Bioinformatics Activities in support of several projects being undertaken in support of Global Polio Eradication Program. Perform assembly & Mapping activities, including genome assembly services for all sequencing platforms in the GSL (Sanger, Roche454, Illumina, Ion Torrent, MinION, and PacBio). Provide single platform assembly using software packages to include CLCbio, Celera Assembler, MIRA, velvet, and BWA. Conduct Genomics analysis such as SNP/indel detection, gene structure comparisons, gene absence/presence determination, and protein sequence comparisons utilizing software packages such as kSNP, BLAST, and custom software. Perform variant detection techniques, including Amplicon or Deep Sequencing, to determine consensus sequences. Conduct Metagenomics techniques to identify species of microorganisms from an uncultured DNA sample utilizing BLAST/Megan, metagenefinder, QIIME, MG-RAST, and 16S databases utilizing RDP and Greengenes software packages. Provides legacy sequencing data retrieval. Analyze genetic sequencing data utilizing new methodologies or existing techniques that have been revised Collaborate on genetic analysis projects and studies with internal and external partners. Assist laboratory scientists (with varying levels of computational expertise) in the design and implementation of bioinformatics tools that support the automation of data analysis, especially for next-generation sequencing data and large data sets. Advise senior scientists on applying a variety of bioinformatics analysis tools used to compare and categorize polio and picornavirus isolates and virus populations. Request NGS Sequencing for Illumina MiSeq and NovaSeq; PacBio RSII and Sequel; Oxford Nanopore MiniON. This description does not encompass all tasks; employees may perform other related duties as required. Requirements Required Experience and Skills Minimum 3 years of experience in the capacity of a bioinformatician. Experience with automation support; QMS & CLIA support; ELIMS integrations; Testing and curating new technologies, e.g., Nanopore; website development; communications and user experience Strong experience using applications such as BLAST/Megan, metagenefinder, QIIME, MG-RAST, and 16S databases such RDP and Greengenes. Experience with Matlab. Experience with de novo assembly and reference mapping. Experience with RocheAVA, CLCbio, VIP, and VarScan software packages Experience working for the federal government or in a public health setting preferred. Strong attention to detail. Ability to work independently and as part of a team in a fast-paced setting. Ability to work with a diverse interdisciplinary team. Excellent written and verbal communication skills. Effective organization skills. Advanced experience with comparative genomics methods, including SNP/indel detection, gene structure comparisons, gene absence/presence determination, and protein sequence comparisons. Ability to pass required Federal background screening, obtain and maintain government clearance. Must be legally authorized to work in the United States without the need for employer sponsorship, now or at any time in the future Preferred Qualifications Experience maintaining epidemiological and laboratory data using SAS, or R, REDCap, Microsoft Access, Excel, EpiInfo. Experience developing scripts and software for data manipulation, cleaning, analysis and visualization with Python, R, BASH, and SQL. Proficient in developing bioinformatics pipelines through workflow tools, including Snakemake or Nextflow, on Linux-based high-performance computing environments. Ability to convert existing datasets from diverse file formats (e.g. Microsoft Excel, Access, SQL, and ASCII files) into SAS datasets. Experience with bioinformatics associated with viral diseases at CDC. Previous experience in federal government or public health and molecular epidemiologic research. Education and Training Master's degree in Bioinformatics, Computational Biology, Computer Science, Microbiology, Biology, or closely related field, plus a minimum of 3 years of experience in the capacity of a bioinformatician. Physical Requirements Prolonged periods of sitting at a desk and working on a computer. May need to lift 25 pounds occasionally. Who We Are Tanaq Management Services (TMS) strives to deeply understand and analyze our clients' vision, needs, and requirements so we may provide alternative solutions, empowering them to choose the best resolution. We aim to achieve excellence by delivering on our commitments to our clients, employees, and partners. Our Commitment to Non-Discrimination Tanaq Management Services is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to disability, status as a protected veteran or any other status protected by applicable federal, state, or local law. Tanaq complies with the Drug-free Workplace Act of 1988 and E-Verify. If you are an individual with a disability and need assistance completing any part of the application process, please email accommodation@tanaq.com to request a reasonable accommodation. This email is for accommodation requests only and cannot be used to inquire about the status of applications. Notice on Candidate AI Usage Tanaq is committed to ensuring a fair and competitive interview process for all candidates based on their experience, skills and education. To ensure the integrity of the interview process, the use of artificial intelligence (AI) tools to generate or assist with responses during phone, in person and virtual interviews is not allowed. However, candidates who require a reasonable accommodation that may involve AI are required to contact us prior to their interview at accommodation@tanaq.com. 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Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description The Senior Scientist will perform complex testing in compliance with laboratory test methods and procedures to support the manufacturing and timely delivery of product to customers (75 to 100%). The Senior Scientist will receive general instructions about required tasks and results expected. Work will be well defined and will be reviewed for accuracy upon completion. The Senior Scientist is expected to apply standard practices and techniques in specific situations and to recognize discrepancies in results and follow operations through a series of detailed steps and processes. The Senior Scientist should be able to serve as an expert in technical areas (15-25%). Additionally, the Senior Scientist has accountability and ownership to maintain laboratory instruments in their qualified state as well as troubleshoot instrumentation in the event of instrument issues. ESSENTIAL FUNCTIONS: Major responsibilities will include: 1. Operating in accordance with current GMPs. This includes the ability to understand and apply SOPs and use GMPs for documenting, testing and maintaining accurate laboratory records. 2. Performing increasingly complex testing to support product release 3. Supporting product development, validation and test method transfer activities 4. Initiation and investigation of non-conforming laboratory test results as well as the communication of stability and quality issues to the next level of management 5. Providing initial and final review of data generated by peers and contract laboratories 6. Performing daily calibrations/verifications and routine maintenance of laboratory instrumentation and equipment according to current SOPs. 7. Support the Instrument Lifecycle Management Process 8. Support the Software Lifecycle Management Process 9. Assisting in various other duties which contribute to the organization and function of the laboratory. 10. Responsibility for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance. 11. Maintain up to date knowledge on the latest applicable laboratory techniques, advances and technology. 12. Performing other related duties as assigned by management. Additional Information Best Regards, Sneha Shrivastava ************