Associate scientist jobs in Bonita Springs, FL - 614 jobs
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Clinical Scientist
Ttg Talent Solutions 4.5
Associate scientist job in Coral Springs, FL
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 AssociateScientists (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.
$105k-129k yearly est. 1d ago
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Senior Gummy Formulator
Gummyworks
Associate scientist job in West Palm Beach, FL
Senior Gummy Formulator - Gummy Manufacturing
At GummyWorks, we go beyond manufacturing, we build partnerships. As a leading gummy manufacturer, we specialize in bringing innovative, high-quality gummy supplements to market. Our team is dedicated to delivering exceptional products while maintaining strong client relationships.
About the Role
We are seeking a Senior Formulator with experience in gummy product development and manufacturing. This role is responsible for leading formulation projects from concept through scale-up, ensuring products meet technical, sensory, and regulatory requirements. The ideal candidate has hands-on R&D experience and understands how to translate lab formulas into commercial-scale production.
Responsibilities
Formulation Development
Develop and optimize gummy formulations containing vitamins, minerals, botanicals, proteins, creatine, or other functional actives.
Work with hydrocolloids and sweetener systems
Conduct testing on ingredient stability, compatibility, and sensory properties.
Scale-Up & Manufacturing Support
Transition bench-scale prototypes into pilot and full-scale production.
Troubleshoot issues during cooking, depositing, drying, and packaging.
Collaborate with production teams to ensure formulas are efficient, consistent, and manufacturable.
Regulatory & Documentation
Ensure all formulations comply with FDA and GMP standards.
Work with QA/Regulatory teams on Supplement Facts Panels, ingredient lists, and Certificates of Analysis.
Maintain accurate formulation records and technical documentation.
Innovation & Ingredient Evaluation
Assess new raw materials for performance, cost, and scalability.
Stay current with trends in functional ingredients and gummy delivery systems.
Collaborate with suppliers and flavor houses to support product innovation.
Cross-Team Collaboration
Provide technical guidance to internal teams and clients as needed.
Support sales/business development with formulation expertise during new project discussions.
Mentor junior staff and promote best practices in formulation.
Qualifications
Bachelor's or Master's in Food Science, Chemistry, Chemical Engineering, or related field.
5+ years of experience in gummy, confectionery, or nutraceutical formulation and scale-up.
Strong knowledge of hydrocolloids, sweetener systems, flavors, and active ingredient stability.
Familiarity with sensory evaluation, stability testing, and troubleshooting manufacturing processes.
Understanding of FDA and GMP regulations for dietary supplements and foods.
Excellent problem-solving and communication skills.
Bilingual skills is a plus
Full Time In Person Position
Equal Opportunity Employer Statement: GummyWorks is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Join a rapidly growing company and make an impact with us at GummyWorks!
Think this could be a great fit for you? Apply now!
📩 Email your resume to *******************.
$65k-111k yearly est. 5d ago
Formulation Scientist
Irving Knight Group
Associate scientist job in Fort Lauderdale, FL
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)
$60k-70k yearly 4d ago
Food Scientist
HR Soul
Associate scientist job in Odessa, FL
Here at HR Soul our solutions amplify the performance of people and the soul of company culture. From strategic planning with CEO's, partnering with HR leaders on key projects, building high performing teams to coaching and recruiting the future of our client's organization.
If your happy place is somewhere between a lab bench, a flavor wheel, and a spark of culinary creativity - you're going to love this one.
Our client, a globally respected flavor house with deep roots, rich heritage, and a passion for craftsmanship, is looking for a Food Technologist/Scientist to join their U.S. Applications team. This role blends hands-on formulation, innovation, sensory science, and cross-functional collaboration to bring new flavor experiences to life across North and Latin America.
This is a fantastic opportunity for someone who thrives at the intersection of science and imagination, and isn't afraid to roll up their sleeves in the lab.
Why This Role Exists
You'll be a key contributor to the company's innovation pipeline by developing flavor applications, supporting customer projects, and ensuring technical excellence from concept through delivery. Your work directly influences product quality, customer satisfaction, and the global R&D strategy, no small task, but definitely a rewarding one.
What You'll Do
Product Development & Application
Create and optimize beverage and food prototypes using proprietary flavor systems.
Lead hands-on formulation and bench work (70-80% of your time).
Evaluate ingredient functionality, feasibility, and cost considerations.
Maintain strict adherence to GLP, documentation standards, and internal quality processes.
Sensory Evaluation & Technical Accuracy
Conduct sensory panels and daily evaluations to assess flavor performance and stability.
Maintain meticulous formulation, project, and sensory documentation.
Prepare technical summaries and present recommendations to stakeholders.
Customer & Cross-Functional Collaboration
Work with Sales, R&D, and Marketing to troubleshoot and adapt formulations for customer needs.
Collaborate with global innovation teams for alignment and knowledge sharing.
Prepare prototypes and support customer meetings with technical insights.
Trend Awareness & Innovation
Track emerging food & beverage trends across the Americas.
Explore new ingredients, technologies, and processes to fuel innovation.
Participate in ideation sessions and contribute to global R&D initiatives.
Lab Operations, Safety & Compliance
Maintain safe, clean, well-organized lab spaces.
Follow all GMP, safety, and environmental protocols.
Support continuous improvement of lab processes and documentation systems.
What You Bring
3-5+ years in food, flavor, or beverage application development.
Strong knowledge of flavor systems, beverage formulation, and processing technologies.
Hands-on sensory evaluation expertise.
Excellent documentation, data analysis, and communication skills.
Experience in global or cross-cultural environments.
Proficiency with formulation software, Excel, and relevant systems.
Bilingual skills (English + Portuguese, Spanish, or French) strongly preferred.
Ability to travel up to 30%.
Education
BS or MS in Food Science, Chemistry, Biology, or related field.
Sensory, food safety, or GMP certifications are a plus.
Who You'll Work With
You'll collaborate closely with R&D, Commercial, Sales, Quality, Marketing, Operations, and global innovation teams, plus customers, suppliers, and co-packers.
If you're energized by experimentation, inspired by flavor, and motivated by technical excellence, this might be your next big move.
Diversity Commitment
At HR Soul, we embrace a rich tapestry of backgrounds and experiences within our workplace. We actively encourage applications from women, individuals of color, members of the LGBTQ+ community, people with disabilities, ethnic minorities, immigrants, and veterans.
Equal Opportunity Employment Statement
HR Soul proudly upholds its status as an Equal Opportunity Employer. We prohibit discrimination against any employee or candidate based on various attributes, including but not limited to race (encompassing characteristics historically associated with race such as hair texture and style), color, gender (including pregnancy and related conditions), religion or belief, national origin, citizenship, age, disability, veteran status, union membership, ethnicity, gender identity, gender expression, sexual orientation, marital status, political affiliation, or any other protected characteristics as required by applicable laws.
Inclusivity Commitment
HR Soul and its partners are fully committed to ensuring that all qualified individuals are included. We provide reasonable accommodations for applicants and employees with disabilities. If you need assistance during the job application or interview process, or require accommodations to perform essential job functions, please reach out via our contact page: Contact HR Soul.
Your Rights
HR Soul is dedicated to ensuring that all applicants are aware of their rights concerning workplace discrimination, which is unlawful.
Application Agreement
By applying for this position, you authorize HR Soul to exclusively consider you as a candidate for the specified opportunity. You affirm that the information you provided about your qualifications is true and that you have not misrepresented yourself. Additionally, you agree to keep confidential any details regarding the position that you may learn from HR Soul, sharing such information only as necessary to support your application process. In exchange, HR Soul pledges to make reasonable efforts to represent you throughout the job screening and resume distribution stages.
Salary Transparency Statement
Compensation for this position (and others) at HR Soul is based on multiple factors, including:
The candidate's skill set, experience, and education
Required licenses and certifications
Geographic location of the office
Additional business and organizational considerations
In line with local regulations, HR Soul provides a salary range that reflects a reasonable estimate of the base pay for this role in areas where salary disclosure is mandated.
$37k-64k yearly est. 1d ago
FISHERIES & WILDLIFE BIO SCIENTIST III - 77000506
State of Florida 4.3
Associate scientist job in Panama City Beach, FL
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:
$1.7k weekly Easy Apply 12d ago
Scientist I
Lupin Pharmaceuticals
Associate scientist job in Coral Springs, FL
Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women's health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way.
Responsibilities
Role Summary
Conducts routine and non-routine laboratory activities following with minimal supervision. Assures that quality standards are met. Prepares protocols and reports and documents activities following cGMP rules.
Essential Duties and Responsibilities
Conduct standard and advanced laboratory activities with minimal supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Lupin, FDA and other governing bodies.
Independently set up and operate lab equipment, conduct instrument and analytical method troubleshooting; research and recommend corrective actions for out-of-specification and out-of-trend results.
Execute approved method transfer protocols, develop and validate cleaning validation methods
Prepare and maintain accurate records in lab notebooks of all testing performed. Analyze data, identify trends and perform basic statistical calculations
Write protocols, reports, methods, standard operation procedures, and submission documents with supervision
Conduct manufacturing activities for MDI/DPI/Nasal drug products with limited supervision.
Support the evaluation and introduction of new technologies
Independently train other scientists
Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicate effectively with team members and internal or external customers. Work effectively with other functional groups. Lead small project tasks effectively, with some supervision.
Establish and maintain effective relationships with team members.
Conduct lab work in accordance with SOPs; follow Corporate safety rules and procedures.
Comply with all Corporate guidelines and policies
Qualifications
Education & Experience
PhD in analytical chemistry or related discipline with 0-2 years, MS in Chemistry with 3-5 years, or BS with a minimum of 7 years analytical research experience in pharmaceutical or related field.
Must possess broad analytical chemistry knowledge in HPLC, GC, UV, FTIR and other related analytical technologies and/or basic knowledge of development and manufacturing MDI/DPI/Nasal products.
knowledge and understanding of the FDA cGMP requirements as they apply to the Pharmaceutical industry. Good understanding of USP methodologies and ICH guidelines
Strong English language skills including writing ability and oral communication.
Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran's status, or any other classification as required by applicable law.
Physical Requirements
The physical requirements of the position generally include: standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing. In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply. This position may require lifting up to 15 pounds occasionally. Generally work is performed in an office environment.
Search Firm Representatives Please Read Carefully
Lupin USA, and its Affiliates does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms for any current openings at our company without a valid written search agreement in place will be deemed the sole property of Lupin. No fee will be paid in the event a candidate is hired by Lupin as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, No phone calls or emails
$48k-78k yearly est. Auto-Apply 60d+ ago
Product Development Scientist
Treatt Usa
Associate scientist job in Lakeland, FL
The Product Development Scientist role:
Responsible for developing and leading scaleup of new products to commercialization. Creative and self-motivated, the Product Development Scientist plays a key role in introducing novel ideas and techniques to the product development and commercialization process - leading directly to improved commercial results for the company.
Duties & Responsibilities:
Research and develop creative and novel products with a focus on extracts and distillates - bringing them to commercial fruition.
Utilize and maintain a range of laboratory and pilot-plant equipment (introducing new equipment and techniques where necessary) during product development.
Identify unique raw materials for the development of new products.
Work with the Innovation, QC teams, VP of Innovation, and Category Managers in the planning of R&D project priorities.
Provide Senior Innovation Manager-Coffee and Tea with ongoing and consistent communication of status of R&D efforts and commercial implications of R&D work.
Lead in planning, monitoring and documentation of plant trials leading to successful commercialization of new products.
Execute shelf life and stability studies of new product development.
Support the Production Supervisor to determine, define and improve product tolerance limits of new and existing products.
Lead projects relating to quality or cost improvement.
Lead Continuous improvement projects as pertinent.
Lead projects and evaluation of alternate raw material sources with detailed reports of findings
Participate in sensory evaluation of R&D projects, new products, reformulations, ingredient substitutions, and competitive products.
Maintain and share accurate records of lab work, and documentation of used ingredients, formulation modifications and provide statistical evaluations and reports.
Develop product and raw material specifications suitable for QA, QC, Regulatory, and Customer
Display understanding of HACCP, GMP, and Acidified Foods Filing
Demonstrate proficient use of internal Systems (JDE, STARS, SharePoint, GICP etc.)
Coordinate with Quality Control in scheduling the use of laboratory facilities and equipment to ensure the appropriate levels of R&D, application and QA testing are performed.
Stay abreast of current, worldwide R&D efforts and transfer new knowledge to Treatt product lines.
Continually explore and identify ways to tailor Treatt product lines to appeal to untapped markets.
Provide/Support Capex planning by identifying and costing out potential solutions that may grow business.
Provide both technical and non-technical articles and reports for internal publication.
Cultivate sales opportunities with current customers and other industry contacts by building strong partnering relationships with key technical personnel in these organizations.
Participate in customer call and/or product demonstrations as needed.
Work with customers as needed on new product developments and reformulations.
Partner with sales team members to identify and analyze consumer market trends that might provide increased sales and product development opportunities.
Act in the best interest of Treatt at all times.
All other duties as customary or as delegated.
Work primarily independently or with minimal supervision to complete required tasks.
Education & Traininig:
A bachelor's degree in chemistry, Food Science or a related Scientific field, plus a minimum of 1 years lab and product development experience in a closely affiliated field.
Knowledge & Experience:
A proven independent worker with strong creativity and problem-solving skills.
An in-depth understanding of fundamental chemistry principles.
Demonstrate knowledge of regulations, policies, procedures and processes in food science and product development.
Superior ability to research and analyze information and data to arrive at valid conclusions and plans of actions.
Effective communication skills at all levels - both orally and in writing.
Basic knowledge in the use of various laboratory equipment and methodologies. Including: Gas chromatography, mass spectrometry and other analytical measurement methods a plus
Ability to use various spreadsheets, word-processing and database computer software.
Environment:
Normal laboratory and manufacturing working conditions.
$57k-89k yearly est. 60d+ ago
Associate Scientist - R&D
Clinical Diagnostic Solutions 4.8
Associate scientist job in Plantation, FL
Clinical Diagnostic Solutions, Inc. (CDS) is a company that provides total hematology solutions for the physician office laboratory, clinic, small hospital, and veterinary office markets. At CDS, our mission is to provide the highest quality experience to our valued customers. Our employees achieve this through our cultural goals of working together through Teamwork, high Quality in the work we do, being Innovative and Courageous, always Results Oriented, and most importantly - being Customer Oriented.
Under supervision, uses fundamental concepts, practices, and procedures of particular field of specialization to perform scientific, R&D tasks of some complexity requiring application and adaptation of established techniques, procedures, and criteria. Participates in new product development, optimization, validation, and transfer into production. Prioritizes work schedules to support team objectives.
Job Responsibilities:
Participates in method development and technical innovation within the research team and supports project timelines
Performs method optimizations, validations and participates in technology transfer to production
Performs routine operation, maintenance, calibration and troubleshooting of laboratory instruments such as pH, conductivity meters, osmometers, spectrnphotometers, hematology analyzers and nucroscopes
Evaluates and selects methods, applies protocols and scientific techniques to accomplish study objectives
Drafts and updates protocols, test methods and standard operating procedures as applicable
Proactively collaborates and supports the team, communicates problems as they arise
Provides solution/s to problem/ s of limited complexity, exercises judgment within defined policies to determine appropriate action
Collects, analyzes and compiles data. Summarizes for interpretation and discussion
Drafts statistical and narrative reports as applicable
Recognizes and reports experimental variances
Is able to coordinate a small project or a small component of a larger project according to set deliverables
Maintains good laboratory records and documentation for experimental work and results Maintains workplace safety and environmental practices
Maintains clean workplace including laboratory bench and glassware
Supports the department with QC technical investigation activities as needed
Works in the spirit of continuous improvement
Engages in inter and intra-departmental activities/studies Performs other related duties as required or as directed. The omission of specific duties does not preclude the supervisor from assigning duties that are logically related to the position.
Qualifications:
Knowledge of scientific approach and methodologies.
Ability to design small studies, gather, organize and analyze statistical data and generate reports
Excellent oral and written communication skills
Ability to investigate and analyze information and to draw conclusions
Skill in the use of personal computers and related software applications such as Word/Excel/Powerpoint/Teams
Knowledge of current technological developments/trends in area of expertise is desirable but not required
Capable of adjusting to dynamic work environment and changing priorities
Willing to take on new challenges and implement new ideas
Must be Comfortable handling blood products
Willing to embrace a learning environment, is open to suggestions, new ideas and innovation
Ability to grasp methods fast and willingness to change course as applicable
Familiar with GLP, GMP practices and capable of working in a regulated medical device company (ISO and FDA)
Must have strong analytical skills
Must be a team player and driven individual Must value innovation, accuracy and accountability
Minimum Requirements:
Bachelor's degree with 2-5 years or Associates degree with 5-8 years' experience that is directly related to the duties and responsibilities specified.
EOE
$49k-76k yearly est. 60d+ ago
Entry-Level Scientist
Brown and Caldwell 4.7
Associate scientist job in Tampa, FL
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
$58k-79k yearly 10d ago
Retail Associate Manage KISSIMMEE | Pleasant Hill Rd
Imobile 4.8
Associate scientist job in Kissimmee, FL
We're a national Wireless Preferred Retailer with 200+ retail stores across the U.S. Since '93, we've been providing superior service and quality wireless products featuring the latest in technology. As a recognized leader in the wireless retail industry, we consistently deliver the solutions and service our customer's demand! Do you think you have what it takes to be an Archer? If so, keep reading!
Arch Telecom's Retail Associate Managers (RAM) work as part of a Retail Team to bring the brand to life. They live and breathe the brand and Arch Telecom's Core Values. Our RAMs are brand ambassadors, they create energy and excitement around our products and services. They thrive in a fast-paced fun environment where customer needs are their first focus. They immerse themselves in meaningful connections with our customers by building new and deepening existing relationships. They continuously work to build expertise in uncovering our customers' needs and have a passion to educate, demonstrate and recommend device and service solutions. This role is a learning role, where you will be expected to work with your team to build required skills as well as assist the Retail Store Manager in all operational duties.
What you'll do in your role?
Learn and build proficiency in customer service, while concurrently providing a best in class customer experience and building loyalty by:
* Helping customers pick up right where they left off in their shopping journey, whether online, through Customer Care or in-store
* Exploring individual needs and providing hands-on demonstrations of the latest and greatest technology in-store.
* Side-by-side selling to find personalized solutions beyond the bare-bones device and service plan that keep our customers connected to the people and lifestyle they love, including anything from unique accessories to up and coming Internet of Things (IOT) devices.
* Guide your customers through their purchasing experience thoughtful questions, informative answers and sharing your expertise.
* Assist Retail Store Manager is daily operations and coaching.
Become proficient in the use of digital tools designed to enhance interactions and onboarding to actively demonstrate:
* How our ever-expanding coverage stacks up in our customer's neighborhood, providing them with a lightning fast LTE network!
* Why plans and services will let our customers live unlimited, feel the love, stay connected and go further.
* How we're redefining how wireless is done, down to device and account inspection, review and troubleshooting.
Complete training on in-store experience, new skills and processes, knowledge of systems and reference resources.
Build relationships with and partner with employees across channels, including business and customer service to:
* Collectively own the customer experience and resolve issues, creating a seamless, run-around-free environment.
* Successfully identify and handoff small business leads.
* Develop strong peer relationships where we are all accountable for the company's success.
* Be willing to have a good time while providing first class customer experience
The ideal candidate will bring:
* Leadership!
* Competitive drive and demonstrates the confidence to succeed in a fast-paced sales environment.
* Willingness to lead your team, sharing best practices, while serving customers and providing resolutions to issues.
* Being effective with operational, financial and performance management.
* Amazing communication skills, to your team and customers.
* Prior wireless sales experience.
What's in it for you?
* Employee Stock Ownership Program (ESOP)
* Competitive hourly pay
* Bonus earnings
* Automatic raises when reaching attainable milestones
* Exciting opportunities for career advancement
* A culture of care & excellence
* Health Benefits for Full Time Employees
What "must haves" do you need?
* Be at least 18 years of age
* High school degree or GED
* Ability to stand for long periods of time
* Ability to lift objects weighing up to 25lbs
* Reliable transportation
* Full Time (40 hours)
Diversity & Inclusion is a foundational principle of Arch Telecom. Embracing a diverse workforce is a significant contributor to our success as an organization. Employees with diverse perspectives, backgrounds, and experiences allow us to better reflect the communities whom we serve and result in a superior customer and employee experience. We embrace the diversity that makes our employees unique, and we welcome everyone to our team. YOU BE YOU!
Apply Now: *******************
Inquiries: **************************
$45k-68k yearly est. 10d ago
Senior Embryologist
CNY Fertility Center
Associate scientist job in Sarasota, FL
Job Description
Job Title: Senior Embryologist
Reports to: Lab Director
FLSA Status: Exempt
Summary: CNY Fertility is a renowned fertility center offering advanced treatments like IVF, IUI, and egg freezing. With a patient-centered approach and cutting-edge technology, we support individuals and couples on their journey to parenthood. Our Senior Embryologist will be a detail-oriented, team player, technically skilled and highly motivated individual, to carry out the mission of CNY Fertility.
Required Duties and Responsibilities: Include the following. Other duties may be assigned.
Daily quality control, media preparation and dish preparation.
Microscope and pipettor use.
Use of other lab equipment to complete procedures: balance, pH meter, CO2 monitor, labeler etc.
Oocyte retrieval and denuding of oocytes.
Embryo and oocyte thawing/embryo and oocyte freezing.
Fertilization checks and embryo transfers.
Have a well-developed understanding of all aspects of running an Embryology lab including but not limited to: equipment maintenance and troubleshooting, QC/QA/QM/QI.
ICSI and conventional fertilization techniques.
Schedule procedures, complete tasks and navigate patient charts.
Understanding of cryopreservation and storage specimens.
Assist in cleaning and stocking inventory for the laboratory.
Perform PGT and load samples. Ability to interpret PGT reports and call patients with results.
Communicate with patients across various platforms such as web correspondences and phone calls.
Perform PESA/TESE sperm retrievals.
Supervise entire embryology staff, including overseeing PTO and scheduling of staff.
Participate in the alarm response team.
Qualifications:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education/Experience:
Bachelor's degree in biology, or related field. At least four years of experience in clinical embryology setting.
Language Ability:
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization.
Math Ability:
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percentage and to draw and interpret bar graphs.
Reasoning Ability:
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. The ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Knowledge, Skills and Other Abilities:
Excellent oral and written communication skills.
Must be able to lift 25lbs.
Excellent computer literacy.
Adequate vision or corrective lenes for sample identification.
Ability to multitask in fast paced environments.
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
There is some risk of exposure of bodily fluids or contagious diseases.
Weekend and holiday rotation is required.
Physical Demands:
The physical demands 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.
While performing the duties of this job, the employee is regularly required to stand; walk; use hands; reach with hands and arms and talk or hear. The employee is occasionally required to sit.
$55k-88k yearly est. 17d ago
Embryologist I
SGF Tampa Bay, LLC
Associate scientist job in Tampa, FL
Enjoy what you do while contributing to a company that makes a difference in people's lives. Shady Grove Fertility, one of the premier fertility centers in the United States, continually seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward.
If you're an Entry Level Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments.
We currently have an opening for a full-time Embryologist I to work in our fast paced, high volume, Embryology Lab located at our Westshore, FL office. This is a full-time position working Monday through Friday, 7:00am-4:00pm. Rotating weekends and Holidays required.
How You'll Contribute:
We always do whatever it takes, even if it isn't specifically our “job.” In general, the Embryologist is responsible for:
Identification, assessment and culture of oocytes; sperm preparation and insemination of oocytes
Assessment and selection embryos for transfer; embryo vitrification, storage and warming
Oocyte vitrification, storage and warming
The position involves preparation of all media used with human gametes.
The position involves diagnostic semen analysis
Preparation and care of gametes/embryos throughout the laboratory process: IVF, ICSI, VIT, ET, Thaw and PGD
Cryopreservation and thawing of embryos at varying stages of development
Assessing fertilization and zygote quality following insemination
Records and reports results in Artworks
TBSA, PESA, TESA and TESE collection
Oocyte denuding and ICSI insemination
PGD biopsy
Responsible for embryo discharge and storage
Responsible for donor sperm/embryo tracking under FDA regulations
What You'll Bring:
Must have appropriate college degree and graduated with a “B” average or greater in a relevant laboratory science; 3.0 or above overall GPA strongly preferred.
Minimum 2 years of Embryology Experience
Must demonstrate the ability to function effectively without direct supervision, and to perform laboratory services in accord with the Laboratory Philosophy and Operating Standards.
Proven ability to access, input, and retrieve information from a computer.
Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.).
Ability to work as part of a multidisciplinary team.
Ability to work in a high standard, stressful environment.
Ability to communicate accurately and concisely.
Excellent interpersonal skills.
More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful.
What We Offer:
Competitive pay + bonus
Comprehensive training
Medical, dental, vision, and 401(k) matching
Generous paid time off and holidays
Retirement plan
Tuition assistance
Ability to make an impact in the communities we serve
At Shady Grove Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values - Empathy, Patient Focus, Integrity, Commitment, and Compassion (EPICC) - guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team!
To learn more about our company and culture, visit here.
How To Get Started:
To have your resume reviewed by someone on our Talent Acquisition team, click on the “Apply” button. Or if you happen to know of someone who might be interested in this position, please feel free to share the job description by clicking on an option under “Share This Job” at the top of the screen.
$55k-88k yearly est. 4d ago
Senior Embryologist
SGF Orlando, LLC
Associate scientist job in Orlando, FL
Enjoy what you do while contributing to a company that makes a difference in people's lives. Shady Grove Fertility, one of the premier fertility centers in the United States, continually seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward.
If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments.
We currently have an opening for a full-time Senior Embryologist to work in our fast paced, high volume, Embryology Lab located in our Orlando, FL office. The schedule is working Monday - Friday 7:00 AM to 4:00 PM with rotating weekends/holiday. Approximately 1 weekend/month
How You'll Contribute:
We always do whatever it takes, even if it isn't specifically our “job.” In general, the Senior Embryologist is responsible for:
Identification, assessment and culture of oocytes; sperm preparation and insemination of oocytes (conventional insemination and ICSI)
Assessment and selection embryos for transfer; embryo vitrification, warming and storage
Oocyte vitrification, warming and storage
Preparation and care of gametes/embryos throughout the laboratory process: IVF, ICSI, VIT, ET, Warming and Embryo Biopsy
Vitrification and warming of embryos at varying stages of development
Assessing fertilization and zygote quality following insemination
Familiarity with data entry into an EMR
Familiarity with MESA, PESA, TESA and TESE collection
Experience with regulatory guidelines and inspections (e.g. CLIA, FDA, TJC, CAP)
What You'll Bring:
Minimum 5 years' experience in Embryology.
Must have a Bachelor's degree or higher in a relevant laboratory science.
Must demonstrate the ability to function effectively without direct supervision, and to perform laboratory services in accordance with the Laboratory Philosophy and Operating Standards.
Proven ability to access, input, and retrieve information from a computer.
Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.).
Ability to work as part of a multidisciplinary team.
Ability to work in a high standard, stressful environment.
Ability to communicate accurately and concisely.
Ability to develop interpersonal working relationships with colleagues
Must be authorized to work in the U.S.A.
More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful.
What We Offer:
Competitive pay + bonus
Comprehensive training
Medical, dental, vision, and 401(k) matching
Generous paid time off and holidays
Retirement plan
Tuition assistance
Ability to make an impact in the communities we serve
At Shady Grove Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team!
To learn more about our company and culture, visit here.
How To Get Started:
To have your resume reviewed by someone on our Talent Acquisition team, click on the “Apply” button. Or if you happen to know of someone who might be interested in this position, please feel free to share the job description by clicking on an option under “Share This Job” at the top of the screen.
$54k-87k yearly est. 5d ago
Senior Embryologist
Us Fertility
Associate scientist job in Orlando, FL
Enjoy what you do while contributing to a company that makes a difference in people's lives. Shady Grove Fertility, one of the premier fertility centers in the United States, continually seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward.
If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments.
We currently have an opening for a full-time Senior Embryologist to work in our fast paced, high volume, Embryology Lab located in our Orlando, FL office. The schedule is working Monday - Friday 7:00 AM to 4:00 PM with rotating weekends/holiday. Approximately 1 weekend/month
How You'll Contribute:
We always do whatever it takes, even if it isn't specifically our “job.” In general, the Senior Embryologist is responsible for:
Identification, assessment and culture of oocytes; sperm preparation and insemination of oocytes (conventional insemination and ICSI)
Assessment and selection embryos for transfer; embryo vitrification, warming and storage
Oocyte vitrification, warming and storage
Preparation and care of gametes/embryos throughout the laboratory process: IVF, ICSI, VIT, ET, Warming and Embryo Biopsy
Vitrification and warming of embryos at varying stages of development
Assessing fertilization and zygote quality following insemination
Familiarity with data entry into an EMR
Familiarity with MESA, PESA, TESA and TESE collection
Experience with regulatory guidelines and inspections (e.g. CLIA, FDA, TJC, CAP)
What You'll Bring:
Minimum 5 years' experience in Embryology.
Must have a Bachelor's degree or higher in a relevant laboratory science.
Must demonstrate the ability to function effectively without direct supervision, and to perform laboratory services in accordance with the Laboratory Philosophy and Operating Standards.
Proven ability to access, input, and retrieve information from a computer.
Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.).
Ability to work as part of a multidisciplinary team.
Ability to work in a high standard, stressful environment.
Ability to communicate accurately and concisely.
Ability to develop interpersonal working relationships with colleagues
Must be authorized to work in the U.S.A.
More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful.
What We Offer:
Competitive pay + bonus
Comprehensive training
Medical, dental, vision, and 401(k) matching
Generous paid time off and holidays
Retirement plan
Tuition assistance
Ability to make an impact in the communities we serve
At Shady Grove Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team!
To learn more about our company and culture, visit here.
How To Get Started:
To have your resume reviewed by someone on our Talent Acquisition team, click on the “Apply” button. Or if you happen to know of someone who might be interested in this position, please feel free to share the job description by clicking on an option under “Share This Job” at the top of the screen.
$54k-87k yearly est. 60d+ ago
Senior Vulnerability Researcher/Reverser/Dev
Nightwing Intelligence Solutions
Associate scientist job in Indialantic, FL
Nightwing provides technically advanced full-spectrum cyber, data operations, systems integration and intelligence mission support services to meet our customers' most demanding challenges. Our capabilities include cyber space operations, cyber defense and resiliency, vulnerability research, ubiquitous technical surveillance, data intelligence, lifecycle mission enablement, and software modernization. Nightwing brings disruptive technologies, agility, and competitive offerings to customers in the intelligence community, defense, civil, and commercial markets.
At Nightwing, we value collaboration and teamwork. You'll have the opportunity to work alongside talented individuals who are passionate about what they do. Together, we'll leverage our collective expertise to drive innovation, solve complex problems, and deliver exceptional results for our clients.
About Cybersecurity, Intelligence and Services
The Cybersecurity, Intelligence and Services (CIS) business provides technically advanced full-spectrum cyber, data operations, systems integration and intelligence mission support services to meet our customers' most demanding challenges. Our capabilities include cyber space operations, cyber defense and resiliency, vulnerability research, ubiquitous technical surveillance, data intelligence, lifecycle mission enablement, and software modernization. CIS brings disruptive technologies, agility, and competitive offerings to customers in the intelligence community, defense, civil, and commercial markets
Job Summary
Our team covers the full life cycle from emulation, reverse engineering, vulnerability research, and CNO/CNE tool development for various operating systems. Our mission covers a wide range of targets, anything from major consumer electronics to proprietary one-off systems. If it runs code, we have probably looked at it (or will soon.). In addition, the position will provide deliverables for real-world use in relatively short turn-around times. Projects will be undertaken in small teams with close coordination with customers to quickly enhance capabilities or resolve issues in existing tools for real-world applications. Working as part of a team you will also need to be familiar with source management tools such as GIT and team coordination tools like the Atlassian suite of work products. All candidates must be US citizens and be able to obtain and maintain a government security clearance.
This position is an onsite role.
Responsibilities to Anticipate
We seek a qualified engineer that can perform as a team member on activities involved with research, reverse engineering, development, testing, maintenance, and modification of complex classified and unclassified software applications.
Basic Qualifications
TS/SCI Clearance Required
Typically requires a Bachelor's in Science, Technology, Engineering, or Mathematics (STEM preferred) and a minimum of 5 years of prior engineering experience or equivalent experience unless prohibited by local laws/regulations
Vulnerability research experience of public targets
Reverse engineering utilizing any of IDA/Ghidra/BinaryNinja
Utilizing full system emulation for research and analysis
Understanding of network protocols (TCP/IP stacks, wire-level protocols, routing protocols, or others)
Experience with source management tools
Experience with assembly language (x86/64, ARM, PPC, Mips, etc.)
Requires advanced knowledge of work area typically obtained through advanced education combined with experience
May have practical knowledge of project management
Practical to substantial knowledge of RTX projects, programs or systems with the ability to make enhancements and leverage in daily work
Preferred Qualifications
C/C++/Python
Capture the Flag (CTF) experience
Fuzzer development
Understanding of network protocols (TCP/IP stacks, wire-level protocols, RF communications, BGP, routing protocols, or others)
Linux or other OS reversing
What We Offer
Whether you're just starting out on your career journey or are an experienced professional, we offer a total rewards package that goes above and beyond with compensation; healthcare, wellness, retirement and work/life benefits; career development and recognition programs. Some of the benefits we offer include parental (including paternal) leave, flexible work schedules, achievement awards, educational assistance and child/adult backup care.
In addition to competitive salaries, CODEX offers excellent benefits for you and your family: competitive medical, dental and vision plans, child, elderly and dependent-care programs, mental health resources, tuition assistance, employee discount programs, 401k matching, flexible work schedules (depending on program), a peer recognition and reward system and performance-based bonuses.
Additional Information
Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products.
ERIP Eligibility - This requisition is eligible for an employee referral award. ALL eligibility requirements must be met to receive the referral award.
#CODEX
At Nightwing, we value collaboration and teamwork. You'll have the opportunity to work alongside talented individuals who are passionate about what they do. Together, we'll leverage our collective expertise to drive innovation, solve complex problems, and deliver exceptional results for our clients.
Thank you for considering joining us as we embark on this new journey and shape the future of cybersecurity and intelligence together as part of the Nightwing team.
Nightwing is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.
$57k-82k yearly est. Auto-Apply 60d+ ago
FISHERIES & WILDLIFE BIO SCIENTIST III - 77000506
State of Florida 4.3
Associate scientist job in Florida
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:
$1.7k weekly Easy Apply 12d ago
Scientist I
Lupin Pharmaceuticals
Associate scientist job in Coral Springs, FL
Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women's health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way.
Responsibilities
Role Summary
Conducts routine and non-routine laboratory activities following with minimal supervision. Assures that quality standards are met. Prepares protocols and reports and documents activities following cGMP rules.
Essential Duties and Responsibilities
Conduct standard and advanced laboratory activities with minimal supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Lupin, FDA and other governing bodies.
Independently set up and operate lab equipment, conduct instrument and analytical method troubleshooting; research and recommend corrective actions for out-of-specification and out-of-trend results.
Execute approved method transfer protocols, develop and validate cleaning validation methods
Prepare and maintain accurate records in lab notebooks of all testing performed. Analyze data, identify trends and perform basic statistical calculations
Write protocols, reports, methods, standard operation procedures, and submission documents with supervision
Conduct manufacturing activities for MDI/DPI/Nasal drug products with limited supervision.
Support the evaluation and introduction of new technologies
Independently train other scientists
Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicate effectively with team members and internal or external customers. Work effectively with other functional groups. Lead small project tasks effectively, with some supervision.
Establish and maintain effective relationships with team members.
Conduct lab work in accordance with SOPs; follow Corporate safety rules and procedures.
Comply with all Corporate guidelines and policies
Qualifications
Education & Experience
PhD in analytical chemistry or related discipline with 0-2 years, MS in Chemistry with 3-5 years, or BS with a minimum of 7 years analytical research experience in pharmaceutical or related field.
Must possess broad analytical chemistry knowledge in HPLC, GC, UV, FTIR and other related analytical technologies and/or basic knowledge of development and manufacturing MDI/DPI/Nasal products.
knowledge and understanding of the FDA cGMP requirements as they apply to the Pharmaceutical industry. Good understanding of USP methodologies and ICH guidelines
Strong English language skills including writing ability and oral communication.
Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran's status, or any other classification as required by applicable law.
Physical Requirements
The physical requirements of the position generally include: standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing. In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply. This position may require lifting up to 15 pounds occasionally. Generally work is performed in an office environment.
Search Firm Representatives Please Read Carefully
Lupin USA, and its Affiliates does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms for any current openings at our company without a valid written search agreement in place will be deemed the sole property of Lupin. No fee will be paid in the event a candidate is hired by Lupin as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, No phone calls or emails
$48k-78k yearly est. Auto-Apply 60d+ ago
Associate Scientist - R&D
Clinical Diagnostic Solutions Inc.
Associate scientist job in Plantation, FL
Job Description
Clinical Diagnostic Solutions, Inc. (CDS) is a company that provides total hematology solutions for the physician office laboratory, clinic, small hospital, and veterinary office markets. At CDS, our mission is to provide the highest quality experience to our valued customers. Our employees achieve this through our cultural goals of working together through Teamwork, high Quality in the work we do, being Innovative and Courageous, always Results Oriented, and most importantly - being Customer Oriented.
Under supervision, uses fundamental concepts, practices, and procedures of particular field of specialization to perform scientific, R&D tasks of some complexity requiring application and adaptation of established techniques, procedures, and criteria. Participates in new product development, optimization, validation, and transfer into production. Prioritizes work schedules to support team objectives.
Job Responsibilities:
Participates in method development and technical innovation within the research team and supports project timelines
Performs method optimizations, validations and participates in technology transfer to production
Performs routine operation, maintenance, calibration and troubleshooting of laboratory instruments such as pH, conductivity meters, osmometers, spectrnphotometers, hematology analyzers and nucroscopes
Evaluates and selects methods, applies protocols and scientific techniques to accomplish study objectives
Drafts and updates protocols, test methods and standard operating procedures as applicable
Proactively collaborates and supports the team, communicates problems as they arise
Provides solution/s to problem/ s of limited complexity, exercises judgment within defined policies to determine appropriate action
Collects, analyzes and compiles data. Summarizes for interpretation and discussion
Drafts statistical and narrative reports as applicable
Recognizes and reports experimental variances
Is able to coordinate a small project or a small component of a larger project according to set deliverables
Maintains good laboratory records and documentation for experimental work and results Maintains workplace safety and environmental practices
Maintains clean workplace including laboratory bench and glassware
Supports the department with QC technical investigation activities as needed
Works in the spirit of continuous improvement
Engages in inter and intra-departmental activities/studies Performs other related duties as required or as directed. The omission of specific duties does not preclude the supervisor from assigning duties that are logically related to the position.
Qualifications:
Knowledge of scientific approach and methodologies.
Ability to design small studies, gather, organize and analyze statistical data and generate reports
Excellent oral and written communication skills
Ability to investigate and analyze information and to draw conclusions
Skill in the use of personal computers and related software applications such as Word/Excel/Powerpoint/Teams
Knowledge of current technological developments/trends in area of expertise is desirable but not required
Capable of adjusting to dynamic work environment and changing priorities
Willing to take on new challenges and implement new ideas
Must be Comfortable handling blood products
Willing to embrace a learning environment, is open to suggestions, new ideas and innovation
Ability to grasp methods fast and willingness to change course as applicable
Familiar with GLP, GMP practices and capable of working in a regulated medical device company (ISO and FDA)
Must have strong analytical skills
Must be a team player and driven individual Must value innovation, accuracy and accountability
Minimum Requirements:
Bachelor's degree with 2-5 years or Associates degree with 5-8 years' experience that is directly related to the duties and responsibilities specified.
EOE
$47k-80k yearly est. 22d ago
Fisheries & Wildlife Bio Scientist III - 77000506
State of Florida 4.3
Associate scientist job in Florida
Working Title: FISHERIES & WILDLIFE BIO SCIENTIST III - 77000506
Pay Plan: Career Service
77000506
Salary: $1,730.77 biweekly + benefits
Posting Closing Date: 01/23/2026
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.
$1.7k weekly Easy Apply 5d ago
FISHERIES & WILDLIFE BIO SCIENTIST III - 77000506
State of Florida 4.3
Associate scientist job in Panama City, FL
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:
How much does an associate scientist earn in Bonita Springs, FL?
The average associate scientist in Bonita Springs, FL earns between $40,000 and $96,000 annually. This compares to the national average associate scientist range of $53,000 to $109,000.
Average associate scientist salary in Bonita Springs, FL