field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
Job Description 
The Analyst I prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Quality Assurance programs and SOP’s.
Analyst I responsibilities include, but are not limited to, the following:
<ul>
<li>Demonstrates and promotes the company vision</li>
<li>Regular attendance and punctuality</li>
<li>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include:
<ul>
<li>Preparation of samples using standard techniques</li>
<li>Performing chemical analysis using standard techniques</li>
<li>Calculating data</li>
<li>Recording and reporting data and any unusual test occurrences to the supervisor</li>
<li>Performing routine instrument maintenance</li>
</ul>
</li>
<li>Responsible for performing job functions in compliance with Eurofins’ EHS and QA standards</li>
<li>Responsible for general housekeeping in his/her work area</li>
<li>Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems.</li>
<li>Works under close supervision using routine and standard methods</li>
<li>Aliquots and weighs samples</li>
<li>Washes glassware</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned&nbsp;</li>
</ul>
The ideal candidate would possess:
<ul>
<li>Ability to use calculator/mathematical formulas and concepts</li>
<li>Ability to complete work within time and quality constraints</li>
<li>Can work independently following written or verbal instructions</li>
<li>Cooperate and coordinate both orally and in writing</li>
<li>&nbsp;Able to follow and learn appropriate protocols in one or more of the following disciplines:
<ul>
<li>Organic preparation</li>
<li>Metals preparation and analysis</li>
<li>Gas Chromatography</li>
<li>Gas Chromatography/Mass Spectrometry</li>
<li>Radio Chemistry</li>
<li>Wet Chemistry</li>
<li>High Resolution preparation and analysis</li>
<li>Low Resolution preparation and analysis</li>
</ul>
</li>
</ul>
Qualifications 
Basic Minimum Qualifications:
<ul>
<li>BS or BA in chemistry or related field; 3 years laboratory experience may substitute for degree.</li>
<li>Laboratory experience is a plus</li>
<li>Previous production-oriented work helpful (awareness and ability to meet deadlines)</li>
</ul>
 Additional Information 
Requirements:
<ul>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English</li>
</ul>
Position is full-time Tuesday - Saturday 8am - pm. Candidates currently living within a commutable distance of Altamonte Springs, FL are encouraged to apply.&nbsp;
Pay rate: $18/hr
Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. we offer excellent benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.
*The benefits package offered will vary based on the employee's full-time or part-time regular status.
To learn more about Eurofins, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.
We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.
Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!
Find out more in our career page: <a href="https://careers.eurofins.com/" target="_blank">https://careers.eurofins.com/</a>
Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.
Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Laboratory Analyst - Eurofins Environment Testing Southeast - Orlando (Altamonte Springs) FL

<h3>Job Description</h3>
Job DescriptionCompany Description 
Fort Walton Machining, Inc.&nbsp;was formed in 1987 as a specialized custom manufacturing operation, specifically to service Eglin Air Force Base and its prime contractors. It began as a small company with only two employees, but its mission—even then, as it remains today—was to provide highly technical, precision machining with zero defects, delivered on time, and to the complete satisfaction of its customers.
Commitment to that mission quickly earned the company a reputation for “walking the walk,” not just “talking the talk.” As evidence of this, Fort Walton Machining became a certified “Dock to Stock” supplier for one of its major customers as early as 1991.
Certified to AS9100 Quality Standards, as well as government and military standards such as MIL-I-45208A, the company played a significant role in the Air Force AMRAAM project from 1991 to 1993. The long-term vision was always to expand into commercial markets while continuing to serve the military and its prime contractors.
In early 1995, the company formed a business alliance with a major corporation in the medical industry, which led to additional business opportunities with partners in the British Isles and Japan. As a result of these diverse experiences, Fort Walton Machining has grown into an international service company, capable of supporting customers around the world.
Job Description 
Conducts established activities of a chemical laboratory technician by performing the following duties for an industrial organization.
Essential duties and Responsibilities include the following as they relate to mil-spec painting, anodizing types I, II, and III, chem film class 1A and 3, passivation and phosphate coatings.&nbsp; Other duties may be assigned.
<ul>
<li>Test solutions used in anodizing and Chem-film processes for chemical concentrations.</li>
<li>Maintain chemical inventory stock to ensure adequate supplies.</li>
<li>Calibrate, setup, adjust and operate laboratory equipment and instruments such as microscopes, spectrophotometer, pH meter and other lab equipment.</li>
<li>Add chemicals or raw material to process solutions to correct or prepare chemical solutions according to standard formulas.</li>
<li>Record test results in computer and maintain records, reports, files and related documentation.</li>
<li>Order laboratory supplies, materials, or equipment.</li>
<li>Maintain established procedures concerning quality assurance.</li>
<li>Clean and maintain laboratory equipment and facility.</li>
<li>Follow written procedures for Chemical hygiene safety.</li>
</ul>
Qualifications 
Education and/or Experience
Associate’s degree (AS) from a two-year College/University, related experience and/or training in chemistry relating to industrial painting, anodizing, chem-film, passivation, and phosphate coatings preferred.
Physical Demands
While performing the duties of this job the employee is regularly required to stand; walk; use hands to finger, handle or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear.&nbsp; The employee is frequently required to sit.&nbsp; The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds.&nbsp; Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
 Additional Information 
Additional Information
All your information will be kept confidential according to EEO guidelines.
Fort Walton Machining, Inc. is a drug-free workplace.&nbsp;Testing for illegal drugs is required prior to hire and may be conducted periodically during employment.
Reasonable Accommodation:&nbsp;Fort Walton Machining, Inc. will provide reasonable accommodation to all applicants and employees. If you need an accommodation to complete the application process, please contact Dan Bowman at 850 244-9095.
Equal Employment Opportunity:&nbsp;Fort Walton Machining, Inc. provides equal employment opportunities to all qualified applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, citizenship status, disability, protected veteran status, or any other legally protected status. We prohibit discrimination in all aspects of employment, including recruitment, hiring, compensation, benefits, training, promotions, and termination.
We comply with all applicable laws and regulations, including but not limited to Title VI and Title VII of the Civil Rights Act, the Vietnam Era Veterans' Readjustment Assistance Act (VEVRAA), Section 503 of the Rehabilitation Act, and the Americans with Disabilities Act (ADA).

Chemical Laboratory Technician

<h3>Job Description</h3>
Job Description
6-month contract-to-hire JOB DESCRIPTION
As an Entry-Level Chemist, you will conduct pilot testing techniques to evaluate the feasibility and performance of new chemical processes and products. You will prepare and maintain detailed documentation of experimental procedures, observations, and results, analyze data, and generate reports to support research and development projects. Collaboration with senior chemists and cross-functional teams will be essential to ensure accurate and efficient testing. The ideal candidate will have a Bachelor’s degree in Chemistry or a related field, strong attention to detail, excellent organizational skills, experience with documentation and data management, a basic understanding of pilot testing techniques and laboratory procedures, the ability to work independently and as part of a team, and strong communication skills, both written and verbal. 
REQUIRED SKILLS AND EXPERIENCE
Required Skills &amp; Experience - Internship or associate or bachelor’s degree in chemistry preferred, but your open to no degree if candidate is qualified - At least one year in an Analytical role involving testing of chemicals o Manufacturing testing or end process testing - Experience in medical manufacturing, pharmaceutical, or cannabis industries preferred but open to ANY manufacturing testing environment. - Excellent documentation skills 
NICE TO HAVE SKILLS AND EXPERIENCE
Preferred, not required - QA/QC experience is a plus - GC (Gas Chromatography) testing - HPLC (High-Performance Liquid Chromatography) testing

QA Chemist/Analyst

<h3>Job Description</h3>
Job Description
Elite Group Staffing and Headhunting Firm is hiring an Analytical Chemist for a confidential client in the hemp processing industry located in Fort Lauderdale, Florida. This is a full-time, onsite role ideal for candidates with hands-on experience in HPLC and GC instrumentation and a passion for quality control and regulatory compliance.
 
The Analytical Chemist will perform chemical analysis of hemp-derived products using advanced chromatographic techniques. This role includes equipment maintenance, data analysis, and oversight of the Certificate of Analysis (COA) process to ensure compliance with FDA and 2018 Farm Bill regulations.
 
Key Responsibilities:
• Conduct cannabinoid testing using Shimadzu LC-2030 and Agilent 1200 HPLC
• Operate and maintain LC and GC systems
• Prepare samples and generate quality system-compliant data
• Troubleshoot instrumentation and ensure proper calibration
Maintain accurate records and follow SOPs and safety protocols
• Manage COA databases and coordinate product sampling and testing
• Monitor regulatory compliance for hemp products
 
Qualifications:
• Minimum 1 year of experience in an analytical laboratory
• Proficiency with Shimadzu LC-2030, Agilent 1200, and Agilent GC systems
• Strong analytical and problem-solving skills
• Experience with method development, qualification, and validation
• Ability to work independently and collaboratively
• Excellent attention to detail and organizational skills
 
Preferred:
• Bachelor’s degree in Chemistry or related field
• Experience in GMP-regulated environments
• Familiarity with hemp industry regulations
• Strong verbal and written communication skills
 
Why Apply:
• Work with cutting-edge instrumentation in a growing industry
• Join a team committed to product safety and innovation
• Competitive compensation and opportunity for growth
Company DescriptionOur Vision Our vision is to become the leading provider of qualified personnel in the industry, by delivering exceptional value to our clients through innovative recruiting solutions and outstanding customer service. Our Approach At Elite Group, we take a holistic approach to staffing and headhunting services, focusing not only on temporary, contract and direct placement, but also on employee engagement and development. We believe that a happy and engaged workforce is key to business success. Our Expertise Our team of HR professionals and recruiters have a diverse range of experience across various industries and sectors, allowing us to offer tailored solutions that meet the needs of any business. We specialize in areas such as Accounting and Finance, Administrative, Banking and Financial Services, Construction, Human Resources, Real Estate, Supply Chain, and Logistics. With the goal of providing our clients with the best in class personnel. 
<h3>Company Description</h3>
Our Vision\r\nOur vision is to become the leading provider of qualified personnel in the industry, by delivering exceptional value to our clients through innovative recruiting solutions and outstanding customer service.\r\n\r\nOur Approach\r\nAt Elite Group, we take a holistic approach to staffing and headhunting services, focusing not only on temporary, contract and direct placement, but also on employee engagement and development. We believe that a happy and engaged workforce is key to business success.\r\n\r\nOur Expertise\r\nOur team of HR professionals and recruiters have a diverse range of experience across various industries and sectors, allowing us to offer tailored solutions that meet the needs of any business. We specialize in areas such as Accounting and Finance, Administrative, Banking and Financial Services, Construction, Human Resources, Real Estate, Supply Chain, and Logistics. With the goal of providing our clients with the best in class personnel.

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionSenior Resident Project RepresentativePosition Overview
KEITH is hiring a Senior Resident Project Representative to act as the owner’s on-site representative for a $300M airport project at Fort Lauderdale-Hollywood International Airport (FLL). The RPR will be responsible for monitoring contractor performance, ensuring quality compliance, and representing the interests of the client throughout construction.
Key Responsibilities:
<ul>
<li>Serve as the day-to-day liaison between the construction team, design professionals, and the owner.</li>
<li>Observe all phases of construction including site preparation, structural, architectural, MEP, and finishes.</li>
<li>Ensure contractor compliance with approved drawings, specifications, codes, and regulatory standards.</li>
<li>Track progress against schedule and report deviations, risks, or issues.</li>
<li>Maintain accurate records including daily logs, photographs, and as-built documentation.</li>
<li>Facilitate resolution of field conflicts and RFIs in collaboration with designers and contractors.</li>
<li>Provide oversight for punch list development, commissioning, and project closeout.</li>
</ul>
Qualifications:
<ul>
<li>10+ years of relevant experience in building construction inspection and resident project representation.</li>
<li>Strong background on complex, multi-phase capital projects, preferably in aviation or public facilities.</li>
<li>Demonstrated expertise in construction observation, field coordination, and QA/QC practices.</li>
<li>Ability to manage multiple stakeholders and maintain professionalism in high-pressure environments.</li>
<li>Familiarity with FAA and airport authority standards a plus.</li>
<li>Excellent reporting, documentation, and problem-solving skills.</li>
</ul>
We offer competitive benefits, including:
<ul>
<li>100% PAID Medical, Dental, and Vision</li>
<li>Employer matched 401K - 100% Vested on Day 1 of contribution!!!</li>
<li>Paid Parental leave and Life Insurance</li>
<li>PTO, Holidays, and more!</li>
</ul>
 ...
Powered by JazzHR
uthjET2TDQ

Senior Resident Project Representative

<h3>Job Description</h3>
Job DescriptionDescription:
Job purpose
 
The Quality Control Microbiologist (QCM) is responsible for performing and managing quality control testing results for human tissue donors, recovered, and acquired tissue, and final processed grafts. Must perform applicable QC testing and related functions in accordance with standard operating procedures, all applicable federal and state regulatory and accrediting standards requirements. Communicates directly with contracted laboratories and internal departments to ensure testing results are available, accurate and communicated in a timely manner.
 
Duties and responsibilities
 
<ol>
<li>Perform Quality Control (QC) testing of tissue samples including, but not limited to, Cell Viability testing, bioburden of recovery cultures, sterility testing, in-process bioburden, method suitability, gram staining, biochemical testing, and microbial identification using VITEK 2.</li>
<li>Perform QC release testing of microbiology media, materials, and reagents. </li>
<li>Review test results and manage Biomaterial Tracking System (BTM) according to internal standard procedures to ensure proper management, tracking, and disposition of grafts. </li>
<li>Communicates directly with outside laboratories (if needed) to obtain records and internally with Operations and Quality Assurance to ensure appropriate samples are available for testing and results are properly communicated. </li>
<li>Maintain proper documentation and trend analysis of QC test results.</li>
<li>Support environmental monitoring (EM) of the facility by reading environmental monitoring plates, processing samples for identification, maintain records and trend analysis.</li>
<li>Support water system testing of the facility by testing for total organic carbon (TOC), bioburden, endotoxin, and conductivity. Reading plates and processing samples for identification.</li>
<li>Perform laboratory cleaning and maintenance of equipment as needed. </li>
<li>Support and execute qualification / validation protocols of QC testing methods as applicable.</li>
<li>Review testing reports, protocols, and procedures to ensure compliance with internal requirements and applicable regulations.</li>
<li>Assist Manager in maintaining the laboratory stock of media and reagents and ordering laboratory supplies.</li>
<li>Participate in the on-call weekend alternating schedule.</li>
</ol>
General Responsibilities
<ol>
<li>Create, review, and edit QC procedures according to AATB, FDA and USP guidelines.</li>
<li>Maintain knowledge of appropriate federal and state regulatory and statutory requirements as well as accrediting body requirements.</li>
<li>Responsible for reporting all variances, errors, and deviations to QA management.</li>
<li>Participate in the investigation complaints and deviations including the formulation and implementation of corrective actions.</li>
<li>Participate in audits and inspections, as needed.</li>
<li>Maintain trend analysis and metrics of testing results.</li>
<li>Support accreditation and licensing activities.</li>
<li>Perform other duties as assigned by the QC Manager and/or Director of Quality Control.</li>
</ol>
 
Requirements:
Qualifications
 
Education/Experience: Bachelor’s in Science, Microbiology degree preferred or Associate in Science with two years of experience. An equivalent combination of education and experience in a regulated environment (e.g., Biologics, Microbiology, Pharmaceutical, etc.) will be considered. 
 
Laboratory Skills: Aseptic techniques, bioburden, sterility, growth promotion, gram staining, microbial identification, and microbiology testing. 
 
Other Skills: Excellent interpersonal, verbal, and written communication skills required. 
Must demonstrate excellent organizational and record keeping skills. 
Must be detail oriented with the ability to multi-task in a high-pressure environment. 
Must gain knowledge of all regulations, laws, and/or standards that govern the tissue banking industry within the first year of employment. 
Computer and Equipment: Proficient in Microsoft Office. 
Working knowledge of Vitek® 2, Sievers M9 Laboratory TOC Analyzer, Conductivity Meter and Cell Analyzers. 
 
 
Working conditions
 
Primarily, a fast pace, lab-oriented work environment. Evening and weekend work may be required.
 
Physical requirements
 
While performing the duties of this job, the employee is regularly required to sit or stand for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds.
 
Direct Reports
No direct reports.

Quality Control Microbiologist

<h3>Job Description</h3>
Job Description
Pest Control Technician - Wildlife
Stark Exterminators is looking to hire a full-time Wildlife Technician to provide uncompromised service to Arrow's residential and commercial wildlife control customers through exclusion, trapping, and removal of wildlife. Exclusion includes sealing, caulking, or installation of sheet metal to soffits, gutter lines, roof ridges, vents, voids etc. This work is often done from rooftops or ladders and may require basic carpentry
Our technicians enjoy a company vehicle and other benefits including:
<ul>
<li>generous time off, </li>
<li>11 paid holidays, </li>
<li>401(k) with company match, Roth IRA, </li>
<li>medical, dental and vision insurance, </li>
<li>high deductible HSA, </li>
<li>telemedicine, </li>
<li>disability, cancer, and accident insurance. </li>
<li>health &amp; wellness suite </li>
<li>company-paid + additional, optional, life insurance. </li>
</ul>
 
ABOUT OUR FAMILY OF BRANDS 
Stark Exterminators is part of the Arrow Exterminators family of brands. We have been a family-owned and operated business since our start in 1964. Over the years, we have grown rapidly, and we now have the privilege of servicing 12 states. To ensure the quality and satisfaction of our customers, we have several offices in each state we are in to offer a more personalized approach to our communities. Ranked by revenue, Atlanta-based Arrow Exterminators is the sixth-largest pest and termite control company in the United States! We instill family values in the company culture to create a welcoming work environment and a successful company. We attribute our success to passionate, highly trained team members who are committed to protecting everyone's quality of life.
As Arrow grows and exceeds industry expectations, we are always looking for new talent to bring on board. We know our team has a lot of options and we are humbled that they choose to work with us. That's why we offer competitive compensation, a robust benefits package, and a family-oriented company culture.
A DAY IN THE LIFE OF A WILDLIFE TECHNICIAN
Your primary focus will be to identify, remove, prevent, or repair anything damaged by wildlife. Your first course of action will be to ask questions on the issue your customer is experiencing. Problem-solving will help you form an in-depth inspection of the customer's home to find the source of the issue. Your wealth of knowledge about wildlife will help you determine the best solution and explain to the customer your next steps. Upon the completion of your service, whether it be exclusion, trapping, or removal, you will be responsible for collecting payment due and proposing additional services that would benefit them. Your independence and accountability will help you as you run and schedule your own services. 
Minimum Qualifications:
<ul>
<li>Ability to pass and maintain any state regulatory agency-required licensing/certification exams</li>
<li>Able to pass internal technical exams</li>
<li>Possess a current Driver License's in the state where you work, the ability to operate a motor vehicle, and maintain a driving record consistent with company standards</li>
<li>High school diploma or equivalent</li>
<li>Able to work a 40-hour (minimum) workweek</li>
<li>Willing to work evenings and weekends as needed</li>
</ul>
 
ARE YOU READY TO JOIN OUR TEAM?
If you feel that you would be right for this position, please fill out our initial 3-minute, mobile-friendly application so that we can review your information. We look forward to meeting you! #StarkExterminators
We are an Equal Opportunity Employer
(The job description is not an exhaustive statement of all the duties, responsibilities, or qualifications of the job, nor is it intended to limit opportunities for necessary modifications).
Stark Exterminators as a PestVets Company is committed to hiring and participating in acts of service for Veterans and active-duty members of the U.S. Military.
 
Stark Exterminators is a Drug-Free Workplace and performs Pre-employment Drug Screens and Background Checks on all employees
 Job Posted by ApplicantPro

Pest Control Technician - Wildlife

<h3>Job Description</h3>
Job Description
Position: Contents Cleaning Technician 
Pay: $15.00 -$18.00/hr&nbsp;
Job Description:
Clean and deodorize a variety of household items in a warehouse setting. &nbsp;Wrap furniture and manipulate in/out of storage during the cleaning process. &nbsp;Pack clean items into boxes. Assist with general warehouse cleaning as needed. 
Limpia un variedad de productos de casas en un marco de almacen. Envuevle muebles y traerlos a/desde almacinamiento durante el proceso de limpiar. &nbsp;Empacan cosas limpias en cajas. Ayuda a limpiar el almacen cuando es necesario. 
Requirements:
-Able to pass a drug screen
-Able to lift 50lbs
-Comfortable working with a variety of chemicals/cleaning products 
-No felony convictions 
-Puede pasar un analisis de drogas
-Puede levantar 50 libras
-Esta comodo a tabajar con un variedad de quimicos/productas limpieazas
-No codenas de crimen
Special consideration for candidates who are English/Spanish bilingual.
Consideracion especial para personas bilinguales ingles/espanol

Contents Cleaning Technician

<h3>Job Description</h3>
Job Description
We are a fast-growing medical device company developing advanced Software as a Medical Device (SaMD) solutions for interventional cardiology and structural heart procedures. Our flagship technology integrates real-time fluoroscopy with pre-procedure 3D CT annotations to provide precise intra-procedural guidance, enhancing safety and clinical outcomes.
Our innovation combines CT preprocessing, fluoroscopy preprocessing, AI-driven detection and tracking, anatomical landmark detection, and personalized DRR-based network training with cutting-edge registration protocols. We operate with a small, highly skilled in-house engineering team, supplemented by specialized contractors across several continents.
Summary: We are seeking a dynamic Director of Technology, Research &amp; Development to lead a team of engineers in our start-up medical device company. This role involves overseeing the R&amp;D pipeline, ensuring alignment with regulatory and market demands, and spearheading the development of groundbreaking technologies that enhance our company's growth and competitive advantage. The position is fully remote and reports directly to the Founder.
Stand out candidates should have experience in one or more of the following:
<ol>
<li>Heart CT imaging</li>
<li>Heart real time fluoroscopy.</li>
<li>Registration of the two modalities</li>
<li>Working with AI for segmentation and detection</li>
<li>Understanding 3D to 2D geometrical consideration</li>
</ol>
Responsibilities
1. Strategic Leadership:
<ul>
<li>
<ul>
<li>Lead and manage a remote team of freelancers and employees in the R&amp;D department.</li>
<li>Oversee the research and development pipeline, ensuring alignment with business goals and market needs.</li>
<li>Drive innovation in medical device technologies to maintain competitive advantage.</li>
<li>Collaborate closely with executive leadership, including product development, regulatory, and commercial teams, to ensure alignment across departments.</li>
<li>Ensure compliance with regulatory standards and guidelines.</li>
<li>Report regularly to the Founder on R&amp;D progress, challenges, and opportunities.</li>
</ul>
</li>
</ul>
2. Research and Development Oversight:
<ul>
<li>Oversee all stages of product research and early development, from ideation through feasibility and prototyping.</li>
<li>Manage the development of the user interface for procedural workflow integration.</li>
<li>Drive efficient design, testing, and validation of new devices in compliance with industry standards and regulations (e.g., FDA, ISO 13485)</li>
<li>Oversee data storage and management systems, ensuring compliance with healthcare data security regulations (e.g., HIPAA, GDPR).</li>
<li>Coordinate data engineering tasks, including structured pipelines for AI training datasets.</li>
</ul>
3. Technology Innovation and Advancement:
<ul>
<li>Develop and optimizeAI-based detection and tracking algorithms, ensuring robustness in procedural conditions.</li>
<li>Promote a culture of innovation and scientific excellence within the organization.</li>
<li>Partner with external stakeholders (clinical sites) for collaborative innovation and research.</li>
</ul>
4. Regulatory and Quality Collaboration:
<ul>
<li>Ensure all research activities align with medical device regulations and quality system requirements.</li>
<li>Support regulatory strategy development by providing technical and scientific input.</li>
</ul>
5. Talent and Organizational Development:
<ul>
<li>Recruit, develop, and retain top engineers and technical talent.</li>
<li>Foster team collaboration, mentoring, and continuous professional development.</li>
</ul>
Ideal Candidate Profile:
<ul>
<li>Advanced degree (Ph.D. or Master's) in engineering, biomedical sciences, or a related field.</li>
<li>10+ years of leadership experience in R&amp;D within the medical device or life sciences industry.</li>
<li>Demonstrated success in bringing medical devices from concept through commercialization.</li>
<li>Background in software development, image registration and AI</li>
<li>Strong understanding of FDA regulations, ISO standards, and global medical device requirements.</li>
<li>Visionary leader with excellent communication, strategic thinking, and stakeholder management skills.</li>
<li>Ability to work and manage in a remote environment.</li>
</ul>
We are currently expanding our team. As a start-up, we are fast paced and have a shared goal to succeed in developing unmet healthcare needs in the most efficient way. If you share this vision and are interested in joining us - please apply. We look forward to hearing from you.

Director of Technology, Research and Development

<h3>Job Description</h3>
Job DescriptionJob Title: Associate Scientist I/II – Pharmaceutical R&amp;D Location: Weston, FL (Greater Ft. Lauderdale Area) Department: CMC – Research &amp; Development Job Type: Full-Time | On-site Job Summary A growing pharmaceutical organization is seeking a motivated Associate Scientist I or II to join its R&amp;D team. This hands-on role involves supporting laboratory operations, performing analytical testing, and assisting in the development and manufacturing of inhalation drug products. Key Responsibilities Perform lab testing of raw materials, intermediates, and finished products to assess quality, identity, strength, and purity. Operate lab instruments such as HPLC, UPLC, UV-Vis, and FTIR; process and analyze resulting data. Support formulation and production of inhaled pharmaceutical products. Prepare reagents and solutions; document results in lab notebooks and reports. Execute equipment calibrations, qualifications, and approved method transfers. Comply with all cGMP, FDA, EH&amp;S, and internal SOPs. Collaborate with project teams to meet timelines and deliverables. Participate in training and mentoring of junior team members as needed. Qualifications Bachelor’s degree (BSc) in Chemistry, Pharmacy, or related field with 2–3 years of pharmaceutical R&amp;D experience — OR — Master’s degree (MSc) with 1–2 years of experience Hands-on experience with analytical instrumentation (e.g., HPLC, UPLC, FTIR) Understanding of FDA regulations and GMP compliance Strong documentation and communication skills Able to work both independently and as part of a team Preferred Skills Experience working with inhalation products Familiarity with method development, sample prep, or blend uniformity testing Experience in training or mentoring lab staff What’s Offered Exposure to cutting-edge pharmaceutical R&amp;D A collaborative and growth-oriented team environment Opportunities for technical and professional advancement

600 Science Jobs