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<h3>Job Description</h3>
We are a group of people united by a strong purpose.
 
We want you to get to know us, and Giuseppe, our very own artificial intelligence.
We love good food, but above all, we love the planet, and that's why, to protect it, we reinvent the food industry, one delicious bite at a time, elevating what we eat, through our technology and based on plants.
 
Our recipe has three mega-important components: science, technology, and of course, disruptive talents who work daily to create a better future.
At NotCo we are not and do not seek to be the perfect company, but rather the right one. We are here to produce changes, and that is why we dare, fail, and sometimes achieve incredible successes.
 
We are currently looking for a Product Development Scientist for our NotCo B2B Research &amp; Development located in San Francisco, California, requiring an active on-site presence. This position will report to our R&amp;D Sr. Team Lead and the incumbent will work cross-functionally to ensure R&amp;D activities are successfully deployed locally. 
 
Responsible for the:
<ul>
<li>Independently conducts day-to-day product development activities as directed by the manager across multiple projects. This includes supporting activities related to the full product lifecycle process (from product concept to successful commercial launch as needed)and supporting process development, scale-up and technology transfer</li>
<li>Supports the design and execution of bench-top tests, pilot-plant trials and full-scale formulations to deliver high-quality food products that meet and exceed the sensory, cost, and other performance targets </li>
<li>Proactively proposes and uses sensory and analytical analysis to guide and validate the development process</li>
<li>Maintains detailed documentation, experiment tracking and outcomes, and documents finished goods and ingredient specifications</li>
<li>Provides feedback to project lead regarding relevant technical and process information</li>
<li>Communicates proactively and effectively with cross-functional teams, clearly articulating perspectives and trade-offs related to new product development goals</li>
<li>Utilizes NotCo’s proprietary AI technology to develop and improve food products</li>
<li>Supports formula validation activities as well as process development, scale-up and technology transfer</li>
<li>Engages in client communications and workshops, bringing technical </li>
<li>Maintains detailed documentation across all R&amp;D activities in a timely manner</li>
</ul>
 
 
Qualifications / Requirements: 
<ul>
<li>Bachelor’s degree in Food Engineering, Food Science, Engineering in Biotechnology or a similar discipline.</li>
<li>2 + years of Food R&amp;D experience is desired, preferably across both food and beverage categories.</li>
<li>Be agile, adaptable, and thrive in a dynamic and changing culture; works relentlessly to overachieve, anticipate obstacles, and create plans to overcome them.</li>
<li>Adapts easily to changing priorities and direction based on new project learnings and team priorities.</li>
<li>Demonstrated competency to effectively communicate (oral &amp; written) cross-functionally with solid collaboration skills.</li>
<li>Comfortable in client-facing situations and able to communicate complex topics clearly and simply.</li>
<li>Excel in a startup environment, is excited to create new procedures and processes from scratch and has a strong entrepreneurial mindset.</li>
<li>Be a problem solver, have a general manager mindset, and take the initiative to get the job done</li>
<li>Possess strong planning, project management, and execution skills, and the ability to articulate where and how you have used them.</li>
<li>Rigorous data-driven/analytical capability and ability and presence to present data effectively to a leadership team</li>
<li>Work well in teams and cross-functional groups in a matrixed environment, both regionally and globally</li>
<li>Possesses strong computer skills, including a high level of proficiency in MS Office, specifically Excel</li>
<li>Authorization to work in the U.S. is required</li>
<li>Ability to travel up to 50% of the time, including international travel and extended trips.</li>
</ul>
 
 
NotCo is committed to fair and equitable compensation practices. The pay range for this role is $65,000 - $75,000. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor.
 
 
We are an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Product Development Scientist

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

Analytical Services Chemist III

<h3>Job Description</h3>
The Plant Chemical Engineer is responsible for supporting chemical-related functions in the production of insulated metal panels. The Chemical Plant Engineer is also involved in process improvements, along with managing the laboratory functions. This position also requires the chemical engineer to manage projects on an independent basis.

Essential Functions 
<ul>
<li>The role includes but is not limited to the following responsibilities:</li>
<li>Responsible for chemical process, equipment, day-to-day production, quality issues and process optimization.</li>
<li>Ensures quality assurance testing is performed on incoming raw materials and finished products.</li>
<li>Maintains organized, detailed records of material testing of results for auditing purposes, for both internal and external bodies.</li>
<li>Maintains strict chemical stock control, including writing and enforcing stocking policies that are in in line with company requirements which also includes FIFO on material usage and forecasting models.</li>
<li>Implements, maintains, reviews and administers standard operating procedures for chemical areas, including generating new procedures for the laboratory and laydown production areas.</li>
<li>Implements, maintains and reviews laboratory and operator training while maintaining a detailed training matrix, including records of the training along with sign-offs.</li>
<li>Ensures follow-up and refresher training takes place as required.</li>
<li>Ensures chemical areas are in compliance with chemical safety and environmental responsibilities, along with relevant risk assessments.</li>
<li>Assists in new product development efforts and product/material testing.</li>
<li>Provides support to manufacturing and operations with process/product improvement projects.</li>
<li>Attends regular meetings within the department.</li>
<li>Provides day-to-day troubleshooting and technical assistance to the site local operations team.</li>
<li>Develops, monitors, and effectively uses control charts and operational indicators, such as SPC, set-up sheets and check sheets.</li>
<li>Prepares oral and written technical and progress reports regarding KPIs.</li>
<li>Submits all required/requested reports to the Divisional Chemical Engineering Manager in a timely manner.</li>
<li>Reports to the Divisional Engineer on the analysis of process parameters, process capability and tests relating to the manufacture of a quality product.</li>
<li>Participate in formulating quality/performance standards or product/processes.</li>
<li>Conducts audits of laboratory and laydown areas to drive housekeeping, record keeping and continual process improvements.</li>
<li>Maintains a calibration program of tank farm, lab and laydown equipment.</li>
<li>Ensures site-wide compliance with all city, state and federal permit regulations regarding chemicals.</li>
<li>Manage Lab Technician to ensure all duties and responsibilities are followed according to established procedures.</li>
<li>Perform other work-related duties as assigned by the Divisional Chemical Engineering Manager.</li>
</ul>
 
Knowledge, Skills, and Abilities 
<ul>
<li>Interpersonal skills; strong verbal and written communication skills</li>
<li>Problem-solving skills</li>
<li>Decision-making skills</li>
<li>Analytical skills</li>
<li>Creative thinking</li>
<li>Attention to detail</li>
</ul>
 
Education and Experience 
<ul>
<li>Minimum of a bachelor’s degree in chemical engineering or a related field or the equivalent combination of education and significant prior relevant professional experience and demonstrated ability to perform independent work.</li>
<li>Minimum 3 years of industrial experience.</li>
<li>Significant experience working with multidisciplinary teams in achieving complex project objectives; demonstrated strength in partnering with outside organizations successfully.</li>
<li>Significant experience working effectively under deadlines, reasoning effectively under broadly defined objectives and limited information, coordinating workload on multiple complex projects simultaneously, and meeting deadlines with conflicting priorities.</li>
<li>Experience working across organizational work units, utilizing effective teamwork and customer service skills.</li>
<li>Advanced verbal and written communication and interpersonal skills necessary to effectively collaborate in a team environment, author complex technical analyses, and present technical information to external sponsors and customers.</li>
<li>Must have strong technical and engineering aptitude.</li>
<li>Willingness to learn.</li>
</ul>
 
Physical Requirements 
<ul>
<li>Ability to interact effectively with employees and other individuals.</li>
<li>Ability to function effectively with moderate to high levels of stress in a demanding and dynamic environment.</li>
<li>Able to wear prescribed personal protective equipment and appropriate clothing.</li>
<li>Lift up to 50 lbs.</li>
<li>Effectively read, write, speak, and communicate in English fluently.</li>
<li>Ability to sit and stand for extended periods of time. Ability to walk, bend, climb, crouch, lean, reach, and other physical movements as required to effectively and efficiently perform duties.</li>
<li>Work in conditions typical of a manufacturing environment, including noise, extreme temperatures and humidity, odors, dust, etc.</li>
<li>Effectively use a computer, monitor, keyboard, mouse, as well as commonly used equipment and software to complete necessary functions.</li>
<li>Finger dexterity, visual acuity, discernment of sounds, color, and texture.</li>
<li>Must be able to use tools, equipment, machinery, etc.</li>
<li>Must be reliable and dependable.</li>
<li>Must have the physical and mental ability to drive a standard forklift successfully. AWIP will certify.</li>
<li>Must have omnidirectional spatial awareness necessary to operate CombiLift forklift.</li>
<li>Ability to travel by automobile, airplane, and other modes of economy-class public transportation are required.</li>
</ul>

Working Environment 
While performing the duties of this job, the employee is regularly exposed to work near moving mechanical parts, dusty conditions, high noise environments, chemicals used in the process, and extreme temperatures. The facility is an industrial manufacturing plant.
This position is designated safety sensitive.
 
AWIP is committed to providing equal opportunity for employees and applicants in all aspects of the employment relationship, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, veteran status, disability, age, religion or any other classification protected by law. In that regard, U.S. applicants and employees are protected from discrimination based on certain categories protected by Federal and State law, as applicable.

Chemical Engineer

<h3>Job Description</h3>
Design a career and build your future... Because it matters!
 
GIS Specialist 
McMillen Inc. is looking for a GIS Specialist with 10+ years of professional experience to lead geospatial workflows for hydropower, watershed, and environmental projects. This position offers the opportunity to apply advanced GIS and data management skills across disciplines including hydrology, geomorphology, and ecology. The successful candidate will oversee spatial data integration, analysis, and visualization to support complex modeling, regulatory, and design projects. This role requires a balance of technical expertise, project management ability, and a passion for transforming geospatial data into actionable insights that inform sustainable water-resource and infrastructure solutions.
 
Responsibilities:
<ul>
<li> Lead GIS workflows supporting hydropower relicensing, dam removal, watershed modeling, hydraulic analysis, and environmental compliance projects.</li>
<li> Manage, process, and QA/QC large spatial datasets (LiDAR, topobathymetric surveys, DEMs, orthophotos, UAV-SfM) for use across engineering, geomorphic, and ecological disciplines.</li>
<li> Build geodatabases and automated geoprocessing workflows (ModelBuilder, Python, SQL) to ensure efficient, reproducible analyses and defensible regulatory documentation (FERC, NEPA/CEQA, ESA).</li>
<li> Conduct hydrologic and terrain analyses—watershed delineation, change detection, floodplain mapping, sediment characterization, and habitat suitability modeling.</li>
<li> Prepare and translate inputs and outputs for 1D/2D hydraulic, sediment transport, and habitat models, ensuring spatial consistency and model-ready datasets.</li>
<li> Develop basemaps, dashboards, and story maps to communicate modeling results and monitoring data to clients, regulators, tribes, and the public.</li>
<li> Produce high-quality cartographic and visualization products for technical reports, permitting, and stakeholder engagement.</li>
<li> Maintain metadata, QA/QC, and data management standards to support transparency, repeatability, and defensible technical deliverables.</li>
<li> Collaborate closely with engineers, geomorphologists, hydrologists, and biologists to integrate GIS analyses into design, modeling, and decision-making.</li>
<li> Mentor junior staff in geospatial methods, database management, and quality assurance practices.</li>
<li> Serve as GIS lead in proposal development, project planning, and data-management strategy for multi-disciplinary teams.</li>
</ul>
 
Qualifications:
<ul>
<li> Minimum of 10 years of experience applying GIS and spatial analysis in support of engineering, hydrology, or environmental science projects.</li>
<li> Bachelor’s degree in Geography, GIS, Environmental Science, or related field required; Master’s degree or graduate GIS certificate preferred.</li>
<li> Advanced proficiency in ArcGIS Pro or QGIS for terrain analysis, cartography, and spatial data management.</li>
<li> Proven ability to manage, process, and QA/QC large geospatial datasets (LiDAR, DEMs, topobathymetric surveys, orthophotos, UAV-SfM).</li>
<li> Strong understanding of hydrologic, geomorphic, and environmental datasets, and their application in watershed, habitat, and infrastructure studies.</li>
<li> Demonstrated experience building and maintaining geodatabases and automated workflows using ModelBuilder, Python, or SQL.</li>
<li> Familiarity with 1D/2D hydraulic, sediment transport, or habitat modeling and preparation of model-ready spatial inputs and outputs.</li>
<li> Skilled in developing high-quality cartographic and visualization products for technical reports, permitting, and stakeholder communication.</li>
<li> Excellent data management, documentation, and metadata practices ensuring transparency and reproducibility.</li>
<li> Experience mentoring junior GIS staff and contributing to proposal development and project planning.</li>
<li> Strong written and verbal communication skills, with the ability to collaborate across disciplines and convey technical concepts to varied audiences.</li>
</ul>
 
Compensation Package:
<ul>
<li>Pay Range: $47 hr. – $76 hr. (DOE) </li>
<li>Benefits: McMillen provides a full Benefits Program consisting of Medical, Dental, Vision, Life, Disability, FSA, EAP, 401(k) and match, 9 Paid Holidays, generous PTO, opportunity for Stock Ownership and Wellness Reimbursement.</li>
</ul>
 
Company Bio: McMillen, Inc. designs and builds solutions that shape the future of water resources. As an employee-owned firm, we take pride in every project because we know our work truly matters. Our people thrive on solving complex challenges, pushing boundaries, and refining their craft. We don’t look for the complacent or the comfortable. We seek problem solvers, innovators, and experts who are always striving to be better. We support continuous learning, cutting-edge technology, and a balanced work-life environment so our employees can build careers they’re proud of.
We are focused in the dams, energy, fisheries, natural resources, and infrastructure markets. With staff across the United States, Canada, Europe, and beyond, we bring global best practices to our clients. Our people integrate engineering, environmental, and construction expertise to deliver practical, results-driven outcomes. From concept to completion, projects are guided through feasibility studies, permitting, design, construction, and commissioning, ensuring technical precision and real-world functionality.
 
EEO: McMillen, Inc. is an EEO/Affirmative Action Employer and will make all employment related decisions without race, color, religion, sex, national origin, disability or protected veteran status.
Visa sponsorship, including renewal during employment, will not be provided for this position.
 
No recruiters, please.

GIS Specialist

<h3>Job Description</h3>
Direct Hire Fulltime position for a Sr. Scientist (cosmetics/personal care products exp.) in Carrollton, TX
 
Position Summary:
<ul>
<li>The Research Innovation and Development Scientist III will be a strong contributor to development activities and serve as a developer of formulation products applied in different delivery systems for various markets. </li>
<li>This position will formulate a wide range of personal care products incorporating the company’s cosmetics raw materials. </li>
<li>The RID Scientist Ill will need to be experienced with experimentation on the bench with conventional and/or non-conventional/creative approaches with new formula bases, raw ingredients and processing techniques that will lead to unique product claims and benefits.</li>
</ul>
 
Essential Duties and Responsibilities: 
<ul>
<li>Create expert level formulations of a variety of personal care products, cosmetics, medical devices and OTC from concept to finished product.</li>
<li>Prepare complete finished product formulations independently from project charters by understanding the requirements and the complete development process including scale up.</li>
<li>Determine and perform design of experiment to evaluate new and/or alternate raw materials through bench trial.</li>
<li>Develop new formulas using existing and new technologies in the personal care medical devices and OTC product area to support company-wide growth and future brand strategies.</li>
<li>Ensure that formulas meet expected performance, safety and regulatory requirements so that they can be produced in manufacturing.</li>
<li>Create innovative formulations in a capable affective manner to answer trends in market and meet project requirements.</li>
<li>Develop new formulas using existing and new technologies in the personal care medical devices and OTC product area to support company-wide growth and future brand strategies.</li>
<li>Ensure that formulas meet expected performance, safety and regulatory requirements so that they can be produced in manufacturing.</li>
<li>Conduct stability testing to ensure formula and/or formula/package robustness. Prepare laboratory batches for studies and evaluations.</li>
<li>Develop specifications for new and/or reformulated products, ensuring product quality.</li>
<li>Serve as Lab Applications representative on cross-functional teams.</li>
<li>Remain up to date and current on trends in the retail market and trends on formulations materials, ingredients, cost, etc.</li>
<li>Customer support and interaction on a regular basis and problem solving.</li>
</ul>
 
Essential Skills and Qualifications:
<ul>
<li>Bachelor's degree in chemistry, engineering, or other technical degree</li>
<li>8-12 years of experience in cosmetics/personal care product formulation.</li>
<li>Minimum 10 years of combined experience in topical formulations, R&amp;D, innovation, ingredient interaction chemistry, and supporting scale-up/manufacturing.</li>
<li>Extensive knowledge of skin care formulation chemistry and understanding of skin care, OTC drugs, personal care products, and medical devices (experience with regulated products preferred).</li>
<li>Expertise in developing stable, aesthetically pleasing formulations and adhering to CGMPs, safety guidelines, and GLP documentation standards.</li>
<li>Working knowledge of FDA regulations.</li>
<li>Strong analytical, problem-solving, and project management skills.</li>
<li>Excellent communication, interpersonal, and presentation skills.</li>
<li>Independent worker with strong organizational skills and a proactive, results-oriented approach.</li>
<li>Ability to manage multiple projects efficiently and deliver high-quality formulations.</li>
<li>Thrives in a fast-paced environment, readily adapts to change, and possesses strong intellectual curiosity for continuous improvement.</li>
<li>Ability to perform under pressure on projects with tight deadlines.</li>
<li>Proficiency in MS Office Suite with a willingness to learn new software applications.</li>
</ul>

Sr. Scientist (with cosmetics/personal care products exp.)

<h3>Job Description</h3>
THE COMPANY:
Formulated Solutions is redefining the Pharmaceutical and Self-Directed Consumer Healthcare CDMO experience through creativity and invention; delivering our world class Marketing Partners unmatched formulations, innovative packaging and cost effective, reliable supply.
Formulated Solutions is and shall always be a company of people with the knowledge and dedication to provide our Marketing Partners with a single source solution for delivering quality and innovative products to market. We shall embrace changes and new opportunities as a vehicle to continually develop and grow sustainable relationships. As a company we shall never accept anything less than a culture that fosters creativity, growth, and profitability for both our Partners and the company.
 
PRIMARY PURPOSE:
The Analytical Laboratory Supervisor is responsible for overseeing daily operations, staff, and projects to ensure compliance and efficiency. Key responsibilities include supervising and training lab personnel, ensuring quality control and regulatory adherence, managing workflow and scheduling, and handling administrative duties and budgets. The role requires a strong background in chemistry, often with experience in analytical techniques and specific pharmaceutical industry practices.
 
MAJOR DUTIES AND RESPONSIBILITIES:
<ul>
<li>Routinely reviews and releases environmental testing, raw materials, in-process/bulk/intermediate, finished product, stability, and method validation/transfers.</li>
<li>Creates COAs for finished goods batches.</li>
<li>Oversee daily operation of QC Laboratory.</li>
<li>Occasionally performs testing, and accurately records raw data, analyzes data, and calculates and interprets the results.</li>
<li>Order supplies ensuring that the laboratory is adequately supplied.</li>
<li>Manage the reference standards/materials program.</li>
<li>Plan daily technical activities in order to meet established timelines. Provide input to establish project timelines.</li>
<li>Qualify, calibrate, and maintain laboratory equipment, including review of activities and data.</li>
<li>Support general laboratory maintenance.</li>
<li>Support site and Technical Operations validation and assessment activities such as reviewing and approving protocols and reports.</li>
<li>Write, review, and revise SOPs as required.</li>
<li>Ensure testing is performed accurately and in compliance with GLP, GMP, USP, SOP and other approved test methods</li>
<li>Proactively investigate and identify areas of improvement.</li>
<li>Investigate, support, validate and implement new laboratory procedures and techniques.</li>
<li>Provide monthly lab metrics to management.</li>
<li>Maintain a level of technical knowledge and understanding of Analytical testing consistent with current scientific literature.</li>
<li>Perform scientific literature searches and evaluations as needed.</li>
<li>Design, within a defined scope, experiments or a series of experiments to address specific project goals.</li>
<li>Train laboratory personnel in lab techniques as required.</li>
<li>Responsible for Cleaning Validation and Method Validation activities.</li>
<li>Follow cGMP, cGLP and OSHA guidelines with regards to work practices and safety.</li>
<li>Other duties which may be assigned sometimes by site management.</li>
</ul>
 
JOB REQUIREMENTS:
<ul>
<li>A minimum of a BS in Chemistry or related field</li>
<li>Minimum of 5 years’ experience preferably in the pharmaceutical industry</li>
<li>Capable of preparing cGMP and other laboratory documents</li>
<li>Excellent knowledge of computer systems and software</li>
<li>Good knowledge of cGMP and FDA regulations</li>
<li>Excellent interpersonal, organizational, communication skills</li>
</ul>
 
WORK ENVIRONMENT:
<ul>
<li>GMP Manufacturing and Laboratory Environment</li>
<li>May be exposed to laboratory chemicals and solvents</li>
</ul>

Laboratory Supervisor

<h3>Job Description</h3>
The R&amp;D Scientist II plays a key role in advancing innovative medical devices based on regenerative technologies. This position combines hands-on laboratory research with product development responsibilities, including experimental design, material characterization, prototype development, and compliance with design control requirements. The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing. This role bridges early discovery and applied development, requiring both strong scientific skills and practical problem-solving.
Key Responsibilities
<ul>
<li>Plan, execute, and analyze laboratory experiments involving biomaterials, regenerative matrices, and medical device components. </li>
<li>Contribute innovative ideas for new products, testing methods, or process improvements to enhance R&amp;D capabilities. </li>
<li>Develop, build, and refine prototypes to meet defined specifications and clinical needs. </li>
<li>Generate accurate technical documentation, reports, and protocols in compliance with FDA, ISO, and Design Control requirements. </li>
<li>Characterize materials and prototypes using analytical, biochemical, and mechanical testing methods. </li>
<li>Perform risk assessments, troubleshoot technical issues, and propose solutions to improve product performance or process robustness. </li>
<li>Support technology transfer from R&amp;D to manufacturing, including process documentation, validation support, and training of personnel. </li>
<li>Collaborate with cross-functional teams (Manufacturing, Quality, Regulatory, Marketing, and Clinical) to align product development with business and clinical requirements. </li>
<li>Engage with external consultants, and customers to gather feedback and translate needs into product features.</li>
<li>Mentor and provide technical guidance to junior staff on laboratory practices, data analysis, and project tasks.</li>
<li>Present findings and project updates to management, peers, and cross-functional stakeholders. </li>
<li>Maintain laboratory operations, including equipment calibration, safety compliance, and method updates. </li>
</ul>
 
Qualifications
<ul>
<li>MS with 1–2 years or BS with 3–5 years in Biomedical Science, Materials Science, Chemistry, or related field.</li>
<li>Experience in medical device research and development, biomaterials, or regenerative technologies preferred. </li>
<li>Knowledge of laboratory techniques for material characterization, tissue-derived biomaterials, or device testing.</li>
<li>Familiarity with Design Controls, GLP/GMP, and ISO standards. </li>
<li>Proficiency with experimental design, data/statistical analysis, and technical problem-solving. </li>
<li>Experience with CAD, prototyping tools, or modeling software is a plus. </li>
<li>Strong organizational skills with the ability to manage multiple studies and projects simultaneously. </li>
<li>Excellent communications and presentation skills for cross-functional collaboration. </li>
</ul>
Demonstrated ability to work independently, manage multiple priorities, and deliver high-quality results.

Research And Development Scientist

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

Quality Control Chemist III / Lab Lead

<h3>Job Description</h3>
Essential Job Duties:&nbsp;
<ul>
<li>Responsible for accurate measurement, sampling, operations, and custody transfer of various crude oil types being gathered and transported; following measurement manual procedures and guidelines.</li>
<li>Responsible to reconcile system/segment line balance, batch changes, and system utilization and quality control.</li>
<li>Performs (L) ACT and tank inspections with associated documentation.&nbsp;</li>
<li>Responsible for measurement security at field locations and stations within area of responsibility.</li>
<li>Responsible for monitoring SCADA/HMI interface, generating tickets (internally/externally)</li>
<li>Read and understand station flow diagrams, gate maps, and pipeline drawings.</li>
<li>Perform duties with “One-Call” pipeline response system as needed, to include identifying/locating company pipelines/assets by probing, mapping, and/or flagging methods.</li>
<li>Responsible for launching/receiving scrapers/pigs, valve inspections, and ROW maintenance including line marker replacement.&nbsp;&nbsp;</li>
<li>Position requires manual dexterity and visual acuity, ability to lift 50 lbs., and work outside in all weather conditions, and extended hours.</li>
<li>Other duties as required </li>
</ul>
Education and Ability
<ul>
<li>High School Diploma or GED.</li>
<li>Strong computer skills (Microsoft Suites, STAR)</li>
<li>Strong interpersonal and communication (verbal and written) skills.</li>
<li>Valid driver’s license and clean driving record.</li>
<li>Self-motivated and able to work with little supervision.</li>
</ul>
Experience
<ul>
<li>2 years of oilfield pipeline/station measurement experience.</li>
<li>Preferred experience with (L) ACT meter operations and station equipment, and meters calibration.</li>
<li>Preferred experience with crude oil analyzing equipment.</li>
<li>Preferred experience with flow computers, Coriolis Meters, and displacement meters.</li>
</ul>
 
Physical Demands
<ul>
<li>Position requires manual dexterity and visual acuity, ability to lift 50 lbs., and work outside in all weather conditions, and extended hours.</li>
<li>Must be able to climb large storage tank stairs, with measurement equipment, and work at elevated heights.&nbsp;</li>
</ul>

Measurement Technician

<h3>Job Description</h3>
About Us
At One Physics, our mission is to transform the health and safety of our communities by providing comprehensive medical physics and radiation safety solutions to our clients. Our organization is comprised of leading technical and diagnostic professionals in the medical physics field, coupled with a best-in-class business and client services support team behind the scenes. We share a passion for excellence, dedication to client and patient care, and a commitment to industry leadership.
 
The Role
We are searching for a highly skilled Chief Therapy Medical Physicist to join our dedicated team of experts. Our candidates must be well-trained in Radiation Oncology and be able to work in a collaborative team environment.
 
Clinic Information:
<ul>
<li>This position is located in Norfolk, VA market and will be also supporting surrounding areas.</li>
<li>This clinics you will support have both Varian and Elekta equipment.</li>
<li>Treatment planning systems include Mosaiq, Monaco, Aria &amp; Eclipse.</li>
<li>This role will lead a great team of several physicists, dosimetrist (onsite and remote), and physicians.</li>
</ul>
 
What You’ll Do
<ul>
<li>Perform weekly and monthly radiation measurements, as well as yearly calibration on all treatment units.</li>
<li>Monitor equipment in the Radiation Oncology Department to ensure that it is functioning correctly and safely.</li>
<li>Maintain regulatory agency records and reports.</li>
<li>Analyze alternative treatment plans and supervise dosimetry treatment planning functions.</li>
<li>Implement assessment/treatment and care based on the developmental stages of the patient.</li>
<li>Perform additional duties, as needed.</li>
</ul>
 
What You’ll Need
<ul>
<li>Master’s Degree and/or PhD in Medical Physics.</li>
<li>A board certification by the American Board of Radiology in Therapeutic Medical Physics, or board eligibility as demonstrated by graduation from a CAMPEP accredited residency in therapy physics.</li>
<li>7+ years of clinical Therapy Medical Physics experience preferred.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to interpret regulations.</li>
<li>A willingness to go “above and beyond” for clients and fellow colleagues.</li>
<li>Demonstrate initiative, organization, and ownership of daily tasks and projects.</li>
<li>Ability to problem solve by seeking, developing, and implementing viable solutions.</li>
</ul>
 
Physical Requirements
<ul>
<li>Requires ability to use and move equipment.</li>
<li>Requires a variety of physical activities including sitting, standing, walking, stopping, lifting, carrying.</li>
<li>Exposure to radiation, communicable diseases, and other conditions common to radiation therapy setting.</li>
<li>Occasional evening or weekend work.</li>
</ul>
 
Benefits 
<ul>
<li>Competitive compensation.</li>
<li>PTO plan with paid company holidays.</li>
<li>Health Insurance (Medical, Dental, Vision and Prescription).</li>
<li>401(k) Plan with company match after 1 year of employment.</li>
<li>Group Life &amp; Voluntary Life Insurance.</li>
<li>Short Term &amp; Long Term Disability.</li>
<li>Flexible Spending Account (FSA).</li>
<li>Health Spending Account (HSA).</li>
</ul>
 
Final offer amounts are determined by multiple factors, including geographic location, as well as candidate experience, education level and expertise. If you have questions on compensation, please ask your recruiter. Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.
 
We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class.

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