Associate scientist jobs in Winston-Salem, NC

ProKidney is seeking an experienced Research Associate for our Cell Therapy Process Development team. The ideal candidate will have a strong background in cell therapy or biopharmaceutical development, process optimization, and technology transfer. In this role, you will lead or support the development and improvement of cell therapy manufacturing processes, contributing to the advancement of cutting-edge therapies. This is a great opportunity for individuals who are passionate about making an impact in the evolving field of cell therapy. Responsibilities: * Design and execution of experiments to optimize and improve processes for cell therapy manufacturing, including but not limited to media preparation, cell expansion and harvest, and product formulation. Analyze experimental data and present results in a clear and actionable manner to stakeholders. * Provide technical expertise in the development and implementation of new techniques and technologies. Support troubleshooting and process improvement initiatives. * Work closely with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing, to ensure the successful transfer of process into GMP clinical and commercial manufacturing. * Support the characterization and validation of cell therapy processes, ensuring compliance with regulatory guidelines and internal standards. Conduct process performance qualification (PPQ) studies and support clinical trial material production. * Ensure that all process development activities adhere to GMP and applicable regulatory standards. Support regulatory filings and audits as needed. * Preparation and review of technical documentation, including process development reports, batch records, SOPs (Standard Operating Procedures), and change controls. * Assist to identify potential risks in process development and manufacturing and implement strategies for mitigation, ensuring the successful advancement of cell therapy programs. Qualifications: * Bachelor's or Master's degree in Cell Biology, Biotechnology, Biochemical Engineering, or a related field. * 2 plus years of experience in cell therapy and /or biopharmaceutical process development. Ability in execution and troubleshooting experiments, analyzing/ reporting/presenting data. Experience in aseptic techniques is essential. * Demonstrated ability to effectively work in cross functional teams, meet deadlines, and prioritize multiple projects. * Strong problem-solving abilities, critical thinking, and the ability to collaborate with cross-functional teams. Strong verbal and written communication skills, including technical writing. * Understanding of GMP, GLP, and regulatory requirements for the development of cell-based therapies. Experience with regulatory submissions and support for inspections is a plus. * Demonstrated troubleshooting and problem-solving skills. * Understanding of basic statistics and working knowledge of statistical software (e.g. JMP). * Must be comfortable handling human tissues. * There will be occasional weekend work. ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law. Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship. Create a Job Alert Interested in building your career at ProKidney? Get future opportunities sent straight to your email. Create alert

Senior Scientist Real-World Evidence Winston-Salem, North Carolina **Reynolds American is evolving at pace into a global multi-category business. Our purpose is to create A Better Tomorrow by Building a Smokeless World.** **To achieve our ambition, we are looking for colleagues who are ready to join us on this journey! Tomorrow can't wait, let's shape it together!** **REYNOLDS AMERICAN has an exciting opportunity for a Senior Manager Real-World Evidence in Winston-Salem, NC.** The Senior Scientist Real-World Evidence, will provide expertise in managing the planning, execution, monitoring, and closing of clinical research to support regulatory submissions and real-world experiences of our products. In this position, the individual will collaborate on projects and programs related to actual use observational studies to support regulatory submissions for current and future market products. Additionally, this position will contribute to generating scientific evidence to support tobacco harm reduction initiatives. This role will participate in cross-functional collaborations and build relationships with internal and external partners to influence regulatory science strategy and deliver evidence generation. Further, this role will bring ingenuity and creativity to independently develop and recommend solutions to complex problems. This person will deliver evidence generation while maintaining high scientific standards and integrity, and adhering to all applicable regulations and procedures. This position requires strong technical, project management, and communication skills. A strong background in observational and/or clinical research is desired. **Your key responsabilities will include:** + Significantly contribute to the operational planning and execution of clinical studies (e.g., actual use trials, pragmatic trials) for tobacco products intended for FDA regulatory submissions. + Act as the primary liaison between clinical research teams, vendors, and cross-functional stakeholders. + Develop and manage detailed project plans, timelines, budgets, and resource allocations. + Assist in the generation of scientific evidence to influence regulatory science strategy + Project management across multiple projects with internal and external stakeholders + Provide insight into scientific study design and data interpretation across a variety of social and behavioral scientific disciplines + Regulatory science engagement through publications, conference presentations, and external collaborations + Regulatory writing and scientific and regulatory engagement **What are we looking for?** + Advanced degree (Ph.D. or M.S.) in epidemiology,chemistry, biology, toxicology, pharmacology, clinical or social science, or other relevant discipline + 2+ years relevant scientific experience resulting in a thorough knowledge of concepts, principles and strategic relevance as pertains toconducting randomized controlled trials and observational research studies + Experience working in a regulated industry, such as tobacco/nicotine, pharmaceutical, and/or medical device + Demonstrated ability to manage and execute multiple projects + Strong organizational, writing, presentation, and communication skills, with the ability to interface with other functions within (and external to) the Company + Ability to conceive, plan and conduct work streams aligned with, and in support of, regulatory strategy + Strong ability to apply critical thinking to ambiguous or complex scientific challenges + Extensive experience navigating tobacco regulatory frameworks and proficiency in biostatistics or data interpretation is considered beneficial **WE ARE REYNOLDS AMERICAN-A member of the BRITISH AMERICAN TOBACCO GROUP** At Reynolds American, we are committed to our Purpose of creating A Better Tomorrow. This is what drives our people and our passion for innovation. **See what is possible for you at REYNOLDS AMERICAN.** **BELONGING, ACHIEVING, TOGETHER** Collaboration and teamwork underpin everything we do here at Reynolds American. We know that collaborating with colleagues is what makes us stronger and best prepared to meet our business goals. **BENEFITS OVERVIEW** **Benefit Information** The following is a general summary of the competitive compensation and benefit plans we offer: - 401(k) plan that offers opportunity to save on pre- and post-tax basis up to 50 percent of eligible compensation. o Company matches 100 percent of employee pre-tax/Roth (401k) contributions up to six percent o Company contributes an additional three percent to 401(k) whether employee participates or not - Comprehensive health- and welfare-benefits package (including medical, dental, vision, and prescription drugs) - Health Savings Account start-up contribution for employees who elect the high deductible health plan - Flexible spending accounts for both Health Care and Dependent Care allowing employee to use pre-tax dollars to pay for qualified expenses during the calendar year - Employee assistance program offering 8 free counselling sessions, per issue, each calendar year for employees and their dependents - Company paid life insurance of 1x annual base pay ($50,000 minimum) - Company paid accidental death or dismemberment insurance of 2x annual base pay ($50,000 minimum) - Voluntary insurances offered at group rates: employee and dependent life insurance, AD&D insurance, critical illness, accident coverage, disability buy-up, and auto & home insurance - Tuition reimbursement and student loan support - Dependent Scholarship Programs - Free confidential personal financial counselling service - On-site health centers and 24/7 fitness centers at certain company locations - A charitable giving matching grants program that enables employees to direct and double their donations to qualifying charitable organizations of their choice - Health-care concierge service - Volunteer service opportunities - Extensive training opportunities - Company vehicle for eligible employees - Mobile phone allowance for eligible employees - Paid Leave: o Sick and Personal Time (exempt employees may be excused with pay for brief absences; non-exempt employees receive up to 6 days) o Vacation (levels Below Senior Director receive 15 days (pro-rated during first year of service); Senior Director and Officers receive 25 days (pro-rated during first year of service)). o Holidays (Nine company recognized and two annual personal holidays to be used at the employee's discretion) o Paid Parental Leave + temporary reduced work schedule opportunity o Funeral Leave o Short-Term Disability Leave o Long-Term Disability Leave o Jury Duty Leave o Military Leave o Released Time for Children's Education o Community Outreach Leave o Other paid leave benefits, as required by state or local law - Your journey with us isn't limited by boundaries; it's propelled by your aspirations. Join us at Reynolds American and become a part of an environment that thrives on internal advancement, where your career progression isn't just a statement - it's a reality we're eager to build together. Seize the opportunity and own your development; your next chapter starts here. - You'll have access to online learning platforms and personalized growth programs to nurture your leadership skills - We prioritise continuous improvement within a transformative environment, preparing for ongoing changes Our organization offers a level of challenge, responsibility, and creativity for motivated employees who want to grow their careers. We are also committed to valuing different perspectives, experiences, and talents to improve the company's potential for optimally achieving its business objectives! Reynolds American Inc. and its affiliated companies is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other status protected by law. Only applicants requiring reasonable accommodation for any part of the application and hiring process should contact us directly via email at *******************

We are currently seeking an experienced Research Associate to join the Cell Therapy Process Development team. This role offers an exciting opportunity to lead or support the development and improvement of cell therapy manufacturing processes, contributing to the advancement of cutting-edge therapies. The ideal candidate will possess a strong experience in cell therapy or biopharmaceutical development, process optimization, and technology transfer, and be passionate about making an impact in the evolving field of cell therapy. Responsibilities + Design and execute experiments to optimize and improve processes for cell therapy manufacturing, including media preparation, cell expansion and harvest, and product formulation. Analyze experimental data and present results in a clear and actionable manner to stakeholders. + Provide technical expertise in the development and implementation of new techniques and technologies. Support troubleshooting and process improvement initiatives. + Collaborate closely with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing, to ensure the successful transfer of processes into GMP clinical and commercial manufacturing. + Support the characterization and validation of cell therapy processes, ensuring compliance with regulatory guidelines and internal standards. Conduct process performance qualification (PPQ) studies and support clinical trial material production. + Ensure all process development activities adhere to GMP and applicable regulatory standards. Support regulatory filings and audits as needed. + Prepare and review technical documentation, including process development reports, batch records, SOPs (Standard Operating Procedures), and change controls. + Identify potential risks in process development and manufacturing, and implement strategies for mitigation, ensuring the successful advancement of cell therapy programs. Essential Skills + Aseptic technique and operation + Experience in cleanroom and sterile processing + Cell culture and cell therapy expertise + Process development knowledge + Understanding of GMP standards + Proficiency in laboratory work and decontamination procedures + Ability to troubleshoot and analyze batch records + Knowledge in molecular biology and biopharmaceutical processes Additional Skills & Qualifications + Bachelor's or Master's degree in Cell Biology, Biotechnology, Biochemical Engineering, or a related field. + 2+ years of experience in cell therapy and/or biopharmaceutical process development. + Strong problem-solving abilities and critical thinking skills. + Ability to effectively work in cross-functional teams, meet deadlines, and prioritize multiple projects. + Strong verbal and written communication skills, including technical writing. + Understanding of GMP, GLP, and regulatory requirements for cell-based therapies. + Experience with regulatory submissions and support for inspections is a plus. Work Environment The role is based in a lab and office setting, specifically within a cleanroom environment with level 10k and 100k specifications. Responsibilities include maintaining sterile gowning certification and adhering to sterile gowning procedures. Job Type & Location This is a Permanent position based out of Winston Salem, NC. Pay and Benefits The pay range for this position is $70000.00 - $75000.00/yr. See company website for details on what is offered for FTE's. Workplace Type This is a fully onsite position in Winston Salem,NC. Application Deadline This position is anticipated to close on Dec 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

The Joint School of Nanoscience and Nanoengineering (JSNN) at North Carolina Agricultural and Technical State University (NC A&T) invites applications for a full-time research scientist position. We are looking for a highly motivated and talented research scientist to join our team in the field of nanomaterials. This is a DoD-initiated multiple year project with extensive industry support. The applicants are expected to have a Ph.D. degree in Nanoscience/Nanoengineering, Materials Science/Engineering, Chemistry, or a related discipline from an accredited institution with solid background in nanomaterials and abundant experience in nanoparticle synthesis such as metal nanoparticles, co-shell nanoparticles, ceramic nanoparticles, and hybrid nanoparticles, as well as nanoparticle characterization and application. The research scientist will carry out research in the field of nanomaterials particularly nanoparticles including material design, synthesis, characterization, and application, publish peer-reviewed journal articles, write and submit research report and grant proposals, disseminate research results and foster research collaborations, mentor and train graduate and undergraduate students, as well as additional duties under the supervision of the PI. The research scientist will enjoy a dynamic and collaborative working environment. This is a renewable position subject to satisfactory performance and availability of funding. US citizenship or lawful permanent residency is required. Primary Function of Organizational Unit North Carolina Agricultural and Technical State University (NC A&T) is a public land grant doctoral university and a constituent member of the University of North Carolina (UNC) system with an enrollment of over 15,000 students. NC A&T is classified as "R2-High Research Activity" by the Carnegie Foundation and is poised to achieve "R1-Very High Research Activity" Status. The Joint School of Nanoscience and Nanoengineering (JSNN) is an academic collaboration between NC A&T and the University of North Carolina at Greensboro (UNCG). JSNN is a $56.3 million, 105,000 square foot state-of-the-art science and engineering education and research facility. JSNN builds on the strengths of the two universities to offer innovative and cross-disciplinary M.S. and Ph.D. graduate programs in the emerging areas of nanoscience and nanoengineering. JSNN partnered with Georgia Tech and was awarded a National Nanotechnology Coordinated Infrastructure (NNCI) grant titled "Southeastern Nanotechnology Infrastructure Corridor (SENIC) by the National Science Foundation. JSNN and SENIC have provided great opportunities to conduct competitive nanoengineering research at NC A&T. The Department of Nanoengineering is dedicated to educating the next generation of leaders in nanotechnology, advancing the understanding of nanoscale phenomena and applications, and serving society through education, outreach, and development of cutting-edge technologies. Committed to excellence in teaching, research, and community engagement, the department strives to achieve national distinction and preeminence in the field. Minimum Requirements (1) Ph.D. in Nanoscience/Nanoengineering, Materials Science/Engineering, Chemistry, or related discipline from an accredited institution. (2) Solid background in nanomaterials and abundant experience in nanoparticle synthesis. (3) Self-motivated and independent researcher. (4) Good communication skills. (5) Publication record. (6) Experience in mentoring students. Preferred Years Experience, Skills, Training, Education (1) Previous experience in nanoparticle synthesis such as metal nanoparticles, co-shell nanoparticles, ceramic nanoparticles, and hybrid nanoparticles, as well as nanoparticle characterization and application. (2) Proficiency in analytical tools like SEM, TEM, DSC, and other nanomaterial characterization techniques. (3) Excellent critical thinking, writing, communication, teamwork, and organization/management skills. Required License or Certification N/A Is this position eligible for a remote or hybrid work arrangement, consistent with university and state policies. On-site (Employees are primarily in the office and/or have a critical job requirement that requires dedicated office space on-site)

is located in Winston-Salem, NC and it is onsite Monday thru Friday Title: Senior Food Scientist This role will be the resident expert for sauce, dips, and syrups using scientific principles to research, develop and improve current as well as new products. Position requires a person who is strong in practical and technical and analytical skills along with sauce development experience. This position is in a lab within a manufacturing facility. Primary Tasks: Independently leads medium to high complexity projects to deliver formulas that are cost-effective, processing optimized, and preferred by customers. Applies scientific principles to understand the chemical, physical, and sensory properties of food ingredients, ensuring safety and quality. Co-develops projects with key customers Leverages internal and external consultants along with preferred vendors to drive projects forward and deliver approved formulas within agreed upon timelines Supports Sales as representative of R&D during customer meetings/calls Documents formulas, feedback, and cutting notes ensure learnings are readily available Collects, records, analyzes, and presents data and recommendations during development and stability testing Reporting Structure: Reports to Director of Innovation Additional Responsibilities: Mentors junior team members Acts as on-site technical resource for Production and Quality Acts as backup for Director of Innovation Remains engaged in flavor, ingredient, and category trends to enable suggestion of new projects Qualifications & Skills: Bachelor's degree in food science, food technology, or food chemistry. Advanced degree is strongly preferred. At least 5 years of experience developing CPG products. Dressing and sauce R&D experience is strongly preferred. Strong understanding of principles of food science and ingredient functionality. Expertise in one food science discipline preferred. Intermediate computer skills (Word, Excel, Outlook, Teams, etc.) and willingness to learn new systems. Project management experience; working knowledge of stage gate, costing, and typical R&D workflows. Other: Ability to communicate technical information and research findings clearly and concisely both verbally and in writing Continuously curious, creative, eager to grow knowledge base Ability to adapt to unforeseen circumstances and view setbacks as learning Skilled at influencing without direct authority and championing ideas within a cross functional team Ability to direct and handle multiple tasks at one time and work within a project timeline. Ability to travel Willingness and ability to consume dressing and sauce products including nuts, soy, eggs, dairy, sesame, shellfish, wheat, and mustard. Ability to occasionally lift 40lbs Must be willing to work weekends, holidays, and varying shifts, as required.

is located in Winston-Salem, NC and it is onsite Monday thru Friday Title: Senior Food Scientist This role will be the resident expert for sauce, dips, and syrups using scientific principles to research, develop and improve current as well as new products. Position requires a person who is strong in practical and technical and analytical skills along with sauce development experience. This position is in a lab within a manufacturing facility. Primary Tasks: Independently leads medium to high complexity projects to deliver formulas that are cost-effective, processing optimized, and preferred by customers. Applies scientific principles to understand the chemical, physical, and sensory properties of food ingredients, ensuring safety and quality. Co-develops projects with key customers Leverages internal and external consultants along with preferred vendors to drive projects forward and deliver approved formulas within agreed upon timelines Supports Sales as representative of R&D during customer meetings/calls Documents formulas, feedback, and cutting notes ensure learnings are readily available Collects, records, analyzes, and presents data and recommendations during development and stability testing Reporting Structure: Reports to Director of Innovation Additional Responsibilities: Mentors junior team members Acts as on-site technical resource for Production and Quality Acts as backup for Director of Innovation Remains engaged in flavor, ingredient, and category trends to enable suggestion of new projects Qualifications & Skills: Bachelor's degree in food science, food technology, or food chemistry. Advanced degree is strongly preferred. At least 5 years of experience developing CPG products. Dressing and sauce R&D experience is strongly preferred. Strong understanding of principles of food science and ingredient functionality. Expertise in one food science discipline preferred. Intermediate computer skills (Word, Excel, Outlook, Teams, etc.) and willingness to learn new systems. Project management experience; working knowledge of stage gate, costing, and typical R&D workflows. Other: Ability to communicate technical information and research findings clearly and concisely both verbally and in writing Continuously curious, creative, eager to grow knowledge base Ability to adapt to unforeseen circumstances and view setbacks as learning Skilled at influencing without direct authority and championing ideas within a cross functional team Ability to direct and handle multiple tasks at one time and work within a project timeline. Ability to travel Willingness and ability to consume dressing and sauce products including nuts, soy, eggs, dairy, sesame, shellfish, wheat, and mustard. Ability to occasionally lift 40lbs Must be willing to work weekends, holidays, and varying shifts, as required.

Labcorp is looking for a Validations and Reagent Research Associate to join their team in Burlington, NC. In this role you will develop new products and improve existing products following Design Control and Good Manufacturing Practices (GMP). **Essential Duties and Responsibilities:** + Develop new products and product improvements. Responsible for but not limited to leading discussions regarding design projects, preparation of verification and validation reports, preparation of research plans, designing experiments, outlining research procedures to follow, determining critical steps, conducting assigned experiments, and analyzing data. Research Associates are expected to be able to organize design projects. + Plan schedule of research according to company's timetable and establishes daily and weekly routines necessary to meet project timetable. This includes maintaining regular and consistent attendance as well as making experimental arrangements when unexpected absences occur. Research Associates are expected to be able to manage design projects, making sure critical path delays are identified so they can be resolved. + Participate in design control and regulatory activities. Serve on project teams and review teams as assigned. Prepare Risk assessments, FMEAs, risk reports, project plans, design inputs, design component specifications, protocols and reports as assigned or required for their projects. Prepare and support submissions to regulatory agencies as assigned. + Analyze data critically, looking for trends and determining when additional testing is needed. + Able to prepare all components required for production of strip lots, as well as analyze strip performance. Able to formulate a test strip lot and be able to make decisions as to levels to test and decide on an acceptable formulation for a clinical lot. + Adhere to GLP, GMP, ISO 13485 and any other regulatory requirements applicable to current project. This includes but not limited to completion of documentation, maintaining proper labeling of reagents and components, proper labeling and storage of raw data, and proper use of PPE required for task. + Troubleshoot problems with existing tests and tests under development. This includes aiding Formulations, QC, and Production departments with technical issues and participating in root cause analysis of complaints and product development issues. + Present experimental analysis, experimental data, complaint analysis, new and improved processes to project teams, design review teams, management, and affected departments. Presentation should be organized to facilitate transfer of important facts. Presentation should also be appropriate for audience. + Other job duties maybe assigned as needed. **Education and/or Experience:** + Bachelor's degree from college or university program in Biological or Chemical Science; and greater than two years related experience and/or training; or equivalent combination of education and experience. **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here (************************************************************** **.** **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site (**************************************************** or contact us at Labcorp Accessibility. (Disability_*****************) For more information about how we collect and store your personal data, please see our Privacy Statement (************************************************* .

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Essential Duties and Responsibilities: * Demonstrates strong client service skills, teamwork, and collaboration * Applies GMP/GLP/ISO 17025 compliance standards in all areas of responsibility, as appropriate * Recognizes errors, identifies root causes, and applies process improvements * Assists in Method Development and execute method validation protocols * Oversees sample preparation and analyses in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, ICP, pH, moisture, Karl Fischer, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.) * Assists in Method Development and executes method validation protocols * Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision * Makes recommendations for technical improvements, as needed * Provides analysis support for method validation as needed * Ensures that the quality policy program is understood, implemented, and maintained at all levels of the organization; identifies, prevents, or corrects any departures from the quality system * Performs work for both routine and non-routine work as specified by a separate and applicable technical job description for the individual * Develops and implements operational improvements * Coaches, trains, and develops others within the group with respect to their personal development and effective implementation of operational improvements * Coordinates workflow and performs daily monitoring to meet TAT * Conducts semiannual performance reviews, interviews applicants, keeps training records up to date for assigned employees, and performs succession planning in preparation for growth * Confronts and addresses problems, concerns, and performance issues * Coaches and develops individuals and teams to maximize performance * Fosters motivation and positive morale * Monitors and approves employees' time worked through the time-entry system * Expands self-awareness and develops leadership skills as defined; attends applicable leadership training based on identified needs * Performs and/or assigns other duties as requested to ensure the smooth operation of the department * Provides analysis support for method validation as needed * Evaluates, reviews, and approves data by other analysts * Trains new analysts in laboratory techniques and procedures * Writes, edits, and updates SOPs, WI and other documentation * Documents results appropriately in notebooks, LIMS, or on testing forms * Possesses strong computer, scientific, quality orientation, and organizational skills * Provides clear feedback * Communicates (oral and written) effectively and shows attention to detail * Keeps accurate records, follows instructions, and complies with company policies Qualifications * Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) * 7+ years of related experience * 1 - 3 years supervisory experience Additional Information * Position is full-time, Monday - Friday 8am to 5 pm * Ability to work overtime as required. * Tasks require repetitive motion and standing for long periods of time. * May be required to respond to off-shift operational issues. * Candidates currently living within a commutable distance of Winston-Salem, NC are encouraged to apply. * Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays * #LI-EB1 * Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Applies GMP/GLP in all areas of responsibility, as appropriate Applies the highest quality standard in all areas of responsibility Demonstrates and promotes the company vision Demonstrates strong client service skills, teamwork, and collaboration Proactively plans and multitasks to maximize productivity Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Regular attendance and punctuality Applies 17025 compliance standards in all areas of responsibility, as appropriate Performs complex analyses and non-routine testing in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, GC-MS, ICP, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.) Operates and maintains job-related equipment as required Performs advanced troubleshooting of laboratory equipment Performs supporting verification, calibration, and maintenance tasks (e.g., balance calibration and pipette verifications) Performs laboratory tasks as assigned following supervisor direction, SOPs, WI, and other documentation Assists other staff in the edits and updates of SOPs, WI, and other documentation Follows all Good Documentation Practices appropriately, including digital platforms Maintains working areas appropriately (cleaning, disinfecting, etc.) Possesses strong organizational skills Provides clear feedback Keeps accurate records, follows instructions, and complies with company policies Proactively checks and stays current with all training across multiple learning platforms Provides instruction/training to new staff Recognizes errors, identifies root causes, and applies process improvements Provides analysis support for method validation as needed Evaluates, reviews, and approves data by other analysts Independently drafts, edits, and updates SOPs, WI, and other documentation Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision Makes recommendations for technical improvements, as needed Assists in Method Development and executes method validation protocols Assist in method transfer from the MDV group Write validation protocols and reports Communicates effectively with client staff members Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) 7+ years of related experience Additional Information Position is full-time, Monday - Friday 8am to 5 pm Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Candidates currently living within a commutable distance of Winston-Salem, NC are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Essential Duties and Responsibilities: Demonstrates strong client service skills, teamwork, and collaboration Applies GMP/GLP/ISO 17025 compliance standards in all areas of responsibility, as appropriate Recognizes errors, identifies root causes, and applies process improvements Assists in Method Development and execute method validation protocols Oversees sample preparation and analyses in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, ICP, pH, moisture, Karl Fischer, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.) Assists in Method Development and executes method validation protocols Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision Makes recommendations for technical improvements, as needed Provides analysis support for method validation as needed Ensures that the quality policy program is understood, implemented, and maintained at all levels of the organization; identifies, prevents, or corrects any departures from the quality system Performs work for both routine and non-routine work as specified by a separate and applicable technical job description for the individual Develops and implements operational improvements Coaches, trains, and develops others within the group with respect to their personal development and effective implementation of operational improvements Coordinates workflow and performs daily monitoring to meet TAT Conducts semiannual performance reviews, interviews applicants, keeps training records up to date for assigned employees, and performs succession planning in preparation for growth Confronts and addresses problems, concerns, and performance issues Coaches and develops individuals and teams to maximize performance Fosters motivation and positive morale Monitors and approves employees' time worked through the time-entry system Expands self-awareness and develops leadership skills as defined; attends applicable leadership training based on identified needs Performs and/or assigns other duties as requested to ensure the smooth operation of the department Provides analysis support for method validation as needed Evaluates, reviews, and approves data by other analysts Trains new analysts in laboratory techniques and procedures Writes, edits, and updates SOPs, WI and other documentation Documents results appropriately in notebooks, LIMS, or on testing forms Possesses strong computer, scientific, quality orientation, and organizational skills Provides clear feedback Communicates (oral and written) effectively and shows attention to detail Keeps accurate records, follows instructions, and complies with company policies Qualifications Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) 7+ years of related experience 1 - 3 years supervisory experience Additional Information Position is full-time, Monday - Friday 8am to 5 pm Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Candidates currently living within a commutable distance of Winston-Salem, NC are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

TAT Technologies (Greensboro Facility) is part of a multi-site, global aerospace company dedicated to our customer experience of exceeding expectations. We are the leading APU leasing and repair station for key commercial and military aircraft solutions with over 50 years of experience in the industry. We have an ambitious and fast-growing environment that believes in the power of team collaboration with the deep-rooted belief that there is no substitution to personal relationships and interactions. We offer a flexible work environment enabling talented individuals to fulfill their development goals through drive, energy, and passion for the customer. TAT Technologies is looking for qualified LG Analytical Technicians. This is a Monday - Friday, 1st Shift (7:00am - 3:30pm) position. These techs will perform the following duties: Must understand the purpose and scope of each process area, including disassembly, machining, inspection, measurement, paint inspection, and reassembly. Must be familiar with and follow FAA requirements related to inspection and repair. Must be able to read and interpret OEM repair manual instructions. Have an aptitude for detailed mechanical work and methodical trouble-shooting is essential. Is expected to practice exemplary conduct and work ethics at all times. Function as a compatible team is imperative to our overall success, and the Associate must participate with initiative, positive approaches to problem solving/prevention, and commitment to quality. Becomes proficient in precise measurement and use of instruments such as micrometers, dial indicators, etc. Practices safe and appropriate use of repair tools. Learns to write concessions. Learns reassembly techniques. Becomes familiar with manuals. Keeps abreast of relative Service Bulletins. Completes all WO paperwork relative to task. Achieves efficiency and broader understanding of reference materials. Accesses and follows instructions in a timelier manner. Knows and follows FAA/ISO guidelines. Knows and follows safety requirements. Requirements One to two years of mechanical repair experience. Familiarity with aviation industry is advantageous. Ability to interpret and follow repair instructions from OEM manuals. Understanding of FAA regulations helpful. An aptitude for detailed mechanical work and methodical trouble-shooting is essential. Writing skills and accuracy are required for documentation. Ability to safely and properly operate Shop equipment and precise measuring equipment. Benefits Piedmont Aviation Component Services, a subsidiary of TAT Technologies, is dedicated to providing an inclusive, fun, and unique workplace. We believe in acknowledging and appreciating the value of our team members. One way we value our team is by providing a comprehensive and expansive benefits offering to include Major Medical, Dental, Vision, Life, 401K with company matching, STD, LTD, accidental coverages, EAP, and more. Insurance carriers vary based on location. TAT Technologies is dedicated to providing an inclusive, fun, and unique workplace. We believe in acknowledging and appreciating the value of our team members. One way we value our team is by providing a comprehensive and expansive benefits offering to include Major Medical, Dental, Vision, Life, 401K with company matching, STD, LTD, accidental coverages, EAP, and more. Insurance carriers vary based on location. Equal Employment Opportunities - TAT TECHNOLOGIES is committed to maintaining a supportive, healthy, and productive work environment free from discrimination, harassment, or bullying, and complying with all legislative requirements. This includes equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran.

The Cell Therapy Process Development Scientist will play a critical role in the development and optimization of robust and reproducible processes for the manufacturing of ProKidney's cell therapy product, Rilparencel, which is in phase three clinical trial. The process development scientist will design and execute studies and implementation of cutting-edge technologies for commercial production. You will work in a fast-paced, highly collaborative environment, engaging with various internal teams, external partners, and key stakeholders to ensure the seamless transition of processes from the laboratory to clinical and, eventually, commercial production. This role offers an exciting opportunity to make a direct impact on the development of life-saving therapies while applying your scientific expertise to solve complex challenges in cell therapy. Key Responsibilities Design and execute studies to develop and optimize cell therapy manufacturing processes, including cell expansion, selection, purification, formulation, and cryopreservation. Analyze and interpret experiment results. Write and review study reports. Design and implement process improvements that reduce cost, improve efficiency, and enhance product quality, while maintaining compliance with regulatory requirements. Work closely with Manufacturing teams to ensure smooth technology transfer and the successful execution of GMP manufacturing runs, ensuring process robustness and troubleshooting any issues that arise. Perform process risk assessment using tools including FMEA. Design and execute experimental plans to characterize and validate critical process parameters (CPPs) of cell therapy products. Participate in project teams and contribute technical expertise to support the transition from pre-clinical to clinical and commercial manufacturing. Stay current with the latest trends, technologies, and regulatory developments in the cell therapy field. Contribute to scientific publications, presentations, and internal knowledge sharing. Qualifications Degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Cell Biology, Bioengineering, or a related discipline. PhD with 2+ years experience, MS with 8+ years experience, or BS with 12+ years experience in bioprocess or cell therapy process development. Extensive hands-on experience with cell expansion, cell selection and cell purification. Proven track record of contributing to successful technology transfer of manufacturing processes. Experience in QbD and process characterization including the use of DoE (Design of Experiments) and statistical analysis. Knowledge of analytical methods such as flow cytometry, PCR, ELISA, cell counting, and other assays for cell therapy characterization. Excellent problem-solving skills and the ability to troubleshoot complex process-related challenges. Strong communication skills, with the ability to articulate complex technical information to both technical and non-technical stakeholders. Self-motivated, detail-oriented, and able to manage multiple priorities effectively in a fast-paced, dynamic environment. Strong interpersonal skills and the ability to work collaboratively in a cross-functional, multidisciplinary team. Preferred Qualifications Experience in preparing regulatory filings. Familiarity with data analysis software (e.g., JMP). Experience in GMP regulations. ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law. Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.

We are currently seeking an experienced Research Associate to join the Cell Therapy Process Development team. This role offers an exciting opportunity to lead or support the development and improvement of cell therapy manufacturing processes, contributing to the advancement of cutting-edge therapies. The ideal candidate will possess a strong experience in cell therapy or biopharmaceutical development, process optimization, and technology transfer, and be passionate about making an impact in the evolving field of cell therapy. Responsibilities * Design and execute experiments to optimize and improve processes for cell therapy manufacturing, including media preparation, cell expansion and harvest, and product formulation. Analyze experimental data and present results in a clear and actionable manner to stakeholders. * Provide technical expertise in the development and implementation of new techniques and technologies. Support troubleshooting and process improvement initiatives. * Collaborate closely with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing, to ensure the successful transfer of processes into GMP clinical and commercial manufacturing. * Support the characterization and validation of cell therapy processes, ensuring compliance with regulatory guidelines and internal standards. Conduct process performance qualification (PPQ) studies and support clinical trial material production. * Ensure all process development activities adhere to GMP and applicable regulatory standards. Support regulatory filings and audits as needed. * Prepare and review technical documentation, including process development reports, batch records, SOPs (Standard Operating Procedures), and change controls. * Identify potential risks in process development and manufacturing, and implement strategies for mitigation, ensuring the successful advancement of cell therapy programs. Essential Skills * Aseptic technique and operation * Experience in cleanroom and sterile processing * Cell culture and cell therapy expertise * Process development knowledge * Understanding of GMP standards * Proficiency in laboratory work and decontamination procedures * Ability to troubleshoot and analyze batch records * Knowledge in molecular biology and biopharmaceutical processes Additional Skills & Qualifications * Bachelor's or Master's degree in Cell Biology, Biotechnology, Biochemical Engineering, or a related field. * 2+ years of experience in cell therapy and/or biopharmaceutical process development. * Strong problem-solving abilities and critical thinking skills. * Ability to effectively work in cross-functional teams, meet deadlines, and prioritize multiple projects. * Strong verbal and written communication skills, including technical writing. * Understanding of GMP, GLP, and regulatory requirements for cell-based therapies. * Experience with regulatory submissions and support for inspections is a plus. Work Environment The role is based in a lab and office setting, specifically within a cleanroom environment with level 10k and 100k specifications. Responsibilities include maintaining sterile gowning certification and adhering to sterile gowning procedures. Job Type & Location This is a Permanent position based out of Winston Salem, NC. Pay and Benefits The pay range for this position is $70000.00 - $75000.00/yr. See company website for details on what is offered for FTE's. Workplace Type This is a fully onsite position in Winston Salem,NC. Application Deadline This position is anticipated to close on Dec 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Labcorp is looking for a Validations and Reagent Research Associate to join their team in Burlington, NC. In this role you will develop new products and improve existing products following Design Control and Good Manufacturing Practices (GMP). Essential Duties and Responsibilities: * Develop new products and product improvements. Responsible for but not limited to leading discussions regarding design projects, preparation of verification and validation reports, preparation of research plans, designing experiments, outlining research procedures to follow, determining critical steps, conducting assigned experiments, and analyzing data. Research Associates are expected to be able to organize design projects. * Plan schedule of research according to company's timetable and establishes daily and weekly routines necessary to meet project timetable. This includes maintaining regular and consistent attendance as well as making experimental arrangements when unexpected absences occur. Research Associates are expected to be able to manage design projects, making sure critical path delays are identified so they can be resolved. * Participate in design control and regulatory activities. Serve on project teams and review teams as assigned. Prepare Risk assessments, FMEAs, risk reports, project plans, design inputs, design component specifications, protocols and reports as assigned or required for their projects. Prepare and support submissions to regulatory agencies as assigned. * Analyze data critically, looking for trends and determining when additional testing is needed. * Able to prepare all components required for production of strip lots, as well as analyze strip performance. Able to formulate a test strip lot and be able to make decisions as to levels to test and decide on an acceptable formulation for a clinical lot. * Adhere to GLP, GMP, ISO 13485 and any other regulatory requirements applicable to current project. This includes but not limited to completion of documentation, maintaining proper labeling of reagents and components, proper labeling and storage of raw data, and proper use of PPE required for task. * Troubleshoot problems with existing tests and tests under development. This includes aiding Formulations, QC, and Production departments with technical issues and participating in root cause analysis of complaints and product development issues. * Present experimental analysis, experimental data, complaint analysis, new and improved processes to project teams, design review teams, management, and affected departments. Presentation should be organized to facilitate transfer of important facts. Presentation should also be appropriate for audience. * Other job duties maybe assigned as needed. Education and/or Experience: * Bachelor's degree from college or university program in Biological or Chemical Science; and greater than two years related experience and/or training; or equivalent combination of education and experience. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Essential Duties and Responsibilities: Demonstrates strong client service skills, teamwork, and collaboration Applies GMP/GLP/ISO 17025 compliance standards in all areas of responsibility, as appropriate Recognizes errors, identifies root causes, and applies process improvements Assists in Method Development and execute method validation protocols Oversees sample preparation and analyses in support of product assessment and quality control on products utilizing one or more analytical techniques (e.g., HPLC, GC, ICP, pH, moisture, Karl Fischer, mass spectrometry, smoking machines, or other special purpose equipment and/or multiple wet chemistry and physical techniques.) Assists in Method Development and executes method validation protocols Performs all testing with good dexterity, good laboratory techniques, and a high degree of accuracy and precision Makes recommendations for technical improvements, as needed Provides analysis support for method validation as needed Ensures that the quality policy program is understood, implemented, and maintained at all levels of the organization; identifies, prevents, or corrects any departures from the quality system Performs work for both routine and non-routine work as specified by a separate and applicable technical job description for the individual Develops and implements operational improvements Coaches, trains, and develops others within the group with respect to their personal development and effective implementation of operational improvements Coordinates workflow and performs daily monitoring to meet TAT Conducts semiannual performance reviews, interviews applicants, keeps training records up to date for assigned employees, and performs succession planning in preparation for growth Confronts and addresses problems, concerns, and performance issues Coaches and develops individuals and teams to maximize performance Fosters motivation and positive morale Monitors and approves employees' time worked through the time-entry system Expands self-awareness and develops leadership skills as defined; attends applicable leadership training based on identified needs Performs and/or assigns other duties as requested to ensure the smooth operation of the department Provides analysis support for method validation as needed Evaluates, reviews, and approves data by other analysts Trains new analysts in laboratory techniques and procedures Writes, edits, and updates SOPs, WI and other documentation Documents results appropriately in notebooks, LIMS, or on testing forms Possesses strong computer, scientific, quality orientation, and organizational skills Provides clear feedback Communicates (oral and written) effectively and shows attention to detail Keeps accurate records, follows instructions, and complies with company policies Qualifications Bachelor's degree in Chemistry, Biology, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) 7+ years of related experience 1 - 3 years supervisory experience Additional Information Position is full-time, Monday - Friday 8am to 5 pm Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Candidates currently living within a commutable distance of Winston-Salem, NC are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

The Electrical and Computer Engineering Department in NC A&T State University invites applications for a full-time, post-doctoral research associate position in Autonomous Vehicles, Robotics, Perception, Control, and Navigation. The applicants are expected to have a strong theoretical and experimental background with evidence of skills related to transportation technologies, control of autonomous vehicles, sensing, perception, and artificial intelligence. This is a non-tenure-track, year-to-year appointment, renewable annually for up to two years subjected to satisfactory performance, availability of resources, and the needs of the Department. We thus look for applicants that have a demonstrated track record in the applications of multi-agent systems. Programming and practical experiences with embedded real-time systems are desired. This position will carry out research on sensor fusion, perception, and control of autonomous vehicles for different applications such as transportation systems and self-driving vehicles as well as autonomous ground and air vehicles. The employee will be a member of a research group at ACCESS Laboratory, supporting projects through original research, collaboration with other team members, and mentoring of students. The employee will also contribute to additional proposal efforts, thereby strengthening North Carolina A&T State University's ability to attract external funding. The employee will confer on overall research direction and strategy but will exercise a considerable amount of independent judgment and original thinking in carrying out research that contributes to original knowledge and advances the University's reputation in research. The employee will publish research results, in collaboration with the Professor, in recognized journals. The employee will share student mentoring with research team members and will participate in departmental seminars and other professional activities as assigned. The candidate will be also working with both graduate and undergraduate students in a mentoring role, and will be involved in conducting workshops, and seminars. The candidate will enjoy a dynamic and collaborative working environment. Primary Function of Organizational Unit North Carolina A & T State University is a public land grant high research activity institution that is committed to dedicated teaching and learning, scholarly and creative research, and effective engagement and public service. The University enrolls over 15,200 students. Nationally recognized for its leadership and excellence in STEM education and research, N.C. A&T is classified as "R2-High Research Activity" in the Carnegie Classifications and is poised to achieve "R1-Very High Research Activity" status. It also holds Carnegie's earned credential in Community Engagement and the Association of Public and Land-Grant Universities (APLU) Innovation and Economic Prosperity designation. With an annual economic impact of $2.4 billion, N.C. A&T plays a vital role as a higher-education economic driver in North Carolina's Piedmont Triad region and across a state that is ranked No. 1 in the nation for the second straight year as "best for business" by the CNBC financial network. The College of Engineering, with over 2,800 students, has EAC ABET accredited undergraduate programs in Architectural, Bio-, Biological, Civil, Chemical, Computer, Electrical, Industrial, and Mechanical Engineering, as well as a CAC ABET-accredited program in Computer Science. On the Graduate level, the College has 8 Masters of Science Degree programs, and 5 Doctoral programs. The 5 research cluster areas of the College of Engineering (COE) are Autonomous Systems, Cybersecurity and Resilience, Energy and Sustainability, Healthcare Applications and Complex Systems and Networks. The College welcomes team members who thrive in an environment that embraces diversity and inclusion within the student body, faculty, and staff. Additional information about the College and the University can be found at ***************** The Department of Electrical and Computer Engineering is the largest department in the College of Engineering and provide highly competitive graduate and undergraduate education in its four degree programs. The four programs are a BS in electrical engineering, a BS in computer engineering, an MS in electrical engineering, and a Ph.D. in electrical engineering. The Department of Electrical and Computer Engineering is committed to be a place of excellence in education, research and community service, and to achieve national recognition, distinction and preeminence. Additional information can be found at **************************************************** Autonomous Cooperative Control of Emergent Systems of Systems (ACCESS) Laboratory aims to address fundamental problems in modeling, analysis, control, and improvement of complex systems. Researchers at ACCESS laboratory achieve this goal by systematically developing tools and techniques for analysis and synthesis of complex systems. Additional information can be found at ************************** Minimum Requirements 1. Ph.D. awarded within the last five years in Electrical and Computer Engineering, Computer Science, or related area, specializing in Control and Robotics. 2. A strong theoretical and experimental background with evidence of skills related to autonomous vehicle technology and transportation technology. 3. The candidate is expected to have good skills in writing scientific papers and technical reports. 4. Possess a high level of initiative and the ability to multitask involving different research problems. 5. Possess good organizational skills; detail oriented. 6. Demonstrated integrity, dependability, and competence. 7. Able to work independently requiring minimal supervision. 8. Able to make presentations utilizing excellent oral communication and facilitation skills. 9. Strong critical thinking, analytical, writing, communication, and interpersonal skills. Preferred Years Experience, Skills, Training, Education 1- Experience with ROS 2. Experience with Autoware 3- Good programming skills such as Python, C++, and ROS, 4- Experience with development and deployment of AI models 5- Knowledge and experience with computer vision, 6- Experience with edge devices 7- Experience with high computing performance systems 8- Project management skills. Required License or Certification Is this position eligible for a remote or hybrid work arrangement, consistent with university and state policies. On-site (Employees are primarily in the office and/or have a critical job requirement that requires dedicated office space on-site)

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. 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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, a place to call home, apply with us today! Job Description Senior Laboratory Technician responsibilities include, but are not limited to, the following : Performs sample preparation on tobacco products using smoking machine and wet chemistry techniques; provides support to analytical chemists Performs some less complex routine analyses in support of product assessment and quality control on tobacco products utilizing Liquid Chromatography, and/or multiple wet chemistry techniques Accurately documents result in notebooks and laboratory LIMS, in compliance with good documentation practices Performs instrument calibration, and recognizes errors Adheres to highest quality standards; ensures compliance with quality system requirements Communicates effectively with client staff members and co-workers Qualifications The ideal candidate would possess : Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies At least one-year related laboratory or quality control experience; familiarity with standard lab concepts, practices, and procedures Basic Minimum Qualifications : High school diploma or equivalent Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, Mon-Fri 8:00am-5:00pm. Candidates currently living within a commutable distance of Winston-Salemm, NC are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

ProKidney is seeking an experienced Research Associate for our Cell Therapy Process Development team. The ideal candidate will have a strong background in cell therapy or biopharmaceutical development, process optimization, and technology transfer. In this role, you will lead or support the development and improvement of cell therapy manufacturing processes, contributing to the advancement of cutting-edge therapies. This is a great opportunity for individuals who are passionate about making an impact in the evolving field of cell therapy. Responsibilities: Design and execution of experiments to optimize and improve processes for cell therapy manufacturing, including but not limited to media preparation, cell expansion and harvest, and product formulation. Analyze experimental data and present results in a clear and actionable manner to stakeholders. Provide technical expertise in the development and implementation of new techniques and technologies. Support troubleshooting and process improvement initiatives. Work closely with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing, to ensure the successful transfer of process into GMP clinical and commercial manufacturing. Support the characterization and validation of cell therapy processes, ensuring compliance with regulatory guidelines and internal standards. Conduct process performance qualification (PPQ) studies and support clinical trial material production. Ensure that all process development activities adhere to GMP and applicable regulatory standards. Support regulatory filings and audits as needed. Preparation and review of technical documentation, including process development reports, batch records, SOPs (Standard Operating Procedures), and change controls. Assist to identify potential risks in process development and manufacturing and implement strategies for mitigation, ensuring the successful advancement of cell therapy programs. Qualifications: Bachelor's or Master's degree in Cell Biology, Biotechnology, Biochemical Engineering, or a related field. 2 plus years of experience in cell therapy and /or biopharmaceutical process development. Ability in execution and troubleshooting experiments, analyzing/ reporting/presenting data. Experience in aseptic techniques is essential. Demonstrated ability to effectively work in cross functional teams, meet deadlines, and prioritize multiple projects. Strong problem-solving abilities, critical thinking, and the ability to collaborate with cross-functional teams. Strong verbal and written communication skills, including technical writing. Understanding of GMP, GLP, and regulatory requirements for the development of cell-based therapies. Experience with regulatory submissions and support for inspections is a plus. Demonstrated troubleshooting and problem-solving skills. Understanding of basic statistics and working knowledge of statistical software (e.g. JMP). Must be comfortable handling human tissues. There will be occasional weekend work. ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law. Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.

At Labcorp, we advance science, technology and innovation and are recognized as one of the most respected companies in the world. We believe in the power of science to change lives. We are a leading global life sciences company that delivers answers to crucial health questions -because we know that knowledge has the potential to make life better for all. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people's lives. Join us in our pursuit of answers. We have an excellent career opportunity for a Research Associate I on our R&D DNA Identification team in Burlington, NC. Position Summary: The Research Associate I will be part of the R&D DNA Identification team that leads development and optimization of DNA testing procedures for HLA testing and other DNA, RNA, and antibody-based assays. The position will require assay development, validation, implementation, and troubleshooting. This includes development of Next Generation Sequencing tests for PacBio and Illumina platforms. Other methods include, but are not limited to, Sanger sequencing, qPCR, Enzyme Immunoassay, STR, bioinformatics, and probe capture. Other Essential Responsibilities: Conduct research on projects with limited oversight through the development process and transfer optimized and developed products to operations. Write standard operating procedures, validation plans, and summaries. Work closely with R&D and Clinical directors, Operations, and other scientific staff in a team environment. Analyze and critique results, note deviations and design relevant experiments. Review primary scientific literature to help develop and troubleshoot experiments. Give presentations to colleagues. Generate reports sufficient for submission to peer-reviewed journals. Coach and assist laboratory staff with newly developed procedures. Qualifications: Previous research experience in molecular techniques such as DNA isolation, PCR, probe/bait capture assays, and Next Generation Sequencing. Familiarity with validation and implementation in a CAP/CLIA Laboratory. Familiarity with assay design and assay performance optimization. Ability to work effectively independently. Education Requirements: Bachelor of Science degree with a minimum of 3 years' relevant experience in HLA, R & D, or equivalent; OR Master of Science degree with a minimum of 1 years' experience in HLA, R & D, or equivalent. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Why People choose to work at Labcorp: At Labcorp, it is our people that make us great - it is what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.