Research and development technician jobs in North Carolina - 589 jobs

Applied AI Data Scientist hackajob on-demand focuses on matching talented contractors like you with organisations seeking specific skills for their projects. We use our platform to connect you with exciting contract opportunities and discuss projects on behalf of the companies we partner with. Must be located in Dallas, TX or Charlotte, NC - role is on-site 5 days/week What You'll Get to Do: Perform statistical analysis, clustering, and probability modeling to drive insights and inform AI-driven solutions Analyze graph-structured data to detect anomalies, extract probabilistic patterns, and support graph-based intelligence Build NLP pipelines with a focus on NER, entity resolution, ontology extraction, and scoring Contribute to AI/ML engineering efforts by developing, testing, and deploying data-driven models and services Apply ML Ops fundamentals, including experiment tracking, metric monitoring, and reproducibility practices Collaborate with cross-functional teams to translate analytical findings into production-grade capabilities Prototype quickly, iterate efficiently, and help evolve data science best practices across the team What You'll Bring with You: Solid experience in statistical modeling, clustering techniques, and probability-based analysis Hands-on expertise in graph data analysis, including anomaly detection and distribution pattern extraction Strong NLP skills with practical experience in NER, entity/ontology extraction, and related evaluation methods An engineering-forward mindset with the ability to build, deploy, and optimize real-world solutions (not purely theoretical) Working knowledge of ML Ops basics, including experiment tracking and key model metrics Proficiency in Python and common data science/AI libraries Strong communication skills and the ability to work collaboratively in fast-paced, applied AI environments

Delta, founded in 1971, is a global leader in switching power supplies and thermal management products with a thriving portfolio of smart energy-saving systems and solutions in the fields of industrial automation, building automation, telecom power, data center infrastructure, EV charging, renewable energy, energy storage and display, to nurture the development of smart manufacturing and sustainable cities. As a world-class corporate citizen guided by its mission statement, “To provide innovative, clean and energy-efficient solutions for a better tomorrow,” Delta leverages its core competence in high-efficiency power electronics and its ESG-embedded business model to address key environmental issues, such as climate change. Delta serves customers through its sales offices, R&D centers and manufacturing facilities spread over close to 200 locations across five continents. Delta has 158 sales offices, 72 R&D centers and 48 manufacturing facilities worldwide. Throughout its history, Delta has received various global awards and recognition for its business achievements, innovative technologies, and dedication to ESG. Since 2011, Delta has been listed on the DJSI World Index of Dow Jones Sustainability™ Indices for 11 consecutive years. In 2021, Delta was also recognized by CDP with leadership level ratings for its substantial contribution to climate change and water security issues and named Supplier Engagement Leader for its continuous development of a sustainable value chain. Power Electronics R&D Engineer - EV Power We are seeking a highly skilled and motivated R&D Engineer to join our team focused on developing cutting-edge on-board chargers for electric vehicles (EVs). The ideal candidate will have a deep understanding of various power conversion topologies, magnetics and wide band gap devices, with a strong background in both theoretical and practical aspects of power electronics. Key Responsibilities: - Design and develop innovative on-board charger solutions for EV applications. - Research and implement power factor correction topologies, including both hard-switching and soft-switching techniques. - Develop and optimize dual-active-bridge (DAB) and resonant DC-DC topologies. - Work on single-stage AC-DC topologies, including resonant and DAB configurations - Work on wireless power chargers for next generation autonomous charging fleet - Work on Ultra-wide range DC-DC chargers and high step-down auxiliary battery charging applications - Explore and implement new bidirectional devices like bi-GaN and bi-SiC in various applications such as Vienna rectifiers, Current Source Inverters (CSI), and single-stage isolated AC-DC converters. - Collaborate with cross-functional teams overseas to ensure seamless integration of new technologies into existing and new products. - Conduct simulations (Simplis, PLECS, ANSYS, Matlab/Simulink) and prototype testing to validate design concepts and ensure performance meets required specifications. - Stay up-to-date with the latest advancements in power electronics and EV charging technologies. - Prepare technical reports, presentations, and documentation to communicate findings and support product development. Qualifications: - Master's or Ph.D. degree in Electrical Engineering, Power Electronics, or a related field. - Proven experience in power electronics design and development, specifically in EV on-board chargers. - Strong knowledge of power factor correction topologies (both hard-switching and soft-switching). - Expertise in DAB and resonant DC-DC topologies, single stage AC-DC topologies, wireless power charging - Knowledge of EMI noise source and propagation phenomenon, experience with EMI filter design - Proficiency in working with wide band gap devices such as SiC and GaN. - Familiarity with new bidirectional devices (bi-GaN and bi-SiC) and their applications. - Hands-on experience with simulation tools such as MATLAB/Simulink, Simplis, PLECS, or similar. - Excellent problem-solving skills and the ability to work independently and as part of a team. - Strong communication skills, both written and verbal. Preferred Qualifications: - Experience in the automotive industry, particularly in EV charging systems. - Knowledge of industry standards and regulations related to EV charging. - Experience with hardware design and testing (6 kW, 11 kW, 22 kW), including PCB layout and thermal management. What We Offer: - Competitive salary and benefits package. - Opportunity to work on cutting-edge technology in the rapidly growing EV industry. - Collaborative and innovative work environment. - Professional development and career advancement opportunities such as IP generation. Equal Opportunity Employer: We are an equal opportunity employer and value diversity in our company. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

As part of the Analytical Production Securitization Industrialization team in the Engineering and Industrialization department, the Associate Process Scientist will perform projects to support the manufacturing of BACT/ALERT Culture Media products. Within this role the Associate Process Scientist will be required to interface with Manufacturing, Quality Control, Quality Assurance / Validation, R&D, Purchasing, Supply Chain, and other functions as required in order to ensure successful project achievements to facilitate quality production that meets on-time customer demands. The position will primarily operate as project lead on multiple projects that will ensure cost savings and raw material securitization initiatives. This position directly impacts delivering lower cost BACT/ALERT product by lowering upstream raw material costs while ensuring supply chain continuity and supporting Quality Control and Operations functions to manufacture quality product. Primary Duties: 1.Analyzes chemical and/or biologically derived raw materials for secondary/alternate sourcing projects for site securitization and/or cost savings initiatives. 2.Executes hands on laboratory testing at the bench scale, within final product, and through large scale validation activities. 3.Management of multiple projects will be required, whereby assessments are generated to assess interim progress and effectiveness. 5.Executes project leadership is necessary in order to guide timelines, adjust expectations, and collaborate cross-functionally. 6. Perform all work in compliance with company quality procedures and standards. 7. Performs other duties as assigned. Education, skills and experience: * B.S. in Biochemistry or closely related field required with 2 years of experience in a regulated industry required * Or in lieu of a Bachelor's degree, 6 years of experience in a regulated industry, will be accepted * M.S. in Biochemistry or closely related field preferred * Engineering/science role within medical device/diagnostic or pharmaceutical preferred * Project Management experience preferred * Experience working in a cGMP environment preferred * FDA regulated cGMP industry experience preferred * Functional skills including critical thinking, adaptability, time management, communication, problem-solving and digital literacy. * Manage and meet competing deadlines, requiring careful prioritization and time management to ensure all tasks are completed on time. * Troubleshooting issues to identify and resolve problems efficiently * Solution oriented in the face of conflict * Drive for Results: Drive for Results while successfully removing barriers * Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared objectives * Written Communications - including the ability to communicate technical data in written form Working Conditions and Physical Requirements: Ability to remain in stationary position, often standing, for prolonged periods. Ability to ascend/descend stairs, ladders, ramps, and the like. Ability to wear PPE correctly most of the day. Ability to adjust or move objects up to 50 pounds in all directions. Domestic travel required 10% of the time International travel required 5% of the time The estimated salary range for this role is between $75,000 and $114,400. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bio Merieux's bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate's experience and will be presented in writing at the time of the offer.In addition, bio Merieux offers a competitive Total Rewards package that may include:*A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options*Company-Provided Life and Accidental Death Insurance*Short and Long-Term Disability Insurance*Retirement Plan including a generous non-discretionary employer contribution and employer match.*Adoption Assistance*Wellness Programs*Employee Assistance Program*Commuter Benefits*Various voluntary benefit offerings*Discount programs*Parental leaves #LI-US Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bio Merieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bio Merieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site or contact us at [emailprotected]. BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at , by email at [emailprotected], or by dialing 711 for access to Telecommunications Relay Services (TRS).

Job Title: Chemist Duration: 06 Months Pay Rate: $25/hr on W2 Shift: 7:00AM-5:30PM (Mon -Thurs) but there is some flexibility in start time Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory. Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs. Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting. Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency. Aid other group members as required. Ensure that equipment and working areas are maintained with good safety and housekeeping practices. Re-stock chemicals and consumables used in analysis. Performs other related assignments and duties as required and assigned. Skills: Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy - UV/Vis, NIR, IR, or AA/AE). Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position. Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting. Lift and maneuver equipment and materials weighing up to 20 pounds. Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums. Use small hand and power tools to perform incidental maintenance. Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces. Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required. Education: The incumbent must have a BA or BS degree in Chemistry or closely related science. Minimum of 1-year relevant experience preferred.

HOURLY R&D TECHNICIAN - 1ST GUILFORD TEXTILES, KENANSVILLE, The primary responsibility of this position is the processing of R&D sample orders and all support functions. This includes but is not limited to preparation, finishing, lamination, inspection of sample orders, all associated record keeping of technical parameters, and distribution of samples to internal and external customers. The technician will have responsibility for cutting, labeling, mounting, and distributing samples to the Lear Sales and Engineering teams to submit to customers for new business consideration. Great attention to detail and pride in workmanship is absolutely critical. The Role: Your work will include, but not be limited to: The technician is expected to assist as needed to process samples through any and all equipment as needed. The ideal candidate will have experience on a variety of equipment and/or the ability and willingness to learn new processes and equipment The technician will execute carton requisitions from receipt to closure and is expected to maintain requisitions to a minimal level Responsibility for sample embossing and welding operations. The associate will participate in regularly scheduled sample preview and review meetings and is expected to contribute independent point of view. Advantages of working for Lear at the Kenansville Plant: Medical Benefits 401k Advancement to leadership Employee 24/7 Resource System Employee Discounts Your Qualifications: Ability to follow departmental work instructions, standards of operations (SOPs), verbal and written directions Adapt to using multiple tools and equipment Attend sample review meetings Background in PLC ladder logic troubleshooting. Ability to troubleshoot AC and DC drives Must be High School Graduate or have a GED. Must have intermediate functional knowledge of Basics, English and metrics units, measuring systems, and conversions Intermediate functional knowledge of Microsoft Excel and Word and other custom oftware. Must be able to pass Background and Drug Screening Ability to lift up to 50 pounds and to stand for a prolonged amount of time. Please include resume WORKING CONDITIONS The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job Constantly work under tight time constraints Occasionally work mandatory overtime May occasionally have exposures to extreme wet and/or humid conditions, heat/cold temperatures, and loud machine/equipment The employee is occasionally exposed to vibration, fumes or airborne particles PERSONAL PROTECTIVE EQUIPMENT REQUIREMENTS Required during production duties: Eye protection Hearing Protection Steel toe/ Non-Slip shoes Reflective Vest (where applicable) NOTICE The above job profile does not include all essential and nonessential duties of this job. Other job duties may be assigned as needed. All employees with disabilities are encouraged to contact the Human Resources Department to review and discuss the essential and nonessential functions of the job. The employee with a disability can evaluate the job in greater detail to determine if she/he can safely perform the essential functions of this job with or without reasonable accommodation. DISCLAIMER Job profiles are not intended, nor should they be construed to be, an exhaustive list of all responsibilities, tasks, skills, efforts, working conditions or similar behaviors, attributes or requirements associated with a job. A job profile is not a comprehensive job description. It is intended for the sole purpose of acquainting a person who is unfamiliar with such position with a brief overview of the position's general direction and scope. Lear Corporation is an EEO/Affirmative Action employer, and all qualified applicants will receive consideration for employment without regard to race, sex, national origin, disability, veteran status, or any other status in accordance with law.

Agency Dept of Environmental Quality Division Waste Management Job Classification Title Industrial Hygiene Consultant (NS) Number 60034645 Grade NC16 About Us The primary mission of the North Carolina Department of Environmental Quality (DEQ) is to provide science-based environmental stewardship for the health and prosperity of all North Carolinians. The North Carolina Department of Environmental Quality (DEQ) is the lead stewardship agency for the protection of North Carolina's environmental resources. The organization, which has offices from the mountains to the coast, administers regulatory programs designed to protect air quality, water quality, and the public's health, and works to advance in all-of-the-above energy strategy that fits North Carolina's needs. DEQ also offers technical assistance to businesses, farmers, local governments, and the public and encourages responsible behavior with respect to the environment through education programs provided at DEQ facilities and through the state's school system. DEQ touches the lives of all North Carolinians in many ways to enhance and ensure our quality of life. Description of Work This is an anticipated vacancy. This position is expected to be available on March 01, 2026. The primary purpose of the Industrial Hygiene Consultant position is to provide technical and program support as an environmental toxicologist to the Underground Storage Tank Section, Superfund Section and on an as-needed basis to the Hazardous Waste Section, Solid Waste Section, and Brownfields Program, within the Division of Waste Management. The position frequently interacts with staff, the public, and regulated community. Key Responsibilities: • Responsible for determining health based clean up levels for soil, groundwater, surface water, sediment, and indoor air stemming from contaminated sites. • Responsible for reviewing human health and ecological risk assessments, reports, and inquiries. • Responsible for evaluating and calculating human health and ecological risk target levels. • Responsible for Quality Assurance and Quality Control reviews of analytical data and issuance of Health Risk Evaluations. • Responsible for calculating levels from vapors as part of structural vapor intrusion analysis and conducting other toxicological evaluations and duties as needed. Knowledge Skills and Abilities/Management Preferences Recruitment Range: $55,823 - $94,912 Important: This posting closes at 11:59:59 PM the night BEFORE the End Date above. The Division of Waste Management is responsible for protecting the public health and environment through assuring that solid and hazardous waste and underground storage tanks are managed properly, and existing contamination is cleaned up across the State of North Carolina. This is accomplished through the Hazardous Waste, Solid Waste, Superfund and Underground Storage Tank Sections, and the Brownfields Redevelopment Section. Click here to learn more about the Division of Waste Management | NC DEQ. If you have student loans, becoming a state employee includes eligibility for the Public Service Loan Forgiveness Program. Visit *********************** to learn more. This position currently qualifies for a hybrid telework option with routine office and remote workdays. The NC Department of Environmental Quality trusts our employees to be self-motivated and successful in hybrid/remote roles. Telework options are subject to change at the discretion of management. Minimum Education and Experience Some state job postings say you can qualify by an “equivalent combination of education and experience.” If that language appears below, then you may qualify through EITHER years of education OR years of directly related experience, OR a combination of both. See the Education and Experience Equivalency Guide for details. Bachelor's degree in industrial hygiene, occupational safety & health, biology, chemistry, physics, mechanical engineering, chemical engineering, or a closely related curriculum from an appropriately accredited institution and three years of progressive experience in industrial hygiene inspections: or an equivalent combination of education and experience. EEO Statement The State of North Carolina is an Equal Employment Opportunity Employer and dedicated to providing employees with a work environment free from all forms of unlawful employment discrimination, harassment, or retaliation. The state provides reasonable accommodation to employees and applicants with disabilities; known limitations related to pregnancy, childbirth, or related medical conditions; and for religious beliefs, observances, and practices. Recruiter: Valerie Delores Moses Recruiter Email: ************************

Primary Purpose: Maintain a quality environment through proper cleaning processes that meet the requirements of the contract.. Offices: Dust, Vacuum, Sweep and Mop Floors, Clean Tables and Empty Trash Outside of Building: Remove Trash and Debris Restrooms: Clean, Sanitize, Remove Trash and Restock Breakrooms: Sweep, Mop, Clean Tables and Remove Trash Entrance and Exit Doors: Clean Windows, Sanitize Door Handles, Vacuum Mats, Sweep Around Doors and Clean Thresholds Conference Rooms: Dust, Vacuum, Sweep and Mop Floors, Clean Tables and Empty Trash Lab: Sweep and Mop Floors, Clean Tables and Empty Trash Requirements: Background Check Drug Testing Must be 18 years of age or older Must be able to lift 40 pounds for the entire shift Must be able to stand for the entire shift Must be able to climb stairs during the entire shift Must be capable of bending, pushing, pulling and squatting during the entire shift Must be capable of pushing a manual broom and mop Must be detailed oriented Must have reliable transportation arrangements Must be comfortable working in a commercial setting Must be willing to wear all required PPE during the entire shift Must be willing to follow all safety protocols Benefits: Weekly Pay Insurance Packages Opportunity to Advance Continuous Training One Week of Vacation After One Year Physical Demands and Work Environment Must be able to lift 40 pounds during the entire shift Must be able to stand for the entire shift Must be able to climb stairs during the entire shift Must be capable of bending, pushing, pulling and squatting during the entire shift Must be capable of pushing a manual broom and mop

: Aspida is a tech-driven, nimble insurance carrier. Backed by Ares Management Corporation, a leading global alternative asset manager, we offer simple and secure retirement solutions and annuity products with speed and precision. More than that, we're in the business of protecting dreams; those of our partners, our producers, and especially our clients. Our suite of products, available through our elegant and intuitive digital platform, focuses on secure, stable retirement solutions with attractive features and downside protection. A subsidiary of Ares Management Corporation (NYSE: ARES) acts as the dedicated investment manager, capital solutions and corporate development partner to Aspida. For more information, please visit ************** or follow them on LinkedIn. Who We Are: Sometimes, a group of people come together and create something amazing. They don't let egos get in the way. They don't settle for the status quo, and they don't complain when things get tough. Instead, they see a common vision for the future and each person makes an unspoken commitment to building that future together. That's the culture, the moxie, and the story of Aspida. Our business focuses on annuities and life insurance. At first, it might not sound flashy, but that's why we're doing things differently than everyone else in our industry. We're dedicated to developing data-driven tech solutions, providing amazing customer experiences, and applying an entrepreneurial spirit to everything we do. Our work ethic is built on three main tenets: Get $#!+ Done, Do It with Moxie, and Have Fun. If this sounds like the place for you, read on, and then apply at aspida.com/careers. What We Are Looking For: Aspida is looking for a Product Development Analyst to join our Retail Annuities team. In this role, you'll help shape and manage annuity solutions that deliver value to clients and drive growth for the business. You'll work across multiple product lines, supporting development and ongoing management, while ensuring our offerings remain competitive, client-centric, and aligned with Aspida's mission of providing innovative retirement solutions. This position reports to the AVP & Product Development Leader and is required to be onsite 3 days a week at our Durham, NC headquarters. What You Will Do: Lead analytical projects that inform product strategy and execution. Support initiatives across the full product lifecycle-from concept and market research to business case development, platform specifications, implementation, and launch. Collaborate with cross-functional teams to deliver on business objectives. Partner with marketing and distribution to educate and train on new product concepts and positioning. Assist in product approvals, onboarding, and business development opportunities with strategic partners. Prepare concise, insightful updates for senior leadership on product ideas, market trends, and project progress. Research competitor offerings and monitor developments in the annuity marketplace, including new product launches and industry trends. Research and development regarding new markets and new partnership opportunities What We Provide: Salaried, DOE Relocation available Full-Time Full Benefits Package Available What We Believe: Not sure if you meet every qualification? We still encourage you to apply! We value inclusivity, welcoming candidates from diverse backgrounds, including non-traditional paths. Unique experiences enrich our team, and the willingness to dream big makes you an exceptional candidate! At Aspida Financial Services, LLC, we are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. As such, Aspida does not and will not discriminate in employment and personnel practices on the basis of race, sex, age, handicap, religion, national origin or any other basis prohibited by applicable law. Hiring, transferring and promotion practices are performed without regard to the above listed items. Requirements What We Require: Bachelor's degree in relevant field. 3-5+ years in financial services, preferably with exposure to annuities or retirement products. Strong analytical, research, and quantitative skills. Excellent written and verbal communication skills-able to convey ideas clearly and persuasively. Familiarity with annuity product design, positioning, and distribution channels is a plus. Comfort using data and analytics to inform decisions; experience with Excel and business case development desirable. High energy, curiosity, and a passion for delivering results.

Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our company in a full-time, entry-level position that will rotate between our Chemistry, Manufacturing and Controls (CMC) and Research & Development (R&D) departments during this 2 year rotational program. This position is well suited for those looking for an entry-level position that is excited to learn all aspects of biotechnology drug development from early-stage research through drug product manufacturing. Candidates will be expected to accomplish defined work, as well as assist in approaching and solving complex scientific problems. Candidates should have demonstrated laboratory or manufacturing experience, with solid communication, technical aptitude, and problem-solving skills. Experience working in regulated, pharmaceutical/biotechnology R&D (GDP, GLP) and/or manufacturing environments (cGMP) is strongly preferred, but not required. Why Locus? Change the future of medicine and address a serious and unmet patient need by developing completely novel therapeutic modalities. Fast-track your career by tackling large & meaningful projects and learning a breadth of techniques and skillsets in the wet lab and manufacturing suites Work with a team of exceptionally talented and hardworking individuals while striving to achieve a common mission Partner with the most highly respected pharmaceutical companies in the world Bonus pool eligibility Health, dental, vision, life insurance, 401(k), and PTO Free access to fitness center and classes Responsibilities will include: Designing and/or executing formulation development activities Designing and/or executing bench-scale process development activities, including set-up and operation of development-scale bioreactors, filter trains, tangential flow filtration (TFF) equipment, and chromatography equipment Development of analytical strategies to inform formulation and process development activities Design and deploy automated workflows for molecular biology and microbiology assays, including liquid handling automation, next-generation sequencing (NGS) library preparation, and high-throughput screening of phage activity to accelerate research timelines and improve experimental reproducibility. Support the development of data infrastructure and bioinformatics pipeline for R&D and CMC operations, including DNA sequence analysis, sequence assembly, and comparative genomic analysis. Molecular biology and synthetic biology- Cloning, NGS library preparation, characterization of novel genetic engineering tools, and generation and analysis of novel engineered phage clones Microbiology - Culturing both aerobic and obligate anaerobic organisms. Utilizing a range of bacterial strains to produce and characterize activity of phage Independent management, planning, and execution of multiple projects, including reviewing, interpreting, and recording results. Supporting tech transfer of new products and processes to ensure smooth transition from R&D to process development to GMP manufacturing Forming strong relationships with all stakeholders, including technicians, associates, project and program managers, and scientists to enable successful tech transfer Supporting Scientists in all aspects of pharmaceutical development Assisting in the preparation of batch records, protocols, SOPs, deviations, technical reports, presentations, and other CMC documents to support drug development, including INDs, BLAs, and other applications Gaining aseptic gowning and fill qualification Performing material handling and staging Practicing real-time documentation (such as batch records) during production run and maintain accurate records/logs according to GDP Supporting Qualification and Validation activities Identifying, communicating, and troubleshooting process issues Supporting team effort in the effective and timely completion of root cause investigations and CAPA Supporting a high-performance teamwork environment Rotations may include any of the following functions: Research and Development including but not limited to phage discovery, phage engineering, and strain engineering. High Throughput Development (Automation) Bioinformatics Material Sciences & Technology cGMP Manufacturing Analytical Development Quality Control Clinical Lab Quality Assurance Project Management Office Clinical Operations Job requirements Education: Technical certificate or degree (e.g. BTEC Biomanufacturing), or graduation from an accredited college/university with a Bachelor's to a Master's degree in Biology, Chemistry, Biochemistry, Chemical Engineering, Biophysics, Pharmaceutical Technology or related field, with some lab experience (required) Experience and Expertise: Familiarity with general laboratory techniques such as pipetting, serial dilutions, aseptic technique and proper decontamination procedures Experience in research, pharmaceutical, biotechnology, and/or sterile production environment Experience executing SOPs and documenting work Strong mechanical aptitude Excellent oral and written communication skills Technical writing ability Thrives in a fast-paced, entrepreneurial and collaborative environment. Openly shares knowledge/information needed to accomplish a task or solve a problem Preferred Qualifications: At least two years' experience between academic or industry research Experience in biologics (upstream, downstream, aseptic fill/finish) with working knowledge of FDA regulations and GMP systems Experience with DNA sequence analysis, including homology searching, sequence assembly and primer design Ability to assist in the design of experiments and interpretation of results Motivation to learn new processes that contribute to the company's overall desire to get products into the clinic Technical proficiency with designing and executing standard molecular biology experiments (PCR, transformation, Gibson cloning) Experience with microbiology skills like growth curves, anaerobic microbiology, streaking and banking strains *The level of the position will be based on the successful candidate's qualifications. About Locus Biosciences Locus Biosciences is a clinical-stage biotechnology company developing precision antibacterial products to address critical unmet medical needs in treating bacterial infections and microbiome indications. The Locus platform engineers bacterial viruses called bacteriophages to specifically kill target pathogens while leaving non-target bacteria (i.e., the rest of the patient's microbiome) unharmed and to deliver biotherapeutic payloads to the body sites where they are needed. Locus's lead program is an engineered bacteriophage product targeting Escherichia coli bacteria in the urinary tract, currently being tested in an active Phase 2/3 clinical trial. Locus has collaborations with BARDA and CARB-X to develop engineered bacteriophage products targeting E. coli infections and Klebsiella pneumoniae infections, respectively. For more information about Locus visit ************************** SHIFT: Full-Time Days, with occasional evening and weekend work Job Type: Full-time, onsite Job Location: Research Triangle Park, North Carolina Direct applicants only. No agencies please. All done! Your application has been successfully submitted! Other jobs

**Lead R&D Data** **Scientist** Labcorp Genetics (formerly Invitae) is dedicated to bringing comprehensive genetic information into mainstream medicine to improve healthcare for billions of people. Our team is driven to make a difference for the patients we serve. We are leading the transformation of the genetics industry, by making clinical-grade genetic information affordable and accessible to guide health decisions across all stages of life. The genomics insights team leverages clinical genomic expertise, our massive genetics, laboratory and linked public/private datasets, and the latest AI/ML technologies to improve diagnosis, clinical care, and treatment options. We design and develop robust, quantitative, and scalable systems for variant interpretation and disease insights. Our research findings are broadly disseminated to improve testing guidelines, optimize reimbursement rates, and educate the healthcare ecosystem. We are seeking a Lead R&D Data Scientist to join our team and contribute to these initiatives. **Duties and Responsibilities:** + Lead and deliver the translation of complex biological and clinical questions into actionable analysis plans. + Architect and implement robust data pipelines that integrate large-scale genomic, phenotypic, laboratory, and real-world clinical datasets. + Conduct repeatable data analysis and modeling with a high degree of scientific and statistical rigor, for complex tasks such as understanding patient trajectories, elucidating varianteffect, andidentifyinggenotype-phenotype associations. + Write clean, maintainable, and well-documented code following best practices for version control, testing, and scalability. + Prepare technical reports, peer-reviewed publications, and conference presentations to share research outcomes with internal stakeholders and the broader scientific community. + Collaborate closely with both internal and external stakeholders to drive impactful research and development initiatives. + Ensurehigh standardsof data privacy, security, and compliance aremaintainedin all projects. **Qualifications:** + Mastersdegree, or equivalent industry experience in Computer Science, Statistics, Data Science, Computational Biology, ora relatedfield. + 5+ years of hands-on experience in data science and statistical methods, as applied to large biomedical datasets. + Experience working within a collaborative technical team with strong software engineering practices. + Proficiencyin modern programming languages (Python and SQL), shell scripting, and version control (Git). + Experience with data management, ETL, and business intelligence tools. + Excellent communication skills for presenting research findings to diverse audiences. **Preferred Qualifications:** + Ph.D + Experience with big data technologies (Snowflake, Databricks, etc.) and visualization/dashboarding (Looker, Dash, etc.). + Experience with high performance computing (SGEetc.). + Experience in the development and validation of complex computational models for biological data, in particular machine learning and bioinformatics techniques. + Understanding ofdata privacy, security, and ethical considerations in clinical and biological research. + Previouspublished work in genetics, functional genomics, or clinical research. **This position is not eligible for visa sponsorship.** **Application window closes: 02/14/2026** **Pay Range: $100,000.00 - $155,000.00 a year** **Schedule/Shift: M-F, 8-5 EST** All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers. Compensation may also include discretionary short- and long-term incentive packages **.** **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 (************************************************* .

About this role: Wells Fargo has embarked on a multiyear transformation journey aimed at building a centralized capability to store, manage and analyze Financial Crimes Compliance Operations (FCO) data to fulfill the Bank's BSA / AML regulatory, compliance and risk commitments. Wells Fargo is seeking a candidate with deep expertise in product management, data, BSA/AML, operations, and technology to develop key data assets associated with the transformation effort. The BSA/AML Data Transformation team delivers to our stakeholders curated data products, which are valuable, understandable, and trustworthy (among other attributes) to our stakeholders, the Operations and Risk analytics communities. These products directly support their ability to leverage Wells Fargo data assets for insight generation. Success in this role will enable faster delivery of the program's objectives, which include standing up data products to drive our regulatory, compliance, and risk commitments. In this role, you will: Lead complex data product initiatives, including those that are cross-functional with broad impact, and act as key participant in large-scale planning, driving data enablement and capabilities across platforms and utilities Review and analyze complex multi-faceted, larger scale or longer-term data product initiatives that require in-depth evaluation of multiple factors, including intangibles or unprecedented factors to drive data enablement strategies and roadmaps, while adhering to data governance and standards Make decisions in complex and multi-faceted situations requiring solid understanding of data, analytics, and integration needs of line of business partners to inform prioritization, roadmap, and architecture design, that influence and lead broader work teams to meet deliverables and drive new initiatives Strategically collaborate and consult with peers, colleagues, and mid-level to senior managers to ensure data product solutions are built for optimal performance and design analytics applications across multiple platforms, resolve data product issues, and achieve goals; may lead projects, teams or serve as a peer mentor Provide strategic input on new use case intake, prioritization, product roadmap definition, and other critical business processes Manage complex datasets continuously focusing on the consumers of the data and their business needs, while adhering to set data governance Create and maintain data product roadmaps throughout the data product life cycle with detailed specifications, requirements, and flows for data capabilities Design and maintain innovative data products, enabling data availability for data intelligence, analytics, and reporting Serve as a strategic liaison between data management, product teams, data engineering, and architecture teams throughout the data product life cycle Location: 141753-NC-Three Wells Fargo Center, Charlotte *This position does not offer relocation benefits Required Qualifications: 5+ years of data product or data management experience, or equivalent demonstrated through one or a combination of the following: work experience, training, military experience, education Desired Qualifications: Strong knowledge of BSA/AML data use cases and associated data products Proficiency in SQL and SAS Knowledge of the modern data stack and experience with data and analytics technologies such as Teradata, Hadoop, Google Big Query, Tableau, Alteryx, Spark, etc. Demonstrated strengths in strategic solutioning, planning, and secondary management, as well as cross functional collaboration Knowledge of ROI assessments and goal planning Experience working closely with senior and executive leadership Ability to translate and summarize complex data into understandable, actionable information and recommendations Proficiency with all Microsoft Office applications and the ability to construct PowerPoint presentations for executive communications Outstanding verbal, written, and interpersonal communication skills Ability to execute in a fast-paced, high-demand, environment while balancing multiple priorities Job Expectations: Ability to travel up to 10% of the time This position offers a hybrid work schedule Position does not provide Visa sponsorship Posting End Date: 19 Jan 2026 *Job posting may come down early due to volume of applicants. We Value Equal Opportunity Wells Fargo is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other legally protected characteristic. Employees support our focus on building strong customer relationships balanced with a strong risk mitigating and compliance-driven culture which firmly establishes those disciplines as critical to the success of our customers and company. They are accountable for execution of all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable Wells Fargo policies and procedures, appropriately fulfilling risk and compliance obligations, timely and effective escalation and remediation of issues, and making sound risk decisions. There is emphasis on proactive monitoring, governance, risk identification and escalation, as well as making sound risk decisions commensurate with the business unit's risk appetite and all risk and compliance program requirements. Candidates applying to job openings posted in Canada: Applications for employment are encouraged from all qualified candidates, including women, persons with disabilities, aboriginal peoples and visible minorities. Accommodation for applicants with disabilities is available upon request in connection with the recruitment process. Applicants with Disabilities To request a medical accommodation during the application or interview process, visit Disability Inclusion at Wells Fargo. Drug and Alcohol Policy Wells Fargo maintains a drug free workplace. Please see our Drug and Alcohol Policy to learn more. Wells Fargo Recruitment and Hiring Requirements: a. Third-Party recordings are prohibited unless authorized by Wells Fargo. b. Wells Fargo requires you to directly represent your own experiences during the recruiting and hiring process.

The Scientist III/ Sr. Scientist is responsible for developing and validating analytical methods to support drug formulation development in a GMP-compliant laboratory. This role involves performing validations, stability testing, and forced degradation studies while ensuring data integrity and regulatory compliance. The scientist will independently manage projects, including literature reviews, experimental design, execution, and reporting. Responsibilities also include authoring technical documents such as method validation protocols, development reports, and SOPs, as well as troubleshooting analytical instrumentation like HPLC and GC. Additionally, the role requires mentoring junior scientists, collaborating with cross-functional teams such as Formulation R&D, Quality Control, and Quality Assurance, and maintaining a safe, well-organized laboratory environment. Essential Functions · Develop and validate analytical methods to support formulation drug development under minimal supervision · Perform routine testing including stability testing, solubility studies, and Drug-Excipient Compatibility studies as and when needed · Ability to own projects independently including literature review, material sourcing, design experiments, executing/delegating tasks and providing data to customers · Perform forced degradation studies · Author product development reports and investigation reports · Author/ Co-author analytical methods, validation and transfer protocols, instrument qualification protocols, validation/qualification reports, SOPs, etc. · Execute routine instrument troubleshooting, peer review of laboratory notebooks, maintenance of logbooks · Maintain laboratory equipment, including calibration scheduling, acquisition, and basic maintenance programs · Maintain a GMP-compliant analytical laboratory and safe working environment, maintain lab inventory · Review laboratory notebooks, data packs, and reports under minimal supervision. Trend stability data. · Present data to the customers, attend client meetings as needed under minimal guidance · Supervise, mentor, train and develop junior scientists Supervisory responsibilities: Direct Reports: No; Indirect Reports: Yes Key Relationships (examples: Depts or Individual positions that this position will be working closely with): · Process Development/ Formulation R&D · Quality Control · Quality Assurance Travel requirements: N/A Education and Experience · B.S., with 8+ years', M.S., with 6+ years' experience, Ph.D.: focus in chemistry, biology, pharmaceutics · 4+ years' experience in a GMP laboratory setting · Proven track record developing and validating GMP-compliant HPLC and GC methods to assess drug product stability · Experience developing methods for topical drug products is a plus · Experience diagnosing and troubleshooting HPLC instrumentation, and addressing OOS and OOT results · Experience with the operation of HPLC and GC · Experience with Empower 3 software · Experience with UV, FTIR, KF, optical microscopy, PSD, viscosity, and rheological methodology a plus Knowledge, Skills, and Abilities · Knowledge of cGMP regulations and ICH, USP, and FDA guidelines · Speaks, writes, listens, and presents information in a logical and articulate manner appropriate for the audience · Technical report writing proficiency preferred · Experience with software such as MasterControl and MS Office preferred · Thorough when performing work, conscientious about attending to detail, and uses logical thinking that is well-organized and methodical Physical Demands and Work Environment While performing the duties of this job, there may be certain physical demands required for the position. · Occasionally required to lift/carry up to 20lbs · Requires standing/walking for extended periods in a climate-controlled lab environment · Frequent bending, lifting, pushing, pulling, carrying, and sitting may be required · May be exposed to moderate noise levels in a climate-controlled lab environment Other Duties You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.

We've been pioneering a world of possibilities to bring surfaces to life for well over 200 years. As experts in making coatings, there's a good chance you're only ever a few meters away from one of our products. Our world class portfolio of brands - including Dulux, International, Sikkens and Interpon - is trusted by customers around the globe. We're active in more than 150 countries and have set our sights on becoming the global industry leader. It's what you'd expect from the most sustainable paints company, which has been inventing the future for more than two centuries. Job Purpose Support Research, Development and Innovation with technical data management and administrative functions following defined standard operating procedures (SOPs). Will serve as the point of contact for formula implementation into the enterprise resource planning system. Will facilitate administrative tasks for the team to include ordering office and lab supplies as well as equipment. Must work within established timelines. Key Responsibilities * Transfer North American Industrial Coatings Wood product information from formulation to finished product into SAP, ensuring availability to all appropriate sites. * Initiate new raw material requests for all designated sites. * Organize and maintain the North America Research and Development SharePoint site and lab archives. * Ensure that the Research, Development and Innovation documentations are updated, distributed, and archived according to instructions. * Prepare activity status reports as required. * Order office and lab supplies and equipment. * Facilitate onboarding of new hires with access to SharePoint site, mailing lists, SAP, and other necessary software platforms. * Maintain and promote a safe work environment, complying with safety policies and procedures. Must follow safe work practices for personnel and equipment safety, in both the laboratory and in the field. End results are zero or minimum safety incidents. Job Requirements * High school diploma or equivalent. Undergraduate degree in Science, Engineering, or related field preferred. * 2 years' experience providing administrative support in a technical environment. * Ability to read, comprehend and follow safety instructions and safety guidelines. * Effective organizational and time management skills. * Strong verbal and written communication skills with the ability to interact with customers, enter data into the system, and read instructions. * Proficient in Microsoft Office. Experience using SAP preferred. * Must be able to use calculator, telephone, typewriter/keyboard and various office machines on a daily basis. * Must be fluent in English. French and/or Spanish language skills desirable. Rewards and Benefits The salary range for these skills is $55,000.00 - $60,000.00 based upon experience. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range. This salary range may also be modified in the future. This position is eligible for overtime for hours worked more than forty (40) in a given work week. Perks for Joining AkzoNobel! Medical insurance with HAS Dental, Vision, Life Insurance Accidental Death and Dismemberment Benefits Annual Bonus 401(K) retirement savings with 6% company match Generous Vacation, Personal and Holiday Pay Paid Parental leave Active Diversity and Inclusion Networks Career Growth Opportunities on a Regional and Global Scale Tuition Reimbursement Career Growth Opportunities Employee Referral Bonus #LI-VS1 All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status. Requisition ID: 50411

Vulcan Elements is manufacturing American rare-earth permanent magnets for a secure, resilient future. With a focus on national security and economic resiliency, we serve critical industries such as defense, aerospace, and automotive powering a high-technology future. Vulcan Elements is building a team of ambitious professionals committed to Mission Focus, Technical Excellence and Transparency. As a R&D Technician - Metals, you will accomplish a broad set of tasks in a research and development environment. You will operate equipment, optimize processes alongside engineering, prepare materials, load & unloaded materials, and maintain a safe, orderly working environment. You will work alongside a team of materials & process engineers, magnetics engineers, and technicians to accomplish company milestones. Description Contribute to the buildout of Vulcan's pilot and R&D line, including equipment installation, commissioning, and continuous equipment and facility improvements Operate vacuum furnaces, induction melting systems, and electrolysis cells to produce molten and solid metals. Prepare raw materials, charge systems, and consumables according to process instructions. Execute startup, steady-state operation, shutdown, and cleaning procedures. Monitor critical process parameters (temperature, voltage, current, pressure, time, chemistry) to ensure operation remains within specification. Respond to alarms, deviations, and abnormal operating conditions in accordance with procedures. Develop, build, and implement new prototype equipment, tooling, and processes alongside engineering, including electromechanical, chemical, and/or analytical/test equipment. Establish standard operating procedures alongside engineering. Responsibilities and tasks outlined are not exhaustive and may change as determined by the needs of the business Qualifications High School Diploma or GED at a minimum Strong communication and planning skills Able to lift and carry 50 lbs. Comfortable with hands on work requiring extended physical activity and standing Comfortable operating, troubleshooting, and maintaining sophisticated manufacturing equipment. Comfortable reading equipment schematics, both electrical and plumbing, to troubleshoot mechanical issues Must be a U.S. Person due to required access to U.S. export-controlled information or facilities. Preferred Qualifications Experience running vacuum furnaces, casting machines, atomizers, or other related metal manufacturing equipment Experience with Welding, Plumbing, or CAD Experience with hot metal

Who We Are FedUp Foods, one of the nation's early producers of kombucha through the Buchi brand and one of the largest functional beverage manufacturers in America, offers a diverse portfolio of organic private label functional beverages for top global retailers. Position Summary The Food Scientist will coordinate and create new products and enhance existing products while remaining aligned with the strategy, commitments, and goals of the organization. You will work directly with the Product Development team. An ideal applicant will be highly skilled, consistently punctual, and enjoy working with a variety of individuals who share similar values and goals. General Duties/Responsibilities Project manage the product development process from benchtop to commercialization. Create, refine, and mix recipes according to customer specifications and requests. Schedule and manage sensory evaluations and tasting panels. Coordinate shelf life studies and pilot batch production. Document, communicate, and track development progress and outcomes. Support food safety compliance including GMP and SQF policy adherence. Manage and organize incoming samples and sample analysis. Coordinate sensory evaluation of new ingredient samples. Maintain thorough documentation of batch and experiment records. Conduct testing and data analysis on prototypes. Draft product specifications and standard operating procedures. Maintain a running action plan for product development. Ensure formulation data and reports are securely controlled. Communicate internally and with clients on progress, timing, and change management. Assist in the review of product label changes. Maintain a clean and organized test kitchen and order supplies as needed. Schedule and brew pilot batches of varying scale. Stay current with trends, new products, flavors, and fermented beverages. Collaborate effectively with team members to complete projects on time. Receive cross-training on production flavoring duties as needed. Food Safety and Quality Responsibilities Follow GMP policy and encourage compliance within the team. Understand SQF policies related to pest control, visitors, allergens, and sanitation. Demonstrate awareness of Management's Commitment to SQF and food safety. Report food quality or safety issues to the Quality Assurance Manager for CAPA review and resolution. Required Skills/Abilities Knowledge of ingredient functionality, sensory evaluation, and QA principles. Strong project management and organizational skills. Team-oriented with the ability to work independently in a fast-paced environment. Education and Experience Bachelor's degree in food science required. 2+ years of R&D experience in a food manufacturing environment preferred. Work Environment/Physical Requirements Ability to stand and walk for prolonged periods. Ability to bend, squat, kneel, push, pull, and walk on uneven surfaces occasionally. Ability to work in hot, cold, and wet environments. Ability to lift, push, or pull up to 30 pounds. Our Values Agility • Collaboration • Communication • Lifelong Learning • Community • Gratitude Our Benefits Health Insurance (80-90% of individual premium covered) Group Term Life Insurance (100% company-covered) Short-Term Disability (100% company-covered) Long-Term Disability (50% company-covered) Voluntary Dental, Vision, Life & Accident Insurance 401(k) with Employer Match 9 Paid Holidays PTO & Sick Time We are committed to fair, equitable, and market-rate compensation. New hire offers are typically positioned around the market midpoint for the role (currently $68,900), with final compensation determined based on experience, scope of responsibility, and overall fit. Higher placement within the range is achieved over time through sustained impact and long-term contribution. EEO Statement AKM provides equal employment opportunities to all employees and applicants for employment and without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws Please be advised that as part of our employment process, we conduct background checks on all prospective employees. This may include verification of your employment history, educational background, criminal record, and other relevant information.

Preferred Years Experience, Skills, Training, Education Hands-on experience with confocal microscopy, imageprocessing/analysis, morphometric measurements, gene editing/misexpression in animal models, immunostaining, and or molecular biology. Work Schedule 12pm - 4pm

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Role Overview Complete Technology Transfer activities by performing manufacturing process development for Injectables products to commercial lines. Using experimental design, establish formulation processes, product pathway and select components for successful scaleup. Support client calls, prepare necessary documentation (including but not limited to work orders, protocols, summaries, with minimum supervision), and provides scientific justification as needed and update status of project work. Discover Impactful Work! Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant. Leads technical/scientific process/product/project activities to implement strategies and technical solutions. Drives creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients. Makes decisions that involve direct application of technical knowledge. A Day in the Life. Design, implement, and evaluate studies, lead tech transfer, commercial scale-up and support process validation. Represent the organization on formal technical and scientific forums. Lead and/or participate in problem solving and project work for formulations, equipment and processes. Write/revise work orders for new processes, FORMs, reports, memos, and protocols as required. Independently manage projects, proficient in evaluating and organizing all technical aspects of the project to achieve necessary landmarks and turning points. Support manufacturing operations, change controls, investigations as subject matter expert (SME), resolve accurate CAPAs. Assess material changes and determine change impact. Support development of proposals and timelines for projects, leading relevant client meetings. Review new bid quotes, protocols, technical documents, results, and reports. Keys to Success Education: Bachelor's of Science in Chemistry, Biochemistry, Biology, Pharmaceutical or related physical science. Experience: Bachelors and 3+ years confirmed experience CMO or Pharmaceutical product development experience PREFERRED Equivalency: Equivalent combinations of education, training, and meaningful work experience may be considered. Knowledge, Skills, Abilities: Advanced knowledge of variety of aspects of a subject area and working knowledge of principles and concepts in other relevant technical subject areas. Excellent knowledge of scientific methodology and development as related to the pharmaceutical industry. Detailed knowledge of Good Manufacturing Practices. Strong proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint). Excellent critical and logical thinking skills. Effective written, interpersonal, and presentation skills, including leading technical discussions with internal and external clients. Ability to work on multiple projects simultaneously. Proficiency at developing knowledge and skills in pharmaceutical processes, equipment, instrumentation, and procedures. Capability to keep current with scientific literature and industry trends relating to process technologies. Ability to develop technical solutions. Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand and walk; ability to lift and/or carry light objects of up to 25 lbs. for brief periods.

Gelest, Inc., part of the Mitsubishi Chemical Group, is hiring a Development Chemist to join our team in Morrisville, PA. This role offers the opportunity to contribute to our mission of delivering innovative specialty chemical solutions to customers worldwide. The Development Chemist will play a key role in designing, developing, and optimizing chemical processes for specialty chemical products. This hands-on role involves synthetic organic chemistry, process development from lab to pilot scale, and data acquisition and analysis to ensure safe, reliable, and cost-effective manufacturing. The Development Chemist will collaborate closely with Product Development, Engineering, Production, and Quality teams to translate laboratory discoveries into scalable processes that meet business and regulatory requirements. PRINCIPAL ACCOUNTABILITIES: Design and perform laboratory experiments involving synthetic organic reactions, route evaluation, optimization, and troubleshooting. Generate and analyze process data to identify improvement opportunities. Scale laboratory processes to pilot and full production, ensuring robust transfer of technology and clear documentation. Utilize analytical techniques (GC, NMR, FTIR, MS) to characterize materials, monitor reactions, and assess process performance. Document experiments, observations, and recommended improvements in lab notebooks and technical reports. Support process hazard assessments, safety reviews, and compliance with environmental, health, and safety regulations. Maintain awareness of industry developments, new technologies, and specialty chemical manufacturing best practices. Perform other duties as assigned. KNOWLEDGE/ EXPERIENCE/SKILLS: To perform the job successfully, an individual should demonstrate the following competencies: Bachelor's degree in Chemistry, Chemical Engineering, or a related field. Master's degree preferred. 1-3+ years of experience in specialty chemical synthesis, chemical process development, or scale-up preferred. Hands-on experience with laboratory techniques and equipment preferred. Background in synthetic organic chemistry, including multi-step synthesis and reaction mechanism understanding is preferred. Experience with process development, including reaction kinetics, heat, and mass transfer, mixing, and scale-up considerations is preferred. Hands-on experience with analytical instrumentation (GC, NMR, FTIR, MS) is preferred. Excellent written and verbal communication, including technical reporting. Commitment to maintaining a safe and compliant work environment. Must be able to wear required PPE (safety shoes, glasses, gloves, hard hat; respirators as needed). Must be able to climb ladders and stairs to collect samples and observe processes. Must be able to lift up to 50 pounds and operate a forklift. Must be able to work 2nd shift: Four (4) 10-hour shifts, Monday-Thursday, 12:30 PM - 11:00 PM Supplemental Company Information: Gelest, located in Morrisville, PA-conveniently accessible from Interstate 95, Route 1, and the PA/NJ Turnpikes-offers a rewarding career with competitive pay and a comprehensive benefits package, including: Generous paid time off Medical, Dental, Vision, and optional supplemental plans for employees and their families 401(k) with a competitive company match Company-paid Life Insurance, AD&D, Short-Term Disability, and Long-Term Disability Eligibility for an annual performance bonus Company-provided uniforms, work boots, and PPE The salary range for this position is $27.00 (entry level) - $35.00 per hour. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills, internal peer equity, as well as market and business considerations may influence base pay offered. This salary will be subject to a geographic adjustment (according to a specific city and state), if an authorization is granted to work outside of the location listed in this posting.

HOURLY R&D TECHNICIAN - 1ST GUILFORD TEXTILES, KENANSVILLE, The primary responsibility of this position is the processing of R&D sample orders and all support functions. This includes but is not limited to preparation, finishing, lamination, inspection of sample orders, all associated record keeping of technical parameters, and distribution of samples to internal and external customers. The technician will have responsibility for cutting, labeling, mounting, and distributing samples to the Lear Sales and Engineering teams to submit to customers for new business consideration. Great attention to detail and pride in workmanship is absolutely critical. The Role: Your work will include, but not be limited to: * The technician is expected to assist as needed to process samples through any and all equipment as needed. The ideal candidate will have experience on a variety of equipment and/or the ability and willingness to learn new processes and equipment * The technician will execute carton requisitions from receipt to closure and is expected to maintain requisitions to a minimal level * Responsibility for sample embossing and welding operations. * The associate will participate in regularly scheduled sample preview and review meetings and is expected to contribute independent point of view. Advantages of working for Lear at the Kenansville Plant: * Medical Benefits * 401k * Advancement to leadership * Employee 24/7 Resource System * Employee Discounts Your Qualifications: * Ability to follow departmental work instructions, standards of operations (SOPs), verbal and written directions * Adapt to using multiple tools and equipment * Attend sample review meetings * Background in PLC ladder logic troubleshooting. * Ability to troubleshoot AC and DC drives * Must be High School Graduate or have a GED. * Must have intermediate functional knowledge of Basics, English and metrics units, measuring systems, and conversions * Intermediate functional knowledge of Microsoft Excel and Word and other custom oftware. * Must be able to pass Background and Drug Screening * Ability to lift up to 50 pounds and to stand for a prolonged amount of time. * Please include resume WORKING CONDITIONS The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job * Constantly work under tight time constraints * Occasionally work mandatory overtime * May occasionally have exposures to extreme wet and/or humid conditions, heat/cold temperatures, and loud machine/equipment * The employee is occasionally exposed to vibration, fumes or airborne particles PERSONAL PROTECTIVE EQUIPMENT REQUIREMENTS Required during production duties: * Eye protection * Hearing Protection * Steel toe/ Non-Slip shoes * Reflective Vest (where applicable) NOTICE The above job profile does not include all essential and nonessential duties of this job. Other job duties may be assigned as needed. All employees with disabilities are encouraged to contact the Human Resources Department to review and discuss the essential and nonessential functions of the job. The employee with a disability can evaluate the job in greater detail to determine if she/he can safely perform the essential functions of this job with or without reasonable accommodation. DISCLAIMER Job profiles are not intended, nor should they be construed to be, an exhaustive list of all responsibilities, tasks, skills, efforts, working conditions or similar behaviors, attributes or requirements associated with a job. A job profile is not a comprehensive job description. It is intended for the sole purpose of acquainting a person who is unfamiliar with such position with a brief overview of the position's general direction and scope. Lear Corporation is an EEO/Affirmative Action employer, and all qualified applicants will receive consideration for employment without regard to race, sex, national origin, disability, veteran status, or any other status in accordance with law. Location Code: 0781 Nearest Major Market: Fayetteville