Regulatory Scientist (Technical Expert 3)
AgHires
Company Description: At Syngenta Seeds Field Crops, we're shaping the future of agriculture and empowering farmers to meet the ever-growing demand for food and fuel. We're a global Ag Tech powerhouse, headquartered in the United States, with passionate, local experts collaborating with farmers to deliver solutions that create market opportunities. We unite precision breeding, advanced biotechnology trait choice, and digital platforms for unmatched in-field performance. Our seeds help mitigate risks such as disease, insect, weed, and extreme weather pressures, all while promoting sustainable farming practices that protect and enhance our planet. Join our mission of revolutionizing food security and transforming agriculture. Job Description: Syngenta's Traits Characterization and Product Safety (TC&PS) group is committed to applying world-class science and winning innovation to offer farmers safe, cost-effective solutions that address the demands of a rapidly changing world. We are looking for a scientist with experience in molecular biology and sequencing to join our Molecular Characterization Team. As a Regulatory Scientist (Technical Expert 3), you will design, execute, and oversee molecular characterization studies, and prepare safety study reports following Good Laboratory Practice Standards (GLPS) to support regulatory submissions of Syngenta's genetically modified (GM) crops and products developed through New Genomic Technologies (NGT), such as gene editing. You will provide technical guidance and scientific advice across broad areas of expertise, and will work with cross-functional teams to support development of GM and NGT crop products and to interpret and apply safety assessments required by regulatory authorities for product approval and maintenance. Accountabilities: Independently plan, execute, and coordinate the delivery of studies conducted by the Molecular Characterization Team (MCT) in compliance with all safety, GLPS, and regulatory requirements. Document experiments and results, interpret data, and write and review complex technical documents (protocols, reports, Standard Operating Procedures, guidance documents). Provide technical expertise and guidance on the application of molecular biology and sequencing technologies for characterization of GM and NGT products (e.g. sequencing, applications of gene editing technologies such as CRISPR-CATCH, real-time PCR). Evaluate new and state-of-the-art molecular (DNA, RNA) characterization technologies and establish validated methodologies to enable the expansion of tools available for characterizing various data sets. Play an active role in identifying, solving, and managing a variety of technical issues or challenges. Identify risks to Syngenta products and contribute to the development, communication, and implementation of risk management and mitigation plans. Communicate complex technical issues with stakeholders, provide techno-regulatory expertise, and prepare technical documents as required by regulatory authorities. Lead projects and/or represent TC&PS in multi-disciplinary regional or global product development teams, providing key input into the development of regulatory and safety strategies. Stay at the forefront of technological and techno-regulatory advancements to enhance and maintain technical expertise, deliver maximum value for Syngenta, and establish yourself as a trusted subject matter expert. Play an active role in identifying operational bottlenecks and establishing efficient ways-of-working through process development and optimization. Qualifications:
PLEASE NOTE:
PhD degree, or equivalent combination of education and experience, with at least 6 years of professional experience in Plant Biology, Molecular Biology, Genomics or related discipline. Demonstrated proficiency in Next Generations Sequencing (NGS), data handling, pipeline optimization and development, and Bioinformatic analyses, Linux environment, and desired experience in relevant programming languages (e.g. Bash scripting, Python). Demonstrated proficiency in molecular biology laboratory techniques, encompassing DNA and RNA extraction from plants, cloning, PCR, and sequencing (e.g. Sanger, Illumina, PacBio, Oxford Nanopore), with desired experience in CRISPR-Cas technologies. Demonstrated proficiency for designing, conducting, interpreting and reporting molecular characterization studies, preferably of GM or NGT crops, using standard methodologies (sequencing, real-time PCR), and proven record of solving difficult and complex technical problems. Understanding of regulatory science and study requirements for the molecular characterization of GM and NGT products and their safety assessments is desirable. Experience as GLP study director or monitor of GLPS or familiarity with quality management systems is preferred. Experience working with external collaborators and contract research organizations is desirable. Additional Information: What We Offer: A culture that celebrates belonging and collaboration, promotes professional development and strives for a work‑life balance that supports the team members. Offers flexible work options to support your work and personal needs. Full Benefit Package (Medical, Dental & Vision) that starts your first day. 401k plan with company match, Profit Sharing & Retirement Savings Contribution. Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. #J-18808-Ljbffr AgHires- ...quality oversight—serving as a technical resource and mentor while... ...pathological conditions, using expert knowledge of normal cell morphology... ...Support quality assurance, regulatory compliance, proficiency testing... ...Science Required Experience 3 Years Clinical - Clinical...Regulatory
- Overview: The Medical Laboratory Scientist III performs routine and... ..., quality control, regulatory, administrative, staff development... ...or crosses disciplines as a technical expert. Trains new employees in the... ...Anthropology Required Experience: 3 Years Clinical - Clinical...RegulatoryRelocation package
$66k - $171.6k
...world.Responsibilities : The Scientist - TSMS PAR will initially focus... ..., specifically regarding technical transfer and process validation... ...Product Reviews, Change Controls, Regulatory Submissions, Deviations,... ...STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.Additional...RegulatoryFull timeH1bWork at officeVisa sponsorshipWork visaMonday to FridayFlexible hours- ...treatment protocols and ensure compliance with regulatory standards. In addition, this position... ...therapy. Troubleshoots and resolves technical issues with radiation therapy equipment,... ...and experiences you'll need to succeed: 3 years of experience [Required] American...RegulatoryFull timeLocal areaShift work
$90k - $110k
...Serve as Project Manager and/or Technical Lead on projects. Lead/... ...estimates). Review deliverables for regulatory compliance, participate in... ..., Professional Wetland Scientist) Salary Range $90,000.00 - $... ...on E-Verify, please visit #J-18808-Ljbffr Utah Channel 3RegulatoryWork at officeFlexible hours- ...Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers... ...every day. Join us!**What the Clinical Scientist does at Worldwide**As a member of the Clinical... ..., and supports the development of key regulatory deliverables such as clinical study...RegulatoryRemote jobWork at officeWorldwide
$84.58 - $121.59 per hour
...maintenance. Perform routine safety checks and ensure compliance with regulatory standards. Patient Safety: Ensure the accurate delivery of... ...Radiology. Professional Experience Requirements: Two to three (2-3) years of clinical experience preferred. Experience with...RegulatoryHourly payFull time- ...Development team, the Clinical Scientist is responsible for... ...internal and external experts and in support of the... ...scientific guidance and technical expertise within teams,... ...advisory boards, and regulatory meetings). Accountable... ....A.) in Life Sciences 3-5 years of experience...RegulatoryLocal area
- ...seeking a highly accomplished Scientist III is a key individual... ...that support product decisions, technical improvements, and project milestones... ..., Operations, Quality, Regulatory, and Commercial teams to align... ...related Life Sciences field with 3+ years of relevant industry...RegulatoryContract workWork at officeFlexible hours
$128.6k - $210k
...components of the Clinical Study Reports and may support development of regulatory documents; may perform quality review Maintains compliance in... ...preferred (PhD/MD/PharmD/MSc). We are seeking ≥ a minimum of 3 years of pharmaceutical clinical drug development experience....RegulatoryLocal area$200k
...assignments. Clinical Laboratory Scientist (Technical Specialist), GS-12.... ...medical laboratory technology, regulatory and accrediting agency requirements... ...Specialist CLS, providing expert authoritative advice and... ...experience within the past 3 years. Reference For more...RegulatoryWork at officeFlexible hoursShift work- ...seeking a Project Environmental Scientist/Planner in our Raleigh, NC... ...permitting; coordinate with regulatory agencies and clients; conduct... ...environmental documents and supporting technical analyses. Assist with work... ...for H-1B, L-1, TN, O-1, E-3, H-1B1, F-1, J-1, OPT, CPT...RegulatoryFull timeTemporary workH1bWork at officeFlexible hoursNight shift
- ...ideal candidate will have 5-10 years in analytical development, a strong grasp of small molecule methods, and be able to navigate regulatory environments. Benefits include a competitive salary of $125,000-$165,000, bonus eligibility, and comprehensive health packages....Regulatory
- ...experienced Medical Laboratory Scientists II (MLS II) to join a high-... ...Evenings — Monday-Friday | 3:00 PM–11:00 PM (rotational weekends... ...independent judgment, strong technical expertise, and a commitment... ...in compliance with regulatory standards. The MLS II may...RegulatoryPermanent employmentFull timeLocal areaRelocation packageMonday to FridayShift workWeekend workDay shiftAfternoon shift
- ...Consultants, Inc. is seeking a Senior Water Resources Scientist in Raleigh, NC to provide technical leadership for municipal stormwater programs. You... ...agency clients on Clean Water Act compliance, develop regulatory documentation, and manage watershed initiatives. The...RegulatoryRemote job
- AgHires is seeking a Regulatory Scientist in North Carolina to join their Molecular Characterization Team. The ideal candidate will have a PhD and at least 6 years of experience in molecular biology or genomics, overseeing studies that support the regulatory approval of...RegulatoryFlexible hours
- ...pharmaceutical products and raw materials. In this role, you will work within a GMP-regulated laboratory, ensuring methods meet regulatory standards while supporting quality control and product release. The ideal candidate will hold a degree in Chemistry or a related...Regulatory
- ...assume responsibility for one or more laboratory projects or functions such as performance improvement, safety, quality control, regulatory, administrative, staff development, and computer systems. Trains new employees and/or students in the theoretical and operational...RegulatoryRelocation package
- ...products and raw materials. Working within a GMP‑regulated laboratory, you will play a key role in ensuring analytical methods meet regulatory standards and support quality control and product release. Key Responsibilities Develop and validate analytical methods in...Regulatory
- ...instrumentation, etc. May assume responsibility for one or more laboratory projects or functions - i.e. PI, safety, quality control, regulatory, administrative, staff development, computer (LIS, HIS, hospital intranet, PC applications), etc. Trains new employees and/or...RegulatoryRelocation package
- ...Health Commercial LLC is seeking a Clinical Scientist specializing in Oncology. This role... ...ideal candidate will engage with external experts and manage project scopes, objectives, and deliverables while adhering to regulatory guidelines. Competitive benefits including...RegulatoryFlexible hours
- ...will perform field data collection, participate in agency meetings, and assist in regulatory document preparation. An ideal candidate will have a BA/BS in related fields and a strong technical writing background, with knowledge of ESRI ArcGIS preferred. This role includes...Regulatory
- ...development projects. The ideal candidate will have a Master's Degree in Life Sciences and a strong understanding of clinical trials and regulatory submissions. This role involves coordinating data, writing clinical documents, and ensuring effective communication across...Regulatory
- ...opportunity for a Senior Water Resources Scientist to join our expanding national Water... ...discretion. In this role, you will provide technical leadership and project management for... ...implementation strategies, supporting regulatory negotiations and enforcement responses,...RegulatoryWork at officeRemote workWork from homeHome office
$28 - $37 per hour
...x 10-hour shifts: 9:00 PM – 7:00 AM ~3 x 12-hour shifts: 7:00 PM – 7:00 AM ~... ...Adhere to all CLIA, CAP, and laboratory regulatory requirements Ensure proper specimen handling... ...Medical Technologist/Medical Laboratory Scientist certification required Bachelor’s...RegulatoryHourly payPermanent employmentLocal areaShift workNight shift$75k - $80k
...development, and manufacturing projects. Develop and validate analytical test methods in accordance with industry standards and regulatory requirements. Operate, calibrate, and maintain laboratory equipment such as HPLC, GC, FTIR, UV-Vis, and other analytical instruments...RegulatoryFull time- ...functional team of internal and external experts and in support of the clinical director.... ...data. Provide scientific guidance and technical expertise within teams, across departments... ..., scientific advisory boards, and regulatory meetings). Write, review, edit, and approve...Regulatory
- Syneos Health/ inVentiv Health Commercial LLC is seeking a Clinical Scientist in Ophthalmology. This role is crucial for developing medical plans, conducting medical reviews, and ensuring regulatory compliance while collaborating with various teams. The ideal candidate...RegulatoryFlexible hours
- ...with federal, state and local regulations. Prepare applicable permit applications, risk assessments and technical documents including proposals, reports and regulatory agency correspondence. Design systems and environmental protection plans. Projects may include Phase I/...RegulatoryLocal area
- ...Principal Clinical Scientist What if your expertise in clinical trial design and regulatory science could directly shape how AI reasons about clinical evidence influencing... ...regulatory expectations Provide structured expert feedback that directly improves how AI models...RegulatoryHourly payOngoing contractContract workFreelanceRemote workFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Scientist (Technical Expert 3). Be the first to apply!
- machine learning research scientist Raleigh, NC
- drug safety scientist Raleigh, NC
- remote scientist Raleigh, NC
- graduate scientist Raleigh, NC
- operations research scientist Raleigh, NC
- senior scientist Raleigh, NC
- applied scientist Raleigh, NC
- water quality scientist Raleigh, NC
- analytical scientist Raleigh, NC
- qc scientist Raleigh, NC


