Scientist jobs in Cary, NC

**1\. Role Overview**Mercor is seeking applied data science professionals to support a strategic analytics initiative with a global enterprise. This contract-based opportunity focuses on extracting insights, building statistical models, and informing business decisions through advanced data science techniques. Freelancers will translate complex datasets into actionable outcomes using tools like Python, SQL, and visualization platforms. This short-term engagement emphasizes experimentation, modeling, and stakeholder communication - distinct from production ML engineering. **2\. Key Responsibilities** ● Translate business questions into data science problems and analytical workflows ● Conduct data wrangling, exploratory analysis, and hypothesis testing ● Develop statistical models and predictive tools for decision support ● Create compelling data visualizations and dashboards for business users ● Present findings and recommendations to non-technical stakeholders **3\. Ideal Qualifications** ● 5+ years of applied data science or analytics experience in business settings ● Proficiency in Python or R (pandas, NumPy, Jupyter) and strong SQL skills ● Experience with data visualization tools (e.g., Tableau, Power BI) ● Solid understanding of statistical modeling, experimentation, and A/B testing ● Strong communication skills for translating technical work into strategic insights **4\. More About the Opportunity** ● Remote ● **Expected commitment: min 30 hours/week ● Project duration: ~6 weeks** **5\. Compensation & Contract Terms** ● $75-100/hour ● Paid weekly via Stripe Connect ● You'll be classified as an independent contractor **6\. Application Process** ● Submit your resume followed by domain expertise interview and short form **7.About Mercor** ● Mercor is a talent marketplace that connects top experts with leading AI labs and research organizations ● Our investors include Benchmark, General Catalyst, Adam D'Angelo, Larry Summers, and Jack Dorsey ● Thousands of professionals across domains like law, creatives, engineering, and research have joined Mercor to work on frontier projects shaping the next era of AI

Job DescriptionDescriptionThis position is ideal for an early-career machine learning scientist to join the AI & Machine Learning team as a Machine Learning Scientist, supporting photo-based diagnostics and remote treatment monitoring. Partnering with other machine learning specialists and product marketing, you'll provide technical solutions to complex problems in computer vision and 3D data analysis to support Align's product portfolio. This role is key to building out Align's core technology capabilities. Role expectations Use data science and machine learning to solve complex, multidisciplinary challenges in applied research and turn technology know-how into execution in a dynamic business environment Develop algorithms and models in collaboration with business partners, product managers, and software engineers to solve key business initiatives Design and implement machine learning techniques to improve treatment planning, customer engagement, and device manufacturing based on historical data Collaborate effectively with other data science teams globally to ensure technology re-use and transfer of new capabilities to drive innovation Quickly learn and assimilate new business processes, ideas and concepts to formulate conclusions and deliver results. Identify features and data needed for machine learning solutions. Help to deliver a vision for our product evolution using machine learning Stay current on the emerging directions in AI-technologies and support the development of the AI/ML roadmap Stay current on specific AI-technologies and apply them in an appropriate manner to applicable projects What we're looking for What we're looking for 5+ years of relevant experience 2+ years of machine learning research practice (including graduate work) Masters degree or higher in Computer Science, Statistics, Machine Learning, Statistical Data Modeling or related field. Knowledge of machine learning theory and practice. 2+ years in a data-science-oriented programming language such as Python or R Strong interpersonal, oral, written, and visual communication skills, with ability to present findings concisely and effectively. Ability to collaborate effectively with developers, program management, and internal customers on objectives, requirements and design constraints in a distributed development environment. Able to solve complex, multidisciplinary challenges in applied research and turn technology know-how into execution in a dynamic business environment Experience in developing software in an Agile SDLC Experience in collaborative work with users and other technical teams Strong background in Computer Vision, Pattern Matching, or Medical Applications. Pay TransparencyIf provided, base salary or wage rate ranges are the range in which Align reasonably expects to set a candidate's pay for the posted position. Actual placement depends on the individual skills and experience level of a candidate plus the total compensation and equity across team members. For other locations outside of the primary location, the base salary range will be adjusted geographically. For Field Sales roles, the salary listed is the base pay only and does not include the applicable incentive compensation plan. A cost of living adjustment may be added to base pay for higher cost areas in the U.S. Our internship hourly rates are a standard pay determined based on the position and your location, year in school, degree, and experience. General Description of All BenefitsWe are pleased to provide a general description of the benefits Align offers to full-time employees in this position. Family Benefits. Align offers employees and their eligible dependents medical (with a Health Savings Account option for some plan offerings), dental, and vision in accordance with those plans. Align also offers to employees: Discounts on Invisalign and Vivera to employees and their eligible dependents after 90 days of employment Back-up Child/Elder Care and access to a caregiving concierge Family Forming Benefits - Available to Employees, and their spouse or domestic partner, covered under one of Align's health plans Breast Milk Delivery and Lactation Support Services Employee Assistance Program Hinge Health Virtual Physical Therapy - Available to all employees and eligible dependents (age 18+) enrolled in an Align medical Plan Employee benefits. Align offers its employees: Short-term and long-term disability insurance in accordance with those plans. Basic Life Insurance and Accidental Death and Dismemberment. Voluntary Supplemental Life Insurance for Employee, Spouse/Domestic Partner, and Child(ren) are available for purchase in accordance with those plans. Flexible Spending Accounts - Employees may be eligible to participate in a health care account (including a limited health FSA if enrolled in a HDHP), dependent care account, and a pre-tax commuter benefit plan. 401k plan (with a discretionary Company match of 50% up to 6% of eligible earnings up to a maximum match of 3%.). Employer match vests after two years - 25% year one and 100% at year two. Align offers traditional, Roth, and after-tax options. Employee Stock Purchase Program (Employees must work 20 hours or more and be employed on purchase date to be eligible). Paid vacation of up to 17 days during the first full year of employment (currently accrued at the rate of 5.24 hours each pay-period), which carries over to a maximum cap of 30 days. Annual paid vacation time accrual increases based on tenure. Both exempt and non-exempt employees who work 32 hours or more per week receive prorated vacation accrual based on their regularly scheduled work hours and tenure. Sick time is accrued throughout the year at the rate of one hour for every thirty worked. Employees can carry over unused sick leave each year, up to a maximum balance of 80 hours. 11 Company-designated paid holidays throughout the year. If employed for at least 12 consecutive months, Align will grant up to 6 weeks of paid Parental Leave. If employed for less than 12 consecutive months, Align will grant up to 4 weeks of paid Parental Leave. All parental leave must be completed within one year of the birth or placement of the child. Parental leave is in addition to any state and/or local parental leave benefits. Three days of paid bereavement leave. In some cases, due to travel the amount of paid leave may be extended to 5 paid days off. To the extent applicable state or local law offers more generous benefits, Align complies with any such law. Non-exempt employees will receive full pay for up to 10 days of jury duty. Exempt employees will receive their full salary during any week they serve and perform any work. Other insurance such as legal, critical illness, voluntary accident, long-term care, auto, home and pet insurance are available for purchase. To the extent applicable state or local law offers more generous benefits, Align complies with any such law.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • The incumbent will join the Manufacturing Science and Technology (MSAT) organization supporting biological therapeutics and vaccines. Within MSAT, the candidate will work in the Purification Group, which develops processes for isolation and purification of recombinant proteins, polysaccharides, bioconjugates, and other biologics. • Execution of lab or pilot-scale purifications using column chromatography, Tangential Flow Filtration (TFF), and/or Normal Flow Filtration (NFF), as needed. • Preparation of equipment, solutions, consumable materials, etc. as needed to support experiment execution. • Preparation of technical reports and presentations to communicate results to scientists and management, as required. Qualifications Able to execute experimental protocols, interpret data, and communicate results from experimental studies conducted at lab, pilot, or commercial scales. Additional Information Best Regards, Anuj Mehta ************

Summary of Key Responsibilities: Develop and validate skin permeation and/or LC-MS/MS analytical test methods with minimal guidance from senior laboratory personnel Carry out laboratory work as directed by senior laboratory personnel Conduct routine analytical experiments using established analytical methods and procedures Assist with assembling and review of data packs Prepare detailed protocols and technical reports for development, validation, and post-validation activities Conduct experiments by developing new analytical methods or using established analytical methods including in vitro permeation testing techniques and LC-MS/MS Data entry into spreadsheets, as directed by senior laboratory personnel For LC-MS/MS experiments independently perform full data review of chromatography, transcription checking of spreadsheets, and calculation review of spreadsheets For Skin permeation/IVPT experiments transcription checking and calculation review of spreadsheets Review and maintain laboratory notebooks Assist in training of entry-level employees Manage essential laboratory activities including equipment maintenance schedules, chemical and laboratory supply inventory Required Qualifications and Skills: B.S with 3-8 years of experience, or M.S with 2-6 years of experience: focus in chemistry, biology, pharmaceutical sciences or related scientific discipline 2-5 years of experience in a GxP laboratory setting in the pharmaceutical industry Experience in either LC-MS/MS or IVPT/Skin permeation testing, troubleshooting and validation Demonstrated experience in developing and implementing new technologies, ways of working, and/or tools to improve capability Technical report writing proficiency Experience with other general laboratory instruments and wet chemistry techniques Proficiency in Analyst and/or MassLynx and MS Excel Speaks, writes, listens and presents information in a logical and articulate manner appropriate for the audience Thorough when performing work, conscientious about attending to detail, and uses logical thinking that is well-organized and methodical

Piper Companies is seeking an Associate Scientist for a clinical stage gene therapy start-up located in Durham, North Carolina (NC). This Associate Scientist will have the exciting opportunity to be a part of a fast-growing startup and enjoy a dynamic role where responsibilities evolve with the company's needs, offering variety, impact, and room to innovate. This is an on-site position in Durham, NC. Responsibilities of the Associate Scientist: * Perform molecular and cellular biology techniques (DNA/RNA purification, qPCR/dd PCR, ELISA, SDS-PAGE, JESS/WES). * Maintain and transfect/transduce mammalian cell lines for plasmid and vector characterization. * Design and execute cloning workflows (restriction enzyme cloning, Gibson assembly). * Record procedures and results in ELN to support nonclinical study reports. * Collaborate with cross-functional teams on vector construct development and in vitro testing. Qualifications for the Associate Scientist: * Bachelor's in life sciences with 4-5 years industry experience, Master's with 2-3 years, or PhD with relevant research background. * Skilled in molecular cloning, plasmid prep, PCR assays, and gel electrophoresis. * Hands-on experience with mammalian cell culture, cell line engineering, and transfection. * Familiarity with ELN tools (e.g., Benchling) and molecular biology software for cloning and sequence analysis. * Experience with western blotting techniques * Ability to work independently in a fast-paced lab with minimal supervision. Compensation for the Associate Scientist: * Salary Range: * Comprehensive Benefits: Sick leave if required by law, medical, dental, vision, 401K This job opens for applications on 11/10/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords: Associate Scientist, gene therapy, Benchling, mammalian cell culture, HEK293, DNA purification, RNA purification, molecular cloning, plasmid prep, PCR, qPCR, dd PCR, gel electrophoresis, ELISA, SDS-PAGE, JESS/WES, Gibson Assembly, restriction enzyme cloning, sequence analysis, transfection, transduction, cell line engineering, ELN, in vitro assays, vector characterization, western blotting, protein analysis, biotechnology, nonclinical studies #LI-GP2 #LI-ONSITE

ABOUT GREENLIGHT GreenLight Biosciences is using RNA to create a world where plants, people, and the planet can thrive together. The company is developing highly effective agricultural solutions for farmers and beekeepers that are targeted to specific pests and degrade quickly in the environment. Our pipeline includes products to protect honeybees and a range of fruits and vegetables. The GreenLight platform allows us to research, design, and manufacture across multiple product categories including insecticides, fungicides, and herbicides. For more information, visit ********************** The Associate Scientist, Process Development at GreenLight BioSciences in Durham, NC will serve as a key member and technical leader of the process development team and support their overall mission of delivering high performance RNA production processes and products to the market. Specific responsibilities include: Support early-stage product development by performing laboratory scale fermentation, RNA production and downstream processing; Run 10 L fermentation experiment to produce plasmid DNA using strains developed by strain engineering team; Collect samples from fermentation experiment and assess process metrics such as plasmid DNA titer, plasmid DNA yield and quality; Perform downstream unit operations to recover plasmid DNA; Run 10 L RNA synthesis experiment using the plasmid DNA and assess process metrics such as RNA titer, yield and purity; Troubleshoot and identify opportunities for improvements in RNA production process by doing DoE based optimization experiments; Do statistically designed multifactorial optimization experiment i.e., Design of Experiment (DoE); Design, plan, execute the experiment, collect samples and run analytical methods for RNA titer, yield, analyze the data, fit curves, make model, do model predictions using statistical data analysis tool; Validate the model prediction, test reproducibility and robustness of the optimized RNA synthesis process conditions; Lead development of next generation processes to improve RNA production metrics; Using DoE and rationally designed experiments, identify the parameters limiting performance of RNA synthesis process; Formulate strategies to address the limitations such as developing new processes, identifying better raw materials, etc., to improve RNA production metrics; Create tasks, delegate and supervise team members towards completion of project goals; Develop, author and implement Standard Operating Procedures (SOPs) for process development activities; Write protocols and development reports for the new processes; Document in Quality Management System; train team members on the new protocols; Scale-up and tech transfer bench-scale processes to pilot production scale; Demonstrate scale-up by evaluating the new process in 10 L scale; Train production team members; Perform and report on procedures to quantitatively measure analytes (DNA, RNA, proteins, ions, etc.,) in a variety of matrices for analytical testing support; Run RNA analysis methods such as RNA concentration, RNA purity; Run DNA analysis methods such as restriction digestion and agarose gel electrophoresis; Run HPLC for small molecules, DNA, RNA; Make data driven decisions and identifies root causes to help solve problems and achieve opportunities; Test assays on different lots of DNA, enzyme samples to evaluate batch-to-batch variability; Identify causes for variability using the assay data; Work collaboratively with operations and quality management team members and communicate effectively to accomplish project goals and milestones; Work with cross-functional teams such as Strain Engineering, Manufacturing, QA/QC; and Plan data review meetings, present results and conclusions, suggest directions and next steps REQUIREMENTS: B.S. in Chemical Engineering, Biochemistry or related field, plus 24 months of experience or similar role in strain engineering field for aseptic techniques, bacterial culture, extraction and characterization of DNA, UV/VIS absorbance, gel electrophoresis, sequencing data analysis is required. Such experience must include: 12 months of experience as a research associate or similar role in process development handling lab-scale bioreactors for running fermentation, downstream processing equipment such as cell harvest by centrifugation, TFF, DNA column chromatography purification; 12 months of experience as a research associate or similar role handling analytical equipment such as HPLC to quantify DNA, RNA, organic acids; and 12 months of experience working with electronic lab notebook, laboratory information management system and statistical software such as GMP. Greenlight Biosciences Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type 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. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Job Description To perform experiments, ensuring that projects are completed to plan, while complying with all quality and safety regulations. Assist with study plan writing, data analysis and interpretation, and report writing. Essential Functions: Assist or act as the lead scientist on assigned studies. Draft study plans and contribute to the preparation of reports for sponsors. Review literature and appropriate guidances (FDA and/or EMA) in preparation for studies and to regularly update knowledge by reviewing appropriate literature. Perform experiments (with supervision as needed) in line with in vitro testing such as in vitro permeation and penetration studies, in vitro release testing studies, extractions, stability studies, etc. Assist with data analysis for studies related to in vitro testing. Confer with scientists, study managers, and management to conduct analyses of research projects, interpret test results, or develop nonstandard tests. Crosstrain and assist with research biology activities (e.g. PCR, PK/PD, etc.) as needed. Report any amendments or deviations from Study Plans/SOPs to Lead Scientist and/or Study Director, as appropriate. Maintain laboratory instruments to ensure proper working order and troubleshoot malfunctions with scientists when needed. Adhere to MedPharm Standard Operating Procedures (SOPs) and guidance documents, where applicable. Contribute to the preparation and review of SOPs and Forms where applicable. Where applicable, promptly record all data according to Good Documentation Practices. Adhere to MedPharm Health & Safety Policy and OSHA regulations at all times and to ensure the safety of others in any procedures or tasks performed. Ensure that all documentation, computer data, and records are stored appropriately. Any other duties and/or tasks that may be assigned Powered by JazzHR CgdzTtjodV

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity. To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com Job Description: • The incumbent will join the Manufacturing Science and Technology (MSAT) organization supporting biological therapeutics and vaccines. • Within MSAT, the candidate will work in the Purification Group, which develops processes for isolation and purification of recombinant proteins, polysaccharides, bioconjugates, and other biologics The incumbent responsibilities will include the following: • Execution of lab or pilot-scale purifications using column chromatography, Tangential Flow Filtration (TFF), and/or Normal Flow Filtration (NFF), as needed. • Preparation of equipment, solutions, consumable materials, etc. as needed to support experiment execution • Preparation of technical reports and presentations to communicate results to scientists and management, as required. Qualifications Requirement: • Bachelor's degree or graduate degree in Chemistry, Chemical Engineering or related biotechnology field. Industrial experience is preferred. • Experience with operating and monitoring of Tangential Flow Filtration (TFF), Normal Flow Filtration (NFF), and chromatography systems is desired • Experience with conjugation chemistry is highly desired. Additional Information All your information will be kept confidential according to EEO guidelines. IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-357-1104 ASAP! I look forward to hearing from you!

Locations: This role requires associates to be in-office 1-2 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office engagement with the autonomy of virtual work, promoting a dynamic and adaptable workplace. Alternate locations may be considered if candidates reside within a commuting distance from an office Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law. PLEASE NOTE: This position is not eligible for current or future VISA sponsorship. The Research Scientist-Health Services Research is responsible for Carelon Research research line of business; specific projects ranging from retrospective to large-scale, prospective studies in areas including population health, health economics, clinical effectiveness (drug, procedures, vaccine, and medical device), and implementation sciences. This role will conduct research studies for Elevance Health, Carelon, and external clients. How you will make an Impact: * Leads high quality research project proposal development from early conceptual stages for external and internal submissions. * Provides scientific rigorous input in the design and development of the research studies to fulfill study objectives. * Executes statistical analyses plans independently with effective problem solving and decision making as principal investigator across a broad program of studies related to a therapeutic area /healthcare intervention and/or external collaborator. * Collaborates with project team members to implement the study design and statistical analyses plans utilizing advanced statistical techniques such as propensity score modeling, GEE (generalized estimate equation) difference-in-difference, and graduate-level statistics in performing research study design and analysis. * Conducts review of administrative claims, electronic medical records, and survey and clinical data and statistical output and review of statistical output to ensure the superior quality of research activities and client deliverables. . * Summarizes key findings and generates value messages for incorporation into project deliverables, publications, and presentations. * Prepares study reports and manuscripts for submissions to peer-review journals demonstrating subject matter expertise. * Performs key project functions with minimal oversight. * Responsible for the final quality and accuracy of study deliverables, presentation of study deliverables and facilitation of the collaboration among project team members towards development. * Manage relationships with study champions/clients, communicates scientific decisions, and presents key study insights to the champions, including Elevance Health senior leadership team, internal decision makers, and other external stakeholders/clients. Minimum Requirements: Requires a MS in health sciences or related advanced degree, or clinical degree such as PharmD, or MD, combined with Master level degree and a minimum of 5 years of experience in health service research, biostatistics, epidemiology, health policy, economics or related field; or any combination of education and experience which would provide an equivalent background. Preferred Skills, Experiences and Competencies: * Ph.D. or MD strongly preferred. * Postgraduate or post-doctoral training or relevant experience in conducting observational and/or prospective research studies. * Understanding of the U.S. health care system, population health and implementation sciences strongly preferred. * Successful experience with research grants/funding applications is strongly preferred. * Proficient in statistical software, including SAS, STATA, R, and/or Python strongly preferred. * Proficient in data management tools, including SQL strongly preferred. Job Level: Non-Management Exempt Workshift: 1st Shift (United States of America) Job Family: RDA > Research Data Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

Codetta Bio is a venture-backed life sciences company with innovative solutions to some of the most significant challenges in the life sciences and healthcare industries. We are developing advanced multi-omic biomarker measurement tools supporting data-driven approaches to understanding the unique genetic, environmental, lifestyle, and clinical factors that contribute to individual health and wellness. Guided by an experienced leadership team, Codetta offers a high-energy, collaborative work environment with opportunities for professional advancement. The ideal candidate will be self-motivated, organized with excellent communication skills, as well as excellent writing skills. As this position relies heavily on working with a cross-functional team, time flexibility is important. The candidate must be comfortable in a fast-paced environment where everyone holds each other accountable and have the flexibility to meet during normal work hours and alternative hours as needed. Major Responsibilities: Responsible for manufacturing key bead-based reagents for Codetta Bio product lines Works with cross-function team to develop, qualify and validate methods to support reagent characterization and product release Optimizes reagent manufacture methods and contributes to improvement of process efficiency Responsible for maintaining appropriate documentation, including Batch Records, compliant with ISO9001 and GMP regulations electronically, and via paper record, as indicated Supports final product quality control Present data at regular meetings and contribute to scientific publications Occasional evening or weekend work when Required Qualifications: BS, or MS in chemistry, biochemistry, chemical engineering or related field 2 years experience working in biological reagent manufacturing, preferably in industry Direct experience with buffer formulation, general lab techniques (pipetting, use of pH meter, analytical balances, volumetric glassware), preferably in industry Direct experience with conjugation of protein and nucleic acids as well as surface (bead or other assay solid support) functionalization methods Exceptional organization skills and attention to detail Ability to work independently and manage time effectively Excellent written and verbal communication skills Collaborative and team-oriented Preferred Qualifications: Demonstrated knowledge and understanding of GMP, QA and QC functions associated with the manufacturing of assay-related products and compliance with ISO 9001 or similar. BSL-2 laboratory experience Direct experience with conjugation of protein and nucleic acids as well as surface (bead or other assay solid support) functionalization methods Direct experience with PCR and immunoassay methods and instruments Direct experience with ELNs, Benchling or similar Additional Information At this time, we are unable to sponsor visas for this position. All applicants must be authorized to work in the United States without company sponsorship. Work Location: On-site in Morrisville, NC

Career CategoryEngineeringJob DescriptionJoin Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Be part of Amgen's newest and most advanced drug substance manufacturing plant. The Amgen FleX batch facility combines the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility not only features the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities but also integrates sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027. Associate Engineer, Process Development What you will do Let's do this. Let's change the world. In this vital role you will be a part of the Process Development Drug Substance Technology group at Amgen's FleX Batch Biologics Manufacturing Facility. This role will be immersed in all aspects of operations in a commercial bulk drug substance facility, which includes collaborating with other drug substance teams across our network. Additionally, the Process Development Associate will use out-of-the-box thinking to contribute to technology development and will demonstrate the desire to expand and develop expertise in downstream protein purification, thereby further contributing to the integrated group. Apply a fundamental understanding of Downstream (Purification) Bioprocessing to support biologics technology transfer, process validation, and plant start-up Support continuous process verification, process monitoring, optimization, complex investigation, and product life cycle management Ensure safety and compliance of process development activities Provide process on floor process support as required Provide support for regulatory filing, inspection, and other CMC activities What we expect of you We are all different, yet we all use our unique contributions to serve patients. The scientific professional we seek is a leader with these qualifications. Basic Qualifications: High school diploma / GED and 6 years of Chemical, Biomedical, or related Engineering; Life Sciences; or other relevant sciences' experience OR Associates and 4 years of Chemical, Biomedical, or related Engineering; Life Sciences; or other relevant sciences' experience OR Bachelor's degree Preferred Qualifications: Master's degree in Chemical, Biomedical, or related Engineering; Life Sciences; or other relevant sciences Some experience in a technical role supporting biotechnology processes within regulated environments (i.e., cGMP) Understanding of protein purification/separation principles Understanding of process scale-up, technology transfer, troubleshooting, and complex investigation Strong oral and verbal communication skills, interact effectively with diverse internal and external stakeholders Familiarity in statistical analysis, analytical methods, and product quality attributes related to biological processing What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team.careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary Range -

Essential Responsibilities * Perform dose formulation analysis in support of GLP Toxicology assays * Perform method validations for HPLC and correlating stability studies for analysis of test articles or other chemicals. * Setup, maintenance and daily operation of HPLC system and related equipment. * Aid in the writing and editing of analytical and formulation sections within protocols and reports. * Prepare reagents, vehicles, solutions and suspensions following applicable SOPs, Protocols, and GLPs. * Receipt of controlled and non-controlled chemicals * Assures proper labeling, handling, and storage of all chemicals. * Maintain up-to-date chemical inventory * Perform solubility testing * Perform dose formulation calculations and preparations * Ensure chemical disposal is handled per local, state, and federal regulations * Communicate with Study Directors, Program Managers, and analytical labs to ensure adherence to study protocols Additional Responsibilities * Prepare dose formulations for in vitro and in vivo experiments as needed * Training of junior staff as needed. * Work in a team environment with a professional and positive attitude * Other duties as needed Minimum Acceptable Qualifications * Education: o B.S. in chemistry or related field * Experience: o Two years' experience in a GLP scientific environment * Skills: o Ability to perform basic unit conversion calculations o Experience working under GLP or regulatory requirements o Ability to use, troubleshoot, and maintain standard chromatography laboratory equipment. o Excellent written and oral communication skills o Excellent computer skills working with MS Word/Excel/Powerpoint o Attention to detail o Excellent organizational skills o Ability to exercise independent judgment * This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level. Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

Job DescriptionAt Whitman, Requardt & Associates, LLP, we are "People Focused and Project Driven". We have been in business for 110 years and we are known for our quality work and developing quality employee careers. We are seeking the very best and most talented to join our team - help us take on today's infrastructure challenges, develop advanced vision and innovative ideas, and design solutions for resilient, sustainable, efficient and effective multi-modal infrastructure improving and connecting our Communities, States, Countries, and World. We are currently seeking a Project Environmental Scientist/Planner in our Raleigh, NC office who is looking for growth opportunities and enjoys working on a wide variety of projects. The candidate for this position will lead natural system surveys, field investigations, and delineations including wetland delineations, conducting threatened and endangered species habitat evaluations and surveys, assist, support and prepare National Environmental Policy Act (NEPA) and State Environmental Policy Act (SEPA) documentation, planning and feasibility studies, and public outreach. The candidate will also lead Section 404/401 permitting, coordinate with regulatory agencies and clients, conduct permit compliance monitoring, conduct bat bridge inspections, conduct surveys for invasive species, prepare invasive species management plans, assist with stream stabilization/restoration projects, mentor and train junior staff, and any other services as required by specific projects. The candidate must have knowledge of and experience with the development of NEPA/ SEPA documents for State DOTs, FHWA, or FTA. The candidate would work collaboratively with teams on complex environmental documents, would manage projects and tasks commensurate to experience, and would be responsible for preparing environmental documents and supporting technical analyses. The individual will assist with work planning and scheduling, managing project budgets and scopes, with Business Development, including proposal preparation. The candidate will participate in the planning of transportation related projects. They must be innovative and adaptive at identifying problems and finding solutions. Responsibilities will also include assuring highest quality and deliverable expectations are always maintained. Periodic travel (including overnight) will be required to conduct field work and/or attend project meetings, as needed. Bachelor's degree in Environmental Planning, Biology, Geology, Environmental Engineering, Environmental Science, Natural Resources Management, or related field. Master's degree preferred. 11 - 15 years of experience desired in the environmental compliance discipline but will consider less years' experience for significant relevant experience in environmental documentation (all levels), ecological studies, wetland, and stream delineations, threatened and endangered species studies, environmental permitting, or related environmental compliance. Thorough knowledge of NEPA/environmental planning practices and procedures as well as experience in preparing NEPA documents in accordance with the US DOT guidelines and specific State DOTs' requirements. Broad knowledge of environmental laws and regulations, which include but are not limited to NEPA and the Clean Water Act (CWA). Experience in performing ecological studies, wetland, and stream delineations, threatened and endangered species surveys and studies, and knowledge of CWA permitting processes. Experience with NCDOT Natural Resource Technical Reports, Guidance, and Procedures. Experience obtaining Section 404/401 permits. Experience coordinating with federal and state resource agencies. Ability to handle multiple projects and deadlines. Experience authoring and reviewing environmental documentation. Excellent technical writing and oral communication skills. Positive attitude and ability to interact and communicate/work with multidisciplinary team members. Ability to work independently and as part of a team in coordination with multiple offices. Experience with Microsoft Office (Word, Excel, Outlook), TEAMS and GIS analysis tools is required. Strong plant identification skills. Willingness to continue to learn and grow technically and professionally within the company. Willingness to mentor and train junior staff. Ability to interpret and stay abreast of environmental regulations. Desired Requirements: Certification or professional registration is a plus. Recent, relevant experience working with federal, and regional states regulatory agencies a plus. Experience managing projects, scopes, budgets, and staff with limited oversight/supervision is a plus. Experience in any of the following states, VA, MD, WV, SC, GA, FL, DE and PA is a plus. Benefits: WRA recognizes that employees play an important role in its success. Our commitment to full-time employees is reflected in the comprehensive benefits package we offer: Flexible work schedule options Competitive salary Leave accrual and paid holidays Healthcare benefits Group Life Insurance, as well as additional optional life Insurance, short and long term disability insurance Flexible spending accounts for medical and dependent care reimbursement 401(k) Retirement Plan Tuition Reimbursement Employee Assistance Program Parental and maternity leave benefits WRA is an equal opportunity/affirmative action employer and complies with all applicable anti-discrimination laws. Applicants must be currently authorized to work in the United States on a full-time basis without the need for employment-based visa sponsorship now or in the future. WRA will not sponsor applicants for U.S. work visa status for this opportunity. (no sponsorship is available for H-1B, L-1, TN, O-1, E-3, H-1B1, F-1, J-1, OPT, CPT or any other employment-based visa) ***** Not accepting resumes from 3rd party recruiters for this position ***** Position # 2529 #LI - Mid-Level #Onsite

Groundwater & Environmental Services, Inc. (GES), an industry leader with a reputation for excellence in providing environmental consulting, engineering, compliance, and technical field services to clients in diverse market sectors, seeks a Mid to Senior Level Biologist or Environmental Scientist to support fieldwork and environmental remediation project activities. Position Description * Direct or Perform work associated with environmental permitting which may include stream cross sections, long profiles, BEHI/NBS, and/or other environmental sampling (chemical and biological). * Direct or Perform Stream Assessment (perennial/intermittent/ephemeral), Stream Reach Condition Studies. * Direct or perform work associated with 401/404 Permitting Documents and Agency Coordination * Familiar with local, state and federal water quality laws (CWA, RHA Section 10, ESA, NHPA, NEPA, etc.) * Exposure to or use of Rosgen Natural Channel Design (Levels I, II, III or IV) and other principals of Natural Channel Design. * Perform HEC/HEC RAS modeling and prepare and submit FEMA CLOMARs/LOMARs, a plus * Develop plans and full plan sets for NCD projects for IRT, State, and local level approvals * Familiarity with local permitting process for development projects * Communicates with clients, third party and regulatory agents regarding project status, schedules and compliance issues. * Ensures adherence to client and corporate contract specifications in all activities including Health, Safety, Security, and Environment. Skills & Requirements * A Bachelor of Science in Engineering, Environmental Engineering or Science, Fluvial Geomorphology, Environmental Studies, or related field is required. Masters of Science a plus. * AutoCAD, Civil3D, and/or Arc Map/Arc Pro experience for preparing plans and plan sets * 4-8+ years of related experience. Experience must include hands on field and office project/task execution (preferably in a responsible position commensurate with employment level) based in environmental consulting field. * EIT or PE preferred * Must possess excellent communication and technical writing skills and be able to independently prepare a complete deliverable report with a focus on QA/QC. Proficient in the use of Microsoft Office suite software. * Experience using GPS equipment and developing data dictionaries for specific GPS data collection efforts to feed into GIS data display and map production. * Willingness to learn new skills and accept challenging task assignments. * Applicants must be eligible to work in the US and have a valid driver's license. When you join Groundwater & Environmental Services, Inc. (GES), you are not a number - you become the reason for our success. You'll have the opportunity to carve your own career path while working shoulder-to-shoulder with some of the most talented and dedicated professionals in the industry. By combining our unique talents and expertise, we help the world's leading organizations solve their most complex environmental challenges. We work hard, and we have a lot of fun while we're at it. Our core values are centered on doing what's right - for our clients, our employees, and our community. Our employees benefit from a supportive, collaborative culture and an entrepreneurial spirit that promotes new ideas and shared learning. Our comprehensive benefits include: medical, dental, vision, prescription card, 401k, FSA, LTD, STD, New Parent Leave, 529 CollegeBound Fund, Tuition Assistance, Bonus Plan, and more. We know that there is life to be lived beyond work. That's why we offer our employees a comprehensive benefits package and champion a culture that embraces work/life balance. Employee benefits are available to regular full-time and part-time employees in accordance with our company policy. Groundwater & Environmental Services, Inc. (GES) believes that diversity and inclusion among our staff is critical to our success, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool. At GES, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and employees without regard to race, color, religion, gender, pregnancy, national origin, age, disability, marital status, sexual orientation, gender identity or expression, military and veteran status, and any other characteristic protected by law.

# Job Description: AI Task Evaluation & Statistical Analysis Specialist ## Role Overview We're seeking a data-driven analyst to conduct comprehensive failure analysis on AI agent performance across finance-sector tasks. You'll identify patterns, root causes, and systemic issues in our evaluation framework by analyzing task performance across multiple dimensions (task types, file types, criteria, etc.). ## Key Responsibilities - **Statistical Failure Analysis**: Identify patterns in AI agent failures across task components (prompts, rubrics, templates, file types, tags) - **Root Cause Analysis**: Determine whether failures stem from task design, rubric clarity, file complexity, or agent limitations - **Dimension Analysis**: Analyze performance variations across finance sub-domains, file types, and task categories - **Reporting & Visualization**: Create dashboards and reports highlighting failure clusters, edge cases, and improvement opportunities - **Quality Framework**: Recommend improvements to task design, rubric structure, and evaluation criteria based on statistical findings - **Stakeholder Communication**: Present insights to data labeling experts and technical teams ## Required Qualifications - **Statistical Expertise**: Strong foundation in statistical analysis, hypothesis testing, and pattern recognition - **Programming**: Proficiency in Python (pandas, scipy, matplotlib/seaborn) or R for data analysis - **Data Analysis**: Experience with exploratory data analysis and creating actionable insights from complex datasets - **AI/ML Familiarity**: Understanding of LLM evaluation methods and quality metrics - **Tools**: Comfortable working with Excel, data visualization tools (Tableau/Looker), and SQL ## Preferred Qualifications - Experience with AI/ML model evaluation or quality assurance - Background in finance or willingness to learn finance domain concepts - Experience with multi-dimensional failure analysis - Familiarity with benchmark datasets and evaluation frameworks - 2-4 years of relevant experience

Summary of Key Responsibilities: • Conducts experiments under limited supervision and maintains excellent notebook documentation in a GMP/GLP laboratory following Good Documentation Practices and ALCOA principles. • Performs In Vitro Release Testing (IVRT) for topical formulations such as Gels, Creams, Ointments, Films and Ophthalmic Solutions as per customer needs. • Prepares solutions for IVRT and High Performance Liquid Chromatography (HPLC) analysis such as Mobile Phase and Buffer. • Calibrates and operates micro and analytical balances for reference standard and reagent weighing. • Calibrates and operates pH meter for Buffer solution adjustments. • Operates data acquisitions system Empower 3. • Compiles data for quantitative analyses using Empower 3 and Microsoft Excel. • Manages daily activities in the laboratory, including chemical inventory and equipment maintenance and troubleshooting • Safely handles and disposes of hazardous materials including Category 3 and 4 potent compounds. • Has capacity to don half face respirator and disposable PPE for hazardous materials. • Provides support to team members as needed. • Works with limited supervision and interact with colleagues efficiently. • Drafts reports, protocols, and methods • Performs logbook and notebook review Required Qualifications and Skills: • B.S. in Pharmaceutical Sciences, Chemistry, Pharmacology, Biochemistry, Biology, or equivalent. • 1-2 years of relevant laboratory experience, university setting or other (GMP experience is preferred). • Possesses technical skills including handling of reference standards and topical products. • Previous experience in dissolution and USP general chapter is preferred. • Experience with general laboratory instruments. • Proficiency in Microsoft Office, use of data acquisitions systems, and document management systems. • Follows instructions meticulously, reads and executes protocols and methods as written. • Methodical, well-organized, conscientious, and thorough • Demonstrates logical thinking and attention to detail. • Has the ability to work with limited supervision and interact with colleagues efficiently.

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity. To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com Job Description • Will assist with cell bank production operations and associated ongoing projects. • Individual will support cell bank operations by executing activities ranging from cell bank production, execution of protocol studies in a lab setting, as well as general daily support including document preparation and review. • Good lab safety awareness and a good foundation in biology or microbiology. • Experience working within a GMP framework with particular regard to manufacturing environments Qualifications Preference would be for an individual with a BS in Biology/Microbiology (or similar). • Lab experience (or small scale fermentation experience) is a very strong preference. • Need someone that wouldn't need to necessarily be taught the basics of GMP and GLP (i.e., good documentation practices, basic Micro lab skills, etc.). • So, a minimum of at least 2-5 years of experience would probably be ideal. If the person has sound lab experience, but not necessarily within the industry, I would not necessarily discount them. Additional Information All your information will be kept confidential according to EEO guidelines. IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-357-1104 ASAP! I want to know more about your preferences. If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!

Groundwater & Environmental Services, Inc. (GES), an industry leader with a reputation for excellence in providing environmental consulting, engineering, compliance, and technical field services to clients in diverse market sectors, seeks a Mid to Senior Level Biologist or Environmental Scientist to support fieldwork and environmental remediation project activities. Position Description Direct or Perform work associated with environmental permitting which may include stream cross sections, long profiles, BEHI/NBS, and/or other environmental sampling (chemical and biological). Direct or Perform Stream Assessment (perennial/intermittent/ephemeral), Stream Reach Condition Studies. Direct or perform work associated with 401/404 Permitting Documents and Agency Coordination Familiar with local, state and federal water quality laws (CWA, RHA Section 10, ESA, NHPA, NEPA, etc.) Exposure to or use of Rosgen Natural Channel Design (Levels I, II, III or IV) and other principals of Natural Channel Design. Perform HEC/HEC RAS modeling and prepare and submit FEMA CLOMARs/LOMARs, a plus Develop plans and full plan sets for NCD projects for IRT, State, and local level approvals Familiarity with local permitting process for development projects Communicates with clients, third party and regulatory agents regarding project status, schedules and compliance issues. Ensures adherence to client and corporate contract specifications in all activities including Health, Safety, Security, and Environment. Skills & Requirements A Bachelor of Science in Engineering, Environmental Engineering or Science, Fluvial Geomorphology, Environmental Studies, or related field is required. Masters of Science a plus. AutoCAD, Civil3D, and/or Arc Map/Arc Pro experience for preparing plans and plan sets 4-8+ years of related experience. Experience must include hands on field and office project/task execution (preferably in a responsible position commensurate with employment level) based in environmental consulting field. EIT or PE preferred Must possess excellent communication and technical writing skills and be able to independently prepare a complete deliverable report with a focus on QA/QC. Proficient in the use of Microsoft Office suite software. Experience using GPS equipment and developing data dictionaries for specific GPS data collection efforts to feed into GIS data display and map production. Willingness to learn new skills and accept challenging task assignments. Applicants must be eligible to work in the US and have a valid driver's license. When you join Groundwater & Environmental Services, Inc. (GES), you are not a number - you become the reason for our success. You'll have the opportunity to carve your own career path while working shoulder-to-shoulder with some of the most talented and dedicated professionals in the industry. By combining our unique talents and expertise, we help the world's leading organizations solve their most complex environmental challenges. We work hard, and we have a lot of fun while we're at it. Our core values are centered on doing what's right - for our clients, our employees, and our community. Our employees benefit from a supportive, collaborative culture and an entrepreneurial spirit that promotes new ideas and shared learning. Our comprehensive benefits include: medical, dental, vision, prescription card, 401k, FSA, LTD, STD, New Parent Leave, 529 CollegeBound Fund, Tuition Assistance, Bonus Plan, and more. We know that there is life to be lived beyond work. That's why we offer our employees a comprehensive benefits package and champion a culture that embraces work/life balance. Employee benefits are available to regular full-time and part-time employees in accordance with our company policy. Groundwater & Environmental Services, Inc. (GES) believes that diversity and inclusion among our staff is critical to our success, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool. At GES, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and employees without regard to race, color, religion, gender, pregnancy, national origin, age, disability, marital status, sexual orientation, gender identity or expression, military and veteran status, and any other characteristic protected by law.

Summary of Key Responsibilities: • Conducts experiments under limited supervision and maintains excellent notebook documentation in a GMP/GLP laboratory following Good Documentation Practices and ALCOA principles. • Performs In Vitro Release Testing (IVRT) for topical formulations such as Gels, Creams, Ointments, Films and Ophthalmic Solutions as per customer needs. • Prepares solutions for IVRT and High Performance Liquid Chromatography (HPLC) analysis such as Mobile Phase and Buffer. • Calibrates and operates micro and analytical balances for reference standard and reagent weighing. • Calibrates and operates pH meter for Buffer solution adjustments. • Operates data acquisitions system Empower 3. • Compiles data for quantitative analyses using Empower 3 and Microsoft Excel. • Manages daily activities in the laboratory, including chemical inventory and equipment maintenance and troubleshooting • Safely handles and disposes of hazardous materials including Category 3 and 4 potent compounds. • Has capacity to don half face respirator and disposable PPE for hazardous materials. • Provides support to team members as needed. • Works with limited supervision and interact with colleagues efficiently. • Drafts reports, protocols, and methods • Performs logbook and notebook review Required Qualifications and Skills: • B.S. in Pharmaceutical Sciences, Chemistry, Pharmacology, Biochemistry, Biology, or equivalent. • 1-2 years of relevant laboratory experience, university setting or other (GMP experience is preferred). • Possesses technical skills including handling of reference standards and topical products. • Previous experience in dissolution and USP general chapter is preferred. • Experience with general laboratory instruments. • Proficiency in Microsoft Office, use of data acquisitions systems, and document management systems. • Follows instructions meticulously, reads and executes protocols and methods as written. • Methodical, well-organized, conscientious, and thorough • Demonstrates logical thinking and attention to detail. • Has the ability to work with limited supervision and interact with colleagues efficiently.