Analytical Scientist II
Senior Scientist Job 25 miles from Fort Mill
Summary of the Position: The Analytical Scientist will be expected to develop and validate new analytical methods with minimum to no supervision as well as to provide technical support to other corporate groups including Quality Control, Quality Assurance, and International Business.
Roles and Responsibilities:
Analytical Scientist reports to Analytical Chemistry (AC) Management.
Performs Quality Control testing and data review to support timely release of product in weekly basis.
Effective development, optimization, and validation of scientifically sound analytical methods to ensure analysis and prompt release of raw materials, finished products, and stability studies.
Proficient in Empower Software and other laboratory software use in QC environment for chromatographic, spectroscopic methods as well as wet chemistry.
Assess testing methodologies and their application to different sample matrix, instrumentation and will include evaluation of testing results from contract laboratories to be sure that the agreed methods and testing parameters were properly followed.
Maintains current knowledge of latest technological and scientific trends and serves as an analytical science resource for the rest of the group. Mentor and train chemists in the proper execution, including interpretation of validation studies.
Responsible for producing hazardous waste from it point of generation. Managing all produced in accordance with RCRA and SCDHEC regulations to include: proper containers, accumulation, labeling, marking, and storage.
Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives.
Communicate effectively with other departments within the organization and function within a team environment.
Regular attendance is required.
Minimum Requirements:
Able to develop analytical methods for chromatographic, spectroscopic, titrimetric, and wet chemistry analyses.
Must be proficient on laboratory instrument trouble shooting.
In-depth knowledge of strategies of analytical method development and specification setting for raw materials and finished products.
Knowledge in most of laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC and test methods.
Knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods, and Mass spectrometry.
Proficient in the selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner.
Experience in effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation, and mechanical manipulation.
Knowledge of statistical techniques, such as data trend analysis and design of experiments, is highly desirable. Proficiency in reviewing and interpretation of laboratory data.
Detailed knowledge of principles of routine laboratory operations.
Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to pharmaceutical and/or nutritional supplement GLP/GMP is strongly desired.
Demonstrated aptitude to function in a dynamic fast-paced environment.
Education and Experience
A Bachelor's degree with 10 years of experience in validation and development of analytical methods for nutraceuticals and/or pharmaceutical samples in a GMP environment. A Master's degree and a minimum of 5 years of technical experience is preferred. Extensive experience may be accepted in lieu of an advanced degree.
A degree in analytical chemistry, biochemistry, chemical engineering, or related fields is strongly preferred.
A need to work on the bench to accomplish tasks along with the Analytical Chemistry team.
Supervisory Responsibilities: None
Advanced AI Research Scientist Associate Manager
Senior Scientist Job 17 miles from Fort Mill
We Are Accenture is helping companies use generative AI to reinvent their enterprise and optimize business functions for breakthrough innovation and competitive advantage. With over 1,600 professionals dedicated to generative AI, leveraging the depth and experience of more than 40,000 AI and data professionals across the company our Generative AI and LLM Center of Excellence (************************************************************************************************************************************* brings together our Experienced Innovation, Strategic Investment, Exceptional Talent, and Power Ecosystem.
You Are
As an Advanced AI Research Scientist, you formulate real-world problems into practical, efficient, and scalable AI and Machine Learning problems.
+ You lead a team and provide guidance to explore and implement new methodologies, model building techniques, and cutting-edge algorithms, and applying these techniques with the right architecture to solve real-world problems.
+ You have a deep understanding and ability to remain at the forefront of generative AI, LLM, and multi-modal models (with a focus on driving innovation by applying these techniques to new business problems, use cases, and scenarios).
+ As needed by the specific problem, you train and/or fine-tune generative AI models and evaluate on the specific problem.
+ As a significant part of this role, you will be justifying the value of innovative generative AI or traditional Machine Learning approaches (or a combination of both) in the business problems, and you'll be expected to construct methodologies that clearly demonstrate their value.
+ You'll also work collaboratively with teams from both the business and technical side, including users, use case representatives, business owners, engineers, architects, and UI designers, to achieve end-to-end project development goals.
The Work
+ Participate internal and external discussions to gather business use case requirements, provide on the spot AI expertise and AI solution options for business problems.
+ Design, develop and implement advanced AI/ML models, especially LLM and other Gen AI models from scratch or existing foundation models via self-supervised learning, transferred-learning, and fine-tuning techniques.
+ Design, develop and implement highly sophisticated Gen AI based applications including generative agent and similar architectures which support multiple Gen AI models to work together for complex tasks.
+ Lead technical teams and grow true AI expertise within broader team including offshore
+ Collaborate seamlessly with diverse, cross-functional teams to accurately identify and prioritize requirements, ensuring that the AI solutions meets the needs and expectations of various stakeholders.
+ Develop and execute an AI solution project plan with team, timeline, and infrastructure dependency.
+ Define and implement a value justification approach to the AI solutions; estimate solution cost with right technological choices; and calculate ROI.
+ Create and maintain comprehensive technical documentation that comprehensibly captures the intricate details of the solution, capture IP, facilitating seamless understanding, knowledge transfer and future development.
+ Collaborate with academia partners to stay on the cutting edge of AI, especially Gen AI technologies, provide through leadership on AI trend, AI use case innovation trend, new AI opportunities, or foreseeable limitation, risks, and concerns.
Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements.
Here's What You Need
+ Minimum of 4 years of experience in designing and developing neural network models, especially deep learning model, and Foundation models.
+ Minimum of 4 years of experience of experience in building, fine-tuning Foundation models including LLMs and multi-modal models.
+ Minimum of 4 years of strong working knowledge of the different technologies, their differences, modalities in the Generate AI space.
+ Minimum of 4 years of working knowledge and familiarity with different LLM driven application architecture patterns.
+ Minimum of 4 years of experience in deep learning and neural networks, in particular training and large language models with popular libraries and GPUs.
+ Minimum of 4 years of working knowledge of computer architecture, and familiarity with the fundamentals of GPU architecture.
+ Minimum of 4 years of proven experience with processor and system-level performance modelling.
+ Minimum of 2 years of experience of technical team management or team mentoring.
+ Bachelor's degree or equivalent (minimum 12 years) work experience. (If Associate's Degree, must have minimum 6 years' work experience)
Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired in California, Colorado, District of Columbia, Illinois, Maryland, Minnesota, New York or Washington as set forth below.We accept applications on an on-going basis and there is no fixed deadline to apply.
Information on benefits is here. (************************************************************
Role Location Annual Salary Range
California $73,800 to $220,400
Colorado $73,800 to $190,400
District of Columbia $78,500 to $202,700
Illinois $68,300 to $190,400
Minnesota $73,800 to $190,400
Maryland $68,300 to $176,300
New York $68,300 to $220,400
Washington $78,500 to $202,700
What We Believe
We have an unwavering commitment to diversity with the aim that every one of our people has a full sense of belonging within our organization. As a business imperative, every person at Accenture has the responsibility to create and sustain an inclusive environment.
Inclusion and diversity are fundamental to our culture and core values. Our rich diversity makes us more innovative and more creative, which helps us better serve our clients and our communities. Read more here (***********************************************************************
Equal Employment Opportunity Statement
Accenture is an Equal Opportunity Employer. We believe that no one should be discriminated against because of their differences, such as age, disability, ethnicity, gender, gender identity and expression, religion or sexual orientation.
All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law.
Accenture is committed to providing veteran employment opportunities to our service men and women.
For details, view a copy of the Accenture Equal Employment Opportunity and Affirmative Action Policy Statement (********************************************************************************************************************************************** .
Requesting An Accommodation
Accenture is committed to providing equal employment opportunities for persons with disabilities or religious observances, including reasonable accommodation when needed. If you are hired by Accenture and require accommodation to perform the essential functions of your role, you will be asked to participate in our reasonable accommodation process. Accommodations made to facilitate the recruiting process are not a guarantee of future or continued accommodations once hired.
If you would like to be considered for employment opportunities with Accenture and have accommodation needs for a disability or religious observance, please call us toll free at ****************, send us an email (************************************************* or speak with your recruiter.
Other Employment Statements
Applicants for employment in the US must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States.
Candidates who are currently employed by a client of Accenture or an affiliated Accenture business may not be eligible for consideration.
Job candidates will not be obligated to disclose sealed or expunged records of conviction or arrest as part of the hiring process.
The Company will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. Additionally, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the Company's legal duty to furnish information.
Staff Scientist
Senior Scientist Job 17 miles from Fort Mill
Job Details Charlotte Office - Charlotte, NCDescription Qualifications
Staff Scientist - Environmental
BL Companies is 100% employee owned, giving us a competitive edge and a unique distinction from most other companies. We offer a competitive benefit package which includes 6 paid holidays plus the week from Christmas to New Years paid, generous PTO, Medical, Dental and Vision insurance, disability insurance, life insurance, 401k matching, and our Employee Stock Ownership Plan. We are an ENR Top 500 firm that provides engineering, architecture, land surveying, and environmental consulting services to the public and private sectors. BL has 18 offices and is expanding.
Our employee owners are capable of being successful working in hybrid environments, and we are now offering opportunities to continue in this setting.
We are looking to hire an environmental scientist with 0-4 years of experience to work with the Environmental Site Assessment and Remediation Group to provide quality services to our clients. This position will provide the opportunity to see, and gain experience in, all aspects of a full-service environmental group including all technical aspects of fieldwork and reporting.
Responsibilities include:
Due diligence tasks including Phase I Environmental Site Assessments, site reviews and opinion letters, Property Condition Assessments, and regulatory file reviews.
Phase II/III Site Investigations including soil and groundwater sampling.
Supervision of drilling subcontractors and subcontractor oversight.
Field logging of soil borings and monitoring well installations.
Field documentation, analysis of environmental data, technical report writing.
Assistance with regulatory reporting and filings.
Adhere to field health and safety protocols and requirements.
Required Experience:
BS Degree in Environmental Science, Geology, Hydrogeology, Environmental Engineering, or related scientific or technical field.
0-4 years of experience in conducting environmental site assessment investigations.
Experience in field sampling of environmental media (soil, water, air, waste).
Ability to draft technical reports and proposal scopes.
Strong oral and written communication skills.
Ability to access remote locations and sites for sampling.
Ability to lift/carry field equipment up to 50 pounds.
Familiarity in AutoCAD and/or GIS preferred.
OSHA HAZWOPER 40-hour Certification preferred.
Flexibility to travel, when needed, to support regional office objectives and project needs.
Research Scientist
Senior Scientist Job 40 miles from Fort Mill
Corvid Technologies is seeking a highly talented Research Scientist. This person will be responsible for research and development of weapons systems and related applications, drawing on an understanding of fundamental physics. Innovative and independent thinking is an absolute must, but must be achieved in the context of collaborative team efforts. Projects will require the ability to start with a problem, create concept solutions, and mature that concept into a prototype that can be tested. Problems will be diverse and multifaceted, ranging from the purely mechanical to the purely computational.
General Requirements:
Ability to obtain a U.S. Security Clearance is required
Must be willing to travel up to 20% of the time
0-5 Years of previous experience
Required Education:
Master's or Doctorate
Desired Backgrounds:
Mechatronics, Embedded Systems, Flight Vehicles, RF
Design, AI/ML
Desired Skills and Experience
Experience in both experimental work and computational tools.
Simulation and design skills.
Innovative and independent thinking.
Knowledge of how to build prototypes.
Possess the ability to evaluate systems and solutions by creating or adapting mathematical models (Models might be either analytical or numerical).
Efficiency in prototyping in Python or other open interpreted language required.
Fluency in C or FORTRAN is desirable.
Why Corvid?
Founded in 2004, we are a group of over 300 engineers and scientists, about 3/4 with master' degrees or Ph.D.'s, that provide end-to-end solutions including concept development, design and optimization, prototype build, test and manufacture. We leverage the predictive capability of our high-fidelity computational physics solvers, indigenous massively parallel supercomputer system, prototyping plant, and ballistics and mechanics lab to investigate a variety of high-rate physics phenomena.
The results are complex engineering solutions for a variety of applications; aircraft, ballistic missile defense, cybersecurity, motorsports, armor development, biological systems, and missile and warhead design and development. These results are achieved with optimal design and cost efficiency due to the predictive capability of Corvid's tools and our in-house, end-to-end integrated approach, which differentiates Corvid from the market.
We value our people and offer employees a broad range of benefits. Benefits for full-time employees include:
Paid gym membership
Flexible schedules
Blue Cross Blue Shield insurance including Medical, Dental and Vision
401k match up to 6%
Three weeks starting PTO; increasing with tenure
Continued education and training opportunities
Uncapped incentive opportunities
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.
Research Scientist
Senior Scientist Job 17 miles from Fort Mill
Lynx Therapeutics is seeking an innovative and highly motivated Research Scientist to join our dynamic research team. In this role, you will be responsible for designing and conducting experiments that contribute to our understanding of therapeutic mechanisms and the development of advanced healthcare solutions. You will work collaboratively with a team of scientists and cross-functional partners to push the boundaries of scientific inquiry and drive impactful research projects.
Key Responsibilities:
Design, execute, and analyze experiments to investigate biological hypotheses relevant to our therapeutic areas.
Develop and optimize laboratory protocols and methodologies to improve research efficiency and accuracy.
Collaborate with interdisciplinary teams to ensure the successful progression of research projects.
Interpret data and present findings in written reports and oral presentations to stakeholders.
Stay current with scientific literature and emerging trends relevant to our areas of research.
Contribute to the preparation of regulatory submissions, scientific publications, and grant applications.
Requirements
Qualifications:
Ph.D. in Biology, Biochemistry, Molecular Biology, or a related field.
2-5 years of postdoctoral research experience or equivalent industrial experience in a relevant scientific area.
Strong proficiency in experimental techniques such as PCR, sequencing, cell culture, and molecular cloning.
Excellent problem-solving skills with a proven ability to analyze and interpret complex data sets.
Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously.
Exceptional written and verbal communication skills, capable of conveying complex scientific concepts clearly.
Benefits
Private Health Insurance
Training & Development
Performance Bonus
Retirement Plan (401k, IRA)
Paid Time Off (Vacation, Sick & Public Holidays)
Family Leave (Maternity, Paternity)
Training & Development
Clinical Research Investigator (MD/DO)
Senior Scientist Job 17 miles from Fort Mill
Clinical Research Investigator (MD/DO) DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our site in Charlotte, NC. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities
Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies.
Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site.
Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies.
Ensures and protects the welfare and safety of participants through ethical conduct.
Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
Exercises meticulous attention to detail in documentation and patient care.
Requirements
Medical license (MD, DO) - Charlotte, NC
2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator)
Bilingual Spanish a plus
Flexible hours - schedule can be tailored as required.
Taxable Fixed Income ABS Sr Research Associate
Senior Scientist Job 17 miles from Fort Mill
The Taxable Fixed Income Senior Research Associate is part of the investment team, and will review investment opportunities by obtaining, organizing and analyzing Taxable Fixed Income market-related information from internal and external sources. Working under general supervision, this job monitors, researches and analyzes markets and trends to support investment decisions and optimize Taxable Fixed Income business.
Key Responsibilities and Duties
* Conducts research analyses on specific organizations, securities, financial products, and the overall economic environment to optimize Taxable Fixed Income business.
* Monitors, researches and analyzes relevant economic, industry, and company data and market trends, preparing reports and developing models to support investment decisions.
* Builds models and acquires, assembles, and normalizes research data sets to support Taxable Fixed Income portfolios.
* Assists in additional studies of industry groups or individual securities by searching for, compiling and analyzing data.
* Develops research methodologies and information sources to improve Taxable Fixed Income research.
* Contributes to all formal reports and research processes (internal ratings, recommendation lists, watch lists, etc.) that enable the efficient and transparent oversight of the asset class.
* Edits and prepares research materials and results for dissemination.
* Identifies opportunities to improve research quality for Taxable Fixed Income portfolio.
Educational Requirements
* University (Degree) Preferred
Work Experience
* 3+ Years Required; 5+ Years Preferred
Physical Requirements
* Physical Requirements: Sedentary Work
Career Level
7IC
Required Qualifications:
* 3+ years ABS research or trading experience
Preferred Qualifications:
* 5+ years ABS research or trading experience
* Subject matter expertise in Consumer, Commercial or Esoteric ABS
* MBA and/or CFA
* Experience in quantitative and financial analysis
* Advanced excel skills
* Knowledge and understanding of Bloomberg, Intex and database skills
* Experience with scripting and/or programming languages such as VBA, SQL, Python, C++
Related Skills
Asset Valuation, Capital Markets, Collaboration, Communication, Credit Analysis, Data Analysis, Financial Modeling, Fixed Income Investments, Investment Research/Analysis, Investments, Market/Industry Dynamics, Research Synthesization, Sector Expertise, Underwriting
Anticipated Posting End Date:
2025-02-26
Base Pay Range: $108,800/yr. - $150,000/yr.
Actual base salary may vary based upon, but not limited to, relevant experience, time in role, base salary of internal peers, prior performance, business sector, and geographic location. In addition to base salary, the competitive compensation package may include, depending on the role, participation in an incentive program linked to performance (for example, annual discretionary incentive programs, non-annual sales incentive plans, or other non-annual incentive plans).
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Company Overview
Nuveen, the investment manager of TIAA, offers a comprehensive range of outcome-focused investment solutions designed to secure the long-term financial goals of institutional and individual investors. Its affiliates offer deep expertise across a comprehensive range of traditional and alternative investments through a wide array of vehicles and customized strategies. For more information about the firm please visit our website at **************
Benefits and Total Rewards
The organization is committed to making financial well-being possible for its clients, and is equally committed to the well-being of our associates. That's why we offer a comprehensive Total Rewards package designed to make a positive difference in the lives of our associates and their loved ones. Our benefits include a superior retirement program and highly competitive health, wellness and work life offerings that can help you achieve and maintain your best possible physical, emotional and financial well-being. To learn more about your benefits, please review our Benefits Summary.
Equal Opportunity
We are an Equal Opportunity/Affirmative Action Employer. We consider all qualified applicants for employment regardless of age, race, color, national origin, sex, religion, veteran status, disability, sexual orientation, gender identity, or any other protected status.
Read more about the Equal Opportunity Law here.
Accessibility Support
TIAA offers support for those who need assistance with our online application process to provide an equal employment opportunity to all job seekers, including individuals with disabilities.
If you are a U.S. applicant and desire a reasonable accommodation to complete a job application please use one of the below options to contact our accessibility support team:
Phone: **************
Email: accessibility.support@tiaa.org
Privacy Notices
For Applicants of TIAA, Nuveen and Affiliates residing in US (other than California), click here.
For Applicants of TIAA, Nuveen and Affiliates residing in California, please click here.
For Applicants of TIAA Global Capabilities, click here.
For Applicants of Nuveen residing in Europe and APAC, please click here.
Process Development Scientist I
Senior Scientist Job 17 miles from Fort Mill
A career with MilliporeSigma is an ongoing journey of discovery: our 57,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.
Your role
MilliporeSigma is looking for a Process Development Scientist to join the technical branch of the commercial organization in Raleigh-Durham, North Carolina. The Process Development Scientist is part of a worldwide team of engineers and scientists reporting into the technical support group for MilliporeSigma's Process Solutions business. The ideal candidate will be a scientist/engineer with an in-depth knowledge and understanding of bioprocess unit operations. Travel required up to 25% within North America region with some international travel.
Proactively pursuing and performing process development studies for the purification of therapeutic proteins and other modalities using MilliporeSigma technologies such as sterile filtration, depth filtration, tangential flow filtration, viral reduction filtration, as well as, chromatography.
Involvement in selection and sizing, process optimization, and technology transfer activities associated with the purification of new pharmaceuticals with a focus on Phase I-III drug development.
Provide consultation to customers through email, telecon or video chat.
Collaborate and work with customer process development groups in the southeast (NC, FL, GA, SC, VA) with the majority of the work being in Raleigh-Durham.
Work collaboratively with a team of local MilliporeSigma account managers to provide technical expertise to local customers.
Document customer interfacing activities through appropriate electronic systems.
Propose new technical ideas/areas for the larger group to advance state-of-the-art.
Communicate and work effectively in cross-functional teams, influence technical approaches and support strategy execution.
Who You Are:
Minimum Qualifications:
Bachelor's Degree in Chemical Engineering, Pharmaceutical Sciences, Life Sciences, Chemistry or Biochemistry
1+ years of experience within pharmaceutical development or technology implementation
1+ years of experience developing test protocols and executing the studies
Preferred Qualifications:
Master's Degree or PhD
Ability to derive relevant conclusions, based on the experimental results, and effectively communicate this to our customers.
Excellent hands on laboratory skills, working knowledge of Microsoft Excel or other data analysis software
Sound understanding of downstream and/or upstream biomanufacturing process requirements, best practices, and industry standards
Comfortable with making recommendations for future course of action based on experimental results
Relay relevant results to sales, field marketing, etc.
Ability to identify scientific leadership opportunities and execute through lunch & learns, publications, presentations, etc. with a focus on customer collaboration
Ability to cope with change, adjust test plans quickly, and comfortably handle risk and uncertainty
Ability to build effective relationships; both internally and externally
Ability to produce quality written experimental reports and other appropriate documentation
Highly motivated, self-directed, and able to work independently in a field-based position
Demonstrated ability to communicate clearly, concisely and effectively to diverse audiences through both written and oral communications
RSRMS
What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at *************************
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.
Formulations Scientist - Solid Dosage
Senior Scientist Job 17 miles from Fort Mill
Formulations Scientist
Greater Charlotte, NC
Excellent opportunity for a chemist with experience in food, nutraceutical, and/or pharmaceutical formulation development, scale-up.
Primary Responsibilities
Prepare and optimize novel formulations with new product innovation team
Develop, prototype, and test new products and/or materials utilizing lab techniques and instrumentation as appropriate
Assist with technology transfer to manufacturing teams and scale-up from R&D to production
Set-up, operate, and troubleshoot operations equipment
Candidate Qualifications
Minimum of BS degree in Food Science, Chemistry, Biochemistry, or a related field
> 3 years of industry experience in food or dietary supplement development in a GMP regulated environment
Hands-on experience using and troubleshooting processes including tablet press, encapsulation, tablet coating, granulation, and extrusion
Knowledge of solid dosage forms and experience with varied matrices (e.g., powders, tablets, capsules, chews, liquids, etc.)
US citizenship or Green Card required
Salary:
$80-95K annual base salary commensurate with experience
Annual discretionary bonus
Health, vision, dental, and life insurance
401k with company match
Childcare and tuition assistance
Relocation assistance available
APPLY NOW!
Click the Apply link on this posting to submit your application to VRS Recruitment. Please include an updated resume and cover letter.
Reference#: VRS2282
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Principal Scientist - Sterility Assurance
Senior Scientist Job 37 miles from Fort Mill
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Organization Overview:
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Responsibilities:
The Principal Sterility Assurance Scientist is a technical role that assists in development and implementation of the site's sterility assurance programs and provides technical guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy. The Principal Sterility Assurance Scientist develops and implements a technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The principal role is also expected to serve as a mentor within the TSMS team and engage in upstream and external to site activities related to sterility assurance.
Ensure and provide oversight and technical guidance for sterility assurance programs at the manufacturing floor level.
Lead or provide technical oversight for activities related to sterility assurance programs including but not limited to; Airflow Pattern Testing, Environmental Monitoring Performance Qualifications, Aseptic Process Simulations, Cleaning, Sanitization, and Disinfection; Gowning within GMP Classified Areas, Aseptic Processing Techniques, Contamination Control
Lead or assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established.
Lead/assist with support and/or provide technical expertise for developing the site's contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy strategies.
Lead/assist with support and/or provide technical expertise for the facility's cleanroom gowning and aseptic technique strategy/program.
Apply sterility assurance risk management to evaluate manufacturing processes and associated controls with respect to potential introduction of microbial, endotoxin, and particulate contamination.
Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities for continuous improvements.
Lead or provide technical support for root cause investigations associated with sterility assurance programs.
Participate and/or provide technical sterility assurance support during internal and external audits.
Work within cross-functional teams to implement TS/MS objective and deliver on business and quality objectives.
Basic Qualifications/ Requirements:
Bachelor's or Master's Degree in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline.
Demonstrated understanding and relevant experience of scientific principles required for manufacturing of parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance, validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing.
5+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept).
Additional Skills/Preferences:
Possess strong interpersonal skills to work cross-functionally within a team.
Possess strong self-management and organizational skills.
Possess strong oral and written communication skills for communicating to colleagues, management, and other departments.
Experience with data analysis and trending.
Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing, warehouse, or laboratory areas.
Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities.
Additional Information:
Role is Monday through Friday based and will be phased from a project support role to a routine support role as the development facility and processes progress. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hour and / or off-hour work may be required.
Tasks may require repetitive motion and standing or walking for long periods of time.
Travel may be required during the project phase for training and implementation of sterility assurance programs
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups.
#WeAreLilly
Senior Research Associate, Trauma & Acute Care Surgery - Nights
Senior Scientist Job 17 miles from Fort Mill
******2-year work commitment required.******
The position involves almost daily, direct interaction with patients and their families, and exposure to almost every part of the CMC hospital system (ED, OR, ICUs, hospital floor units, labs, etc). Our Sr Research Associates are vital members of our clinical research team that work alongside the Research Director, our Research Coordinators, the Trauma and Acute Care Surgeons and countless other clinicians. Our focus is mainly in the critically ill and injured patient populations. We generally have about 15 different clinical trials open at a given time, ranging from new investigational drugs, medical devices, or changes in patient care practices in pediatric and adult populations.
Some of our clinical trials enroll patients at our Atrium Health Cabarrus, University, and Pineville hospitals, with potential to expand further. Travel to facilities outside Carolinas Medical Center is sometimes required, but travel expenses beyond normal daily commute are reimbursable.
Sr RAs must be self-motivated, detail-driven, and willing to work the described schedule (nights). This position is ideal for candidates seeking clinical research experience to develop a career in clinical research, or apply for Medical School or PA School.
Job Summary
Collects, enters and analyzes research data. Provides reports using computerized databases and information systems. Prepares reports from requests from the director, faculty, study sponsor, and outside collaborators. Designs, implements, and evaluates request using databases as information source.
Essential Functions
Maintains designated applications in research department databases.
Creates new databases, prepares and runs data analysis queries, and uploads local database to the national database center.
Uses existing database to create reports as requested.
Performs data manipulation and migration.
Reviews data quality reports for data submissions and errors.
Ensures data requests are received, have authorizations, are evaluated, and reported.
Prepares specifications and summary reports for data queries and requests.
Performs chart abstraction.
Provides administrative support when needed.
Physical Requirements
Work consistently requires sitting for 5-6 hours. Intact senses of sight, hearing, smell, touch, and manual dexterity. Each employee has the responsibility to work in a safe manner.
Education, Experience and Certifications
Bachelor's Degree in Computer Science or health-related field required but Associates Degree and equivalent work experience will be considered. Training in information systems technologies, desktop application, and databases required. Experience with analytical software and database analysis and reports preferred.
Analytical Scientist II
Senior Scientist Job 25 miles from Fort Mill
Summary of the Position: The Analytical Scientist will be expected to develop and validate new analytical methods with minimum to no supervision as well as to provide technical support to other corporate groups including Quality Control, Quality Assurance, and International Business.
Roles and Responsibilities:
* Analytical Scientist reports to Analytical Chemistry (AC) Management.
* Performs Quality Control testing and data review to support timely release of product in weekly basis.
* Effective development, optimization, and validation of scientifically sound analytical methods to ensure analysis and prompt release of raw materials, finished products, and stability studies.
* Proficient in Empower Software and other laboratory software use in QC environment for chromatographic, spectroscopic methods as well as wet chemistry.
* Assess testing methodologies and their application to different sample matrix, instrumentation and will include evaluation of testing results from contract laboratories to be sure that the agreed methods and testing parameters were properly followed.
* Maintains current knowledge of latest technological and scientific trends and serves as an analytical science resource for the rest of the group. Mentor and train chemists in the proper execution, including interpretation of validation studies.
* Responsible for producing hazardous waste from it point of generation. Managing all produced in accordance with RCRA and SCDHEC regulations to include: proper containers, accumulation, labeling, marking, and storage.
* Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives.
* Communicate effectively with other departments within the organization and function within a team environment.
* Regular attendance is required.
Minimum Requirements:
* Able to develop analytical methods for chromatographic, spectroscopic, titrimetric, and wet chemistry analyses.
* Must be proficient on laboratory instrument trouble shooting.
* In-depth knowledge of strategies of analytical method development and specification setting for raw materials and finished products.
* Knowledge in most of laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC and test methods.
* Knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods, and Mass spectrometry.
* Proficient in the selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner.
* Experience in effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation, and mechanical manipulation.
* Knowledge of statistical techniques, such as data trend analysis and design of experiments, is highly desirable. Proficiency in reviewing and interpretation of laboratory data.
* Detailed knowledge of principles of routine laboratory operations.
* Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to pharmaceutical and/or nutritional supplement GLP/GMP is strongly desired.
* Demonstrated aptitude to function in a dynamic fast-paced environment.
Education and Experience
* A Bachelor's degree with 10 years of experience in validation and development of analytical methods for nutraceuticals and/or pharmaceutical samples in a GMP environment. A Master's degree and a minimum of 5 years of technical experience is preferred. Extensive experience may be accepted in lieu of an advanced degree.
* A degree in analytical chemistry, biochemistry, chemical engineering, or related fields is strongly preferred.
* A need to work on the bench to accomplish tasks along with the Analytical Chemistry team.
Supervisory Responsibilities: None
Coatings Scientist - Application
Senior Scientist Job 28 miles from Fort Mill
Covia is a leading supplier of minerals and material solutions to the industrial and energy markets. Covia's rich legacy includes many achievements across industries and capital success through partnership. Our ability to deliver the right product, to the right place, at the right time, is unmatched. Just as strong is our commitment to building partnerships that help our customers succeed.
Quality and innovation are at the foundation of Covia; but our real strength is our people. Covia employs a diverse and highly skilled team of professionals to convert natural minerals into engineered solutions for our customers. Every member of our team has a valuable opportunity to help shape our future and make a positive impact on the world around us through our commitment to the locations where we live and work.
COVIA IS COMMITTED TO EMBRACING AND PROMOTING DIVERSITY AND INCLUSION (D&I) WHERE WE WORK, WITH WHOM WE DO BUSINESS, AND WHERE WE LIVE. We strive to create an inclusive culture where diversity is valued and respected and where all feel included and engaged. We are intentional in our efforts to bring Team Members together and create opportunities to contribute their unique skills, experiences, and perspectives in the pursuit of Covia's business growth objectives. Enabling all Team Members to perform at their best while being themselves is fundamental to the Clearly Covia Values and Culture.
Covia is looking for a dynamic Coatings Application Scientist who will have a positive impact on the Applications Development Team in Charlotte, NC. As a Coatings Application Scientist, you will support the innovation in the Paint, Coatings, Adhesives, & Sealants markets through formulation design, evaluation, and engagement with paint and coatings customers.
The successful candidate will have the following Key Accountabilities:
Lead the design, installation, commissioning, and on-going maintenance of the coatings laboratory to support coatings formulation applications
Conduct the coatings laboratory projects supporting new product development and commercial growth. Develop technical value propositions. Translate voice of customers (VOC) into key performance attributes. Design and conduct experiments to demonstrate and quantify functional and performance benefits using customer language.
Interface with the technology platform, corporate analytical laboratory, and pilot staff to ensure seamless technology transfer and scale-up.
Support coatings technical product commercialization, assisting in the creation of technical data sheets, brochures, and new product launch packages
Support within a cross-functional team to develop IP strategy in the coatings space. Conduct annual coatings IP landscape study, stay up to date to competitive IP.
Coordinate comparative testing & evaluation of competitive products in the coatings markets.
Supervise lab technicians.
Provide training and technical assistance to Sales, Operations, Marketing and other Covia affiliated employees involved in supplying and servicing the coatings markets. Serve as a resource for customer problem resolving and technical support.
Represent the organization in forums and conferences within specific area of application expertise.
The successful incumbent will have the following Minimum Qualifications:
Bachelor's degree in chemistry or chemical engineering with 10 years' experience in the relevant industry, or Master /Ph. D degree with 5 years of industrial experience
Experience in resin systems and formulations with pigments, fillers, curing agents, activators
Experience in various paint and coating systems, including architectural interior, exterior coatings, industrial coatings, and specialty applications such as solar reflection coatings.
Laboratory experience with chemicals, MSDS, ventilation and safety training
Hands-on ability to execute analytical / laboratory procedures and maintain applicable equipment / systems
Deep knowledge of coating formulations with a structured methodology for building, optimizing, and testing coating formulations is preferred
Experience with Critical to Quality (CTQ) process is preferred
Benefits:
Excellent Healthcare Benefits - medical, vision, dental
401K with company matching
Vacation + Paid Holidays
Disability, Life / AD&D, and Long-Term Care Insurances
Employee Assistance Program
At Covia, we strive for and support a diverse workforce as we firmly believe this lays the foundation of our success. Our compelling culture supports inclusion, individuality and respect within the workplace. We are committed to providing employment opportunities to the most qualified candidate based on work-related factors and without regard to non-work-related factors including race, color, religion, national origin, gender, sexual orientation, gender identity, age, disability, or veteran status.
The organization offers competitive salaries, advancement opportunities, and a full range of benefits.
An Equal Opportunity Employer
IND2
Senior Research Associate, Trauma & Acute Care Surgery - Nights
Senior Scientist Job 17 miles from Fort Mill
******2-year work commitment required.******
The position involves almost daily, direct interaction with patients and their families, and exposure to almost every part of the CMC hospital system (ED, OR, ICUs, hospital floor units, labs, etc). Our Sr Research Associates are vital members of our clinical research team that work alongside the Research Director, our Research Coordinators, the Trauma and Acute Care Surgeons and countless other clinicians. Our focus is mainly in the critically ill and injured patient populations. We generally have about 15 different clinical trials open at a given time, ranging from new investigational drugs, medical devices, or changes in patient care practices in pediatric and adult populations.
Some of our clinical trials enroll patients at our Atrium Health Cabarrus, University, and Pineville hospitals, with potential to expand further. Travel to facilities outside Carolinas Medical Center is sometimes required, but travel expenses beyond normal daily commute are reimbursable.
Sr RAs must be self-motivated, detail-driven, and willing to work the described schedule (nights). This position is ideal for candidates seeking clinical research experience to develop a career in clinical research, or apply for Medical School or PA School.
Job Summary
Collects, enters and analyzes research data. Provides reports using computerized databases and information systems. Prepares reports from requests from the director, faculty, study sponsor, and outside collaborators. Designs, implements, and evaluates request using databases as information source.
Essential Functions
Maintains designated applications in research department databases.
Creates new databases, prepares and runs data analysis queries, and uploads local database to the national database center.
Uses existing database to create reports as requested.
Performs data manipulation and migration.
Reviews data quality reports for data submissions and errors.
Ensures data requests are received, have authorizations, are evaluated, and reported.
Prepares specifications and summary reports for data queries and requests.
Performs chart abstraction.
Provides administrative support when needed.
Physical Requirements
Work consistently requires sitting for 5-6 hours. Intact senses of sight, hearing, smell, touch, and manual dexterity. Each employee has the responsibility to work in a safe manner.
Education, Experience and Certifications
Bachelor's Degree in Computer Science or health-related field required but Associates Degree and equivalent work experience will be considered. Training in information systems technologies, desktop application, and databases required. Experience with analytical software and database analysis and reports preferred.
Senior Research Associate (Contract Contingent)
Senior Scientist Job 17 miles from Fort Mill
ProSidian is looking for “Great People Who Lead” at all levels in the organization. Are you a talented professional ready to deliver real value to clients in a fast-paced, challenging environment? ProSidian Consulting is looking for professionals who share our commitment to integrity, quality, and value.
ProSidian is a management and operations consulting firm with a reputation for its strong national practice spanning six solution areas including Risk Management, Energy & Sustainability, Compliance, Business Process, IT Effectiveness, and Talent Management. We help clients improve their operations.
Linking strategy to execution, ProSidian assists client leaders in maximizing company return on investment capital through design and execution of operations core to delivering value to customers. Visit ***************** or follow the company on Twitter at ************************* for more information.
Job Description
The Senior Research Associate (Contract Contingent) will be responsible for leading efforts of program evaluation and reporting for various government programs that seek to evaluate overall effectiveness and alignment with government mandates within a government agency tasked with assisting and guiding small businesses. This position will specifically entails developing program evaluation protocol and data tools; documenting analysis and processes; and reporting findings to appropriate stakeholders.
Responsibilities and Duties:
Demonstrate theoretical and practical knowledge of research design and analysis.
Assist in the development of research projects including research plan and sample plan.
Assist in the creation of survey instruments
Assist in the management of research projects including programming, data collection, analysis, and reporting.
Export, analyze, query, and clean data from completed surveys in multiple formats.
Assist in preparation of summaries of analysis and reports for stakeholders and internal partners.
Assist in responding to custom/ad hoc requests for research data.
Monitor secondary sources for consumer trends, industry trends, brand/product/category developments, and competitor marketing and research activities and integrate findings into research activities.
Multi-task and demonstrate flexibility to meet needs and deadlines.
Other duties as assigned.
Qualifications
Master's Degree (doctoral degree preferred) in an area related to assessment and measurement
Minimum 5 years of experience in a research setting, professional practice with assessment, evaluation, and/or research as their primary position responsibility
Experience building and/or utilizing analytic databases i.e. PC SAS/SPSS/STATA or other analytical software
Experience designing, conducting and making performance management recommendations from formative and summative evaluations
Experience in designing evaluations of qualitative and quantitative data, analyzing secondary data from administrative records, collecting and analyzing primary data, and using a broad set of methodological designs
Ability to Travel to Client Site
Additional Information
CORE COMPETENCIES
Teamwork - ability to foster teamwork collaboratively as a participant, and effectively as a team leader
Leadership - ability to guide and lead colleagues on projects and initiatives
Business Acumen - understanding and insight into how organizations perform, including business processes, data, systems, and people
Communication - ability to effectively communicate to stakeholders of all levels orally and in writing
Motivation - persistent in pursuit of quality and optimal client and company solutions
Agility - ability to quickly understand and transition between different projects, concepts, initiatives, or work streams
Judgment - exercises prudence and insight in decision-making process while mindful of other stakeholders and long-term ramifications
Organization - ability to manage projects and activity, and prioritize tasks
FOR EASY APPLICATION
USE OUR CAREER SITE LOCATED ON http://*****************/ OR SEND YOUR RESUME'S, BIOS, AND SALARY EXPECTATION / RATES TO ***********************. ONLY CANDIDATES WITH REQUIRED CRITERIA ARE CONSIDERED.
Be sure to place the job reference code in the subject line of your email. Be sure to include your name, address, telephone number, total compensation package, employment history, and educational credentials.
R&D Tax Senior Associate
Senior Scientist Job 17 miles from Fort Mill
Join Frazier & Deeter and be a part of a rapidly growing Top 50 accounting & advisory firm that has been repeatedly named a Best Firm to Work For, a Best Firm for Women and a Pacesetter firm among U.S. accounting firms. With offices in Atlanta, Alpharetta, Charlotte, Las Vegas, London, Nashville, and Tampa, there is a spot for you!
We serve clients of all sizes across the United States and the globe, with a suite of services that grows every year. Our growth mindset and entrepreneurial environment translates into variety and opportunity for our people.
With our emphasis on Investing in Relationships to Make a Difference and a Firmwide Focus on Inclusion, we help each other grow in every aspect of life.
Overview:
Join our R&D Credits and Incentives team as a Senior Associate, where you'll collaborate with a dynamic group of professionals who bring extensive consulting and industry experience to help clients address their complex business challenges. As a trusted advisor, you will support clients in maximizing their R&D tax benefits by advising on credit eligibility, preparing technical documentation, and navigating the evolving landscape of tax incentives. This role provides an excellent opportunity to advance your technical skills, work with a diverse client base, and contribute to strategic problem-solving.
Key Responsibilities:
Provide expert tax advisory services to a variety of clients, including public companies, private companies, and owner-managed businesses. Guide clients on the eligibility of R&D projects, qualifying activities, and relevant tax regulations to maximize R&D tax benefits.
Work with Managers, Senior Managers, and Partners to oversee all phases of the engagement process, including planning, execution of engagement letters, client communications, staffing, scheduling, and job planning.
Develop detailed technical reports that accurately describe and substantiate clients' R&D activities and eligible costs. Review tax working papers to ensure compliance with professional standards and engagement letter terms.
Cultivate and maintain strong relationships with clients, particularly technical and software teams, to understand their projects, gather data, and address specific needs related to R&D tax credits.
Devise strategies to solve complex technical challenges encountered during client engagements, offering innovative solutions that maximize credit opportunities.
Continuously improve your own and the team's technical expertise by staying up-to-date with tax laws, IRS regulations, research credit case law, and R&D database tools.
Keep abreast of local, national, and industry-specific economic issues and trends that may impact clients and their eligibility for credits and incentives.
Qualifications:
2-3 years of relevant experience in R&D tax credits, credits and incentives, or a similar tax-focused role.
Deep understanding of R&D tax issues, including IRS regulations, research credit case law, and the use of R&D databases. Experience analyzing organizations to identify tax savings opportunities.
Proficiency in working with large, complex data sets, using tools such as Excel and data visualization software to create models and provide insights. Familiarity with automation and digitization in a professional services environment.
Ability to write comprehensive technical documents that clearly explain complex R&D activities, with attention to detail and precision.
Knowledge of alternative fee arrangements and pricing strategies, with the ability to assess and suggest pricing options for engagements.
Excellent interpersonal and communication skills, with the ability to explain complex tax concepts to clients and colleagues in a clear and accessible manner.
Preferred Qualifications:
CPA, EA, or other relevant certification is preferred but not required.
Attention External Recruiters: Frazier & Deeter is not accepting any unsolicited resumes for our openings at this time.
#LI - Remote
Formulation Scientist
Senior Scientist Job 51 miles from Fort Mill
The company is a contract manufacturer with over 25 years of experience, specializing in formulation and manufacturing services for both emerging and established personal care brands, major retailers, and distributors. The company converts customer innovations into finished, branded products ready for consumer markets through various channels.
The company creates solutions for lip care, sunscreen, hand sanitizer, topical ointments, hair care, pet care, and various lotions, gels, and creams. With 12 manufacturing lines, the company offers hot- or cold-filled product formulations and labels them into all major packaging categories, including bottles, sticks, tubes, tins, jars, packets, and Bag-on-Valve aerosols. Customers work closely with an in-house Research and Development laboratory and a dedicated team of chemists to develop innovative solutions that meet consumer needs.
All operations take place in an FDA-registered facility, monitored by a highly skilled Quality team to ensure compliance with cGMP standards. For global customers, the company is cleared by Health Canada and other international regulators. Additionally, regular quality and safety audits by customers are successfully completed. Many customers, including the largest ones, have maintained long-term partnerships with the company, with most relationships spanning nearly a decade. The company's growth has largely been driven by referrals from satisfied customers.
The company's success over the past two decades is attributed to consistently delivering quality products on time, ensuring compliance with all relevant regulations and safety guidelines. The company fosters a respectful and supportive culture, from the production floor to senior management, with all team members working together to serve both colleagues and customers.
Compensation for this full-time position includes a competitive base salary, health/vision/dental insurance, 401k plan and PTO benefits.
Position Description
•Research and develop new products according to customer demand and market trends
•Support new products formulation through lab batching, raw material procurements, sample submissions, and lab stability monitoring
•In charge of converting lab batch processes designed by formulator technicians into a technology transfer/GMP compliant processes.
•Establish required product and manufacturability specifications for feasibility and scalability
•Continuously improve existing products including formula modifications, raw materials substitutions and manufacturing instruction improvements to fulfil sales & marketing strategies
•Generate master formulas by inputting approved formulas into ERP system and establishing formulas' BOM, manufacturing procedures, sampling plans, product specifications and instructions for drumming off, storage and filling
•Review and evaluate formulas and compounding procedures
•Troubleshoot manufacturing issues, identified root causes and provided resolutions and corrective and preventive actions (CAPA); lead all production batch adjustment
• Conduct change control request (CCR) for any modifications for master formulas and inform the changes to associated departments including R&D, Quality, Purchasing and Planning to ensure the integrity and consistency of product quality
• Source and test new ingredients to meet marketing and regulatory demands, sourced and qualified alternative ingredients to the current ones with supply issues
• Provide recommendations to Production / Compounding Manager on feasibility of use of raw materials and/or make suggestions for possible changes
• Provide support in preparation of batch records, process characterization reports, verification reports, corrective actions (CAPA) and investigation reports.
• Evaluate raw material for formulation assessment to ensure compliance to regulatory requirements.
• Interaction with raw material manufacturers and other vendors as needed.
• Prepare appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.
• Additional duties as assigned
Experience Requirements
2+ years experience working in the cosmetic, beauty, OTC or a similar industry.
Direct knowledge of product formulation working from a client brief.
Experience/knowledge scaling a batch from the lab to full commercialization.
Additional Information
•This is a fulltime on site position.
•Relocation assistance is available.
•Salary negotiable dependant on experience.
Med Lab Scientist FT Nights
Senior Scientist Job 6 miles from Fort Mill
Medical Lab Scientist Full Time Nights ***$20,000.00 Sign-on Bonus (paid over 2 years)*** Medical Technologist perform various tests to analyze the blood, body fluids and tissues as ordered by Healthcare personnel. Under the general supervision of departmental section supervisors, precisely and accurately, orders, performs and evaluates technical procedures in the different subsections of the clinical laboratory department. Receives, processes, and distributes specimens appropriately and in a timely manner. CLS properly stores specimens for further testing, as needed. Assists with the training of new employees and students. Maintains equipment and supply inventory. Adheres to laboratory and hospital policies (i.e. attendance, continuing education, dress code, infection control, and patient confidentiality) and procedures. Maintains knowledge and practices current regulatory guidelines. Prepares and participates in processes relating to regulatory agencies such as Joint Commission, CAP and AABB. Follows best practice for infection control in accordance with hospital and regulatory guidelines.
THE MEDICAL LAB SCIENTIST FULL TIME NIGHTS CANDIDATE WILL POSSESS THE FOLLOWING EDUCATION, LICENSE/CERTIFICATIONS, AND EXPERIENCE.
For a Medical Technologist to perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Minimum Education: Associate Degree or Bachelor's Degree, professional training required. Must be at least 18 years old.
Minimum Experience: 1 to 2 years of job-related experience, blood bank is preferred.
Required Certifications/Registrations/Licenses: ASCP-MLT or equivalent other current equivalent state licensure or a minimum of 5 years job related experience in lieu of licensure and/or ASCP. BLS certification required.
Engineer/Scientist, Senior (SECRET Clearance Required)
Senior Scientist Job 31 miles from Fort Mill
Position Description: Performs tasks with little or no guidance. Has demonstrated knowledge in area of engineering expertise. Applies engineering principles to investigate, analyze, plan and design, develop, implement, test or evaluate military weapons systems. Reviews and prepares engineering and technical
analyses, reports, change proposals and other technical documentation. Applies systems engineering
experience to perform functions such as system integration, configuration management, quality assurance
testing, or acquisition and resource management. Analyzes, designs, develops, implements, tests, or
evaluates software, components, or systems related to engineering or functional requirements of military
weapons systems, associated support systems. OR; Leads the execution of complex tasks. Applies and
integrates engineering principles to investigate, analyze, plan, design, develop, implement, test or evaluate
military weapons systems. Reviews and prepares engineering and technical analyses, reports, change
proposals and other technical documentation. Applies engineering experience to perform functions such as
system integration, configuration management, quality assurance testing, or acquisition and resource
management. Analyzes, designs, develops, implements, tests, or evaluates software related to engineering
or functional requirements of military weapons systems, associated support systems.
This position will specifically support the F16 FST.
Education: Position requires a MS or MA degree from an accredited college or university in Engineering,
Mathematics, Physics or a related scientific discipline. ALLOWABLE SUBSTITUTION: A BS or BA
degree from an accredited college or university in Engineering, Mathematics, Physics or a related scientific
discipline and an additional four (4) years of recent and relevant experience may be substituted for a MS or
MA degree. These four (4) years of experience are in addition to the required minimum of ten (10) years to
meet the “Experience” requirements below, therefore, requiring a total of fourteen (14) years of experience.
Experience: At least ten (10) years of recent and relevant experience in an engineering position, three (3)
of which must be directly related to naval systems. Demonstrated knowledge in area of engineering
expertise is required.
Benefits:
Medical, Dental, & Vision Plan, short- and long-term disability, accidental death & dismemberment, 401K retirement & matching, Tuition assistance program, direct deposit, leave package and 11 paid federal holidays.
Salary:
The projected salary range for this position is $120,000-$130,000; however, this is not a guarantee of salary. Salary will be set based on experience and contractual requirements.
Med Lab Scientist FT Nights
Senior Scientist Job 6 miles from Fort Mill
Medical Lab Scientist Full Time Nights ***$20,000.00 Sign-on Bonus (paid over 2 years)*** Medical Technologist perform various tests to analyze the blood, body fluids and tissues as ordered by Healthcare personnel. Under the general supervision of departmental section supervisors, precisely and accurately, orders, performs and evaluates technical procedures in the different subsections of the clinical laboratory department. Receives, processes, and distributes specimens appropriately and in a timely manner. CLS properly stores specimens for further testing, as needed. Assists with the training of new employees and students. Maintains equipment and supply inventory. Adheres to laboratory and hospital policies (i.e. attendance, continuing education, dress code, infection control, and patient confidentiality) and procedures. Maintains knowledge and practices current regulatory guidelines. Prepares and participates in processes relating to regulatory agencies such as Joint Commission, CAP and AABB. Follows best practice for infection control in accordance with hospital and regulatory guidelines. THE MEDICAL LAB SCIENTIST FULL TIME NIGHTS CANDIDATE WILL POSSESS THE FOLLOWING EDUCATION, LICENSE/CERTIFICATIONS, AND EXPERIENCE. For a Medical Technologist to perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Minimum Education: Associate Degree or Bachelor's Degree, professional training required. Must be at least 18 years old. Minimum Experience: 1 to 2 years of job-related experience, blood bank is preferred. Required Certifications/Registrations/Licenses: ASCP-MLT or equivalent other current equivalent state licensure or a minimum of 5 years job related experience in lieu of licensure and/or ASCP. BLS certification required.