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Quantitative Researcher - New York, NY. Use advanced statistical methods to develop models used for forecasting, strategy selection, and portfolio construction. Use quantitative methods in financial engineering to develop algorithmic solutions, modeling and visualization of complex data. Maintain/edit algorithms to ensure optimal data processing. 1yr. Exp. Req. Salary: $100,547/yr., Master's - Applied Mathematics and Statistics, Proficiency with Python programming language req. Mail or email resume to: Gabrielle, Human Resources, KHAWK, LLC. 217 E 49th St. New York, NY 10017 or at <a href="mailto:HR@KHAWK.com" target="_blank">HR@KHAWK.com</a>.

Quantitative Researcher

Quantitative Researcher - New York, NY. Research, analyze, design &amp; develop predictive financial modeling systems; create &amp; handle large-scale quantitative datasets for research &amp; development. Minimum requirements: Master's Degree in Electrical &amp; Computer Engineering, Operations Research, Mathematics, Applied Mathematics, Statistics, Computer Science, or related quantitative field + knowledge of: probability; algorithm design, analysis &amp; optimization; numerical analysis skills including machine learning, causal inference, Bayesian inference, hypothesis testing, stochastic process modeling &amp; time series analysis; ability to adapt theory &amp; algorithms to real-world problems in finance; large-scale data analysis; Unix/Linux, Bash &amp; Version Control; Python &amp; C; data analysis tools including NumPy, SciPy &amp; Pandas; &amp; ability to conduct in-depth research projects in a quantitative field, as evidenced by publication of research work in academic journals or conference proceedings. Must pass company's required skills assessment. Base pay: $165k-$325k/year (does not include other forms of compensation/benefits). Note Hybrid work attendance policy: In-office work required at below office address for collaboration days based on each team's requirement; remote work permissible for remainder of same month. Send resume to <a href="mailto:TS-Posting@twosigma.com" target="_blank">TS-Posting@twosigma.com</a> or mail to TS/HR Dept, Two Sigma Investments, 100 6 Ave, 16 Fl, NY, NY 10013. Reference Job ID 13033

Statistical Programmers needed for Ephicacy Consulting Group, Inc located in Iselin, NJ to assist clients submission of statistical programming deliverables for single/ multiple studies located throughout the U.S. Positions require Master's degree in relevant filed along with relevant experience. Salaries range from $140,000 to $143,000. Send resumes to: <a href="mailto:careersusa@ephicacy.com" target="_blank">careersusa@ephicacy.com</a>

Statistical Programmers

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
This role is not available for immediate hire.
Chemical Laboratory Technician responsibilities include, but are not limited to, the following&nbsp;
<ul>
<li>Responsible for processing of incoming food and feed samples for analytical testing in compliance with all applicable standard operating procedures and quality systems as well as care and maintenance of equipment associated with this testing.</li>
</ul>
Qualifications 
The ideal candidate would possess&nbsp;:
<ul>
<li>Strong computer, scientific and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to work independently and as part of a team</li>
<li>Self-motivated, adaptable, high ownership of assigned tasks and results oriented</li>
<li>Ability to work with minimal supervision in a fast paced environment</li>
<li>Ability to learn new analytical laboratory techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions and comply with company policies</li>
</ul>
Basic Minimum Qualifications&nbsp;:
<ul>
<li>Bachelor’s degree in a scientific field. BS in Chemistry preferred.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
​​​​​​Position is&nbsp;Full-Time, First Shift,&nbsp;with&nbsp;additional hours as needed.&nbsp; Candidates currently living in a commutable distance to New Orleans, LA are encouraged to apply.
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Chemical Laboratory Technician

<h3>Job Description</h3>
Job Description
JOB SUMMARY
The Research &amp; Development (R&amp;D) Specialist conducts product development and improvement and process innovation, as well as other R&amp;D activities that may be assigned by the R&amp;D Brand Lead or R&amp;D Manager. These activities include but are not limited to the design, formulation and commercialization of new products, quality improvement of existing products, process improvement and innovation, product costing and sustainability initiatives, and analyses of food materials and finished products. The R&amp;D Specialist works closely with the R&amp;D Brand Lead or R&amp;D Manager to ensure that the goals of product taste superiority, sustainability and food safety are achieved.
ESSENTIAL FUNCTIONS
1.&nbsp;&nbsp;Knowledge of Food Material Properties and Functional Ingredients:
&nbsp;&nbsp;&nbsp;&nbsp;Apply knowledge of food material properties, functional ingredients and food additives when developing product formulas and processes and evaluation of alternative ingredients.&nbsp;&nbsp;Conduct continuous research on food properties and new trends in food material science as relevant to the needs of the assigned project.
2.&nbsp;Culinary Techniques:
Develop and apply classic and contemporary culinary techniques to product and process specifications, resulting into finished products that meet target product acceptability with consistent quality and sustainability.
3.&nbsp;Food Quality and Safety:
&nbsp;&nbsp;Incorporate in-depth knowledge of food quality and safety to product design and development, such as GMP and HACCP.&nbsp;&nbsp;Apply knowledge of food microbiology and food chemistry in the development of product standards and process parameters relative to food safety.&nbsp;&nbsp;Ensure that quality and safety are built into product design.
4.&nbsp;Formulation and Process Development and Optimization:
&nbsp;&nbsp;Design products that meet the requirements of the company and its customers.&nbsp;&nbsp;Develop formulas and processes for new and improved products. Perform timely activities relevant to the product development process for efficient and on-time achievement of product launches as budgeted, which may include but not limited to conceptualization, formulation and prototype evaluation, optimization and standardization, material sustainability evaluation, product cost calculation, commercial translation, and product launch.
5.&nbsp;&nbsp;Food Processing Technology and Commercialization:
Effectively translate formulas and processes from lab scale to commercially prepared food products at the manufacturing and store levels using current food processing technology, as may be required.&nbsp;&nbsp;Work directly with internal commissaries and external toll processors and vendors and store operations to ensure that commercial products meet JFC standards. Prepare product guides, instructional materials, teaching aids and conduct product simulation and training as needed for effective transfer of technical information to end users.
6.&nbsp;&nbsp;Food Packaging Properties and Functions:
Evaluate and select appropriate food packaging based on knowledge of material properties &amp; functions relative to the product application and recommend specifications for such.
7.&nbsp;&nbsp;Preservation and Shelf-Life Principles:
&nbsp;&nbsp;Conduct shelf-life evaluation of raw materials and finished products to ensure food safety and consistent sensory and nutritional quality of products within standardized storage and shelf life.
8.&nbsp;Methods of Analyses of Food Properties:
&nbsp;&nbsp;Conduct variety of applicable microbiological tests and physico-chemical analyses on food products to determine inherent properties and provide analysis of results and recommendation for further product development and improvement.
9.&nbsp;Sensory Evaluation and Sensometrics:
&nbsp;&nbsp;Apply methods of sensory evaluation and sensometrics to support requirements in ensuring consistent product quality and taste superiority. Prepare sensory analysis reports and provide recommendation on technical product specifications as required.
10.&nbsp;Food Nutrition Fundamentals:
Apply knowledge of nutrients in food and food ingredients relative to formulation and process development and improvement.
11.&nbsp;Food Standards, Laws and Regulations:&nbsp;&nbsp;Apply knowledge of federal, state, local and international government and industry regulations pertaining to standards on food safety, nutrition, food preparation and processing in the design and development of food products. Review the proper representation or translation of developed products in merchandising and marketing collaterals through print and media shoots, product and material descriptions, marketing copy and claims.
12.&nbsp;Business Knowledge and Acumen:
Demonstrate awareness on the state of the company’s performance and plans for the future. Openly contribute insights, feedback and suggestions to the R&amp;D team, providing timely solutions to the needs of the business. Recommend process improvements for R&amp;D related functions to R&amp;D Brand Lead and R&amp;D Head as needed.
COMMON KEY RESULT AREAS (KRA):
On top of the above essential functions, the R&amp;D Specialist will perform the following key result areas common to all R&amp;D team members:
1.&nbsp;Documentation and Knowledge Management: Ability to record product and process specifications in technical format with accuracy and comprehensive detail for proper record, communication and transfer of information to target recipients.
2.&nbsp;Technical and Best Practice Research:&nbsp;Pursue continuous improvement and innovation of R&amp;D processes and systems through technical and applied research as well as sharing of best practices in the food science and culinary industry.
3.&nbsp;Issue Resolution:&nbsp;Apply R&amp;D expertise in finding solutions to issues and conditions affecting safety, quality and sustainability of food products and processes as needed by the company.
JOB SPECIFICATIONS
Education
<ul>
<li>Associate’s Degree or Professional Certification in Culinary, Bakery/Pastry, Food Science/Technology, Nutritional Science, Culinology, Chemistry, Chemical Engineering, or any equivalent related course.</li>
<li>Bachelor’s degree preferred.</li>
</ul>
Experience
At least 2 years of work experience in Research &amp; Development (R&amp;D) from manufacturing and/or foodservice industry, or any equivalent combination of education and experience from which comparable knowledge, skills and abilities have been achieved.
<ul>
<li>Professional certifications:</li>
<ul>
<li>Preferred: Food Safety Certification - eg. ServSafe</li>
</ul>
</ul>
Other Qualifications
<ul>
<li>Computer Literacy:&nbsp;&nbsp;Proficient in MS Applications (MS Word, Excel, PowerPoint) and trainable in other software related to food analysis</li>
<li>Physical Effort/Requirements:&nbsp;&nbsp;While performing the duties of this job, the&nbsp;employee will:</li>
<ul>
<li>Stand/walk for the majority 90% of the scheduled work shift.</li>
<li>Lift, reach, pull, push, grasp and use hands frequently.</li>
<li>Bend and/or squat down for the majority of the scheduled shift.</li>
<li>Climb, stoop and/or kneel rarely.</li>
<li>Lift up to 50 pounds occasionally.</li>
<li>Need to see well enough to differentiate product quality parameters, read/compose email, reports and use the computer and be proactive to customers’ feedback affecting quality.</li>
<li>Need to speak and hear well enough to give/receive instructions, feedback and communicate with employees, customers and partners/suppliers.</li>
<li>Be required to work irregular hours, varying work shifts schedules as necessary at work.</li>
</ul>
<li>Work Environment:&nbsp;&nbsp;While performing the duties of this job, the employee is regularly exposed to:</li>
<ul>
<li>Kitchen/production areas with extreme temperatures for product testing/development/training.</li>
<li>Manufacturing plants, warehouse and logistics work areas.</li>
<li>Store and vendor/supplier plant visits, as necessary.</li>
<li>Production and Store kitchen equipment</li>
<li>Hot and cold temperatures and a wet work area.</li>
<li>Wet and slippery floors.&nbsp;</li>
<li>Cleaning chemicals</li>
<li>Possible cuts and burns.&nbsp;</li>
<li>Moderate noise level when working in production, store and suppliers’ work environment.</li>
<li>Tensions and pressures may arise in meeting deadlines and goals.</li>
</ul>
</ul>
This job description has been designed to indicate the general nature and level of work performed by employees in this classification.&nbsp; It is not designed to contain or be interpreted as an exhaustive list of all duties, responsibilities and qualifications required of employees assigned to this job.&nbsp; The duties, responsibilities may differ from the job description, and that the other duties as assigned, may be part of the job.
If the position requires a college/university degree, it must have been issued by an educational institution accredited by the United States Department of Education.&nbsp; Any degree issued by educational institution outside the United States must include documentation validating the equivalency of the degree to the same degree in the United States to be considered acceptable for this company’s purposes.
Reasonable accommodation for people with disabilities maybe requested by calling (626) 369-7118 at least five (5) working days in advance of the scheduled examination/assessment date(s).
APPLICANTS MUST BE AUTHORIZED TO WORK IN THE USA.
This Company is an Equal Opportunity Employer.
 We use eVerify to confirm U.S. Employment eligibility.

Research & Development Specialist

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking an experienced professional with a strong background in analytical method development and technology transfer within a GMP-regulated environment. This role primarily supports our client by performing routine GMP sample testing, method validation, and bioassay execution. In addition to technical responsibilities, this individual will serve as a group leader, overseeing a team of Eurofins PSS employees embedded within the client’s operation.
Primary Responsibilities:
<ul>
<li>Perform complex GMP release and stability assays, including cell-based functional assays such as PCR, ELISA, and NGS.</li>
<li>Support method transfer, qualification, and validation of bioassays for lot release and characterization of cell and gene therapy products and critical materials.</li>
<li>Author and review SOPs, technical reports, and other documentation in compliance with regulatory standards.</li>
<li>Collaborate with cross-functional teams on method development, product/process characterization, comparability studies, and technical investigations.</li>
<li>Analyze, trend, and interpret data to assess and maintain consistent assay performance and method robustness.</li>
</ul>
Leadership Responsibilities:
<ul>
<li>Supervise and support the daily performance of the Eurofins PSS team.</li>
<li>Assist in the recruitment and onboarding of new team members.</li>
<li>Communicate administrative updates and reinforce company vision and values.</li>
<li>Ensure high standards of quality, efficiency, and GMP compliance in all laboratory operations.</li>
<li>Manage shift coverage, scheduling, and resource allocation.</li>
<li>Support employee growth through performance discussions and development planning.</li>
<li>Maintain a balanced role between hands-on technical work and leadership duties.</li>
<li>Cultivate a positive team culture, encouraging collaboration, accountability, and continuous improvement.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in a scientific discipline with 3–8 years of relevant experience, or a Master’s degree with 2–5 years of experience.</li>
<li>Proven experience in analytical method validation in alignment with GMP regulations.</li>
<li>Demonstrated success in the transfer of analytical methods into GMP-regulated laboratories.</li>
<li>Hands-on experience performing routine sample testing in a GMP environment.</li>
<li>Strong knowledge of regulatory expectations related to method lifecycle management (e.g., FDA, EMA).</li>
<li>Excellent written and verbal communication skills; able to work collaboratively within cross-functional teams.</li>
<li>Self-motivated, highly organized, and detail-oriented with strong problem-solving capabilities.</li>
<li>Previous laboratory supervision or leadership experience is preferred.</li>
<li>Experience with potency assays (e.g., cell-based assays, ELISA) is a plus..</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
The position is full-time and permanent,&nbsp;Monday-Friday, 8 am-5 pm,&nbsp;with overtime as needed.&nbsp;Candidates living near or in&nbsp;Cambridge, MA,&nbsp;are encouraged to apply.
Excellent full-time benefits include:
<ul>
<li>Comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our clients’ quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Group Lead - Sample Testing & Method Transfer (GMP)

<h3>Job Description</h3>
Job DescriptionCompany Description 
<ul>
<li>Katalyst Healthcares &amp; Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.</li>
<li>We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.</li>
</ul>
Job Description 
Job Description: Seeking a Contract Scientist to support the siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This temporary position offers the opportunity to contribute to the design and execution of cutting-edge experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will apply their scientific expertise to drive innovation, collaborate across teams, and support the development of Client RNA-based therapies. Responsibilities:
<ul>
<li>Lead research efforts within a cross-functional team to advance siRNA platform development for therapeutic applications.</li>
<li>Resolve key project hurdles and assumptions utilizing available information and technical expertise.</li>
<li>Work autonomously to perform laboratory research or develop methods with minimal supervision, consistently delivering high-quality results.</li>
<li>Demonstrate expertise in a wide range of relevant technologies and methodologies.</li>
<li>Conceive and execute Client scientific research that achieves project goals.</li>
<li>Maintain high productivity in the laboratory, ensuring efficiency in experiment execution.</li>
<li>Analysed and interpret multidisciplinary data, generating conclusions that drive future experimental directions.</li>
<li>Contribute to internal reports, presentations, and potentially intellectual property filings.</li>
</ul>
Requirements:
<ul>
<li>PhD (or equivalent experience) in Cell Biology, Molecular Biology, Biochemistry, or related field. Alternatively, a master's degree with 8 years of significant relevant experience may be considered.</li>
<li>Strong hands-on experience in cell and molecular biology, including mammalian cell culture, mRNA isolation/quantitation by qPCR, sequencing (NGS/Sanger), and protein quantification by ELISA and western blot.</li>
<li>Experience in oligonucleotide therapeutics is a plus.</li>
<li>Familiarity with CNS disease models and DNA/RNA editing tools is highly desired.</li>
<li>Outstanding aptitude for experimental design and execution, efficient assay development and creative problem solving.</li>
<li>Ability to thrive in a dynamic, fast-paced research environment.</li>
<li>Collaborative team player with excellent communication skills.</li>
</ul>
Additional Information 
All your information will be kept confidential according to EEO guidelines.

Scientist III

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, apply with us today!&nbsp;&nbsp;
Job Description 
<ul>
<li>Conduct laboratory-scale cell culture studies (shake flask through fed-batch bioreactor and harvest) to support characterization of cell banks and/or manufacturing bioprocesses</li>
<li>Perform affinity chromatography and viral inactivation in support of lab-scale cell culture activities</li>
<li>Perform cGLP cell banking activities for research use</li>
<li>Coordinate with a broader scientific team to align on scheduling of lab activities</li>
<li>Statistically analyze large data sets and draft technical reports to support commercial filings</li>
<li>Present on technical topics during cross functional meetings.</li>
<li>Provide technical support to Manufacturing during troubleshooting and continuous improvement opportunities</li>
<li>Enjoy working in a fast-paced environment and you have the innate ability to balance multiple projects, prioritize them and execute them independently, while excelling at keeping all impacted parties well advised</li>
<li>Can take on new and sometimes ambiguous challenges, learning quickly</li>
<li>Work in a team environment but can also take ownership of large technical reports and projects</li>
<li>Develop and drive scientific and/or business-related improvement ideas</li>
<li>Understand antibody manufacturing processes</li>
<li>Utilization of Microsoft Suite (Word, Excel, Powerpoint)</li>
</ul>
Qualifications 
<ul>
<li>Bachelor's degree in life sciences required - Chemistry or Biochemistry majors preferred.&nbsp;</li>
<li>Strong cell culture experience and competence required.&nbsp;</li>
<li>Must have the availability to begin working full time as soon as possible.&nbsp;</li>
<li>Authorization to work in the US indefinitely without sponsorship.</li>
<li>Candidates currently living within a commutable distance of&nbsp;Rensselaer, NYare encouraged to apply</li>
</ul>
 Additional Information 
<ul>
<li>
This position is&nbsp;Wednesday-Saturday, 6:00 AM - 4:30 PM.&nbsp;
<ul>
<li>
Training will take place on a Monday-Friday, 8:00 AM - 4:30 PM schedule.
</li>
</ul>
</li>
<li>
Pay: $21.50/hour
</li>
<li>
.#LI-EB1
</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Cell Culture Biochemist - Entry Level

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Job Responsibilities for this role include, but are not limited to:
<ul>
<li>Demonstrates and promotes the company vision</li>
<li>Regular attendance and punctuality Reads, understands and follows management system requirements as relevant to responsibilities, including but not limited to requirements found in the Quality Manual, SOPs, Local Work Instructions and Methods which in turn ensures compliance.</li>
<li>Adhere to all health, safety, and environmental regulations relative to assigned analytical work; maintain and assist others in maintaining a clean, safe work environment.&nbsp;Registration of incoming samples (as needed), maintaining a neat and accurate record system of work performed on a daily basis and as needed for quality control tests or regulatory purposes.</li>
<li>Enter the sample data into Eurofins eLIMS system in a timely and accurate manner.</li>
<li>Complete laboratory testing on all incoming samples in an accurate, efficient and timely manner; ensure sample turnaround time goals are met or exceeded.&nbsp;</li>
<li>Verify results and submit results to the appropriate personnel for transmission, in a timely manner. &nbsp;</li>
<li>Identify process difficulties and report these together with proposed solutions to supervisor.</li>
<li>Maintain a perpetual state of readiness and willingness to respond to the queries and needs of clients, staff, and co-workers.</li>
<li>Maintain cooperative working relationships with all company employees. &nbsp;Communicate orally and in writing to co-workers. &nbsp;This includes “intra” and “inter” departmental employees.</li>
<li>Promote the company image through the exercising of sound and ethical business practices as related to the public and our customers.</li>
<li>Continually strive to improve the quality of work we provide to our clients through existing and new technologies</li>
<li>Identify non-conformances and out-of-specifications &nbsp;</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned</li>
</ul>
Qualifications 
The Educational Background requirements include the following:
<ul>
<li>A High School Diploma&nbsp;</li>
</ul>
The Ideal Candidates carry the following Traits:
<ul>
<li>1-2 years of Laboratory experience is preferred</li>
<li>Computer skills with MS Suite required</li>
<li>Excellent interpersonal and organizational skills</li>
<li>Excellent communication skills</li>
<li>Responsive problem solver and action-oriented</li>
</ul>
Work Environment:
<ul>
<li>Must be able to lift 10 lbs regularly; up to 25 lbs.</li>
<li>Must be able to stand for the entirety of their shift</li>
<li>Must be able available and willing to work overtime as needed</li>
<li>Must be able to work Holidays when called for</li>
</ul>
 Additional Information 
This position is a great opportunity for you to grow your career in a successful, well established lab. We nurture your growth, and strive to provide our already amazing internal employees with tools, knowledge, and room for growth to keep “climbing the ladder”! This is a&nbsp;Full-Time&nbsp;position. The schedule for this role is&nbsp;SECOND SHIFT&nbsp;3pm-11pm&nbsp;Monday-Friday&nbsp;
What we Offer:
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
#LI-EB1
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Senior Lab Technician- Microbiology (2nd Shift)

<h3>Job Description</h3>
Job Description
Position Summary
The RWE biostatistician provides statistical expertise for all observational research project sponsored by the US Evidence Based Medicine in protocol development, Statistical Analysis Plan (SAP) preparation and study report. The role needs to ensure that appropriateness of study design, sample size and statistical methodologies are used and adherence to the established standards and SOPs. The role manages the timely execution of statistical and research methodological components of RWE study protocols in order to meet project objectives and has a thorough understanding of current requirements for statistical standards.
Roles/Responsibilities
Utilize statistical knowledge of and expertise to provide statistical support for RWE studies, with a main focus of real-world observational studies, database examples:
1)US medical and pharmacy claims databases (e.g. MarketScan); 2) US medical record databases (e.g. GE Healthcare); 3) US government public use databases (e.g. NHANES, MEPS)
Participate in study concept, protocol and SAP development and ensure appropriateness of study design, sample size and statistical methodologies proposed.
Specify the structure of the datasets that will be delivered for statistical analysis to ensure that the structure follows any existing company standard for databases pooling.
Mock-up, review, and approve tables, listings and graphs specifications.
Actively participate in project/study team meetings
Establish/negotiate timelines for completion of study-related statistical activities. Ensure the study timelines are met.
Conduct observational data analysis, include data management, statistical programming, interpretation of analyses results, and write-up/review the corresponding sections of RWE study report.
Produce analysis datasets, listings, tables, and figures for research projects, according to specifications, while maintaining documentation and complying with pre-defined project / study standards.
Provide oversight of the biostatistics-related activities for RWE studies subcontracted to a CRO:
Oversee the CROs work on the preparation of analysis plans, development and validation of computer algorithms for inferential analyses, statistical writing of study reports, and other outsourced analyses as appropriate.
Perform quality control procedures to ensure that statistical deliverables conform to the requirements outlined in the SAP
Skills:
Working knowledge and experience with bio statistical analysis and R and/or SAS programming.
Excellent oral and written communication skills in English are a must.
Prior work experience in epidemiology, health economic and outcome research, or clinical research area is a plus.
Specific experience and understanding of outcomes research, drug development is an asset
Familiarity with observational databases desirable; database examples
US medical and pharmacy claims databases (e.g. MarketScan)
US medical record databases (e.g. GE Healthcare)
US government public use databases (e.g. NHANES, MEPS)
Ph.D. in Statistics, epidemiology or related field, or MS with Minimum 2-year experience in pharmaceutical industry; Strong R programming skills.
TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
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