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SCIENCE MANAGER-Eikon Therapeutics, Inc. in Jersey City, NJ seeks Sr. Clinical Project Manager: Oversee the execution of clinical trials in oncology and other therapeutic areas. Ensure effective management of assigned Phase I-III in-sourced global clinical studies. Part-time telecommuting allowed. $198,000/yr. Email res (must reference Job Code #43966) to <a href="mailto:recruitment@eikontx.com" target="_blank">recruitment@eikontx.com</a>.

SCIENCE MANAGER

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

Senior Managing Consultant, IBM Corporation, Armonk, NY and various unanticipated client sites throughout the US (Up to 100% Telecommuting permitted): Oversee Request for Proposals (RFP) and Project Change Request (PCR) development including managing the process end-to-end from developing proposals to estimating complex projects from a solution, resource, and budget perspectives. Develop Key Proposals and Statements of Work (SOWs) to handle deal registration in internal systems. Lead AI value strategy projects leveraging machine learning and artificial intelligence for efficiency. Lead and contribute to global client work across enterprise strategy and AI value projects, working closely with clients to understand their business goals, challenges, and opportunities. Drive company's global efforts to build eminence in automation, cloud, generative AI, Watsonx by developing and presenting comprehensive enterprise strategies to clients to showcase integrated business solutions, automation and technology capabilities (especially with AI/Generative AI/Watsonx) to drive business value and innovation. Develop and maintain VP/SVP or higher relationships with clients to understand their business needs and priorities. Lead a strategy team to develop and manage client project plans, timelines, and resources to ensure successful project delivery. Utilize Project Management, Agile Methodology, Garage Methodology, AI and Generative AI Skills, and Design Thinking Methodology. Required: Required: Bachelor's degree or equivalent in Business Administration, Marketing, Engineering, Computer Science or related and five (5) years of experience as a Data Analyst, Strategy Consultant, Managing Consultant or related. Five (5) years of experience must include utilizing Project Management, Agile Methodology, Garage Methodology, AI and Generative AI Skills, and Design Thinking Methodology. $239003 to $270000 per year. Please send resumes to <a href="mailto:recruitad@us.ibm.com" target="_blank">recruitad@us.ibm.com</a>. Applicants must reference V186 in the subject line.

Senior Managing Consultant

<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 
Become your most extraordinary self!&nbsp; Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. &nbsp;Join Eurofins Discovery Services North America, LLC&nbsp;part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. &nbsp;Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide!
We have a philosophy to support work life balance, career progression opportunities and offer many benefits such as formal mentoring programs, tuition reimbursement, extensive career training programs, competitive health benefits, paid time off and 10 annual paid holidays*. &nbsp;
The Scientific Director, Antibody Discovery for Biotherapeutic Services is a scientific leadership position, responsible for providing guidance for establishing and growing antibody discovery platforms and alignment between our customer base, the industry at large, commercial teams and service operations. This role will be collaborative and influential in a broad network of business functions in support of driving business growth, brand recognition, and alignment with Eurofins core competencies of delivering high quality services to our valued customers. The successful candidate will:
<ul>
<li>Spend time in the lab to define, develop and/or expand antibody discovery platforms in BTX</li>
<li>Develop client and stakeholder relationships through technical leadership and collaboration</li>
<li>Deliver scientific leadership to executive management in developing portfolio strategy, new growth areas and new technology planning</li>
<li>Lead scientific community through external marketing, industry reputation and brand awareness</li>
<li>Provide leadership in establishing and monitoring unit research and development objectives and commercial lifecycle management</li>
<li>Provide technical leadership to lab operations, business development and marketing team</li>
<li>Support client services team in generating proposals, RFPs, study plans and scope of work preparation. Assists pricing team in completing custom pricing and cost analysis</li>
<li>May act as Study Director for specific projects to ensure timely delivery of project updates, data and reports to clients</li>
<li>Understand requirements for work performed within a GxP site in order to work with other organizations within the Eurofins family</li>
<li>Complete required training and support 100% of Employee Health and Safety requirements</li>
<li>Conduct responsible use of confidential IT and business systems, as required</li>
<li>Adhere to department SOP and documentation requirements</li>
<li>Ensure accurate data management and reporting, with the highest integrity, and perform quality control, when required, on project data and reports</li>
<li>Support unit goals and demonstrate Eurofins’ competencies, as defined in the job plan</li>
<li>Provide training to colleagues and external end users, when required</li>
<li>Perform other duties, as assigned</li>
</ul>
Qualifications 
<ul>
<li>Senior-level scientific experience and knowledge in supporting all aspects of antibody discovery</li>
<li>Demonstrated expertise and experience with antibody discovery by hybridoma generation, B- and Plasma cell isolation and V-region sequence recovery, and display systems</li>
<li>Antibody engineering, humanization, germlining, CDR-scanning and affinity maturation</li>
<li>Molecular cloning, including restriction enzyme-based cloning, Gibson assembly cloning and ligation-independent cloning.</li>
<li>DNA and RNA extraction, purification and handling</li>
<li>Experience in analyzing NGS data, pairing heavy and light chains, identifying sequence liabilities and optimization thereof</li>
<li>Demonstrated experience with developing client/external relationships, supporting technical correspondence, drafting and presenting scientific proposals to clients or collaborators</li>
<li>Experience in collaborating with cross-functional teams (research, regulatory, pharmacology, safety) to guide growth and advancement of the platform from concept to pre-clinical development</li>
<li>Experience leading and managing internal scientific teams and directing /influencing external resources</li>
<li>Proven experience with portfolio management, portfolio expansion and research/development in an industry setting</li>
<li>B.S., M.A., or M.S. with 12 years relevant experience</li>
<li>Ph.D. with 7 years relevant experience</li>
<li>Combination of Education and Relevant Experience</li>
<li>Demonstrated experience in working effectively with different stakeholders with an interest in antibody discovery, including Business Development, Client Services and internal contributors</li>
<li>Demonstrated reputation as a key opinion provider and industry influencer via publications, networking and presentation experience</li>
<li>Experience with leading cross-functional teams effectively</li>
<li>Demonstrated experience in strategic planning and managing portfolio growth initiatives</li>
<li>Demonstrated ability to build and lead a Scientific team, and appropriate technical capabilities to support therapeutic and tool antibody discovery</li>
<li>Demonstrated ability to identify and introduce new technology (equipment and techniques) to grow capabilities</li>
<li>Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health</li>
<li>Excellent interpersonal, verbal and written skills, including ability to prepare detailed scientific reports and group presentations</li>
<li>Ability to plan and coordinate multiple projects simultaneously, with appropriate allocation of available resources</li>
</ul>
 Additional Information 
The position is full-time, Monday-Friday, 8:00 a.m.-5:00 p.m., with overtime as needed. Candidates within a commutable distance of Saint Charles, MO are encouraged to apply.&nbsp;
<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 USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.

Scientific Director - Antibody Discovery, Biotherapeutics Services

<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 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins 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. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
The incumbent interacts with Business Development, Proposal Development, and Laboratory Operations with the aim to win proposals. S/he exchanges information with relevant stakeholders (internal/external), documents existing and needed laboratory capabilities and proposes qualified solutions to Management to profitably grow the laboratory business.
Hybrid Role- Hours: Monday-Friday 8am-5pm&nbsp;
Qualifications 
Key Accountabilities
<ul>
<li>Reviews client clinical protocols and provides synopses to ensure the proposals meet the testing needs of the client.</li>
<li>Provide and update testing information to include cost, feasibility, TAT, and methodology to meet tight turnaround times during bidding process.</li>
<li>Provide recommendations for in-house vs. outsourced testing capabilities and relevant process changes to Management to enhance operational and financial performance.</li>
<li>Identify appropriate referral labs as needed and obtain relevant information needed to support clinical trials.</li>
<li>Maintains a current list of referral labs with contact information and areas of specialization.</li>
<li>Communicates directly with referral lab to meet required time frames and testing capabilities.</li>
<li>Negotiates preferred pricing for large volume testing directed to referral lab in conjunction with Management.</li>
<li>Communicate the use of a referral lab to QA allowing adequate time for QA qualification.</li>
<li>Support Proposal Development department with suggestions on optimizing global sample logistics.</li>
<li>Monitor the Central Laboratory test menu, ensuring all data is available accurate and traceable with version control, including costing and pricing, on a global basis.</li>
<li>Maintain database information for bid vs. awarded studies when validation by lab is required.</li>
<li>Communicate effectively with Management to ensure client testing needs are met from bid to awarded study.</li>
<li>Attend client meetings as needed to support sales.</li>
<li>Dialogue with client as requested determining whether additional support is required.</li>
<li>Provide input to satisfaction surveys (sponsors, investigators) and translates findings into actionable recommendations to Management for specific improvements (business practices, service levels, process changes, etc.).</li>
</ul>
Position Specifications and Job Requirements Experience
<ul>
<li>Minimum 5 years in a diagnostic, clinical laboratory</li>
<li>Experience with clinical assay validation protocols</li>
</ul>
Education
<ul>
<li>Bachelor of Science Degree</li>
</ul>
Degree in Medical Technology or Life Sciences preferred
 Additional Information 
Position is full-time,&nbsp;1st shift hours available. 8 AM- 5 PM&nbsp;
Authorization to work in the United States without Sponsorship is required.&nbsp;
Additional information
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Position is Full-Time, 40 hours per week.&nbsp; Candidates currently living within a commutable distance of Lancaster, PA&nbsp;are encouraged to apply.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
<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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Scientific Affairs Liaison

<h3>Job Description</h3>
Job Description
This position is responsible for production and compliance assigned duties. This includes but is not limited to batch and process manufacturing, compliance responsibilities, inventory control, bulk material handling, and packaging. This role will fulfill necessary routine activities assigned by both the Production Supervisor and the Corporate Compliance Manager. Essential Functions &amp; Responsibilities • Works with Production Supervisors, Process Technicians, other Utility, and the Corporate Compliance Manager in the safe handling of the equipment and chemical intermediates in both storage and use in production; • Ascertain proper and sufficient verbal and written to execute daily and long term goals; • Understand and demonstrate compliance with HMIS, SDS’s, HAZCOM, General Safety, HAZWASTE, LO/TO, PSM, PPE protocol, and proper housekeeping; • Inventory Control through cycle counts, batch log &amp; MUS record keeping, and filling or transferring documentation; • Management of Waste Water including: monitor and reporting of tank volumes, compliant and effective loading of the outbound water trailers, sampling tanks and trailers, neutralization when necessary, and weight tickets for outbound trailers. • Management of Storm Water including: Monitor and reporting of storm water in containment areas and reporting to Corporate Compliance Manager, Sampling Storm Water and logging samples into laboratory, compliant and effective discharge of the Storm Water, and completing the cycle of required documentation including the Storm Water checklist back to Corporate Compliance Manager. • Executes tasks and project responsibilities as outlined and assigned from the compliance &amp; PM calendars, production worklist, expected delivery report, and verbal / written instructions from Supervisors and Management. Examples include palletizing drum trailers, offloading bulk tank trailers to tote containers, and staging materials for production as well as assistance with packaging. Other examples including area checklist completion, waste area checklists completion, etc. • Housekeeping Specific assigned areas and duties i.e. Tank Farm floors and area checklist, trash cans around plant, warehouse floors, around vacuum pumps, immediate reporting of any discovered leaks and assistance with proper clean up, daily Top 25 checklist, etc.;

Forklift Operator - Chemical Manuf.

<h3>Job Description</h3>
Job Description
Help us change lives
At Exact Sciences, we’re helping&nbsp;change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.
Position Overview
The Clinical Lab Associate I, Specimen Processing is responsible for performing the day-to-day operations of the Specimen Processing Department including, but not limited to, lab productivity and process line support, such as:&nbsp; accessioning, processing, automation usage, sample racking, lab maintenance, and lab cleaning, as well as other lab support tasks.
The Clinical Lab Associate I, Specimen Processing follows all Laboratory policies and procedures and maintains accurate data reporting practices to ensure consistent and diligent execution of Specimen Processing. This role supports the mission and vision of Exact Sciences Laboratories and shares the responsibility of ensuring the Specimen Processing department operates effectively. The function of this position is performed under the guided direction of the Specimen Processing Supervisor or designee.
Shift: Tuesday - Friday, 8:00pm - 6:30am
Essential Duties
include but are not limited to the following:
<ul>
<li>Perform primary responsibilities listed below completely, timely and accurately:
<ul>
<li>Support and comply with the company’s Quality Management System policies and procedures.</li>
<li>Maintain documentation of problems and problem resolutions following Good Documentation Practices (GDP).</li>
<li>Support department goals that align with organizational priorities.</li>
<li>Work with leadership to identify and progress on individual development goals that align with organizational priorities.</li>
<li>Support operational initiatives including, but not limited to, quality and process improvements, SOP development, department inspections and audits.</li>
<li>Complete all mandatory training assignments and annual competencies within &nbsp;established timelines.</li>
<li>Handle and dispose of all specimens following standard precautions and applicable safety policies.</li>
<li>Understand and comply with all lab and safety regulations.</li>
<li>Support employee engagement initiatives and activities to maintain and improve team morale.</li>
</ul>
</li>
</ul>
<ul>
<li>Meet performance and behavior expectations listed below:
<ul>
<li>Exemplify the core values of Integrity, Teamwork, Accountability, Quality, and Innovation at all times.</li>
<li>Self-motivation with a results-driven approach.</li>
<li>Maintain a high level of professionalism in written and verbal communications.</li>
<li>Act with an inclusion mindset and model these behaviors for the organization.</li>
<li>Maintain regular and reliable attendance.</li>
</ul>
</li>
</ul>
<ul>
<li>Demonstrate the necessary skills and abilities:
<ul>
<li>Ability to work in a fast-paced team environment, adapt to changing workload and circumstances effectively and respond to new information quickly.</li>
<li>Strong critical thinking skills with the ability to make decisions in a fast-paced environment.</li>
<li>Ability to communicate effectively with all levels of the organization through both verbal and written communication.</li>
<li>High level of listening skills and attention to detail with strong organizational and prioritization skills.</li>
<li>Ability to flex hours and work nights and/or weekends as needed to support the success of ES Labs.</li>
<li>Ability to work overtime, as needed.</li>
<li>Ability to lift and move up to 40 pounds for approximately 25% of a typical working day.</li>
<li>Ability to work seated for approximately 50% of a typical working day.</li>
<li>Ability to work standing for approximately 50% of a typical working day.</li>
<li>Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 75% of a typical working day.</li>
<li>Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.</li>
<li>Ability to comply with any applicable personal protective equipment requirements.</li>
<li>Ability to perform repetitive motions.</li>
<li>Understand potential exposure to hazardous materials, tissue specimens and instruments with moving parts, heating and freezing elements.</li>
<li>Tolerate the handling of bodily fluids and solids (e.g., blood, urine and feces).</li>
<li>Ability and means to travel to and work at all other sites within the same city, as needed.</li>
</ul>
</li>
</ul>
Minimum Qualifications
<ul>
<li>High School Degree/General Education Diploma.</li>
<li>Must be 18 years of age or older.</li>
<li>Experience using computers to include Internet navigation, email, Microsoft Office Suite.</li>
<li>Demonstrated ability to perform the Essential Duties of the position with or without accommodation.</li>
<li>Authorization to work in the United States without sponsorship.</li>
</ul>
Preferred Qualifications
<ul>
<li>Associate degree or Bachelor’s degree in Life Sciences, Physical Sciences, or field related to the essential duties of the job.</li>
<li>Experience in a laboratory or similar environment with maintaining sample integrity, following procedures and protocols, and sample collecting/handling.</li>
<li>Knowledge and understanding of CAP, GLP, GDP, CLIA, New York State Department of Health (NYSDOH), and HIPAA.</li>
<li>Experience in troubleshooting automation and performing instrument maintenance.</li>
<li>Lean experience (Kaizen, Kanban, root cause analysis, countermeasure implementation, etc.).</li>
</ul>
#LI-KB1
Salary Range:
$34,000.00 - $54,000.00

The annual base salary shown is for this position located in US - WI - Madison on a full-time basis. In addition, this position is bonus eligible, and is eligible to be considered for company stock at hire and on an annual basis.
Exact Sciences is proud to offer an employee experience that includes paid time off (including days for vacation, holidays, volunteering, and personal time), paid leave for parents and caregivers, a retirement savings plan, wellness support, and health benefits including medical, prescription drug, dental, and vision coverage. Learn more about our benefits.
Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, please contact us here.
Not ready to apply? Join our talent community and stay up to date on what’s new at Exact Sciences.
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state, or federal law. Any applicant or employee may request to view applicable portions of the company’s affirmative action program.
To view the Right to Work, E-Verify Employer, and Pay Transparency notices and Federal, Federal Contractor, and State employment law posters, visit our compliance hub. The documents summarize important details of the law and provide key points that you have a right to know.
PandoLogic. Keywords: Medical Laboratory Technician (MLT), Location: Madison, WI - 53725 , PL: 597710096

Lab Processing Associate - 3rd Shift

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins is the world leader in the bio/pharmaceutical testing market.&nbsp; With over €5.3&nbsp;billion in annual revenues and 55,000 employees across 900 sites in&nbsp;50 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries and to governments.
The Eurofins BioPharma Product Testing (BPT) Group is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide. Eurofins BPT provides comprehensive CMC laboratory services for the world’s largest pharmaceutical and biopharmaceutical companies. The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control.
Job Description 
Job Summary:&nbsp;Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team is seeking candidates with expertise in method development and/or method validation.
<ul>
<li>Applies GMP in all areas of responsibility, as appropriate.</li>
<li>Performing a large variety of analytical tasks for the validation of analytical methods used in the testing of drug products and raw materials by means of various procedures including HPLC, GC, UV/Vis, and dissolution.</li>
<li>Reading, understanding, and interpreting diverse analytical procedures.</li>
<li>Conducting analytical investigations.</li>
<li>Troubleshoot instrumentation and communicate with vendors when required.</li>
<li>Train and mentor junior staff in laboratory procedures.</li>
<li>Manage and discuss projects with clients.</li>
</ul>
Qualifications 
The Ideal Candidate would possess:
<ul>
<li>3-5 years of experience with LC chromatographic validation in a GMP environment.</li>
<li>Excellent communication (oral and written) and attention to detail.</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
</ul>
Minimum Qualifications:
<ul>
<li>Higher education degree in analytical chemistry or other related degree concentration.</li>
<li>BS and 4+ years of experience, MS and 2+ years of experience, or PhD and 1+ years of experience.</li>
<li>Authorization to work in the U.S. without restriction or sponsorship.</li>
</ul>
 Additional Information 
The position is full-time, Monday-Friday, 8am-4pm, with overtime as needed. Candidates within a commutable distance of Lancaster, PA 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 USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

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