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<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is a global leader in providing a unique range of analytical testing services to multiple industries. With over 200,000 analytical methods, Eurofins Scientific helps make life and our environment safer, healthier, and more sustainable. Our network of over 63,000 employees across a network of more than 950 laboratories in 60 countries, strengthens Eurofins Scientific as leader in scientific testing services. In 2024, Eurofins generated total revenues of EUR € 6.9 billion, and has been among the best performing stocks in Europe over the past 20 years.
EAG Laboratories, a Eurofins company has over 40 years’ experience in materials and engineering testing services. EAG&nbsp;is a global leader in scientific services with a portfolio of&nbsp;analytical methods. We offer a consultative multi-disciplinary approach to solving your materials and engineering related product problems. As thought leaders in investigative science, we set the global standard for materials and engineering&nbsp;testing services.
Job Description 
EAG Laboratories, a part of the Eurofins network of companies, is a global leader in advanced microscopy, surface analysis and semiconductor testing services of various types of materials from synthetic biomaterials to nanotechnology, deliver new “super materials” with the potential to transform our world.&nbsp;Our laboratories&nbsp;are&nbsp;at the forefront of this revolution, providing the scientific expertise and analytical techniques to support companies at every phase of the product lifecycle, from R&amp;D to manufacturing.
EAG is looking for a&nbsp;Laboratory Analystto join our lab in Syracuse, NY. The candidate will be responsible for prepping and analyzing solid samples by ICP-MS and/or ICP-OES.Additionally, the candidate will be responsible for process and equipment troubleshooting.&nbsp;
Use of information in this role is subject to the International Traffic in Arms Regulations (ITAR). All accepted applicants must be U.S. Persons as defined by ITAR: U.S. Person is a U.S. Citizen, U.S. Permanent Resident (i.e., "Green Card Holder"), Political Asylee, or Refugee.&nbsp;
Employees are expected to comply with ISO 27001 standard and company requirements for Information security. &nbsp;
Work Schedule: 3:30pm-2:00am M-Th
*This candidate must be comfortable working the 3:30pm-2:00am Shift*&nbsp;
Qualifications 
Skills, Knowledge and Experience:
<ul>
<li>BS degree in materials science or related field.&nbsp;&nbsp;</li>
<li>1+ years of sample preparation, analytical instrument operation and analysis.</li>
<li>Able to cut various metals using bench top sheers, hand held metal snips, precision saws, grinding surfaces layers of materials using a grinder or rotary tool.</li>
<li>Testing and Associated Instrumentation Experience (Microscope, GDMS, ICP-OES, ICP-MS, etc.)&nbsp;</li>
<li>Effectively manages project/assignment requirements, coordinates with partners, and works independently under supervision.</li>
<li>Prioritizes tasks, allocates time effectively, and manages distractions to meet deadlines.&nbsp;</li>
<li>Collaborates effectively with others, including balancing own interests with others' and acknowledging their contributions.&nbsp;</li>
<li>Maintains professionalism and contributes to a safe and harmonious work environment adhering to safety protocols, sharing important information, fulfilling team responsibilities, and resolving interpersonal conflicts effectively.&nbsp;</li>
<li>Under supervision, implements and delivers solutions that meet customer expectations.&nbsp;</li>
<li>Provides customer support, collaborates with others, and contributes to the establishment of effective customer relationships.&nbsp;</li>
<li>Demonstrates a commitment to personal and professional growth by actively seeking opportunities to improve skills and knowledge, embracing new challenges, and learning from experiences and structured learning opportunities.&nbsp;</li>
<li>Leverages available resources for continuous development by effectively utilizing available development resources to enhance capabilities and broaden expertise.&nbsp;</li>
</ul>
We encourage you to apply even if your experience is not a 100% match with the position. We are looking for someone with relevant skills and experience, not a checklist that exactly matches the job description. We want to help you grow and in return, you help us grow into a stronger, more inclusive organization.&nbsp;&nbsp;
Ability and Physical Requirements:
<ul>
<li>Must be able to remain in a stationary position 80% of the time.&nbsp;</li>
<li>Ability to continuously operate a personal computer or lab equipment for extended periods of time (4 or more hours).</li>
<li>Ability to operate a keyboard and other lab equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead</li>
<li>Ability to communicate clearly and understandably ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting.</li>
<li>Ability to handle small and fragile devices with tweezers and /or fingers.</li>
<li>Require close distance visual acuity with or without correction (Glasses, Contacts, etc.)</li>
<li>Must be willing and able to wear PPE such as hard-hat, steel-toed shoes, safety glasses, laboratory coat and/or any other devices or equipment that is required.</li>
<li>Learn new tasks, remember processes, maintain focus, complete tasks independently, make timely decisions in the context of a workflow, ability to communicate with visitors, ability to complete tasks in situations that have a speed or productivity quota.</li>
<li>Ability to move equipment or items up to 50 lbs.</li>
</ul>
The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.&nbsp;&nbsp;
We will consider reasonable accommodations for qualified individuals with disabilities. If you have a disability or special need, we would like to know how we can better accommodate you.&nbsp;
 Additional Information 
Compensation Range:&nbsp;$24-27/per hour with a 15% shift differential for second shift. Salary is commensurate with experience and degree of technical expertise.
What It’s Like to Work Here:
•&nbsp;Teamwork:&nbsp;be inspired by your leaders, be encouraged by your teammates, and be supported in all parts of your journey while you work with us.
•&nbsp;Learning &amp; Development:&nbsp;take on career development programs and goal setting to create big possibilities for your career and life. Develop within the company; be mentored and grow as a leader.
•&nbsp;Diversity &amp; Authenticity:&nbsp;we work hard to embrace diversity and inclusion and encourage everyone to bring their authentic selves to work every day.
Benefits &amp; Perks to Foster Work/Life Balance:
✓ Medical, Dental and Vision Coverage
✓ 401k Company Matching
✓ Paid Time Off
✓ Wellness Program
✓ Education Assistance
✓ …and more!
Eurofins EAG Laboratories is an equal opportunity employer and prohibits discrimination, harassment, and retaliation in all of our employment practices. Eurofins EAG Laboratories recruits, hires, trains, promotes and administers all employment-related matters based on an individual's qualifications, abilities, and efforts.  Applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship status, sexual orientation, gender identity and/or expression, pregnancy, genetic information, disability, military and/or protected veteran status, and/or any other category protected by applicable federal, state, or local law. &nbsp;&nbsp;&nbsp;
If you enjoy being immersed in science or engineering, tackling problems head-on, finding solutions through teamwork, and taking pride in accomplishments, join us today! Check out our other opportunities:&nbsp;<a href="http://www.eag.com/about/careers/&amp;nbsp" target="_blank">www.eag.com/about/careers/&amp;nbsp</a>;
Eurofins USA Material Sciences is a Disabled and Veteran Equal Employment Opportunity employer.
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Eurofins USA Material Sciences is a Disabled and Veteran Equal Employment Opportunity employer.

ICP (Materials Science) Analyst - Second Shift | EAG Laboratories

<h3>Job Description</h3>
Job DescriptionDescription:
We are seeking a knowledgeable and innovative SANY Science Curriculum Coordinator for grades K-12 to lead and enhance our established science programs across all SANY schools. This pivotal role involves refining our current science curriculum to ensure alignment with district, state, and national standards, while fostering scientific inquiry, critical thinking, and a love for discovery among students and educators.
 
Job Goals: The SANY Science Curriculum Coordinator will continue to advance, articulate, implement, and evaluate our comprehensive science program, ensuring it remains research-based, rigorous, and responsive to the diverse learning needs of students across the district.
 
Position Responsibilities:
Curriculum and Instruction: Serve as the SANY leader on curriculum and instruction in science across all K-12 grade levels. Maintain and strengthen the alignment of the science curriculum with state and NGSS (Next Generation Science Standards). Manage, coordinate, and monitor instructional programs while ensuring timely updates to content and pedagogy.
Assessment and Intervention: Evaluate the effectiveness of current science programs in improving student outcomes. Lead data meetings to analyze science performance data and design targeted intervention plans where necessary to improve student achievement.
Staff Development: Lead district-wide professional learning opportunities for science educators. Design and deliver high-quality workshops, training sessions, and coaching that support effective science instruction, inquiry-based learning, and cross-disciplinary integration.
Leadership and Coordination: Collaborate with school leaders and educational stakeholders to ensure effective implementation of science instruction and evidence-based interventions. Work in coordination with other curriculum coordinators to promote interdisciplinary coherence and strategic instructional planning.
Expectations:
<ul>
<li>Demonstrate exemplary instructional leadership by modeling effective science teaching practices and actively engaging in curriculum innovation.</li>
<li>Stay informed of cutting-edge developments in science education, instructional technology, and research-based practices.</li>
<li>Contribute to the development and execution of SANY-wide school improvement plans with a strong focus on science goals.</li>
<li>Adhere to professional standards and conduct as outlined in the SANY Employee Handbook.</li>
</ul>
Respond to staff communications within 72 hours and address administrative concerns in a timely and effective manner. SANY Climate:
<ul>
<li>Promote a positive, respectful, and collaborative environment in all school-related interactions.</li>
<li>Follow the established chain of command for addressing academic and interpersonal matters.</li>
<li>Uphold and exemplify SANY’s core values of positivity, professionalism, and progressive education.</li>
</ul>
Requirements:
Education &amp; Certification
<ul>
<li>Master’s degree in Science Education, Curriculum &amp; Instruction, or a closely related field.</li>
<li>Preferred: Valid New York State teaching certification in Science (Biology, Chemistry, Physics, or General Science).</li>
</ul>
Experience
<ul>
<li>Minimum of 5 years of successful teaching experience in K–12 science.</li>
<li>Demonstrated expertise in science curriculum design, NGSS alignment, and inquiry-based instruction.</li>
<li>Experience leading professional development workshops for science educators.</li>
<li>Proven ability to analyze science assessment data to design interventions and improve student outcomes.</li>
</ul>
Knowledge &amp; Skills
<ul>
<li>Deep knowledge of Next Generation Science Standards (NGSS) and NYS Science Learning Standards. </li>
<li>Strong understanding of STEM integration and cross-disciplinary instructional practices.</li>
<li>Ability to model and coach inquiry-based, lab-based, and technology-supported science instruction.</li>
<li>Skilled in curriculum evaluation, program improvement, and instructional leadership.</li>
</ul>
Additional Expectations
<ul>
<li>Commitment to fostering a culture of scientific inquiry, critical thinking, and discovery. </li>
<li>Willingness to collaborate across multiple grade levels and school sites.</li>
<li>Strong organizational and communication skills for coordinating district-wide science initiatives.</li>
<li>Valid driver’s license and willingness to travel to schools within a 2-hour range, including operation of district vehicles.</li>
</ul>
SANY is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

SANY Science Curriculum Coordinator

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose
The Microbiology Laboratory Technician performs laboratory testing within a fast paced GMP environment in support of one or more of the following areas; raw materials, environmental monitoring, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties.
Responsibilities
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. Works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for department.</li>
<li>Support investigations</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Qualifications 
<ul>
<li>Associates Degree in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree with &lt;2 years pertinent experience or High School Diploma with 2+ years combined experience in Manufacturing, QA, QC, R&amp;D in pharmaceutical or biologics industry.</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Microbiology Laboratory Technician III (Monday-Friday 7am-3:30pm)

<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 
<ul>
<li>Raw Materials Analytical testing could include: compendial testing, HPLC/UPLC, generic testing (e.g., solvents, water, ash, titrations, heavy metals) and compound specific methods</li>
<li>Ability to investigate and troubleshoot equipment related issues</li>
<li>Work with a balance for weighing, pH, pipettes</li>
<li>Preparation of buffer and media</li>
<li>UV</li>
<li>Smart Lab and Trackwise software experience a plus</li>
</ul>
Qualifications 
<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, 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>
<li>Bachelor's degree in physical science (chemistry, physics, etc.), or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, 8:00 am- 5:00 pm Overtime as needed.&nbsp;</li>
<li>Candidates currently living within a commutable distance of Indianapolis, IN, are encouraged to apply</li>
<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>
<li>#LI-EB1</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Analytical Chemist

<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.
Job Description 
Job Summary: Eurofins' BPT Small Molecule Method Development and Validation team is seeking an Scientist to join their team full time in Lancaster, PA. This individual will work in a duel analyst and data reviewer role. The Scientist will be able to:
<ul>
<li>Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus</li>
<li>Execute specialized analyses and method transfer and feasibility testing</li>
<li>Troubleshoot method and instrumentation problems</li>
<li>Use office and instrumentation specific computer software</li>
<li>Develop and execute validation plans</li>
<li>Carry out method transfers and feasibility studies</li>
<li>Train technical staff</li>
<li>Some travel to client sites for technical meetings could be required</li>
<li>Determine if data is compliant and defendable based on industry regulations and methodology</li>
<li>Verify scientific data is of sound quality following all method, industry, and client requirements where applicable</li>
<li>Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations</li>
<li>Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate</li>
<li>Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area</li>
<li>Review methods to ensure procedures are followed</li>
<li>Authorize written reports (e.g., SOP, OMC, client reports)</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Bachelor's degree in chemistry, pharmaceutical science, or other related degree concentration and a minimum of 3 years of experience in a cGMP compliant industry lab.</li>
<li>Master's degree in chemistry, pharmaceutical science, or other related degree concentration and a minimum of 1 year of experience in a cGMP compliant industry lab.</li>
<li>Experience with HPLC and Empower</li>
<li>Authorization to work in the U.S. without restriction or sponsorship</li>
</ul>
 Additional Information 
Position is full-time position, Monday - Friday 8:00am - 4:00pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
<ul>
<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.

Analytical Chemist- Small Molecule

<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.
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&nbsp;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>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>BS or MS degree in analytical chemistry or other related degree concentration.</li>
<li>BS and 4+ years of industry experience, MS and 2+ years of industry experience, or PhD and 1+ years of industry experience.</li>
<li>3-5 years of experience with LC chromatographic validation in a GMP environment.</li>
<li>Authorization to work in the U.S. without immediate or future sponsorship.</li>
</ul>
 Additional Information 
Position is full-time position, Monday - Friday 8:00am - 4pm. Candidates currently living 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.

Senior Chemist- HPLC Method Development & Validation

<h3>Job Description</h3>
Job Description
Sr. Director of Research &amp; Development
Direct Hire | Relocation Offered | Excellent Benefits 
Description
Will be responsible for developing new pharmaceutical products from concept to commercialization that support company growth. Position will also enhance and improve upon current products. Serves as a technical expert that supports product improvements, quality improvements, customer requests, and cost savings initiatives. Is responsible for formulation and generation of representative pilot samples for internal and external customer evaluations &nbsp;
Duties:
<ul>
<li>Formulates new products from development to commercialization within defined company, industry, and regulatory parameters </li>
<li>Evaluates raw materials </li>
<li>Establishes specifications for new and/or reformulated products </li>
<li>Changes existing formulations to improve product cost </li>
<li>Perform scale-up for transition to manufacturing </li>
<li>Develops new technologies related to pharmaceutical processing </li>
<li>Writes necessary documents for manufacturing feasibility </li>
<li>Prepares product registration documentation and product chemistry packages to meet regulatory requirements </li>
<li>Responsible for batch production from pilot scale to process validation </li>
<li>Additional duties as required</li>
</ul>
Knowledge, Skills &amp; Abilities:
<ul>
<li>Minimum of a BS in Chemistry, Pharmacy, or other Science</li>
<li>5+ years of experience in pharmaceutical formulation development</li>
<li>5+ years of experience in pharmaceutical management</li>
<li>10+ years of experience in the pharmaceutical industry</li>
<li>Proven problem-solving skills and track record of successful technical accomplishments</li>
<li>Strong understanding of cGMP guidelines and FDA regulations related to the pharmaceutical industry</li>
<li>Experience with FDA and other regulatory agencies required</li>
<li>Experience with ANDA, ANADA, IND, and INAD submissions preferred</li>
<li>Experience with HPLC testing and other stability testing preferred</li>
</ul>
Experience Level
Expert Level
Pay and Benefits
The pay range for this position is $180000.00 - $220000.00/yr.
Good stuff with this company! Trust me!
Workplace Type
This is a fully onsite position in Minneapolis,MN.
Application Deadline
This position is anticipated to close on Aug 29, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Sr. R&D Director (Pharmaceutical Industry)

<h3>Job Description</h3>
Job DescriptionDescription:
WHY US?
Sterling Labs invests in the success of our team. We are seeking highly motivated individuals who want to invest in their skill sets and careers, be rewarded for their initiative, and thrive in a collaborative environment. Our analytical data has a tremendous impact on protecting human health and the environment. We value teamwork, continuous improvement, growth, and empowered ethical decision-making.
We Preserve the Planet to Protect the Future.
Our Core Values:
<ul>
<li>We strive for Integrity in Everything We Do. We're honest and transparent in our actions and decisions.</li>
<li>We are Customer-Focused. We prioritize our customers' needs and value their feedback.</li>
<li>We are Never Satisfied and are dedicated to continuous improvement. We always seek ways to improve and adapt to changing needs.</li>
</ul>
Sterling Labs' growth has been directly tied to our clients’ needs for 36 years. We are a growth-oriented organization that prioritizes our clients. We partner with manufacturers, engineering firms, and government agencies to provide environmental laboratory data that helps protect the environment. From wastewater sampling and analysis in greater Chicago and Milwaukee to nationwide service with Department of Defense partners, our commitment to our clients drives our growth.
 
Objectives
The GCMS Analyst performs a wide variety of tasks to achieve production and quality goals. Key responsibilities include:
<ul>
<li>Planning daily workflow.</li>
<li>Monitoring the quality of procedures and ensuring proper technique.</li>
<li>Communicating issues and needs to the supervisor.</li>
</ul>
The GC-MS Analyst adheres to Sterling Labs’ standard operating procedures (SOPs) in a culture of safety, honesty, and ethical behavior. Duties are performed under the direction of the supervisor to meet client service requests. The role requires motivation to complete projects successfully and meet client expectations.
Duties of the Position
Primary Analytical Tasks
<ul>
<li>8270/625 SIM</li>
</ul>
Secondary (Backup) Analytical Tasks
8082/608 PCB/ D4059 PCB 
 
Key Responsibilities
<ul>
<li>Manage sample workload to meet reporting deadlines.</li>
<li>Upload and review results in Sterling Labs’ Laboratory Information Management System (LIMS).</li>
<li>Quantify and qualify results according to analytical methods and SOPs.</li>
<li>Prepare a daily Work Status Report in Element 7.</li>
<li>Report accurate and timely data in Element 7.</li>
<li>Produce Level IV PDF data at the time of analytical reporting.</li>
<li>Calibrate instruments accurately per SOPs.</li>
<li>Build sequence and batch data to maximize instrument run efficiency.</li>
<li>Perform daily and ongoing instrument maintenance (e.g., inlet maintenance, column changes, source cleaning).</li>
<li>Prepare standards and reagents for analysis.</li>
<li>Assess sample quality prior to analysis to protect instruments and meet client objectives.</li>
<li>Assist the manager in identifying sources of problems (Corrective Action Reports) and implementing corrective actions.</li>
<li>Assist other analysts and extractors in lab areas as workflow demands require, under the manager's direction.</li>
<li>Maintain good housekeeping habits and assist with sample disposal.</li>
<li>Communicate workload status and data quality issues to the manager.</li>
<li>Complete quarterly studies in a timely manner. </li>
<li>Perform other duties as assigned, including assistance with other analyses and extractions.</li>
</ul>
Instruments Used
<ul>
<li>Gas Chromatography-Mass Spectrometry (GC-MS)</li>
<li>Laboratory Scales</li>
<li>Pipettes</li>
<li>Syringes</li>
<li>PCs</li>
</ul>
 
 
Requirements:
Qualifications
<ul>
<li>B.S. or B.A. degree in Chemistry is preferred.</li>
<li>Familiarity and competence with LIMS.</li>
<li>Experience producing and reviewing Level IV QC data.</li>
<li>Proficiency in Microsoft Office (Word, Excel, Access).</li>
<li>Strong verbal and written communication skills.</li>
<li>Self-motivated, goal-driven, and outcome-oriented.</li>
<li>Previous experience working with Department of Defense environmental samples preferred.</li>
</ul>
Physical Requirements
<ul>
<li>Ability to lift or move up to 25 pounds safely.</li>
<li>Work in cold environments (e.g., cold room/cooler) for short periods.</li>
<li>Wear required Personal Protective Equipment (PPE).</li>
<li>Vision requirements include close, distance, color, peripheral vision, depth perception, and focus adjustment.</li>
<li>Perform physical tasks including standing, walking, sitting, handling objects, reaching, climbing stairs, balancing, stooping, kneeling, crouching, talking, hearing, tasting, and smelling.</li>
</ul>
BENEFITS &amp; COMPANSATION
Understanding that employee well-being is essential to performance, we offer a comprehensive benefits package to full-time employees, including:
<ul>
<li>Healthcare Coverage – Medical, dental, and vision insurance plans</li>
<li>Financial Protection – 401(k) retirement plan, life insurance, short-term and long-term disability coverage</li>
<li>Work-Life Balance – Paid time off, including vacation, sick leave, and holidays</li>
</ul>
Compensation: This is an entry-level role, compensated at $21.00 per hour, paid biweekly, with opportunities for overtime.

Laboratory Analyst, GCMS - SVOC

<h3>Job Description</h3>
Job Description
WE ARE FLORIDA MEDICAL!
Our 459-bed acute care hospital has made excellence in delivering healthcare a priority, and it shows:
<ul>
<li>We are home to the Heart Institute of Florida, where our doctors have worked on the leading edge of cardiac care for more than 40 years.</li>
<li>We are part of the Advanced Neuroscience Network, leading the way in brain and spinal care in Florida.</li>
<li>We have a comprehensive stroke center that offers fast, effective stroke care for a strong recovery.</li>
</ul>
At Florida Medical Center, we are committed to delivering the highest quality care possible to each of our patients. We strive to help patients achieve better outcomes, quicker recovery times, shorter hospital stays and ultimately, better health. As a result of our efforts, Florida Medical Center has received numerous prestigious awards and accolades from trusted organizations including the Florida Agency for Health Care Administration (AHCA) and the American Heart/Stroke Association.
WHAT WE OFFER
<ul>
<li>Essential/stable and growing company with many opportunities for training and advancement within the medical field that all employees and team members (including Full-Time and Part-Time) can benefit from.</li>
<li>Hourly pay is negotiable based on experience. We offer competitive market pay and opportunities for bonus depending on great work performance</li>
<li>Comprehensive Employee Benefits: Full and Part Time employees are eligible for various plans for medical, dental, and vision insurance.</li>
</ul>
Position Summary:
Performs analysis on body fluids and exudates from hospital in-patients and out-patients to provide information for diagnosing and combating diseases. Updates procedures manual, checks quality control of each procedure and of each shift. Oversees the performance of other employees Ensures that the staff maintains their competency to perform test procedures and report test results promptly, accurately and proficiently., checks linearities, statistics, send data to be evaluated and to be compared with other laboratories. Performs and/or review the CAP surveys of the section. Maintains required standards of accreditation. Maintains instruments and equipment in accordance with manufacturer's specifications. Implements and maintains performance improvement program. Monitors, analyzes and justifies expense and revenue within departments. Other duties as assigned.
Responsible for assisting the Laboratory Director and the Medical Laboratory Director in the management and supervision of the Laboratory. Provide administrative direction to all sections. Provide technical direction to those areas in which the Supervisor is licensed. Support the Laboratory Director by assuming the role as a leader in planning, directing and managing the laboratory, designated sections and staff to assure quality service on a 24-hour basis. Responsible for assisting in meeting TJC, AHCA, CAP and AABB, CLIA and OIG/CMS standards, complying with corporate policy and procedure, managing the equipment in the department, promoting teamwork with physicians and all healthcare providers, promoting internal and external customer satisfaction and appropriate resource management. Performs additional duties as needed or assigned
CUSTOMER SERVICE RESPONSIBILITIES:
Performs duties and conducts interpersonal relationships in a manner designed to project a positive image of the department and the hospital. Works with supervisor/manager and other members of section or department to promote a harmonious work environment. Ensures that all contacts with patients, the public, physicians and other hospital personnel are carried out in a friendly, courteous, helpful and considerate manner. Answers telephones in a prompt and courteous manner. Displays concern and provides assistance or explains procedures as appropriate to callers or in face-to-face situations. Dedicated to meeting the expectations and requirements of internal and external customers. Works with customers to identify problem areas and recommend solutions
Additional Information
Qualifications/Requirements
Education
Successful completion a Bachelor's degree in Clinical Laboratory Science, Chemical Science, or Biological Science from an accredited institution, including at least 24 semester hours of academic science (6 hours in biological sciences and 6 hours in chemical sciences) and at least 12 months of training in a clinical laboratory of a hospital accredited by the American Society of Clinical Pathologists (ASCP), or a B.S. in Medical Technology, or an A.A. in Medical Laboratory Science with a full semester of Hospital Training. If the degree is from outside the U.S., an equivalency evaluation may be required to meet staff sign-off requirements.
Required licensures/certifications
<ul>
<li>State of Florida supervisor's license in one or all disciplines.</li>
<li>Supervisor licensure is required, covering at least 5 areas, including Clinical Chemistry, Blood Banking (Immunohematology), and Hematology, satisfying the need for the position.</li>
</ul>
 
Skills and Abilities
<ul>
<li>Ability to perform and to teach students in the threshold and practical aspect of all procedures of the department. Knowledge and understanding of the workflow in the laboratory. Manual dexterity.</li>
<li>Good oral and written communication skills</li>
<li>Minimum of 5 years as a clinical lab technologist, with at least 1 year of leadership experience preferred.</li>
</ul>

Laboratory Supervisor -Full Time

<h3>Job Description</h3>
Job Description
SALARY: $60-65k
LOCATION: New York or Remote
 
Who are we?
We are the originators of influencer marketing.
Influencer is an agency built at the intersection of creativity, data, and technology with a unique ‘people power &amp; platform power’ approach.
From big brand launches to shifting perceptions and from riding fast trends to driving footfall, Influencer builds ideas with impact to deliver outcomes that drive your business forward via an unmatched client experience.
Campaigns are underpinned by Influencer’s game-changing proprietary technologies, which are supercharged by official partnerships and data integrations with the world’s leading social platforms for real-time and accurate reporting. Influencer is an Official Global Marketing Partner of TikTok, Snap, YouTube and Meta.
We believe the more tangible, scaled outcomes that creators produce drive impact beyond just likes and impressions. Influencer is championing the ‘True Human Influence’ movement; on a mission for creator campaigns to be judged in the same way as other media activations.
Founded by OG YouTube creator Caspar Lee &amp; entrepreneur Ben Jeffries, Influencer has been helping brands navigate the ever-evolving influencer marketing landscape since 2015. In that time they have developed valuable knowledge, experience, and technology that have enabled them to deliver thousands of campaigns, for hundreds of brands in markets across the world. Today, Influencer has a team of 170+ of the best talent in the industry, working across Europe, North America, and the Middle East. From Google to Coca-Cola, from Amazon to Microsoft, and from TikTok to Meta - they work with companies, brands, and agencies across every vertical, building meaningful relationships between brands, creators, and their audiences. 
Job Title
Measurement Analyst (Hybrid, Open to Remote) 
Reporting of the role
This role reports to the Associate Director of Measurement
Overview of the job
We’re looking for a sharp, detail-oriented Insights &amp; Measurement Analyst to help shape how we evaluate the impact of influencer marketing campaigns. In this role, you’ll partner closely with the Associate Director of Measurement to build a world-class measurement function - analyzing performance data, identifying key themes in social content, and helping translate creator-driven insights into business impact. You’ll be instrumental in evolving our internal measurement systems, conducting thematic and sentiment analysis, and supporting the delivery of clear, compelling post-campaign reporting for our clients. If you’re fluent in both the language of data and digital culture, and you’re excited by the idea of turning social buzz into business intelligence, we want to hear from you.
 
3 best things about the job 
<ul>
<li>
Work where data meets culture: Dig into the numbers and the memes - turning influencer content, viral moments, and audience sentiment from comment sections into insights that actually move the needle for brands.
</li>
<li>
Help showcase creator stories: Your analysis helps shape the next big brand moments on TikTok, Instagram, and beyond - because behind every great campaign is an even greater insights report.
</li>
<li>
Collaborate with creative minds: Work shoulder-to-shoulder with strategists, creatives, and client teams to dream up smarter campaigns and show off their impact with dashboards and stories that wow clients.
</li>
</ul>
 
Measures of success – In the first few months, you would have:
<ul>
<li>
Developed a strong understanding of the measurement studies in our toolbox, with a focus on sentiment analysis, brand lift, and content effectiveness.
</li>
<li>
Successfully scraped, coded, and charted data, contributing to building world-class, client-facing sentiment reports and decks.
</li>
<li>
Helped organize, archive, and maintain historical campaign data to support our benchmarking initiatives.
</li>
<li>
Been a part of all forms of creator measurement within our full funnel, industry-leading toolkit.
</li>
</ul>
 
Roles &amp; Responsibilities:
<ul>
<li>
Support the development and refinement of our measurement infrastructure and analytics processes.
</li>
<li>
Analyze campaign performance across social platforms using both qualitative and quantitative methods.
</li>
<li>
Conduct creative effectiveness, sentiment and thematic analysis of influencer content and audience responses.
</li>
<li>
Collaborate with strategy, client services, and creative teams to deliver actionable insights and strategic recommendations.
</li>
<li>
Help build and maintain dashboards, benchmarks, and reporting templates.
</li>
<li>
Identify patterns and trends in social behavior that can inform future campaign planning.
</li>
<li>
Assist in developing measurement frameworks tailored to brand goals and KPIs.
</li>
</ul>
 
What you will need:
<ul>
<li>
1–3 years experience in data analysis, social listening, or campaign measurement - ideally in a digital, media, or influencer-focused environment
</li>
<li>
Familiarity with social media analytics tools (e.g., CreatorIQ, Sprout, Talkwalker, or native platform tools)
</li>
<li>
Experience with basic data manipulation and visualization (Excel, Google Sheets, Looker, Tableau, or similar)
</li>
<li>
Strong writing and communication skills - you know how to turn numbers into a narrative
</li>
<li>
Curiosity for internet culture, creator trends, and emerging social behaviors
</li>
<li>
A collaborative mindset and a strong attention to detail
</li>
</ul>
 
Bonus Points: 
<ul>
<li>Experience working in or adjacent to influencer marketing</li>
<li>Comfort with natural language processing tools or basic coding (e.g., Python, SQL)</li>
<li>Exposure to brand lift studies or media mix modeling</li>
</ul>
 
A few of our core benefits:
<ul>
<ul>
<li>
Medical Benefits through Insperity
</li>
<li>
Wellbeing support including EAP &amp; Mental Health cover
</li>
<li>
401K with match opportunity
</li>
<li>
22 days of Paid Time Off (+ Federal Holidays which can be flexed to your needs)
</li>
</ul>
</ul>
 
For more information on our benefits, perks and what makes us unique, please visit our website here
 At Influencer, we’re committed to cultivating an environment that promotes diversity, equity and inclusion. We promote DEI in our workplace and are a global community who believe our unique qualities should be celebrated. We want everyone at Influencer to bring their authentic selves to work everyday, irrespective of age, disability (including hidden disabilities), gender, gender identity or gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, or sexual orientation. We are committed to embedding Diversity, Equity &amp; Inclusion into everything we do at Influencer, making it part of our culture. All we ask is that you have a passion for Influencer Marketing and a desire to be a part of one of the fastest growing companies within this exciting industry.

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