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<h3>Job Description</h3>
JOB DESCRIPTION: Microbiology Technician
DEPARTMENT: Quality
REPORTS TO: Director of Laboratory Services
 
SUMMARY
The Microbiologist position ensures food safety by establishing and maintaining procedures and programs within the food processing facility. This includes analysis of raw materials, finished product and environmental monitoring samples. Assists in audits by ensuring that all food safety system documents are current and accurate, ensuring compliance with regulations and standards. Reports to Director of Laboratory Services
 
KEY RESPONSIBILITIES
 Analysis:
<ul>
<li>Conducts routine and complex analysis of food and environmental samples to detect pathogens and food quality or sanitation microbial indicator organisms. </li>
<li>Conducts investigation and provides corrective actions for food safety failures in both finished goods and environment.</li>
<li>Conducts in-process chemistry testing for products as well as shelf-life development studies.</li>
<li>Participates in laboratory proficiency testing</li>
</ul>
 
Food Safety Program Implementation
<ul>
<li>Assists in developing and implementing food safety programs, ensuring compliance with regulations and standards and good manufacturing practices.</li>
</ul>
 
Data Analysis and Reporting
<ul>
<li>Collects, accurately analyzes and interprets microbiological data, and prepares Certificates of Analysis and reports for internal and external parties.</li>
<li>Responsible for release of production for shipping through positive-release program.</li>
</ul>
 
Laboratory Maintenance and Calibration
<ul>
<li>Maintains and calibrates laboratory equipment, ensuring accuracy and reliability of testing procedures and results. </li>
<li>Assists with media preparation, and test sample disposal.</li>
</ul>
 
Training and Support:
<ul>
<li>May train junior microbiologists, provide technical support to production teams and participate in both internal and external audits.</li>
</ul>
 
REQUIERED SKILLS AND QUALIFICATIONS
Education:
<ul>
<li>Minimum Bachelor’s degree in Microbiology, Food Science, or a related field and experience in food manufacturing plant performing quality or analytical procedures related to production</li>
<li>Familiarity with relevant food safety regulations and standards</li>
<li>Knowledgeable in Good Manufacturing Practices and Good Laboratory Practices policies and procedures.</li>
<li>Excellent written and verbal communication skills for reporting findings and collaborating with others.</li>
<li>Attention to detail is crucial for accurate testing and record-keeping</li>
<li>Able to demonstrate understanding and knowledge of aseptic techniques </li>
<li>Experience with Microsoft Office (Word, Excel, Access, E-mail, internet etc.) computer-based programs. </li>
<li>Must utilize time in an efficient manner and be able to work with minimal supervision. </li>
<li>Must have the ability to read, write and communicate effectively in English. Bilingual in Spanish a plus.</li>
<li>Detail oriented.</li>
<li>Strong organizing skills and able to meet deadlines.</li>
<li>Must be able to prioritize and handle multiple projects at the same time.</li>
<li>Be able to work independently or in a team environment.</li>
<li>Able to work flexible hours and weekends.</li>
</ul>
 
 
OTHER INFORMATION AND REQUIREMENTS
FLSA Status: Non- Exempt
Travel Requirements: No travel.
Driving Requirements: Valid driver’s license and clean driving record as needed for occasional business travel.
 
Physical Demands/work environment
Ability to sit for extended periods of time at a computer workstation; use hands and motor skills on a frequent basis for functions such as keyboard data entry input; clear vision to read and interpret documents, reports, and information on a computer screen, etc. Ability to stand and walk for long periods of time and occasionally required to climb or balance; and stoop, kneel, crouch or crawl. Ability to work in a fast-paced manufacturing environment and withstand strong odors from the foods being processed. Ability to lift 50 lbs. 
Pre-Employment
Applicants must successfully pass a pre-employment background check and drug screen as a condition of any offer of employment to ensure compliance with Drug Free Workplace policies
 
Haliburton proudly supports diversity in the workplace and is an Equal Opportunity Employer and considers qualified applicants for employment without regard to sex, race, color, religion, ethnic or national origin, gender, sexual orientation, gender identity or expression, age, pregnancy, leave status, disability, veteran status, genetic information and/or any other characteristic or status protected by national, federal, state or local law.

Microbiology Technician

<h3>Job Description</h3>
Job Title: Research Scientist of Crystallization R&amp;D 
Department: Crystallization R&amp;D
Location: Onsite, Cranbury NJ
Job Type: Full Time 
Position Reports to: Director or VP of Crystallization R&amp;D
 
Job Summary:
We are seeking a highly motivated and skilled Research Scientist to join our Crystallization R&amp;D Department at Porton J-STAR. In this role, this position is responsible for leading group or contributing individually to search for the right solid form and develop formulations to support preclinical studies including PK, PD, efficacy, tox studies. This role is also responsible for crystallization process development, with goals of controlling final solid form of drug substances with desired solid-state attributes needed for optimum performance as well as drug intermediates for robust purification. The responsibilities of the position include, but are not necessarily limited to, the items listed below.
Responsibilities:
<ul>
<li>Perform activities in phase-appropriate solid form screening &amp; selection and solid-state characterization, such as powder X-ray diffraction, DSC, TGA, SEM, particle size, polarized light microscopy, moisture sorption analysis, solubility, dissolution and stability assessments. </li>
<li>Understand solid form phase mapping of drug candidates to assist in crystallization process development </li>
<li>Carry out experiments in preformulation and developability assessment.</li>
<li>Conduct phase-appropriate crystallization process development for API and intermediates to meet critical quality attributes.</li>
<li>Carry out rational design and control of drug substance physical properties through particle engineering technologies and drug substance-drug product coprocessing. </li>
<li>Learn continuously and apply fundamentals of related instrumentation knowledge (automation, PAT), and simulation tools in effective crystallization process development, from experimental design to operation, data collection, result analysis and presentation.</li>
<li>Implement new technologies, systems and ways of working to enhance both technical rigor and operational efficiency to better meet the demands of diverse drug developmental programs. </li>
<li>Contribute weekly client updates, ensure weekly update and final reports submitted in a timely fashion.</li>
<li>Prepare and submit final technical reports and documentation to clients in accordance with project timelines.</li>
<li>Communicate candidly, clearly and timely with clients, management, peers and group members. </li>
<li>Maintain a safe and clean laboratory environment, comply with cGMP procedures, and company policies.</li>
<li>Contribute to the development, calibration, and maintenance of laboratory instruments and equipment to support crystallization and solid-state research. </li>
<li>Maintain appropriate documentation (batch records and lab notebooks).</li>
<li>Perform other relevant duties as assigned by the management team.</li>
</ul>
Qualifications:
<ul>
<li>MS or BS. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field with a focus on crystallization, solid-state chemistry, or materials science.</li>
<li>1-5 years of experience in solid form studies and preformulation development, crystallization process development.</li>
<li>Good understanding of solid-state chemistry of small molecule drug substances.</li>
<li>Working knowledge of analytical techniques such as PXRD, TGA, DSC, PLM, DVS, HPLC, NMR and PSD.</li>
<li>Experience within the pharmaceutical/biotechnology industry or CDMO industry is required. Experience in both is desirable but not required.</li>
<li>Proven track record meeting aggressive targets as related to safe, timely and successful projects.</li>
<li>Good written, verbal and presentation skills.</li>
<li>Strong communication, organization, and planning skills.</li>
<li>Ability to prioritize and manage numerous activities simultaneously.</li>
<li>Ability to interact in an effective and appropriate manner with diverse population sets.</li>
<li>Experience in working on and positively contributing to scientific teams.</li>
<li>Ability to perform the physical requirements of the position.</li>
</ul>

Research Scientist (Preformulation and Crystallization Process Development)

<h3>Job Description</h3>
About the Opportunity
 
We are looking for a Process Developmet Scientist lll for an innovation-driven, fast-growing oral solid dosage (OSD) CDMO known for its science-first mindset, entrepreneurial culture, and hands-on approach to solving complex drug development challenges. The organization partners with emerging and established biopharma companies to design, develop, and manufacture differentiated oral solid products — from early development through commercial launch. Team members operate in a collaborative, curious, and high-accountability environment where advancing therapies and creating value for patients is the core mission.
 
Core Cultural Values
 
AUTHENTIC – Be vulnerable, build trust
CURIOUS – Ask questions, be adaptable, speak up
ACCOUNTABLE – Own it, meet commitments, communicate transparently
COLLABORATIVE – Engage others, stay open-minded
FLEXIBLE – Listen actively, make thoughtful decisions
CARE – Be passionate, act with integrity
BLAZE TRAILS – Push boundaries, challenge constraints
EXCELLENCE – Learn, improve, create value
FOCUS – Pay attention to details, deliver exceptional service
 
How You Will Make an Impact
 
<ul>
<li>Independently lead development activities across client projects from preclinical through Phase III and registration.</li>
<li>Create phase-appropriate strategies for customer-defined product development programs.</li>
<li>Execute prototype, scale-up, and process transfer activities including manufacturing, data evaluation, troubleshooting, and risk assessments.</li>
<li>Write, review, and approve cGMP documentation (batch records, protocols, SOPs, pharm dev reports, investigations, etc.).</li>
<li>Apply QbD principles, design of experiments, and statistical tools to support drug product development.</li>
<li>Maintain expert knowledge of equipment and processes relevant to pharmaceutical development.</li>
<li>Monitor emerging formulation technologies and conduct literature/patent reviews to inform development plans.</li>
<li>Operate in a GMP environment with diverse compounds (including high-potent and controlled substances).</li>
<li>Collaborate closely with Analytical Development, QA, Project Management, and Validation groups on cross-functional initiatives.</li>
<li>Serve as a technical lead on product development project teams and mentor junior scientists.</li>
<li>Lead continuous process improvements and support scheduling of group activities.</li>
<li>Demonstrate reliable attendance and professional communication with stakeholders while embodying cultural values.</li>
</ul>
 
What You Will Bring
 
<ul>
<li>Bachelor’s degree in Pharmaceutics, Chemistry, Chemical Engineering, or related field with 8+ years of oral solid dosage formulation/process development experience (Master’s with 6+ years acceptable).</li>
<li>Hands-on expertise in formulation and process development for tablets, capsules, and multiparticulates.</li>
<li>Strong theoretical foundation in pharmaceutics and physical organic chemistry.</li>
<li>Proven knowledge of excipient functionality, formulation strategy, and unit operations.</li>
<li>Experience applying statistical DoE for process optimization.</li>
<li>Excellent written, verbal, and technical communication skills.</li>
<li>Familiarity with MS Office and statistical tools such as JMP or Minitab.</li>
<li>Knowledge of GLP/cGMP and regulatory guidance (FDA, ICH, EMEA) related to oral solid dosage.</li>
</ul>
 
Special Conditions
 
<ul>
<li>Some travel required (client meetings, conferences, cross-site collaboration).</li>
</ul>

Process Development Scientist lll

<h3>Job Description</h3>
Duration: 06 Months Contract (possible extension-performance based)
 
Employment Type: W-2 
 
 Key Responsibilities: 
A research technician position is available at Genomic Research Center (GRC) . We are looking for a highly motivated research technician to work independently and in collaboration with other scientists in projects involving human induced pluripotent stem cells reprogramming, cell differentiation, CRISPR editing, and high throughput functional screenings. The successful candidate will be involved in critically timed experiments and long differentiation protocols that require daily attention. The applicant is expected to:
a. Conduct routine wet lab experimental protocols and procedures.
b. Maintain cultured stem cells and stem cell-derived cells
c. Keep an accurate record of experimental setup, SOP protocols, and data quality control notes.
d. Maintain efficient and continuous communication with team members and managers.
e. Support team members with basic routine cell culture procedures including media preparation and reagents aliquoting.
 
Required Skills:
 1: Significant cell culture expertise: maintenance, freezing, thawing, and passaging.
2: Having experience in stem reprogramming, maintenance and differentiation is highly preferred.
3: Biochemistry such as: Western blot, Immunofluorescence, flow cytometry
4: Molecular biology such as: RNA extraction, cDNA synthesis, RT-QPCR 
 
Preferred Skills:
<ol>
<li>Lentivirus production and lentiviral transduction</li>
<li>Gene editing using CRISPR technology </li>
</ol>
 
Education:
BS degree or master’s degree in biological sciences, molecular biology, neuroscience, or biochemistry and significant 2-3 years tissue culture experience are a must. (Or a master’s degree with at least one year of experience). The applicant should already be trained in proper wet lab procedures and should be familiar with using basic lab equipment. Having strong communication, organizational and documentation skills is a must.
 
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit <a href="http://www.ustechsolutions.com" target="_blank">www.ustechsolutions.com</a>.
 
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
 
Recruiter Details:
Name: Jyoti
Email: <a href="mailto:jyoti.bhargav@ustechsolutionsinc.com" target="_blank">jyoti.bhargav@ustechsolutionsinc.com</a>
Internal Id: 25-45347

Scientist I (Research Technician)

<h3>Job Description</h3>
Job DescriptionCompany Description 
At Northwestern Medicine, every patient interaction makes a difference in cultivating a positive workplace. This patient-first approach is what sets us apart as a leader in the healthcare industry. As an integral part of our team, you'll have the opportunity to join our quest for better healthcare, no matter where you work within the Northwestern Medicine system. At Northwestern Medicine, we pride ourselves on providing competitive benefits: from tuition reimbursement and loan forgiveness to 401(k) matching and lifecycle benefits, we take care of our employees. Ready to join our quest for better?
Job Description 
The Health Physicist II reflects the mission, vision, and values of NM, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.
The Health Physicist II, under the direction of the Radiation Safety Officer, assists in the development, implementation, coordination, evaluation and continuous improvement of the radiation and laser safety programs.&nbsp; Responsibilities include general surveillance of overall activities and areas in which radioactive materials/radiation sources and laser equipment are used, supporting compliance with rules and regulations, authorized users and research projects approval as specified by the Radiation Safety Officer or Radiation Safety Committee, consultation on radiation protection with department radiation safety liaisons, determination of need and evaluation of personnel monitoring, and implementation of instructional programs on safe procedures in the use of radiation sources.
Responsibilities:
<ul>
<li>Under the direction of the Radiation Safety Officer, the Health Physicist II will assist in the design, implementation and ongoing maintenance of the radioactive material management programs in all areas of the hospital.</li>
<li>Promotes departmental goals in the protection of employees, staff, physicians, students, guests, and visitors</li>
<li>Provide radiation safety training for occupational radiation workers</li>
<li>Help maintain databases within the department</li>
<li>Have proficiency in the use of meters and instrumentation used in the departments</li>
<li>Perform surveys and wipe tests of all laboratories using radioactive materials in accordance with the Radioactive Materials License</li>
<li>Perform radiological or environmental surveys as required or as directed by the Radiation Safety Officer</li>
<li>Radiation safety functions related to radiopharmaceutical therapies performed on patients</li>
<li>Monitor all intercavitary of interstitial implant patients and high dose therapy patients</li>
<li>Ensure bioassays of personnel are completed in accordance with the Radioactive Materials License</li>
<li>Work with other departments in the hospital to ensure radiation safety compliance</li>
<li>Maintains the meter calibration program under the direction of the RSO</li>
<li>Collect, inventory, and prepare for removal of all radioactive waste generated</li>
<li>Receive and distribute all incoming radioactive materials</li>
<li>Perform quarterly sealed source inventory and semi-annual leak testing</li>
<li>Participates regulatory processes, surveys, inspections, as directed (IEMA, OSHA, DOT, NRC, OIG, DOE, EPA, etc)</li>
<li>Supports emergency response and participates in drills and actual incidents including those that might occur after hours or on the weekends</li>
<li>Aides in the lead apron and lead waste programs</li>
</ul>
Additional responsibilities
<ul>
<li>Coordinate and provide radiation safety training for occupational radiation workers</li>
<li>Lead the preparation and shipment of radioactive materials with approved vendors</li>
<li>Assist Health Physicist III with preparation and shipment of radioactive materials with approved vendors</li>
<li>Coordinate radioactive waste shipments</li>
<li>Support the Laser Safety Officer with the laser safety program, inspections, and training laser users</li>
<li>Perform any required calibrations of the liquid scintillation counter and auto gamma counter</li>
<li>Assist Health Physicist III in lead waste disposal</li>
<li>Mentor Health Physicist I</li>
<li>Assist the Radiation Safety Officer and Health Physicist III as needed</li>
</ul>
Working Conditions:
The Radiation Safety Department is responsible for overseeing the Radiation Safety Program and regulatory functions for the Northwestern Memorial HealthCare Radioactive Materials License.&nbsp; This involves traveling to Northwestern Medicine hospitals throughout the Northwestern Memorial HealthCare system. Health Physicist II has a primary reporting location of Northwestern Memorial Hospital, but all health physicists will also be expected to travel to off-sites to support health physics services.
#NMH1
Qualifications 
Required:
<ul>
<li>Bachelor’s Degree in Radiological Health, Health Physics, Nuclear Medicine, Medical Physics or related field&nbsp; &nbsp;</li>
<li>5 years as Health Physics I or equivalent experience in medical radiation safety in a large hospital or academic medical center</li>
<li>Strong communication and interpersonal skills</li>
<li>Strong problem solving and organizational skills</li>
<li>Must be able to move and load equipment and shielding (up to 50 lbs) and transfer it to locations throughout the hospital/campus</li>
<li>Ability to lift 10 lbs routinely, and to stand for 3 hours</li>
<li>Strong organizational, communications, teaching and writing skills</li>
<li>Identifies quality issues to be addressed and brings to the attention of the Radiation Safety Officer as appropriate</li>
<li>Assists in the design and implementation of process improvements</li>
<li>Collects and monitors data for key quality indicators and process improvement plans</li>
<li>Able to wear a self-contained breathing apparatus (SCBA or PAPR) or other appropriate respiratory equipment as required.</li>
<li>Observe work practices and review written policies and procedures</li>
<li>Demonstrate good body mechanics for lifting</li>
</ul>
Preferred:
<ul>
<li>Master’s Degree in Radiological Health, Health Physics or Medical Physics</li>
<li>National Registry of Radiation Protection Technologist: (NRRPT)</li>
<li>Board eligible for Part I of the CHP exam by the American Board of Health Physics</li>
<li>Medical Laser Safety Officer (CMLSO) or previous laser safety experience</li>
</ul>
 Additional Information 
Northwestern Medicine is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, disability, sexual orientation or any other protected status.
Benefits
We offer a wide range of benefits that provide employees with tools and resources to improve their physical, emotional, and financial well-being while providing protection for unexpected life events. Please visit our&nbsp;Benefits&nbsp;section to learn more.

Health Physicist II-Radiation Safety, Full-time Days

<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 
Employee Responsibilities:
<ul>
<li>Performing stability and release testing in support of large molecule biopharmaceutical products using various analytical techniques including HPLC, SCE, CE, iCE, UV, MFI, Appearance, etc.</li>
<li>Document work as required for cGMP compliance</li>
<li>Perform tests accurately</li>
<li>Troubleshoot method and instrumentation problems</li>
<li>Use Office and instrumentation specific computer software including Empower</li>
</ul>
Qualifications 
The Ideal Candidate would possess:
<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>Theoretical understanding of large molecule biochemistry</li>
</ul>
Qualifications
Minimum Qualifications:
<ul>
<li>Bachelor's degree in biochemistry, biology, chemistry, biology, 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>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 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.

Associate Scientist - Biochemistry

<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.
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
Job Description 
Essential Duties and Responsibilities:
<ul>
<li>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Demonstrates and promotes the company vision</li>
<li>Regular attendance and punctuality</li>
<li>Perform prep/analysis of samples of various matrices for various analytical methods</li>
<li>Analyze/prep samples and QC for routine testing</li>
<li>Review, work up, and assemble all supporting data for work performed</li>
<li>Perform basic maintenance on equipment used for routine work</li>
<li>Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC department</li>
<li>Prepare standard solutions and other reagents as needed</li>
<li>Use word processor and spreadsheet programs on PC</li>
<li>Dispose of all chemical wastes using approved methods</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned</li>
<li>Work overtime as workload requires</li>
</ul>
Qualifications 
Basic Minimum&nbsp;Qualifications
<ul>
<li>Bachelor's Degree in Chemistry, Biology, or related field</li>
</ul>
Ideal Candidates will have:&nbsp;
<ul>
<li>Previous lab experience&nbsp;</li>
<li>Bachelor's in Chemistry, or Chemistry minor&nbsp;</li>
</ul>
 Additional Information 
Requirements:
<ul>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English</li>
</ul>
Position is full-time, Monday - Friday 7:00am -3:30pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.&nbsp;
Pay rate: $18-20/hr depending on experience
Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.
To learn more about Eurofins, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.
We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.
Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!
Find out more in our career page: <a href="https://careers.eurofins.com/" target="_blank">https://careers.eurofins.com/</a>
Company 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 discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research 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 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 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 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.
Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Chemist (PFAS) - 1st Shift - Eurofins Environment Testing - Lancaster, PA

<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:
Generate and analyze precise, reliable, and reproducible data in a timely manner, under the direction of a more senior scientific leader. Demonstrate experimental precision and should possess general understanding of core discipline.
Responsibilities:
<ul>
<li>Completely follow established experimental protocols and assess results with supervision.</li>
<li>Recognize and report experimental variances.</li>
<li>Apply basic scientific principles to research.</li>
<li>Learn and effectively implement new experimental protocols and/or techniques. Maintain laboratory equipment and optimize laboratory operations for efficient use of time and laboratory supplies and reagents, when appropriate.</li>
<li>Consult literature to understand scientific purpose of assignments. Impact projects predominantly through lab and/or pilot plant based activities.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree, or equivalent education.</li>
<li>Theoretical and practical knowledge to carry out job functions.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements understate or local law:&nbsp;​​​
<ul>
<li>
Location: PDS&amp;T Biologics in MA location.
</li>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it&nbsp;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 otherform of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company'ssole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole andabsolute 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>

Associate Scientist, I

<h3>Job Description</h3>
Job DescriptionCompany Description 
Syngenta Seeds is one of the world’s largest developers and producers of seed for farmers, commercial growers, retailers and small seed companies. Syngenta seeds improve the quality and yields of crops. High-quality seeds ensure better and more productive crops, which is why farmers invest in them. Advanced seeds help mitigate risks such as disease and drought and allow farmers to grow food using less land, less water and fewer inputs.&nbsp;&nbsp;
Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions.&nbsp;&nbsp;
Syngenta Seeds is headquartered in the United States.&nbsp;
Job Description 
About Us
Through leading innovations, we help farmers around the world meet the challenge of feeding a growing population and taking care of our planet. To support this challenge, Syngenta is currently seeking a Research Scientist in Durham, NC.
This role will contribute to the effective operation of maize transformation pipeline and support trait research and product development goals
Accountabilities&nbsp;
•&nbsp;&nbsp; &nbsp;Provide scientific expertise and support transgenic event generation pipeline efforts required to deliver business objectives defined by a research program, function, or supervisor.&nbsp; •&nbsp;&nbsp; &nbsp;Responsible for process improvement and new capability development including maize genetic transformation and precision genome engineering. &nbsp;&nbsp; •&nbsp;&nbsp; &nbsp;Lead to design and execute complex experiments to generate scientific/technical data alone or working with scientists in group. &nbsp;&nbsp; •&nbsp;&nbsp; &nbsp;Follow existing processes, procedures and systems to independently design and execute complex experiments&nbsp; •&nbsp;&nbsp; &nbsp;Proactively initiate and implement improvements to established protocols or systems to improve function capability and efficiency in consultation with supervisor •&nbsp;&nbsp; &nbsp;Maintain accurate experimental records and enter data into databases strictly following Syngenta policy and guideline •&nbsp;&nbsp; &nbsp;Actively contribute to process improvement and integration of new technologies.&nbsp; •&nbsp;&nbsp; &nbsp;Provide subject matter guidance to other team members and uses existing procedures to solve process problems or bottlenecks.&nbsp; &nbsp;
Qualifications 
•&nbsp;&nbsp; &nbsp;A minimum of a Masters degree with at least 3 years of relevant experience or a Ph.D. degree with at least 1 year of postdoc experience.&nbsp; •&nbsp;&nbsp; &nbsp;Experience in plant tissue culture and plant transformation. Strong preference for candidates with field crop transformation experience.&nbsp; •&nbsp;&nbsp; &nbsp;Must be eligible to work in the United States without sponsorship support from Syngenta.&nbsp;
Preferred Qualifications
•&nbsp;&nbsp; &nbsp;Expertise in developing and improving plant transformation methods and protocols. •&nbsp;&nbsp; &nbsp;Experience working with genome editing in plant cells.&nbsp; •&nbsp;&nbsp; &nbsp;Track record of delivering research and innovation through journal publications and/or patent applications.&nbsp; &nbsp;
 Additional Information 
What We Offer:
•&nbsp;&nbsp; &nbsp;A culture that celebrates diversity &amp; inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs •&nbsp;&nbsp; &nbsp;Full Benefit Package (Medical, Dental &amp; Vision) that starts your first day&nbsp; •&nbsp;&nbsp; &nbsp;401k plan with company match, Profit Sharing &amp; Retirement Savings Contribution&nbsp; •&nbsp;&nbsp; &nbsp;Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;
3AWL
 Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: &nbsp;<a href="https://www.youtube.com/watch?v=OVCN_51GbNI" target="_blank">https://www.youtube.com/watch?v=OVCN_51GbNI</a> ________________________________________ Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
#LI-DR123

Research Scientist

<h3>Job Description</h3>
Job Description
Hillis-Carnes Engineering Associates (HCEA) is currently seeking a geotechnical engineer, P.E. preferred, to join our team in Annapolis Junction, Maryland and participate on a wide variety of geotechnical projects. Projects are primarily located within Maryland, Virginia, and DC. Candidate will have the opportunity to collaborate with personnel at other HCEA offices throughout the company. 
General Responsibilities:
<ul>
<li>Prepare field reports, internal correspondence, and geotechnical engineering reports.</li>
<li>Perform geotechnical analyses based on site conditions and requirements to support project designs.</li>
<li>Evaluate laboratory and field data for inclusion in reports.</li>
<li>Review and interpret data and test results.</li>
<li>Prepare technical proposals, cost estimates, plans, technical specifications, and reports, including day to day correspondence.</li>
<li>Develop and maintain clients and actively participate in professional and related industry organizations.</li>
<li>Support field instrumentation and monitoring activities.</li>
<li>Support the office's Geotechnical Group and other departments as required.</li>
<li>Follow company safety standards, site safety standards, and provide all required permitting.</li>
<li>Contact vendors; research literature and regulatory requirements; prepare designs.</li>
</ul>
Candidate Qualifications:
<ul>
<li>B.S. Civil Engineering, Geotechnical Engineering, M.S. preferred.</li>
<li>Minimum of 5 to10 years of related experience.</li>
<li>Professional Engineer (PE) preferred.</li>
<li>Enthusiastic, self-starter with desire to provide excellent service to clients.</li>
<li>Strong communication skills (oral and written).</li>
<li>Computer literate (Word, Excel, Outlook, AutoCAD).</li>
<li>Valid driver's license.</li>
<li>Willing to travel and work out of town for short periods of time.</li>
<li>Physical requirements may require lifting to 50 pounds and traverse over rugged terrain.</li>
<li>Ability to successfully meet all pre-employment requirements.</li>
</ul>
HCEA offer a competitive salary and benefits package which includes medical (Health Savings Account available), dental, life, long and short-term disability plans, 401k plan with company match, Employee Stock Ownership Plan (ESOP), Employee Assistance Program, Wellness Program, paid time off, paid holidays and much more. 
HCEA is proudly an Equal Opportunity Employer. Women and Minorities are encouraged to apply for this position.
 Job Posted by ApplicantPro

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