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<h3>Job Description</h3>
Job DescriptionWildlife Technician - Meridian Bird RemovalMeridian Wildlife Services is the fastest-growing safe bird capture company in the country! We are searching for our next Wildlife Technician to help us embrace new adventures daily.Why Join Us?
<ul>
<li>Unforgettable Interactions: Each day offers new adventures and the chance to connect with new people, creating memorable experiences for both our technicians and the customers we serve.</li>
<li>Local Impact, National Reach: Travel locally and nationally, enhancing your skills and broadening your horizons as you provide bird removal services to our customers.</li>
<li>Become an Expert: Our comprehensive training program provides you with the skills needed to excel, covering everything from bird capture techniques to building positive customer relationships.</li>
<li>Grow Fast: We provide clear career paths that require little to no prior experience. Grow with our dynamic team through continuous learning and opportunities for advancement.</li>
</ul>
 About Us:At Meridian, our goal is to provide safe and effective bird removal solutions to our customers in the commercial retail space.Role:As a Wildlife Technician, you will be the friendly face of Meridian. Our technicians uphold food safety standards for our customers while managing and mitigating potential bird-related nuisances in commercial spaces. Making a Difference for Our Customers Become a Trusted Advisor: Walk through customer facilities to identify bird activity and potential problems. Work closely with customers to understand their unique concerns and tailor effective solutions. Embrace the Challenge: No two jobs are the same and every job brings new challenges. One will be resourceful and adaptable, tackling diverse bird-related issues to effectively address customer needs. Empower Our Customers: Share one's knowledge of bird behavior and prevention techniques. This empowers customers to maintain bird-free spaces and achieve lasting results. Core Values: Uphold our core values to deliver exceptional service that builds trust and strengthens customer relationships.
<ul>
<li>Eagerly Optimistic: We approach every assignment with a positive attitude.</li>
<li>Humbly Confident: We're experts, but always open to learning more along the way.</li>
<li>Adapt and Overcome: No bird challenge is too big! We find creative solutions that work.</li>
<li>Commitment to Capture: We finish the job no matter what it takes and guarantee your satisfaction.</li>
<li>Be Above the Bar: We strive to exceed our customers’ expectations in every interaction.</li>
<li>Help First: We're always willing to go the extra mile to assist our customers and teammates.</li>
</ul>
Basic Qualifications and Job Functions Basic Qualifications:
<ul>
<li>High School Diploma or GED.</li>
<li>At least 21 years old.</li>
<li>Valid Driver's License.</li>
<li>Insured and reliable vehicle.</li>
<li>Driving Record free from moving violations.</li>
<li>Mobile smartphone.</li>
<li>Lives within 50 miles of Concord, NH.</li>
</ul>
Job Functions:
<ul>
<li>Lift and carry up to 50 lbs.</li>
<li>Stand, walk, and sit for prolonged periods of time.</li>
<li>Work exposed to outdoor elements.</li>
<li>Frequent bending, kneeling, and reaching.</li>
<li>Ability to work at heights, climb ladders, and use scissor lifts.</li>
<li>Ability to see up close and at a distance.</li>
<li>Ability to travel long distances to our customers’ facilities. All technicians use their personal vehicles to travel to worksites.</li>
</ul>
If one want each workday to be a new adventure, apply now! About Us Frequently Asked Questions Our Services 
<ul>
<li>On average, Part-Time Bird Removal Technicians make $1,000 - $2,200 per month, $28,000-$32,000 annually.</li>
</ul>
<ul>
<li>Compensation is subjective and is only an average of what our Bird Removal Technicians can make. There is no guarantee that any one person will receive any set amount of compensation during any period of time. Compensation is dependent on several variables, including but not limited to, seasonality, location, rank, and off-the-job pay.</li>
</ul>
About Meridian Bird RemovalGuaranteed Bird Removal service is not a new segment of the pest control and wildlife industry, but it’s now easier than ever. We offer four specialized services that remove interior bird issues, help control exterior bird populations, remove nests, and prevent future bird issues. All our services are fast, effective, require no shutdown, and are public relations friendly. Our Services: Interior Bird Removal Interior birds have traditionally been a challenge, and many companies use outdated methods to remove the invaders. Our patented “Bird-N-Free” capture system and process allows us to predictably remove birds from inside any facility. Exterior Population Reduction When nuisance bird populations grow out of control, reducing their numbers can save damage to the exterior of a facility, as well as prevent birds from entering the facility. Nest Removal Nest Removal is a critical component of our bird removal services. To safely perform nest removal, our technicians wear appropriate personal protective equipment and follow a careful set of guidelines to contain all of the nesting materials. Full Facility Inspection Our Full Facility Inspection involves a deep dive into operational practices, facility maintenance, and sanitation issues. By evaluating these three key areas, we are able to give an accurate assessment of your current situation and provide a post-service recommendation to help prevent future bird issues. Meridian Bird Removal is an Equal Opportunity Employer committed to fostering an inclusive and diverse workplace. We welcome and consider all qualified applicants without regard to race, color, religion, sex, national origin, age, disability, veteran status, or any other protected status as defined by the Equal Employment Opportunity Commission (EEOC) guidelines. All employment decisions at Meridian Bird Removal are based on business needs, job requirements, and individual qualifications.

Wildlife Technician - Meridian Bird Removal

<h3>Job Description</h3>
Job Description
STAFF GEOLOGIST / STAFF ENVIRONMENTAL SCIENTIST / STAFF ENVIRONMENTAL ENGINEER
Broadbent &amp; Associates, Inc. of Salt Lake City, Utah is looking to hire an organized full-time Staff Scientist or Engineer to support a wide variety of environmental projects. The position earns a competitive salary, depending on experience. We also offer a comprehensive benefits package, including a bonus program, 100% health insurance premium coverage, dental, vision, a health savings account (HSA), a generous 401(k) retirement plan with safe harbor contribution and company match, vacation, sick leave, ability to earn additional paid time off, disability and life insurance, solid opportunities for advancement, and a friendly and fun work environment. If this sounds like the right opportunity for you, in the environmental and water resource arena, consider applying today!
A DAY IN THE LIFE OF A STAFF SCIENTIST OR STAFF ENGINEER
As a Staff Scientist or Staff Engineer your hard work ensures that we deliver for our clients. Under the supervision of a Principal Geologist, you provide support on a wide range of environmental projects including: collection of surface and groundwater samples, water and wastewater engineering design under supervision of a Professional Engineer, remediation system operation and maintenance, water and wastewater treatment facility monitoring, and water resources investigations. Your primary job function will be to support the Salt Lake City, UT office. You will support field work activities as needed to drive project execution and ensure that appropriate health and safety procedures are being followed.
People skills are essential as you interact regularly with contractors, regulators, and clientele. Though some time is spent in the Salt Lake City, UT office, preparing project reports and completing routine administrative tasks, you are also responsible for conducting field activities such as seeps and spring monitoring, well sampling, and operations or water systems. Collected field data is summarized in reports and presented to Project Managers. Our mission is to complete work safely, on time, and on budget, which makes our clients happy and provides a great sense of accomplishment to our staff.
ABOUT BROADBENT &amp; ASSOCIATES, INC.
Founded in 1987, we are an environmental, water resource, and civil engineering firm. We provide professional services throughout the United States to energy companies, mining operations, agricultural companies, municipalities, private industries, governmental agencies, public and private utilities, and developers. Our mission is to build long-term client relationships by providing sound scientific solutions to comprehensive resource management challenges. We're very client-focused with a commitment to providing services in a time-efficient and cost-effective manner.
We take care of our customers AND employees like family. Our ability to hire and retain long-term skilled key personnel has significantly contributed to our success. We offer competitive pay, opportunities for personal growth, and a great work environment with a sense of camaraderie.
QUALIFICATIONS FOR SCIENTIST/ENGINEER
<ul>
<li>Bachelor's degree in Geology, Environmental Science, Environmental Engineering, Civil Engineering, Earth Science or other related fields</li>
<li>Ability to lift 50 pounds and traverse moderate mountainous terrain with a 30-pound pack</li>
<li>Ability to safely drive two-track trails and use GPS</li>
<li>Technical writing competency</li>
<li>Strong technical and computer skills</li>
<li>Self-starter, quick learner and effective communicator</li>
<li>Ability to work individually and as part of a team</li>
<li>Ability to work consecutive long days in the field under varying adverse weather conditions (hot, cold, windy, and sometimes wet)</li>
</ul>
Are you detail-oriented? Do you have technical writing and research skills? Are you a problem-solver? Are you organized and able to effectively prioritize multiple tasks? Do you have excellent communication skills? Are you energetic, self-sufficient, and motivated? Are you collaborative and team-oriented? If so, you might just be perfect for this position!
WORK SCHEDULE
This full-time Staff position typically works Monday - Friday with occasional traveling and weekend work.
READY TO JOIN OUR TEAM?
We understand your time is valuable and that is why we have a very quick and easy application process. If you feel that you would be right for this position, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!
 
Broadbent is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity or any other factor protected by applicable federal, state or local laws.
 Job Posted by ApplicantPro

STAFF GEOLOGIST / STAFF ENVIRONMENTAL SCIENTIST / STAFF ENVIRONMENTAL ENGINEER

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

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

Lab Processing Associate - 3rd Shift

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description 
Become your most extraordinary self!&nbsp; Our team is intensely proud to be a major provider of services and products to the drug discovery research industry. &nbsp;Join Eurofins Discovery Services North America, LLC&nbsp;part of the Eurofins Discovery ™ group of companies serving global clients in the Pharma and Biotech industries. &nbsp;Work alongside industry experts and collaborate with team members to directly and positively impact human health worldwide!
We have a philosophy to support work life balance, career progression opportunities and offer many benefits such as formal mentoring programs, tuition reimbursement, extensive career training programs, competitive health benefits, paid time off and 10 annual paid holidays*. &nbsp;
The Scientific Director, Antibody Discovery for Biotherapeutic Services is a scientific leadership position, responsible for providing guidance for establishing and growing antibody discovery platforms and alignment between our customer base, the industry at large, commercial teams and service operations. This role will be collaborative and influential in a broad network of business functions in support of driving business growth, brand recognition, and alignment with Eurofins core competencies of delivering high quality services to our valued customers. The successful candidate will:
<ul>
<li>Spend time in the lab to define, develop and/or expand antibody discovery platforms in BTX</li>
<li>Develop client and stakeholder relationships through technical leadership and collaboration</li>
<li>Deliver scientific leadership to executive management in developing portfolio strategy, new growth areas and new technology planning</li>
<li>Lead scientific community through external marketing, industry reputation and brand awareness</li>
<li>Provide leadership in establishing and monitoring unit research and development objectives and commercial lifecycle management</li>
<li>Provide technical leadership to lab operations, business development and marketing team</li>
<li>Support client services team in generating proposals, RFPs, study plans and scope of work preparation. Assists pricing team in completing custom pricing and cost analysis</li>
<li>May act as Study Director for specific projects to ensure timely delivery of project updates, data and reports to clients</li>
<li>Understand requirements for work performed within a GxP site in order to work with other organizations within the Eurofins family</li>
<li>Complete required training and support 100% of Employee Health and Safety requirements</li>
<li>Conduct responsible use of confidential IT and business systems, as required</li>
<li>Adhere to department SOP and documentation requirements</li>
<li>Ensure accurate data management and reporting, with the highest integrity, and perform quality control, when required, on project data and reports</li>
<li>Support unit goals and demonstrate Eurofins’ competencies, as defined in the job plan</li>
<li>Provide training to colleagues and external end users, when required</li>
<li>Perform other duties, as assigned</li>
</ul>
Qualifications 
<ul>
<li>Senior-level scientific experience and knowledge in supporting all aspects of antibody discovery</li>
<li>Demonstrated expertise and experience with antibody discovery by hybridoma generation, B- and Plasma cell isolation and V-region sequence recovery, and display systems</li>
<li>Antibody engineering, humanization, germlining, CDR-scanning and affinity maturation</li>
<li>Molecular cloning, including restriction enzyme-based cloning, Gibson assembly cloning and ligation-independent cloning.</li>
<li>DNA and RNA extraction, purification and handling</li>
<li>Experience in analyzing NGS data, pairing heavy and light chains, identifying sequence liabilities and optimization thereof</li>
<li>Demonstrated experience with developing client/external relationships, supporting technical correspondence, drafting and presenting scientific proposals to clients or collaborators</li>
<li>Experience in collaborating with cross-functional teams (research, regulatory, pharmacology, safety) to guide growth and advancement of the platform from concept to pre-clinical development</li>
<li>Experience leading and managing internal scientific teams and directing /influencing external resources</li>
<li>Proven experience with portfolio management, portfolio expansion and research/development in an industry setting</li>
<li>B.S., M.A., or M.S. with 12 years relevant experience</li>
<li>Ph.D. with 7 years relevant experience</li>
<li>Combination of Education and Relevant Experience</li>
<li>Demonstrated experience in working effectively with different stakeholders with an interest in antibody discovery, including Business Development, Client Services and internal contributors</li>
<li>Demonstrated reputation as a key opinion provider and industry influencer via publications, networking and presentation experience</li>
<li>Experience with leading cross-functional teams effectively</li>
<li>Demonstrated experience in strategic planning and managing portfolio growth initiatives</li>
<li>Demonstrated ability to build and lead a Scientific team, and appropriate technical capabilities to support therapeutic and tool antibody discovery</li>
<li>Demonstrated ability to identify and introduce new technology (equipment and techniques) to grow capabilities</li>
<li>Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health</li>
<li>Excellent interpersonal, verbal and written skills, including ability to prepare detailed scientific reports and group presentations</li>
<li>Ability to plan and coordinate multiple projects simultaneously, with appropriate allocation of available resources</li>
</ul>
 Additional Information 
The position is full-time, Monday-Friday, 8:00 a.m.-5:00 p.m., with overtime as needed. Candidates within a commutable distance of Saint Charles, MO are encouraged to apply.&nbsp;
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.

Scientific Director - Antibody Discovery, Biotherapeutics Services

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description 
The incumbent interacts with Business Development, Proposal Development, and Laboratory Operations with the aim to win proposals. S/he exchanges information with relevant stakeholders (internal/external), documents existing and needed laboratory capabilities and proposes qualified solutions to Management to profitably grow the laboratory business.
Hybrid Role- Hours: Monday-Friday 8am-5pm&nbsp;
Qualifications 
Key Accountabilities
<ul>
<li>Reviews client clinical protocols and provides synopses to ensure the proposals meet the testing needs of the client.</li>
<li>Provide and update testing information to include cost, feasibility, TAT, and methodology to meet tight turnaround times during bidding process.</li>
<li>Provide recommendations for in-house vs. outsourced testing capabilities and relevant process changes to Management to enhance operational and financial performance.</li>
<li>Identify appropriate referral labs as needed and obtain relevant information needed to support clinical trials.</li>
<li>Maintains a current list of referral labs with contact information and areas of specialization.</li>
<li>Communicates directly with referral lab to meet required time frames and testing capabilities.</li>
<li>Negotiates preferred pricing for large volume testing directed to referral lab in conjunction with Management.</li>
<li>Communicate the use of a referral lab to QA allowing adequate time for QA qualification.</li>
<li>Support Proposal Development department with suggestions on optimizing global sample logistics.</li>
<li>Monitor the Central Laboratory test menu, ensuring all data is available accurate and traceable with version control, including costing and pricing, on a global basis.</li>
<li>Maintain database information for bid vs. awarded studies when validation by lab is required.</li>
<li>Communicate effectively with Management to ensure client testing needs are met from bid to awarded study.</li>
<li>Attend client meetings as needed to support sales.</li>
<li>Dialogue with client as requested determining whether additional support is required.</li>
<li>Provide input to satisfaction surveys (sponsors, investigators) and translates findings into actionable recommendations to Management for specific improvements (business practices, service levels, process changes, etc.).</li>
</ul>
Position Specifications and Job Requirements Experience
<ul>
<li>Minimum 5 years in a diagnostic, clinical laboratory</li>
<li>Experience with clinical assay validation protocols</li>
</ul>
Education
<ul>
<li>Bachelor of Science Degree</li>
</ul>
Degree in Medical Technology or Life Sciences preferred
 Additional Information 
Position is full-time,&nbsp;1st shift hours available. 8 AM- 5 PM&nbsp;
Authorization to work in the United States without Sponsorship is required.&nbsp;
Additional information
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Position is Full-Time, 40 hours per week.&nbsp; Candidates currently living within a commutable distance of Lancaster, PA&nbsp;are encouraged to apply.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
</ul>
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Scientific Affairs Liaison

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

Forklift Operator - Chemical Manuf.

<h3>Job Description</h3>
Job DescriptionCompany Description 
<ul>
<li>Katalyst Healthcares &amp; Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.</li>
<li>We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.</li>
</ul>
Job Description 
Job description:
The Biologics CMC Developability team is an integral part of the Biologics CMC Drug Product Development Org. The Biologics CMC Developability team is responsible for- (1) the identification of biophysical- and chemical liabilities in discovery-stage biologic drug candidates to guide lead selection, and (2) for characterization of the key CMC attributes important for biologic drug development. We have an exciting opportunity for a motivated scientist to join the Biologics CMC Developability team.
Responsibilities:
<ul>
<li>
<ul>
<li>Perform in-depth LC-MS based characterization of therapeutic biologic molecules and their post-translational modifications.</li>
<li>Conduct biophysical and biochemical characterization of biologic drug candidates, as needed.</li>
<li>Execute experimental protocols, collect results, and perform data analysis carefully and independently.</li>
<li>Maintain excellent documentation of work including electronic lab notebook and protocols.</li>
<li>Prepare and deliver concise scientific presentations of experimental results.</li>
<li>Oversee maintenance of key laboratory equipment and routine laboratory operations.</li>
<li>Build strong relationships with other team members and across groups.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, and documentation compliance.</li>
</ul>
</li>
</ul>
Requirements:
<ul>
<li>
<ul>
<li>BS or MS in Biochemistry, Biology, Chemistry (or equivalent, e.g., Chemical Engineering, Pharmaceutical Sciences) with 5+ (BS) or 2+ years (MS), or Ph.D. with 0+ years of biopharmaceutical industry experience.</li>
<li>Hands-on experience with protein mass-spectrometry (subunit analysis, peptide mapping, disulfide mapping) and data processing is required.</li>
<li>Experience with biochemical and biophysical characterization of biologic proteins would be desirable.</li>
<li>Experience with liquid handling robots and their programming would be highly beneficial.</li>
<li>Demonstrated track record of independent thinking, creativity, and scientific accomplishment.</li>
<li>Highly responsible and self-motivated. Skills to plan and conduct experiments with high quality and timely deliverables. Able to perform data analysis using MS Excel &amp; GraphPad.</li>
<li>Team player with excellent collaboration and communication skills.</li>
</ul>
</li>
</ul>
Additional Information 
All your information will be kept confidential according to EEO guidelines.

Scientist III

<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>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>Document work as required for GMP compliance</li>
<li>Perform tests accurately</li>
<li>Troubleshoot method and instrumentation problems</li>
<li>Use office and instrumentation specific computer software</li>
<li>Produce written reports (e.g., SOP, OMC, client reports)</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>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>Bachelor's degree in chemistry, analytical chemistry, biochemistry, or other related degree concentration</li>
<li>3 years of related pharmaceutical experience in a cGMP environment</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
The Ideal Candidate Would Possess:
<ul>
<li>Strong computer, scientific, and organizational skills</li>
<li>Experience working with protein chromatography</li>
<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>
</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.
<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>
To learn more about Eurofins, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
#LI-EB1
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Scientist II: Method Development and Validation

<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 
<ul>
<li>Function as an MS subject matter expert within Analytical Development and be viewed as peer to other MS SMEs within Eurofins network</li>
<li>Perform method development, feasibility, qualification and/or validation of methods in support of biopharmaceutical products using primarily Mass spectrometry</li>
<li>Execute identification of unknown compounds with minimal support</li>
<li>Develop and execute validation plans</li>
<li>Troubleshoot method and instrumentation problems</li>
<li>Generate complete, accurate, and concise documentation using electronic systems and laboratory notebook</li>
<li>Author documents (e.g., development reports, methods and client reports)</li>
<li>Give presentations for training and client reviews</li>
<li>Have a strong understanding of current regulatory expectation</li>
<li>Effectively guide more junior scientists on technical issues</li>
<li>Use office and instrumentation specific computer software</li>
<li>Contribute to set up an oligonucleotide testing laboratory and establish processes, workflows and general operations</li>
<li>Developing and validating new QC methods to assess the suitability, stability, and functionality of a range of oligonucleotides through a variety of analytical and functional tests</li>
<li>HPLC and high resolution mass spectrometry method development for oligonucleotide characterization</li>
<li>Installation and verification of equipment, documenting processes, and training operators</li>
<li>Support various analytical instrument operation, maintenance and troubleshooting to sustain analytical performance, data reproducibility and reliability to deliver results to project teams within a timely manner</li>
<li>Champion and implement new and innovative analytical applications and technology</li>
<li>Advise clients on analytical scope to meet technical and regulatory requirements</li>
<li>Handling any customer related queries where necessary and liaising with the team to problem solve these queries if needed</li>
<li>Provide training/mentoring to junior staff</li>
</ul>
Qualifications 
<ul>
<li>B.S. / M.S. degree in Chemistry, Biology, biochemistry or related technical discipline with 4+ years of relevant experience, either post-doctoral or in the bio/pharmaceutical industry</li>
<li>Hands-on experience in use of multiple types of mass spectrometers (GC/MS, LC/MS, HRMS)</li>
<li>Experience with identification of unknown materials</li>
<li>Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude.</li>
<li>Strong organizational and time management skills</li>
<li>Excellent communication (oral and written) and attention to detail</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
<li>Extensive knowledge of oligonucleotide based drug products including ASO, siRNA, mRNA</li>
<li>Subject matter expert analytical chemistry knowledge including theory and application of three or more chromatographic and spectroscopic techniques for identification, purity, and assay of various analytes</li>
<li>Operate and troubleshoot available instruments including HPLC and MS</li>
<li>Experience with an assortment of different HPLC separations which includes IEX, RP, SEC, etc.</li>
<li>Hands-on experience in QC of oligonucleotides</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.
<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>
To learn more about Eurofins, please explore our website&nbsp;<a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

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