Laboratory Assistant jobs at CSL Plasma - 185 jobs

Summer 2026 Intern: Application Lab, Health, Nutrition & Care Newark, NJ If you're looking to grow your network and gain new skills within a global company, an internship with dsm-firmenich could be the program for you. Our summer internships provide students opportunities to work on real business projects and gain invaluable professional experience. As an intern, you'll have exposure to many different areas of a global flavors, fragrances, and ingredients organization that works with some of the biggest brands in the world, along with opportunities to network with your peers and leadership. From engaging events to mentoring opportunities and valuable resume-building experiences, we're committed to preparing you for a fulfilling and enduring career, both at dsm-firmenich and beyond. The 2026 dsm-firmenich Summer Internship Program will run from June 1, 2026 to August 14, 2026. Working Hours: Monday - Friday, 8:00am - 5:00pm Join our HNC Application team as an intern and gain invaluable professional experience. Enhance your skills and contribute to real projects that have visibility across the business through a Summer internship. Come discover all we have to offer! Your Key Responsibilities: * Operate dietary supplements and/or food process equipment with limited supervision. * Generate reliable data during laboratory activity. * Set-up, clean and maintain equipment for experiments by following the SOPs. Ensure all equipment is in a good condition to conduct product developments safely and effectively in a timely manner * Organize raw materials, packaging materials, laboratory and supplies used in formulation development and maintain adequate inventory. We Bring: Opportunities for students to develop skills and expand their professional connections within a company where sustainability is not just a slogan but is at the core of our strategy and purpose. We strive to create inclusive communities within our organization where every employee is equally valued and respected, regardless of their background, beliefs, or identity. Additionally, we provide an environment that encourages curiosity and an open mindset, allowing for personal and professional growth. Together, we can learn from one another to drive progress and create a better future. * Build Your Future Skills: Gain hands-on experience and develop practical skills that prepare you for a successful career. * Expand Your Network: Connect with professionals and peers in a company where sustainability drives every decision and action. * Thrive in an Inclusive Culture: Join a community that values and respects every individual-regardless of background, beliefs, or identity. * Grow Through Curiosity: Work in an environment that encourages open-mindedness, learning, and collaboration to create a better future together. You Bring: * Current students pursuing an undergraduate or graduate degree in Food Science or related scientific major. * The job requires lifting ~25 pounds. The job requires working in a highly regulated health and safety environment, which requires using gloves and safety glasses. The incumbent should not have health restrictions for these safety gears. * Demonstrate ability to be self-motivated with an inherent winning can-do attitude. Ability to follow instructions from senior scientists, read and follow SOPs. * Excellent communications and presentation skills - written and verbal; fluent in English. Knowledge of Microsoft word and excel is essential The hourly rate for this position is $23.00 - $26.00 per hour. Compensation will be dependent on factors that include location, education, training, specific skills, and years of experience. At the end of this internship, you will: * Learn the complete process for formulating and manufacturing gummies, including ingredient selection and quality control. * Gain experience in creating dietary supplement gummies that meet regulatory and nutritional requirements. * Understand the steps involved in tablet formulation and compression, including active ingredient and excipient functionality. About dsm-firmenich: At dsm-firmenich, we don't just meet expectations - we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future. Because real progress only happens when we go beyond, together. Inclusion, belonging and equal opportunity statement: At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve. We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work. Agency statement: We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.

Lancaster, PA, USA Full-time ** Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. **Job Description** The Laboratory Operational Assistant is primarily responsible for performing duties within the central laboratory related to inventory, administrative reporting tasks, management of samples, manual processing and handling of samples, and other miscellaneous tasks as assigned. **Laboratory & Operations Assistant responsibilities include, but are not limited to, the following** **:** + Level I - Minimum + Under the direction of the laboratory management, ensures that lab supplies are ordered and stocked. + Maintains inventory documentation and communicates to laboratory management when there are delays in supply delivery to the lab. + Works within the Purchase Ordering system and communicates to administrative personnel to ensure all paperwork is available for accounts payable. + Follow-up communication with vendors on all pending incoming orders. + Always maintain supply areas in audit-ready conditions. + Fast and accurate process of supplies from receiving to shelves. + Maintain accurate accountability of inventory within the assigned database. + Ensures proper handling of receipts and purchase orders. + Providing support to the Reporting Officer as needed. This may include receipt of client calls for reprinting of reports, executing administrative tasks associated with result cleanings as indicated in query management tool, and other reporting responsibilities as needed. + Provides support to Sample Management as needed, including unpacking, accessioning, flow and storage of samples, and archiving. + Retrieve and provide samples to laboratory as requested. + Perform manual processing of samples in the laboratory, including but not limited to, sample aliquoting, and special handling. + Adhere to policies and protocols in the lab. + Ability to read, interpret, and comply with documents such as internal SOPs, operating and maintenance instructions, and company policies. Perform housecleaning and laboratory cleaning as required. + Work closely with and communicate with other lab assistants to complete daily activities efficiently. + Level II - Fully meets the qualifications of the Level I plus the following: + Perform manual processing of samples in the laboratory, including but not limited to, PBMC isolation, sample aliquoting, and special handling. + Crosstrain appropriate personnel in qualified job tasks. + Level III - Fully meets the qualifications of the Level I and II plus the following: + Under the direction of the laboratory technologists and laboratory supervisor, ensures that lab testing is performed according to established global protocols, timelines and established procedures (SOPs) to generate high-quality, error-free, analytical results. + Perform other laboratory-related tasks such as sample sorting, archiving, instrument maintenance etc. as directed by the laboratory management. + Demonstrate leadership and problem-solving skills through supervision, coaching, mentoring of others as required **Qualifications** **Basic Minimum Education Qualifications** **:** + Level I/II + High School Diploma or GED acceptable, Associate of Applied Science preferred + Level III + Associate of Applied Science acceptable, Bachelor of Applied Science preferred **Basic Minimum Qualifications** **:** + Level I/II + Laboratory experience is beneficial but no prior experience is needed. + Level III + Minimum 1 year clinical laboratory experience is required. + Authorization to work in the United States indefinitely without restriction or sponsorship. **The ideal candidate would possess:** + Energetic and hard working. + Willing to work overtime as needed to accomplish tasks + Strong analytical, logistics, leadership and communication skills: verbal and written. + Self-motivated. + Strong organizational skills. + Knowledge of MS Office Suite and Outlook. + Ability to lift packages greater than 40 pounds. + Ability to work in a fast-paced environment. **Additional Information** Position is full-time working **alternating days (including Saturdays) working 2:00pm - 10:30pm** , with overtime as needed. 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 + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

Lancaster, PA, USA Full-time ** Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. **Job Description** The Laboratory Operational Assistant is primarily responsible for performing duties within the central laboratory related to inventory, administrative reporting tasks, management of samples, manual processing and handling of samples, and other miscellaneous tasks as assigned. **Laboratory Operational Assistant responsibilities include, but are not limited to, the following** **:** + Level I - Minimum + Under the direction of the laboratory management, ensures that lab supplies are ordered and stocked. + Maintains inventory documentation and communicates to laboratory management when there are delays in supply delivery to the lab. + Works within the Purchase Ordering system and communicates to administrative personnel to ensure all paperwork is available for accounts payable. + Follow-up communication with vendors on all pending incoming orders. + Always maintain supply areas in audit-ready conditions. + Fast and accurate process of supplies from receiving to shelves. + Maintain accurate accountability of inventory within the assigned database. + Ensures proper handling of receipts and purchase orders. + Providing support to the Reporting Officer as needed. This may include receipt of client calls for reprinting of reports, executing administrative tasks associated with result cleanings as indicated in query management tool, and other reporting responsibilities as needed. + Provides support to Sample Management as needed, including unpacking, accessioning, flow and storage of samples, and archiving. + Retrieve and provide samples to laboratory as requested. + Perform manual processing of samples in the laboratory, including but not limited to, sample aliquoting, and special handling. + Adhere to policies and protocols in the lab. + Ability to read, interpret, and comply with documents such as internal SOPs, operating and maintenance instructions, and company policies. Perform housecleaning and laboratory cleaning as required. + Work closely with and communicate with other lab assistants to complete daily activities efficiently. + Level II - Fully meets the qualifications of the Level I plus the following: + Perform manual processing of samples in the laboratory, including but not limited to, PBMC isolation, sample aliquoting, and special handling. + Crosstrain appropriate personnel in qualified job tasks. + Level III - Fully meets the qualifications of the Level I and II plus the following: + Under the direction of the laboratory technologists and laboratory supervisor, ensures that lab testing is performed according to established global protocols, timelines and established procedures (SOPs) to generate high-quality, error-free, analytical results. + Perform other laboratory-related tasks such as sample sorting, archiving, instrument maintenance etc. as directed by the laboratory management. + Demonstrate leadership and problem-solving skills through supervision, coaching, mentoring of others as required **Qualifications** **Basic Minimum Education Qualifications** **:** + Level I/II + High School Diploma or GED acceptable, Associate of Applied Science preferred + Level III + Associate of Applied Science acceptable, Bachelor of Applied Science preferred **Basic Minimum Qualifications** **:** + Level I/II + Laboratory experience is beneficial but no prior experience is needed. + Level III + Minimum 1 year clinical laboratory experience is required. + Authorization to work in the United States indefinitely without restriction or sponsorship. **The ideal candidate would possess:** + Energetic and hard working. + Willing to work overtime as needed to accomplish tasks + Strong analytical, logistics, leadership and communication skills: verbal and written. + Self-motivated. + Strong organizational skills. + Knowledge of MS Office Suite and Outlook. + Ability to lift packages greater than 40 pounds. + Ability to work in a fast-paced environment. **Additional Information** Position is full-time working **alternating Saturdays 2:00pm - 10:30pm** , with overtime as needed. 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 + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. **Job Summary** This is a full time - 40 hours/week position. Must be able to start full time day shift within one month of offer. Perform basic laboratory support and record-keeping tasks. Support the functions of the Laboratory Sciences department. ESSENTIAL DUTIES AND RESPONSIBILITIES: Receive, monitor, and maintain inventory and stock levels of assigned areas. Operate lab equipment and perform routine maintenance as needed. May be responsible for preparing lab solutions (e.g., buffers, media/common vehicles, and bleach solutions). Wash and dry glassware and distribute to appropriate locations within the laboratory. Keep glass-washing area clean and organized. May sterilize glassware and other items using an autoclave. Label tubes and perform laboratory set-up/clean-up. Organize and perform inventory of department refrigerators or freezers. Assist in the archiving of equipment/facility records. Assist technical personnel with clerical duties (e.g., filing, making copies, shipments set-up etc.). May record observations and measurements for basic lab/research task. Perform limited troubleshooting and maintenance of instruments as appropriate for assigned area. May generate forms, tables, and hand record data. Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs). Ship, store, and document received supplies (e.g., test articles, bio-hazard boxes, dry ice, reagents, etc.) Assist technical personnel with laboratory supplies expiry check and discard as needed. Perform all other related duties as assigned. The pay range for this position is $21.00/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. **Job Qualifications** QUALIFICATIONS: ⦁ Education: High school diploma or General Education Degree (G.E.D.). ⦁ Experience: None. ⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. ⦁ Certification/Licensure: Must have valid, state-issued, driver's license. ⦁ Other: Must be detail-oriented and have general familiarity with lab procedures. Good verbal communication skills required. Basic computer skills; familiarity with Microsoft Office software. PHYSICAL DEMANDS: ⦁ Employees must be able to regularly lift, move, or manipulate heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or supplies. ⦁ Must be able to perform procedures, which require standing or sitting for long periods of time. ⦁ Must be able to regularly move about the facility to access file cabinets, office machinery, and other buildings. ⦁ Regularly operates a computer and other office productivity machinery, such as a calculator, copy machine, and computer printer. ⦁ Regularly uses laboratory instruments. ⦁ Must be able to work in narrow spaces. ⦁ Must be able to wear safety equipment (PPE), as needed, according to OSHA regulations and company standards. ⦁ Must be able to regularly stoop, bend, kneel, stand, or reach up with hands and arms to manipulate objects on shelves from one and one-half to six and one-half feet above the floor on a repetitive basis each day. ⦁ Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus. ⦁ Must be able to communicate with employees, exchanging accurate information. ⦁ Must regularly move about inside the facility to access supplies which may require going up and down stairs. WORK ENVIRONMENT: ⦁ Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud. ⦁ The noise level in the work environment ranges from low to moderate depending upon the task being performed. Comments: ⦁ This position requires overtime, weekend, holiday, and/or after hours shift coverage as needed. **About Safety Assessment** Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility. **Equal Employment Opportunity** Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit *************** 231803

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description The Laboratory Operational Assistant is primarily responsible for performing duties within the central laboratory related to inventory, administrative reporting tasks, management of samples, manual processing and handling of samples, and other miscellaneous tasks as assigned. Laboratory Operational Assistant responsibilities include, but are not limited to, the following: * Level I - Minimum * Under the direction of the laboratory management, ensures that lab supplies are ordered and stocked. * Maintains inventory documentation and communicates to laboratory management when there are delays in supply delivery to the lab. * Works within the Purchase Ordering system and communicates to administrative personnel to ensure all paperwork is available for accounts payable. * Follow-up communication with vendors on all pending incoming orders. * Always maintain supply areas in audit-ready conditions. * Fast and accurate process of supplies from receiving to shelves. * Maintain accurate accountability of inventory within the assigned database. * Ensures proper handling of receipts and purchase orders. * Providing support to the Reporting Officer as needed. This may include receipt of client calls for reprinting of reports, executing administrative tasks associated with result cleanings as indicated in query management tool, and other reporting responsibilities as needed. * Provides support to Sample Management as needed, including unpacking, accessioning, flow and storage of samples, and archiving. * Retrieve and provide samples to laboratory as requested. * Perform manual processing of samples in the laboratory, including but not limited to, sample aliquoting, and special handling. * Adhere to policies and protocols in the lab. * Ability to read, interpret, and comply with documents such as internal SOPs, operating and maintenance instructions, and company policies. Perform housecleaning and laboratory cleaning as required. * Work closely with and communicate with other lab assistants to complete daily activities efficiently. * Level II - Fully meets the qualifications of the Level I plus the following: * Perform manual processing of samples in the laboratory, including but not limited to, PBMC isolation, sample aliquoting, and special handling. * Crosstrain appropriate personnel in qualified job tasks. * Level III - Fully meets the qualifications of the Level I and II plus the following: * Under the direction of the laboratory technologists and laboratory supervisor, ensures that lab testing is performed according to established global protocols, timelines and established procedures (SOPs) to generate high-quality, error-free, analytical results. * Perform other laboratory-related tasks such as sample sorting, archiving, instrument maintenance etc. as directed by the laboratory management. * Demonstrate leadership and problem-solving skills through supervision, coaching, mentoring of others as required Qualifications Basic Minimum Education Qualifications: * Level I/II * High School Diploma or GED acceptable, Associate of Applied Science preferred * Level III * Associate of Applied Science acceptable, Bachelor of Applied Science preferred Basic Minimum Qualifications: * Level I/II * Laboratory experience is beneficial but no prior experience is needed. * Level III * Minimum 1 year clinical laboratory experience is required. * Authorization to work in the United States indefinitely without restriction or sponsorship. The ideal candidate would possess: * Energetic and hard working. * Willing to work overtime as needed to accomplish tasks * Strong analytical, logistics, leadership and communication skills: verbal and written. * Self-motivated. * Strong organizational skills. * Knowledge of MS Office Suite and Outlook. * Ability to lift packages greater than 40 pounds. * Ability to work in a fast-paced environment. Additional Information Position is full-time working alternating Saturdays 2:00pm - 10:30pm, with overtime as needed. 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 * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. **Job Summary** We are seeking a Laboratory Assistant I for our Safety Assessment site located in Reno, NV. This position will be responsible for performing basic laboratory and record keeping tasks ESSENTIAL DUTIES AND RESPONSIBILITIES: * Wash and dry glassware and distribute to appropriate locations within the laboratory. Keep glass-washing area clean and organized. May sterilize glassware and other items using an autoclave. * Label tubes, devices and containers and perform laboratory set-up/clean-up. * Assist technical personnel with clerical duties (e.g., filing, making copies, etc.). * Monitor inventory and stock assigned areas. * May record observations and measurements for basic lab/research tasks. * Operate basic lab equipment and perform routine maintenance as needed. * Perform limited troubleshooting and calibration of instruments as appropriate for assigned area. * May be responsible for preparing simple lab solutions (e.g., buffers, media/common vehicles). * May generate reports, data, and forms. * Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs). * Perform all other related duties as assigned. **Job Qualifications** * Education: High school diploma or General Education Degree (G.E.D.). * Experience: None. * An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. * Certification/Licensure: None. * Other: Must be detail-oriented and have general familiarity with lab procedures. Good verbal communication skills required. Basic computer skills; familiarity with Microsoft Office software. The pay for this position starts at $19.00/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. **About Safety Assessment** Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility. **Equal Employment Opportunity** Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit *************** 231684

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. **We are PCI.** Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. **JOB DESCRIPTION:** Position Title: Microbiology Laboratory Intern Location: Assembly Drive. Rockford, IL 61109 Department: Lab Shift: 1st Reporting To: _Director, Laboratory_ Responsible For (Staff): _None_ Brief Project Description: The Laboratory will have an intern to learn vital skills and assist in the Microbiology Department in day-to-day testing. This testing will include biological indicator testing, preparation of basic microbiology medium(s), collection of environmental monitoring samples from various packaging environments and water testing (total plate count and coliforms). The Microbiology Laboratory intern will work in conjunction with the Senior Microbiologist and Microbiologist to assist in the daily operations of the Microbiology Laboratory. This is a first shift, M-F position. **ESSENTIAL DUTIES AND RESPONSIBILITIES:** Learn day-to-day operations of the Microbiology Laboratory and assist Microbiologists in daily testing activities (biological indicator, total plate count, coliform testing, etc). Preparation of basic microbiological medium to be used in testing in addition to preparing poured plates for the Microbiologists to be used in testing. Perform environmental monitoring testing in various packaging environments with various testing equipment. Understanding technical writing requirements for working in a Laboratory/GMP environment. Assist in the day-to-day Laboratory activities such as washing dishes, operating the dishwasher, putting away supplies/reagents, operation of the autoclave, etc. Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, and rules. Attendance to work is an essential function of this position Performs other duties as assigned by Manager/Supervisor. Special Demands: + Stationary Position: None + Move, Traverse: 3/4 of the day and up. + Operate, activate, use, prepare, inspect, or place: 3/4 of the day and up. + Install, place, adjust, apply, measure, use, or signal: 3/4 of the day and up. + Ascend/Descend or Work Atop: 3/4 of the day and up. + Position self (to) or Move (about or to): 3/4 of the day and up. + Communicate or exchange information: 3/4 of the day and up. + Detect, distinguish, or determine: 3/4 of the day and up. On an average day, the individual can expect to move and/or transport up to 25 pounds between 1/2 and 3/4 of the day. **QUALIFICATIONS:** **Required** : + Working toward Bachelor's Degree in related field. + College Level Math Skills + Advanced Computer Skills: Ability to perform the most complex computer tasks and operate various computer programs. + Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. + High Reasoning: Ability to solve practical problems and deal with a variety of concrete variables in situations where there is only limited standardization. Ability to interpret a variety of instructions that may be provided in various forms. **Preferred** : + Ability to effectively present information to various people as the job requires. + Ability to work independently and/or part of a team. + Ability to display original thinking and creativity. + Ability to hold oneself in a professional manner. _The hiring rate for this position is $20.00hour plus eligibility for an annual performance bonus. Final offer amounts are determined by multiple factors including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), flexible spending account, and 401(k)._ Join us and be part of building the bridge between life changing therapies and patients. Let's talk future (***************** **Equal Employment Opportunity (EEO) Statement:** _PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._ _At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._ Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how. PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled

Full Time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position/Job Summary The lab assistant position entails calibrations and maintenance of various laboratory equipment for our 760 Exton location located on Pennsylvania Drive. Primarily calibrating freezers, incubators, automation platforms and various other smaller lab equipment's. The position requires an individual to be flexible at the requests of laboratory scientists including buffer prep and various instrument flushing. General laboratory housekeeping is also included. Roles and Responsibilities Ability to read and position various calibration instruments. Ability to keep documentation in a neat and orderly fashion. Ability to lift to 50lbs. Ability to follow safety procedures. Ability to work as a team. Ability to work independently with little supervision. Ability to work the 9am to 5:30pm shift. An 8 hour work shift everyday M-F. Education Requirements: High school diploma or higher. Experience and Skills Prior experience working in a laboratory, particularly with sample preparation, equipment operation, and data recording is preferred. Familiarity with common laboratory equipment and instruments, such as centrifuges, microscopes, pH meters, etc. Knowledge of preparing buffers, media, and other common laboratory reagents. Capable of recording experimental data and using computer software (e.g., Excel, SPSS) for data processing and analysis. Able to manage time and prioritize tasks effectively in a fast-paced work environment. Strong learning ability. Salary and Benefits: Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. An Immunopathology Laboratory Assistant I is performing basic tasks and procedures, primarily in support of the Immunopathology department. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Performs basic tasks of the department which may include handling of tissues, inventory/archive of study materials; reagent and antibody receiving, storing and maintenance, slide labeling; running and maintaining the H&E stainer, loading slide scanners, shipping materials, and general maintenance of the lab. • Collects, documents, reviews, and verifies data on forms, or in electronic data capture systems. • Reviews documentation of functions performed as part of quality control requirements. • Uses and maintain instrumentation and equipment. • Performs all other related duties as assigned. MINIMUM QUALIFICATIONS: Education: High school diploma or General Education Degree (G.E.D.) Experience: No experience required. Certification/Licensure: None Other: Demonstrates ability to consistently and effectively produce high quality results and record accurate study and departmental data. Ability to communicate verbally and in writing at all levels inside and outside the organization. Excellent written and verbal communication skills. Ability to manage multiple tasks and priorities to achieve goals. Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice. Ability to work under specific time constraints. PREFERRED QUALIFICATIONS: Associates (A.A/A.S) degree preferred. The pay for this position starts at $18.00/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility. Equal Employment Opportunity Charles River Laboratories 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, veteran or disability status. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit ***************

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. An Immunopathology Laboratory Assistant I is performing basic tasks and procedures, primarily in support of the Immunopathology department. **ESSENTIAL DUTIES AND RESPONSIBILITIES:** * Performs basic tasks of the department which may include handling of tissues, inventory/archive of study materials; reagent and antibody receiving, storing and maintenance, slide labeling; running and maintaining the H&E stainer, loading slide scanners, shipping materials, and general maintenance of the lab. * Collects, documents, reviews, and verifies data on forms, or in electronic data capture systems. * Reviews documentation of functions performed as part of quality control requirements. * Uses and maintain instrumentation and equipment. * Performs all other related duties as assigned. **MINIMUM QUALIFICATIONS:** + **_Education:_** High school diploma or General Education Degree (G.E.D.) + **_Experience:_** No experience required. + **_Certification/Licensure:_** None + **_Other:_** Demonstrates ability to consistently and effectively produce high quality results and record accurate study and departmental data. Ability to communicate verbally and in writing at all levels inside and outside the organization. Excellent written and verbal communication skills. Ability to manage multiple tasks and priorities to achieve goals. Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice. Ability to work under specific time constraints. **PREFERRED QUALIFICATIONS:** + Associates (A.A/A.S) degree preferred. The pay for this position starts at **$18.00/hr.** Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. **About Safety Assessment** Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility. **Equal Employment Opportunity** Charles River Laboratories 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, veteran or disability status. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit *************** 231688

Lenexa, KS, USA Full-time ** **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** Eurofins Viracor LLC is an equal opportunity employer and encourages individuals from all backgrounds to apply. By submitting your application, you acknowledge and agree to the following conditions: 1. **Drug Screen:** Successful candidates will be required to pass a standard drug screen as part of the pre-employment process. 2. **Background Check:** A thorough background check will be conducted for all potential employees. This may include, but is not limited to, criminal history, education verification, and employment history. 3. **Visa Sponsorship:** Eurofins Viracor LLC does not sponsor employment visas. All candidates must have the legal right to work in Lenexa, KS without requiring sponsorship. Unless approved by HR and supporting parties. **_Basic Function and Scope of Responsibility:_** The Laboratory Assistant is primarily responsible for performing duties related to accessioning, specimen management, problem resolution, and data entry and specimen storage with a high degree of proficiency. **_Essential Job Duties:_** Level I - Minimum + Receive incoming shipments and document appropriately + Examine samples for accuracy and other requirements (sample type, volume, etc.) + Contact client to resolve sample and/or testing related issues or discrepancies + Complete correction requests as needed + Operation of the front end processing automation equipment as assigned by management + Perform data entry into the Laboratory Information Management System (LIMS) + Label samples and deliver them to proper area(s) + Retrieve and re-file samples for testing + Properly store specimens for short term and long term storage + Prepare specimens to be shipped and adhere to all applicable shipping requirements + Aid laboratory personnel in cleaning duties + Maintain quality control and quality assurance records as required + Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies + Adhere to policies and protocols in the lab + Work closely and communicate with other lab associates to complete daily activities efficiently + Ensure adherence to laboratory safety policies + Other duties as assigned by management Level II - Fully meets the qualifications of Level I plus the following: + Manage issues and projects; resolve escalated issues as appropriate. + Demonstrate superior understanding of Laboratory operations Level III - Fully meets the qualifications of Level I and II plus the following: + Demonstrate leadership skills through the supervision, coaching and mentoring of others as required + Ensure department adheres to policies and procedures **Qualifications** **_Essential Knowledge, Skills and Abilities:_** Level I - Minimum + High School diploma or equivalent required + 2 years of clinical laboratory experience preferred + Must be comfortable with raw specimen handling + Ability to read, interpret, and comply with documents such as internal SOPs, operating and maintenance instructions, and company policies + Position may require evening and weekend hours + Intermediate level of proficiency with PC based software programs, with database skills and 1 year data entry experience preferred Level II - Fully meets the qualifications of Level I plus the following: + Demonstrated leadership abilities + Advanced problem solving skills Level III - Fully meets the qualifications of Level I and II plus the following: + Ability to manage direct other Associates as required + Ability to manage daily workload as required + Ability to assist Management in providing overall direction of workflow for Lab Assistants and Support Services as needed + Ability to ensure applicable SOPs are being utilized and followed appropriately + Help with weekly scheduling of staff + Serve as the primary trainer for new Lab Assistants or re-training of existing Lab Assistants + Ability to accurately answer questions when Supervisor is unavailable + Ability to interact with other departments as necessary and develop relationships with other Lab Leadership and Management as it relates to work processes and work flow + Ability to communicate concerns/needs as necessary to Supervisor + Aid Supervisor with areas of improvement in workflow or organization, etc. **_Physical Requirements:_** + Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead + Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting + Ability to stand for extended periods of time as necessary in the laboratory (4 or more hours) + Ability to lift and move items weighing up to 25 pounds. It is advised to obtain assistance for items over 25 pounds. + Physical dexterity sufficient to move body frequently around laboratory equipment and instrumentation + Ability to continuously operate a personal computer for extended periods of time (4 or more hours) + Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, make valid judgments and decisions 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. **Additional Information** **Schedule:** + Mon-Fri 8:00a-4:30p **What we offer:** + Excellent full time benefits including comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.**

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 Eurofins Viracor LLC is an equal opportunity employer and encourages individuals from all backgrounds to apply. By submitting your application, you acknowledge and agree to the following conditions: * Drug Screen: Successful candidates will be required to pass a standard drug screen as part of the pre-employment process. * Background Check: A thorough background check will be conducted for all potential employees. This may include, but is not limited to, criminal history, education verification, and employment history. * Visa Sponsorship: Eurofins Viracor LLC does not sponsor employment visas. All candidates must have the legal right to work in Lenexa, KS without requiring sponsorship. Unless approved by HR and supporting parties. Basic Function and Scope of Responsibility: The Laboratory Assistant is primarily responsible for performing duties related to accessioning, specimen management, problem resolution, and data entry and specimen storage with a high degree of proficiency. Essential Job Duties: Level I - Minimum * Receive incoming shipments and document appropriately * Examine samples for accuracy and other requirements (sample type, volume, etc.) * Contact client to resolve sample and/or testing related issues or discrepancies * Complete correction requests as needed * Operation of the front end processing automation equipment as assigned by management * Perform data entry into the Laboratory Information Management System (LIMS) * Label samples and deliver them to proper area(s) * Retrieve and re-file samples for testing * Properly store specimens for short term and long term storage * Prepare specimens to be shipped and adhere to all applicable shipping requirements * Aid laboratory personnel in cleaning duties * Maintain quality control and quality assurance records as required * Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies * Adhere to policies and protocols in the lab * Work closely and communicate with other lab associates to complete daily activities efficiently * Ensure adherence to laboratory safety policies * Other duties as assigned by management Level II - Fully meets the qualifications of Level I plus the following: * Manage issues and projects; resolve escalated issues as appropriate. * Demonstrate superior understanding of Laboratory operations Level III - Fully meets the qualifications of Level I and II plus the following: * Demonstrate leadership skills through the supervision, coaching and mentoring of others as required * Ensure department adheres to policies and procedures Qualifications Essential Knowledge, Skills and Abilities: Level I - Minimum * High School diploma or equivalent required * 2 years of clinical laboratory experience preferred * Must be comfortable with raw specimen handling * Ability to read, interpret, and comply with documents such as internal SOPs, operating and maintenance instructions, and company policies * Position may require evening and weekend hours * Intermediate level of proficiency with PC based software programs, with database skills and 1 year data entry experience preferred Level II - Fully meets the qualifications of Level I plus the following: * Demonstrated leadership abilities * Advanced problem solving skills Level III - Fully meets the qualifications of Level I and II plus the following: * Ability to manage direct other Associates as required * Ability to manage daily workload as required * Ability to assist Management in providing overall direction of workflow for Lab Assistants and Support Services as needed * Ability to ensure applicable SOPs are being utilized and followed appropriately * Help with weekly scheduling of staff * Serve as the primary trainer for new Lab Assistants or re-training of existing Lab Assistants * Ability to accurately answer questions when Supervisor is unavailable * Ability to interact with other departments as necessary and develop relationships with other Lab Leadership and Management as it relates to work processes and work flow * Ability to communicate concerns/needs as necessary to Supervisor * Aid Supervisor with areas of improvement in workflow or organization, etc. Physical Requirements: * Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead * Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting * Ability to stand for extended periods of time as necessary in the laboratory (4 or more hours) * Ability to lift and move items weighing up to 25 pounds. It is advised to obtain assistance for items over 25 pounds. * Physical dexterity sufficient to move body frequently around laboratory equipment and instrumentation * Ability to continuously operate a personal computer for extended periods of time (4 or more hours) * Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, make valid judgments and decisions 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. Additional Information Schedule: * Mon-Fri 8:00a-4:30p What we offer: * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.

Medpace Reference Laboratories is currently seeking Laboratory Receiving Assistants to work in our Sample Management/Biorepository Department. This individual will be responsible for basic administrative duties as well as the handling and delivery of clinical samples and other materials. 8:00-4:30 PM Saturday Shift Required Responsibilities * Receive biological samples; * Perform sample processing duties (unpack samples, scanning samples, data entry, etc.); * Handle dry ice; and * Prepare sample shipments to be sent to third-party lab * Participate in clinical study projects to facilitate testing timelines and deliverables * Assist with routine maintenance and/or cleaning of equipment * Performs sample retrieval and QC of physical inventory for study-related projects, transfers/shipments, general inventory upkeep, and to maintain database accuracy * Adheres to good documentation practices, and ensures accurate database entry of sample- or subject-related demographics * Communicates professionally with inter-functional groups regarding daily business, project-specific requests, or problem resolution * Coordinates with management, project staff, and other team members to execute assigned responsibilities in a timely manner. Qualifications * High school diploma or equivalent; * Basic computer skills; * Prior sample management, logistics, or health care experience desired; and * Team-worker and detail-oriented with good time management skills. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks * Cincinnati Campus Overview * Flexible work environment * Competitive PTO packages, starting at 20+ days * Competitive compensation and benefits package * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Community involvement with local nonprofit organizations * Discounts on local sports games, fitness gyms and attractions * Modern, ecofriendly campus with an on-site fitness center * Structured career paths with opportunities for professional growth * Discounted tuition for UC online programs Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Princeton, NJ If you're looking to grow your network and gain new skills within a global company, an internship with dsm-firmenich could be the program for you. Our summer internships provide students opportunities to work on real business projects and gain invaluable professional experience. As an intern, you'll have exposure to many different areas of a global flavors, fragrances, and ingredients organization that works with some of the biggest brands in the world, along with opportunities to network with your peers and leadership. From engaging events to mentoring opportunities and valuable resume-building experiences, we're committed to preparing you for a fulfilling and enduring career, both at dsm-firmenich and beyond. We are currently looking for a Creation Lab Technician Intern at our Plainsboro, NJ office. The 2026 dsm-firmenich Summer Internship Program will begin June 1st, 2026 and run through August 14, 2026. Working Hours: Monday - Friday, 8:00am - 5:00pm Join our Taste Creation Lab team as an intern and gain invaluable professional experience. Enhance your skills and contribute to real projects that have visibility across the business through a Summer internship. Come discover all we have to offer! Work side by side with Flavorists in compounding flavors used in newly developed foods, beverages, and supplements. Maintain your own laboratory space while compounding formulas for internal use and submission to clients. Work together with your colleagues as a critical part of the Creation team. Your Key Responsibilities: * Compound formula at a reliable and precise level, for flavorists and internal use and submission to clients. * Maintain, manage and coordinate shipment of flavor samples. * Keep daily compounding record, lab raw material record and other appropriate documentation on all laboratory work performed. * Maintain and replenish laboratory supplies of stock raw materials, solutions, collection oil samples, glassware, and general laboratory equipment, ensuring the laboratory is well-stocked and resourced. * Maintain a clean and well-organized laboratory/work place, and independently operate standard equipment/procedures to the required level. Assure compliance of HS&E procedures and proactively contribute to the improvement of lab safety. * Identify common problems/issues encountered, report when an abnormal phenomenon happen: solubility, stability, color change, etc. Maintain awareness of technology and issues affecting own job. We Bring: * Build Your Future Skills: Gain hands-on experience and develop practical skills that prepare you for a successful career. * Expand Your Network: Connect with professionals and peers in a company where sustainability drives every decision and action. * Thrive in an Inclusive Culture: Join a community that values and respects every individual-regardless of background, beliefs, or identity. * Grow Through Curiosity: Work in an environment that encourages open-mindedness, learning, and collaboration to create a better future together. You Bring: * Currently purusing a Bachelor's degree in Food Science, Chemistry, Biochemistry, Culinary, or related. * Passion for technology. * Self-motivated team player. * Collaboration and team spirit. * Candidates must be available to work full-time beginning on June 1, 2026 - August 14, 2026. * Excellent communication and interpersonal skills. The hourly rate for this position is $23.00 - $26.00 per hour. Compensation will be dependent on factors that include location, education, training, specific skills, and years of experience. About dsm-firmenich: At dsm-firmenich, we don't just meet expectations - we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future. Because real progress only happens when we go beyond, together. Inclusion, belonging and equal opportunity statement: At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve. We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work. Agency statement: We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.

Responsibilities * Prepare samples according to project protocol and/or related SOPs; * Maintain compliant laboratory documentation; * Perform data analysis and data checking; * Interpret results obtained for accuracy and acceptability; * Clean and sterilize laboratory equipment; and * Other duties deemed necessary. Qualifications * A minimum of a Bachelor's degree, with previous experience in a research laboratory; * Knowledge of GLP, cGMP, and ICH guidelines; * Strong organizational and communication (written and oral) skills; and * Knowledge of Microsoft Word, Excel, and Powerpoint. Travel: None Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks * Cincinnati Campus Overview * Flexible work environment * Competitive PTO packages, starting at 20+ days * Competitive compensation and benefits package * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Community involvement with local nonprofit organizations * Discounts on local sports games, fitness gyms and attractions * Modern, ecofriendly campus with an on-site fitness center * Structured career paths with opportunities for professional growth * Discounted tuition for UC online programs Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Role Description Lab Tech 1 - Chemistry SHIFT: Monday-Friday 10:00 pm - 6:30 am The Lab Technician 1 is responsible for performing routine laboratory tests to support the diagnosis and treatment of animal health conditions. Key responsibilities include preparing samples, operating laboratory equipment, and maintaining accurate records. This role supports the Global Diagnostics division at Zoetis and will work closely with internal veterinarians or medical team, and other lab personnel to ensure the highest standards of quality and accuracy in our diagnostic services. Job Duties: * Prepare biological specimens for testing in various departments, including but not limited to, hematology, urinalysis, serology, chemistry, endocrinology, parasitology, cytology, and coagulation * Use high-throughput automated analyzers, microscopes, and other diagnostic equipment to test various sample types, including but not limited to, whole blood, serum, urine, and feces * Set up and execute laboratory tests, review results, and release findings in accordance with ZRL Standard Operating Procedures (SOPs) * Perform routine and non-routine maintenance on analyzers, including but not limited to, daily, weekly, monthly, and as needed maintenance * Perform basic analyzer troubleshooting techniques on one major department analyzer * Review and accept daily Quality Control reports and weekly Levey-Jennings charts * Handle and store all biological specimens in accordance with ZRL Standard Operating Procedures (SOP) * Maintain a clean and organized laboratory workspace * Properly handle and dispose of medical and biohazardous waste while adhering to all applicable regulatory guidelines * Consistently and properly fill out laboratory logs, including but not limited to maintenance logs, environmental logs, and cleaning logs * Maintain several types of records, including but not limited to medical records, courier logs and manifests * Prepare biological specimens for shipment to offsite testing facilities, adhering to all standards set forth by regulatory bodies including the Department of Transportation (DOT) * Receive, store, and log all laboratory and office supplies into designated locations * Operate and maintain secondary laboratory equipment, including but not limited to centrifuges, pipettes, heating blocks, and slide stainers * Understand and follow SOPs and training modules set forth by Zoetis Reference Laboratories Education/Experience: * High School Diploma or equivalent required. * Associate or Bachelor's degree preferred. * Requires 1-2 years of experience in a clinical laboratory setting and experience in performing basic laboratory testing or operations * Proficient knowledge in one of the following preferred: Hematology, Chemistry, Urinalysis, Endocrinology, Parasitology, and Cytology Technical Skills Required: * Strong attention to detail * Proficiency in using laboratory equipment and software. * IT and LIS (laboratory information systems) experience and general comfort level with computer systems, technology, and equipment interfaces. * Team-oriented with excellent collaboration skills * Ability to work independently and as part of a team * Robust organizational and time management abilities * Excellent data entry skills * Strong written and oral communication skills * Ability to complete tasks with minimal supervision * Fluency in English language Physical Position Requirements: * Ability to lift up to 50 pounds * Ability to bend, kneel, stoop, crouch * Ability to walk, sit, or stand for extended periods Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Role Description Lab Tech 1 - Chemistry SHIFT: Monday-Friday 10:00 pm - 6:30 am The Lab Technician 1 is responsible for performing routine laboratory tests to support the diagnosis and treatment of animal health conditions. Key responsibilities include preparing samples, operating laboratory equipment, and maintaining accurate records. This role supports the Global Diagnostics division at Zoetis and will work closely with internal veterinarians or medical team, and other lab personnel to ensure the highest standards of quality and accuracy in our diagnostic services. Job Duties: · Prepare biological specimens for testing in various departments, including but not limited to, hematology, urinalysis, serology, chemistry, endocrinology, parasitology, cytology, and coagulation · Use high-throughput automated analyzers, microscopes, and other diagnostic equipment to test various sample types, including but not limited to, whole blood, serum, urine, and feces · Set up and execute laboratory tests, review results, and release findings in accordance with ZRL Standard Operating Procedures (SOPs) · Perform routine and non-routine maintenance on analyzers, including but not limited to, daily, weekly, monthly, and as needed maintenance · Perform basic analyzer troubleshooting techniques on one major department analyzer · Review and accept daily Quality Control reports and weekly Levey-Jennings charts · Handle and store all biological specimens in accordance with ZRL Standard Operating Procedures (SOP) · Maintain a clean and organized laboratory workspace · Properly handle and dispose of medical and biohazardous waste while adhering to all applicable regulatory guidelines · Consistently and properly fill out laboratory logs, including but not limited to maintenance logs, environmental logs, and cleaning logs · Maintain several types of records, including but not limited to medical records, courier logs and manifests · Prepare biological specimens for shipment to offsite testing facilities, adhering to all standards set forth by regulatory bodies including the Department of Transportation (DOT) · Receive, store, and log all laboratory and office supplies into designated locations · Operate and maintain secondary laboratory equipment, including but not limited to centrifuges, pipettes, heating blocks, and slide stainers · Understand and follow SOPs and training modules set forth by Zoetis Reference Laboratories Education/Experience: · High School Diploma or equivalent required. · Associate or Bachelor's degree preferred. · Requires 1-2 years of experience in a clinical laboratory setting and experience in performing basic laboratory testing or operations · Proficient knowledge in one of the following preferred: Hematology, Chemistry, Urinalysis, Endocrinology, Parasitology, and Cytology Technical Skills Required: · Strong attention to detail · Proficiency in using laboratory equipment and software. · IT and LIS (laboratory information systems) experience and general comfort level with computer systems, technology, and equipment interfaces. · Team-oriented with excellent collaboration skills · Ability to work independently and as part of a team · Robust organizational and time management abilities · Excellent data entry skills · Strong written and oral communication skills · Ability to complete tasks with minimal supervision · Fluency in English language Physical Position Requirements: · Ability to lift up to 50 pounds · Ability to bend, kneel, stoop, crouch · Ability to walk, sit, or stand for extended periods Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Are you ready to take the next step in your career and join a company that truly values your contributions? At Eurofins PSS, we offer more than just a job-we provide a rewarding, enriching, and fulfilling career path with opportunities for growth and advancement. As part of our team, you'll work in state-of-the-art laboratories alongside passionate professionals dedicated to the testing, development, and advancement of life-saving drug products. Together, we're making the world a healthier and happier place to live. Eurofins PSS is a global leader in life sciences, delivering a unique range of analytical testing services that help ensure the safety, authenticity, and accuracy of products and their ingredients. We partner with some of the world's largest companies to make life and our environment safer, healthier, and more sustainable. Our people are our chemistry-and we're looking for talented individuals like you to join us in making a difference. Job Description Team Leadership & Operations * Lead and schedule team members (small team of 5-6) in a client-based lab environment * Train employees, conduct performance reviews, and manage training records * Interview candidates and support succession planning * Foster morale, collaboration, and a positive team culture * Ensure lab operations meet high standards for quality and efficiency Scientific & Technical Work * Execute automated protein purifications using chromatographic techniques, TFF, and AKTA systems * Characterize protein solutions using Agilent HPLC and SDS-PAGE * Perform routine analytical measurements (pH, UV-Vis, HPLC) * Prepare buffers and solutions; maintain inventories and lab equipment * Clean and maintain AKTA systems (including CIP procedures) * Document assay data and contribute to study reports Compliance & Documentation * Maintain accurate records in electronic lab notebooks * Participate in investigations and ensure adherence to GLP and company policies Qualifications * Bachelor's degree in Chemistry, Biochemistry, or a related field * + Minimum 4 years of industry lab experience * OR * Master's degree in a related field * + Minimum 2 years of industry lab experience * Industry leadership experience is required Additional Information * Position is full-time, 8:00 am- 5:00 pm Overtime as needed. * Position is located in Indianapolis, IN. * Excellent full-time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays * #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Indianapolis, IN, USA Full-time ** _Are you ready to take the next step in your career and join a company that truly values your contributions?_ _At Eurofins PSS, we offer more than just a job-we provide a rewarding, enriching, and fulfilling career path with opportunities for growth and advancement._ _As part of our team, you'll work in_ **_s_** _tate-of-the-art laboratories alongside passionate professionals dedicated to the testing, development, and advancement of life-saving drug products. Together, we're making the world a healthier and happier place to live._ _Eurofins PSS is a global leader in life sciences, delivering a unique range of analytical testing services that help ensure the safety, authenticity, and accuracy of products and their ingredients. We partner with some of the world's largest companies to make life and our environment safer, healthier, and more sustainable._ _Our people are our chemistry-and we're looking for talented individuals like you to join us in making a difference._ **Job Description** **Team Leadership & Operations** + Lead and schedule team members (small team of 5-6) in a client-based lab environment + Train employees, conduct performance reviews, and manage training records + Interview candidates and support succession planning + Foster morale, collaboration, and a positive team culture + Ensure lab operations meet high standards for quality and efficiency **Scientific & Technical Work** + Execute automated protein purifications using chromatographic techniques, TFF, and AKTA systems + Characterize protein solutions using Agilent HPLC and SDS-PAGE + Perform routine analytical measurements (pH, UV-Vis, HPLC) + Prepare buffers and solutions; maintain inventories and lab equipment + Clean and maintain AKTA systems (including CIP procedures) + Document assay data and contribute to study reports **Compliance & Documentation** + Maintain accurate records in electronic lab notebooks + Participate in investigations and ensure adherence to GLP and company policies **Qualifications** + **Bachelor's degree** in Chemistry, Biochemistry, or a related field + **+ Minimum 4 years** of industry lab experience + _OR_ + **Master's degree** in a related field + **+ Minimum 2 years** of industry lab experience + **Industry leadership experience** is required **Additional Information** + Position is full-time, 8:00 am- 5:00 pm Overtime as needed. + Position is located in Indianapolis, IN. + Excellent full-time benefits including comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays + _\#LI-EB1_ **Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**