Laboratory Assistant jobs at Zoetis - 120 jobs

Shift: 2am-1030am Lab Accessioner 1 The Laboratory Accessioner helps prepare samples and supports lab operations as requested. The Accessioner is responsible for receiving, labeling, and preparing specimens for laboratory testing while ensuring adherence to standard operating procedures, safety protocols, and quality control guidelines. Job Duties: Accountable for understanding and following the laboratory's standard operating protocols, quality control processes, and safety rules. Receives and accessions specimens into the Laboratory Information Management System. Unpacks specimens and routes specimens by type to various staging areas. Prepares all specimens received for testing in designated laboratory departments or locations such as staging of specimens, centrifuge, etc. Prepares excess specimen samples for storage and resolves and documents problem specimens. Organizes work by matching computer orders with specimen labeling, sorting specimens, checking labeling, logging specimens and arranging reports for delivery. Accountable for keeping work surfaces clean and orderly. Participates in all applicable safety training sessions to ensure thorough understanding and execution of safety procedures, including the use of all applicable safety equipment. Organizes and maintains lab specimen storage. Organizes and monitors lab supplies for appropriate inventory levels. ·Perform other duties as directed by supervisor. Education/Experience: · HS Diploma or GED equivalent required · 1-2 years of experience in data entry preferred · Medical background or experience with laboratory testing terminology or a strong aptitude to learn terminology preferred Technical Skills Required: · Proficiency in Microsoft Platforms (Teams, Outlook, Word etc.) · Detail oriented, flexible, quick to learn · Proficient in data entry · Organizational abilities · Able to work productively, effectively, and independently in a fast-paced environment · Ability to handle multiple tasks systems · Effective verbal and written communications, especially listening skills · Detailed orientated with regards to data entry and excellent typing skills · Strong computer skills and ability to work within windows environment · Must be comfortable in a fast-paced environment with target productivity rates 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 · Ability to use tools such as boxcutters · Ability to wear PPE for extended periods of time 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.

A leading global pharmaceutical company is seeking an experienced individual to join their Global Oncology Medical Affairs team in New Jersey. This role is responsible for shaping the Companion Diagnostics (CDx) strategy and ensuring alignment with medical affairs and precision medicine initiatives. Candidates must possess an MD, PharmD, DO, PhD, or another doctorate alongside a minimum of 10 years in the pharmaceutical industry, with demonstrated leadership in multidisciplinary teams. The position includes competitive compensation and potential for growth in a dynamic environment. #J-18808-Ljbffr

The Associate Analytical Technician supports manufacturing operations by performing laboratory analyses, maintaining analytical systems, and ensuring data integrity. This role is ideal for individuals who are detail-oriented, safety-conscious, and eager to grow in a technical laboratory environment. Key Responsibilities: Train under senior team members to perform routine analyses until proficiency is demonstrated. Collect samples in accordance with the Sample Plan and standard operating procedures. Conduct laboratory analyses to support plant operations and product quality. Evaluate the validity of routine analytical data and take appropriate corrective actions. Monitor analytical systems and escalate issues as needed. Perform basic preventive maintenance and calibration of laboratory instruments. Implement and qualify new analytical equipment and methods. Document, communicate, and archive analytical results and data accurately. Follow Environmental Health & Safety (EH&S) and Operating Discipline Management System (ODMS) procedures. Suggest improvements to laboratory processes, tools, and workflows. Maintain lab cleanliness and inventory through regular housekeeping tasks. Escalate non-routine requests or issues to appropriate team members. Preferred Skills & Qualifications: Understanding of analytical/scientific methods and laboratory best practices. Ability to troubleshoot and adapt to non-routine lab analyses. Familiarity with data systems and statistical evaluation tools. Strong attention to detail and commitment to safety and quality. Effective communication and collaboration skills. Schedule: This Lab Tech position is on a Rotating shift schedule but you will have different hours during training. This position will follow a rotating shift schedule with AM and PM shifts switching every two weeks.

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 Technician I for our Molecular Imaging Team located in Mattawan, MI. A Technician I is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. The pay range for this position is $20.00 to $21.50/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. **Job Qualifications** The following are minimum requirements related to the Technician I position: + Minimum: High School Diploma or GED + Experience: minimum of 1 year of work exerience preferred + Ability to communicate verbally and in writing at all levels inside and outside the organization. + Basic familiarity with Microsoft Office Suite. + Computer skills, commensurate with Essential Functions, including the ability to learn a validated system. + 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 **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 *************** 231424

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 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.**

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.**

Who We Are: Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico's highly innovative technology labs, its commitment to curiosity-driven discovery science and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs. Position Description: We are seeking a Colony Lead to work in a dynamic team environment, reporting to our Vivarium Manager in the Laboratory Animal Resources (LAR) Core. We are seeking a self-motivated individual who is detail-oriented, highly organized, flexible in a fast-paced environment with shifting priorities, capable of adopting new technologies, and has great time-management skills. The person will be responsible for the management of breeding colonies, veterinary care, study support, and assisting with the training program. Responsibilities: * Veterinary Care * Make recommendations as the Attending Veterinarian (AV) designee and perform clinical health assessments and treatments as described in SOPs and IACUC protocols * Observe health conditions of animals, recognize and report common signs of clinical illness and/or irregularities in animal behavior * Make recommendations on treatment based on established health protocols and approved protocols * Surgical or post-procedural observations and support for research staff * Aging colony observations and care under the direction of the AV * Execute colony health surveillance under the direction of the AV * Execute rodent quarantine program in collaboration with the VM and AV * Maintain colony health surveillance, quarantine, and environmental testing results * Breeding Colony Support * Assist in the maintenance of rodent colonies at the direction of Principal Investigator and Core labs * Record keeping: Maintain accurate breeding and health records database * Genotyping: Facilitate sample collection, submission, and processing with external vendors * Perform breeding colony tasks including, but not limited to, setting up matings, sexing, weaning and identification of mice; daily health/pregnancy checks, daily facility checks, cage changes, and sanitation * Provide rotational weekend/holiday coverage as needed * GEMS Procurement & Receiving * Coordinate and receive animal shipments from external GEMs lines, including management of colony data, confirmatory genotyping, and follow up on concerns/discrepancies * In-Vivo Study Support * Assist scientists and Core labs with their projects, which may include independently executing study support, assisting during technical procedures, clinical evaluations or behavioral assessments, performing necropsies or tissue collection, at the direction of research lab or AV * May perform dosing, blood collection, body weight collection in support of research projects * Document experimental data in technical notebooks or approved electronic files including activities undertaken, existing conditions, observed results and variation from expected data patterns * Training * Coordinate LAR team training events and update training records * Train husbandry and/or scientific staff in basic breeding techniques (sexing, weaning, genotyping, synched peak setups, pregnancy/plug checks), and in-vivo technical procedures related to genotyping and animal identification * Train husbandry staff on techniques related to colony health surveillance, weaning and sexing * May provide colony management software training to research staff * SOP & Protocols * Review or assist in the revision of SOPs and IACUC protocols * Perform all other related duties as assigned Position Requirements: * Bachelor's (B.S) or equivalent in animal or life science or related discipline * Minimum of 2 years of experience in the care, handling, and treatment of laboratory animals, including broad skills in husbandry and record-keeping * Experience in rodent colony health, clinical assessment, and veterinary interventions * Experience in the handling, management, and/or breeding of traditional and transgenic rodents * AALAS LAT certification or higher preferred * Attention to detail and accuracy in documentation * Strong written and verbal communication skills * Proficient with Google Suite, MS Suite, MacOS, PC Windows, and colony management software * Effectively collaborate with key support groups, core labs, and PI labs * Must be willing to work onsite 5 days a week The estimated base salary range for this role is $115,000 - $120,000. Actual pay will be based on a number of factors including experience and qualifications. This position is also eligible for two annual cash bonuses.

Information about Eurofins as a whole: * Over 50,000 employees worldwide * Eurofins recently celebrated 30 years of excellence in bioanalytical testing. * The company has grown from 4 employees in a small lab in France to a global network. * 800 state-of-the-art laboratories across 41 countries. * Eurofins is one of the best performing companies in the world. In three decades, the company has grown more than 3,000 times. * Eurofins is now the global market leader in environmental, food, pharmaceuticals and cosmetics testing as well as in agro-sciences CRO (Contract Research Organization) services. Job Description On Call/Flex Laboratory Assistant - flexible hours: evenings, weekends 1. Understand and follow Quality System documents relevant to responsibilities, e.g., Quality Manual, SOPs, Methods, and Local Policies. 2. Adhere to appropriate quality measures, which meet or exceed the standards set by ISO/IEC 17025, government regulatory, and company requirements. 3. Follow all company guidelines and procedures relevant to assigned duties. 4. Adhere to all pertinent health, safety, and environmental regulations. 5. Assist in the daily assaying of samples. Perform testing from a daily work list. 6. Set up batches of samples to weigh and weigh samples. 7. Identify from samples assayed the need for rechecks. 8. Prepare solutions used in the daily testing of designated samples. 9. Maintain a neat and accurate record system; keep accurate records of work performed on a daily basis or as needed for quality control tests or regulatory purposes. 10. Record test data and results for samples in logbook, record book or BookMaster and enter the data or results into eLIMS either manually or through automatic export in a timely and accurate manner. 11. Maintain a safe and clean laboratory; clean work area and glassware used in analyses, dispose of hazardous wastes according to established procedures; assist others in maintaining a clean, safe work environment. 12. Identify method/matrix/analytical difficulties and report these together with proposed solutions to supervisor. 13. Ensure that proprietary methodologies are not disclosed to non-employees except as approved in writing by the Laboratory Manager or appointed designate. 14. Maintain a perpetual state of readiness and willingness to respond to the queries and needs of clients, staff, and co-workers. 15. Remain current on technical, industry, and business advancements and trends as suggested by Department Leader or supervisor. 16. Recommend more accurate or efficient laboratory equipment or procedures. 17. Maintain cooperative working relationships with all company employees. Communicate orally and in writing to co-workers. This includes "intra" and "inter" departmental employees. 18. Promote the company image through the exercising of sound and ethical business practices as related to the public and our customers. 19. Other duties, as assigned. Qualifications Excellent interpersonal, organizational, and analytical skills. Excellent communication skills. Responsive, independent problem solver and action oriented Initial Education Background Basic understanding of ISO 17025 guidelines. High School diploma with 0-3 years experience. Additional Information Candidates currently living within a commutable distance of Des Moines, IA 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee is required to stand; walk; and use hands to find, handle, and feel objects, tools, or controls, and some repetitive motion. The employee is occasionally required to reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and distance vision. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Des Moines, IA, USA Part-time ** **Information about Eurofins as a whole:** + Over 50,000 employees worldwide + Eurofins recently celebrated 30 years of excellence in bioanalytical testing. + The company has grown from 4 employees in a small lab in France to a global network. + 800 state-of-the-art laboratories across 41 countries. + Eurofins is one of the best performing companies in the world. In three decades, the company has grown more than 3,000 times. + Eurofins is now the global market leader in environmental, food, pharmaceuticals and cosmetics testing as well as in agro-sciences CRO (Contract Research Organization) services. **Job Description** On Call/Flex Laboratory Assistant - flexible hours: evenings, weekends 1. Understand and follow Quality System documents relevant to responsibilities, e.g., Quality Manual, SOPs, Methods, and Local Policies. 2. Adhere to appropriate quality measures, which meet or exceed the standards set by ISO/IEC 17025, government regulatory, and company requirements. 3. Follow all company guidelines and procedures relevant to assigned duties. 4. Adhere to all pertinent health, safety, and environmental regulations. 5. Assist in the daily assaying of samples. Perform testing from a daily work list. 6. Set up batches of samples to weigh and weigh samples. 7. Identify from samples assayed the need for rechecks. 8. Prepare solutions used in the daily testing of designated samples. 9. Maintain a neat and accurate record system; keep accurate records of work performed on a daily basis or as needed for quality control tests or regulatory purposes. 10. Record test data and results for samples in logbook, record book or BookMaster and enter the data or results into eLIMS either manually or through automatic export in a timely and accurate manner. 11. Maintain a safe and clean laboratory; clean work area and glassware used in analyses, dispose of hazardous wastes according to established procedures; assist others in maintaining a clean, safe work environment. 12. Identify method/matrix/analytical difficulties and report these together with proposed solutions to supervisor. 13. Ensure that proprietary methodologies are not disclosed to non-employees except as approved in writing by the Laboratory Manager or appointed designate. 14. Maintain a perpetual state of readiness and willingness to respond to the queries and needs of clients, staff, and co-workers. 15. Remain current on technical, industry, and business advancements and trends as suggested by Department Leader or supervisor. 16. Recommend more accurate or efficient laboratory equipment or procedures. 17. Maintain cooperative working relationships with all company employees. Communicate orally and in writing to co-workers. This includes "intra" and "inter" departmental employees. 18. Promote the company image through the exercising of sound and ethical business practices as related to the public and our customers. 19. Other duties, as assigned. **Qualifications** Excellent interpersonal, organizational, and analytical skills. Excellent communication skills. Responsive, independent problem solver and action oriented **Initial Education Background** Basic understanding of ISO 17025 guidelines. High School diploma with 0-3 years experience. **Additional Information** Candidates currently living within a commutable distance of Des Moines, IA 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.** **Physical Demands:** The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee is required to stand; walk; and use hands to find, handle, and feel objects, tools, or controls, and some repetitive motion. The employee is occasionally required to reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and distance vision. **Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.**

100% on-site The Laboratory Intern provides introductory exposure to the overall function of a commercial laboratory through partnerships with laboratory chemists in the execution of daily laboratory testing and tasks Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. The role: Maintain data integrity and employs good documentation practices when performing experiments Compare laboratory data against specifications where applicable to determine if results meet requirements Ensure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentation Ensure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigations Enter data into established reports/templates or software-based systems Adhere to assignments and execute under the guidance of a mentor The candidate: High school diploma or equivalent Current or recent enrollment in an undergraduate or graduate degree program in Biology, Chemistry, Biochemistry, Biotechnology, or related discipline Must be located within 50 miles of the Greenville, North Carolina, site to be considered Why you should join Catalent: Competitive medical benefits and 401K 152 hours PTO + 8 Paid Holidays Dynamic, fast-paced work environment Opportunity to work on Continuous Improvement Processes Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

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.

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.

What you will do Johnson Controls is seeking an HVAC Test Lab Supervisor (1st Shift) to oversee daily operations within our state-of-the-art Engineering Test Lab in New Freedom, PA. In this role, you will lead a union team of 40+ employees, ensuring that all activities are carried out in alignment with company policies, applicable laws, and the union contract. Key responsibilities include supervising staff, planning and assigning work and ensuring new employees have completed onboarding and are properly trained. This is an onsite position, and candidates must either live within commuting distance to New Freedom, PA, or be willing to relocate. How you will do it Supervise the daily operation of key test lab areas balancing the needs of the customers with the available resources. Assists to manage the day-to-day operations, including labor reporting and transactions, maintenance program, 5S and organization and union issues that might arise. Address employee performance and corrective action plans; employee motivation and rewards. Support Health & Safety through participation in Joint Health Safety Committee, weekly safety training, completion of safety audits, and Safety Action Reports. Maintain maintenance and project list to support effective allocation of resources to include assembler, welder, and electrician work. Facilitate the loading/unloading of Industrial HVAC equipment with crane service and lift plan. Ensure the accuracy of timekeeping and production management systems that include LODIS, MRP, and Kronos systems across all 3 shifts. Maintain refrigerant, oil, propane (liquid and vapor), oxygen, acetylene and nitrogen tracking logs each month and order as needed to support testing requirements. Ability to work 1st or 2nd shift schedule as needed to support the business. Hours will be 7:00am - 4:30pm Monday - Friday. Adheres to the Company's Code of Conduct and Business Ethics standards. What we look for Required Bachelor's degree or equivalent combination of education and experience. 6 years experience in management within a manufacturing environment within a union. Continuous improvement Perform their duties in a Union shop environment. Strong people management & communication skills. Excellent computer and data analysis/management skills with proficiency in Microsoft Suite Applications (Word, Excel, Access, and PowerPoint) as well as internet software and e-mail Preferred Bachelor's degree Financial and analytical skills HVAC industry experience HIRING SALARY RANGE: $95,000 - $120,000 (Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, location and alignment with market data.) This position includes a competitive benefits package. For details, please visit the About Us tab on the Johnson Controls Careers site at ***************************************** Johnson Controls International plc. is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, genetic information, sexual orientation, gender identity, status as a qualified individual with a disability or any other characteristic protected by law. To view more information about your equal opportunity and non-discrimination rights as a candidate, visit EEO is the Law. If you are an individual with a disability and you require an accommodation during the application process, please visit here.

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** **Laboratory Supervisor** **responsibilities include, but are not limited to, the following** **:** To supervise and oversee the general operation including testing and reporting of results for the US laboratory including the areas of Chemistry, Hematology, Molecular, Microbiology, Special Chemistry, and Virology testing. Leads the training and technical oversight of staff in quality, service, fiscal productivity and customer/employee satisfaction goals and objectives. + Ensure samples are tested and results reported within expected turn around time. + Functions as the technical expert, performing and maintaining proficiency for procedures and equipment within the section. + Review clinical protocols and lead the development of lab protocols for studies and provide technical guidance to Eurofins Project Management group as well as sponsors as needed. + Works with SME and Team leads to ensure UATs are written and executed for new instrumentation and software. + Oversees writing and execution of new instrument and test validations with the assistance of SMEs and leads. + Troubleshooting and resolving technical and equipment problems. + Plans daily work schedule and assignments for sections ensuring that work is done and reported promptly and accurately; preparing schedules and arranging coverage. + Perform reporting tasks to ensure timely release of validated test results. + Performs review of monthly maintenance and ensures proper documentation. + Recognizes the need for and assumes daily departmental responsibilities, in the case of staffing shortages. + Establishes and monitors preventive maintenance and quality control procedures for all equipment and methods, documenting review as required. + Completes all proficiency testing in the allotted time, reviewing results, taking corrective action and documenting review. + Writes and reviews general and technical laboratory SOPs. + Assists Management in the investigation of quality investigations (CAPAs), both internal and external. + Ensures that time and attendance for subordinates meet departmental expectations. Monitors and approves payroll. + Interviews candidates for technical positions. + Supervises the orientation and training of new personnel. Conducts performance appraisals in a timely manner and documents above or below standard performance, providing supporting documentation. + Makes suggestions for improved work methods and ways to increase efficiency, reduce costs, and solve operational problems. + Understands and follows company policies and procedures. + Works with other departments to plan for and accomplish organizational goals and objectives, and development and execution of organizational projects + Other activities as assigned **Qualifications** **Basic Minimum Education Qualifications** **:** + Associate degree in a laboratory science or medical technology or equivalent education and training with **minimum 6 years** of training and/or experience in high complexity testing + Doctoral degree in chemical, physical, biological or clinical laboratory science from an accredited institution with **minimum 1 year** of laboratory training and/or experience in high complexity testing; OR + Master's degree in a chemical, physical, biological, or clinical laboratory science or medical technology from an accredited institution with **minimum 2 years** of laboratory training and/or experience in high complexity testing; OR + Bachelor's degree in a chemical, physical, or biological science or medical technology from an accredited institution with **minimum 4 years** of laboratory training and/or experience in high complexity testing. AND + **Certification by ASCP, NCA, or AMT REQUIRED.** **Basic Minimum Qualifications** **:** + Minimum 6 years working in a diagnostic, clinical laboratory working with modern automation + Prior managerial experience preferred, but not required + Hematology experince in a clinicla laboraotyr epereince preferred, but not required. + Proficient usage of a commercial grade or customized clinical LIMS + Prolonged usage of analytical and computer systems (>75% time). + Ability to lift up to 20 lbs from time to time + Capable of identifying problems, root causes and solutions, documenting deviations and notifying superiors. + Proficient use of Microsoft Office tools and Ep Evaluator. + Proficient in good laboratory and documentation practices. + Authorization to work in the United States indefinitely without restriction or sponsorship. **The Ideal Candidate Possesses the Following:** + Fluent in English. + Commits to perform work and to behave according to the agreements established in SOPs, within the overall quality system and, where applicable, the specific applicable quality system. + Ability to set concrete goals, taking into account the common interest, does everything to achieve the primary study objectives. + Ability to set and follow priorities, working accurately following set procedures and under deadlines. + Focused on improvement and optimization of processes within the laboratory. + Shows detailed knowledge and skills with regard to the work, keeps up to date and increases professional knowledge, keeping abreast of the latest developments. + Good interpersonal skills **Additional Information** Position is **full-time working Monday - Friday 2:00pm - 10:30 PM, alternating Saturdays** . 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.**

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.

A lab technician works in a laboratory setting and works in various capacities to fulfill required duties. This includes diagnostic testing on bodily fluids, organic matter, and chemicals. They use high-specialized equipment to measure and report their findings. Collects samples and safely store biomedical materials and tools. ESSENTIAL JOB DUTIES: Receives specimens from doctors, laboratories, hospitals, or directly from patients, and performs complex quantitative and qualitative analyses to provide information for use in the diagnosis Documents all quality control and maintains required records Troubleshoot any or all automatic, semi-automatic, or manual equipment within the laboratory and ensure it is in working order Performs Quality Control and maintenance procedures as required Interacts with and/or performs clinical laboratory procedures on patients of all ages RESPONSIBILITIES/KNOWLEDGE/SKILLS: Perform quality control tests in the lab as well as on-site when necessary Assist with testing and calibrating lab equipment in preparation for specific tasks Perform quality control tests on ingredients, completed products and product samples Prepare samples prior to shipping them to outside vendors Follows all company policies and procedures to ensure product integrity and quality control Obtains specimens from clinical laboratory examination directly from any patient of any age, including infants Near visual acuity is required to read detailed instructions and to examine specimens Analyze retrieved data and prepare reports for laboratory manager Perform any other duties that may be necessary for the operation of the corporation and/or hospital Requirements QUALIFICATIONS: High school diploma Associate degree required (Bachelor's degree preferred) Five plus years laboratory experience Ability to communicate effectively PHYSICAL REQUIREMENTS: Varied activities including standing, walking, reaching, bending, lifting. Requires full range of body motion including handling and lifting patient's manual and finger dexterity and eye hand coordination. Requires standing and walking for extensive periods of time Occasionally lifts and carries items weighing up to 50 pounds. Requires corrected vision and hearing to normal ranges Requires working under stressful conditions or working irregular hours Exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a hospital and/or clinic environment

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice (************************************** and Terms of Use (********************************************* . I further attest that all information I submit in my employment application is true to the best of my knowledge. **Job Description** **Please take this** **virtual tour** **to get a sneak peek of one of our Plasma Donation Centers.** About the role: Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a plasma donor screener and perform phlebotomy to support plasma center operations. How you will contribute: · You will answer phones, and greet and focus on our donors, while ensuring the safety of donors and our team. · You will screen new and repeat donors and take and record donor vital signs and finger stick results. · You will use our Donor Information System, prepare donor charts, maintain accurate records, and coordinate donor compensation. · You will help identify operational opportunities for continuous improvement and initiate changes to center processes using company approved procedures. · You will be there for our donors, which includes working a variety of shifts, Saturdays and Sundays, and holidays. What you bring to Takeda: · High school diploma or equivalent · Ability to walk and/or stand for the entire work shift · Will work evenings, weekends, and holidays · Ability to lean, bend, stoop, crouch, and reach above shoulders and below knees · Ability to lift to 5 lbs., and occasional lifting of materials up to 32 lbs. and rarely 50 lbs. · Fine motor coordination, depth perception, and ability to hear equipment from a distance · Because of potential exposure to bloodborne pathogens (risk level 1), 90% of work tasks require prolonged glove wear · 1 or more years minimum experience working in a customer or patient facing role is helpful What Takeda can offer you: Every day at Takeda, we feel good knowing that what we do helps improve the lives of patients with rare diseases. At BioLife, while you focus on our donors, we will support you. We offer a purpose you can believe in, a team you can count on, opportunities for career growth, and a comprehensive benefits program to include retirement benefits, medical/dental, family leave, disability insurance and more, all in a fast-paced, friendly environment. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to provide Better Health and a Brighter Future to people around the world. **BioLife Compensation and Benefits Summary** We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. **For Location:** USA - GA - Snellville **U.S. Starting Hourly Wage:** $16.00 The starting hourly wage reflects the actual starting rate for this position. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. **EEO Statement** _Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law._ **Locations** USA - GA - Snellville **Worker Type** Employee **Worker Sub-Type** Regular **Time Type** Part time **Job Exempt** No

Laboratory Associate II Per Diem PCR Department Louisville, KY As a Per Diem Laboratory Associate at IDEXX, you will be a key contributor at one of the largest veterinary diagnostic companies in the world. You will perform laboratory testing that helps veterinarians diagnose and treat pets. You will join a fast-paced work environment that encourages teamwork, quality, and offers opportunities for personal growth. This is a per diem, as-needed position. IDEXX reference laboratories is a global network united by a shared commitment to enhancing pet care where the true strength in our name is the people behind it. Our reference laboratories make it possible for our customers to discover more with our unrelenting commitment to innovation, personalized support, guidance, and expertise, while providing the most complete and advanced menu of diagnostic tests along with technology and tools. In this Role: You will be using automated analyzers, microscopes, and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries, and diseases in support of veterinarian animal treatment. You will be performing diagnostic tests on blood, urine, fecal, or pet biopsy samples that we receive in our lab by the thousands, every day. You will be responsible for setting up and running lab tests and reading and releasing results according to SOPs (Standard Operating Procedures). What You'll Need To Succeed: Ideally, you will have experience working in a laboratory. Experience setting up, running and reading lab test and operating laboratory equipment (microscopes and / or clinical diagnostic analyzers) would be a plus. You have a positive attitude and love to bring that energy into the lab every day to support your colleagues You are looking forward to working in a team You concentrate on the details and can work reliably and precisely You have a great sense of team spirit and responsibility You possess a High School diploma or equivalent combination of education and experience is required. A 2-, 3- or 4-year degree in a Science-related field is preferred. It is not required to work in our lab, but if you were a Veterinary Technician (RVT, LVT, CVT) or Medical Laboratory Technician (MLT or MT), this experience and education would be a plus. Able to meet the physical requirements that go with working in a lab - standing and sitting for extended periods of time, phone & computer use, extended reach, lifting up to 50lb, and specific vision ability - close, color, depth perception, and ability to adjust focus. This is a laboratory, so there is potential exposure to biohazards, agents known to cause zoonotic diseases, and hazardous chemicals. Schedule: This is a Per Diem position, scheduling will be done on an as-needed basis. Hours and schedule are not a guarantee and are based on the staffing needs of the lab The shifts and hours may vary slightly depending on business needs. Reliable and dependable attendance is an essential function of the position. Why IDEXX? We're proud of the work we do, because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. This position will be based out of our LOUISVILLE, KY location. Does this sound like the opportunity for you? Apply today!