Laboratory Technician jobs at Zoetis - 240 jobs

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.

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 - CA - Victorville U.S. Starting Hourly Wage: $19.00 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. LocationsUSA - CA - VictorvilleWorker TypeEmployeeWorker Sub-TypeRegularTime TypePart time Job Exempt No

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

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.

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.

The Laboratory Assistant Manager is responsible for the day-to-day operations of the laboratory, including staff supervision, assisting with budgeting, and placing orders for lab supplies. They develop and implement policies and procedures to ensure the safety of laboratory personnel and the quality of lab results. The Laboratory Assistant Manager also coordinates with other departments within the hospital or clinic to ensure smooth operation of the laboratory. ESSENTIAL JOB DUTIES: To oversee and manage all aspects of the laboratory, including personnel, equipment, and operations. To develop and implement policies and procedures to ensure the efficient and effective operation of the laboratory. To ensure that all laboratory personnel are properly trained and qualified to perform their duties. To maintain a safe and clean working environment in the laboratory. To monitor and control inventory levels of supplies and materials needed for the operation of the laboratory. To prepare reports on the activities of the laboratory as required by management or regulatory agencies. RESPONSIBILITIES/KNOWLEDGE/SKILLS: Supervise and coordinate the work of laboratory technicians and other staff. Plan and oversee the laboratory's budget, including purchases of equipment and supplies. Develop and implement policies and procedures for the operation of the laboratory. Ensure that the laboratory meets all applicable safety regulations. Keep abreast of new developments in the field of laboratory science and incorporate them into the lab's operations as appropriate. Train new employees in the use of lab equipment and procedures. Perform various tests and analyses using lab equipment, as needed. Prepare reports on the results of tests and analyses conducted in the laboratory Requirements QUALIFICATIONS: High School Diploma Training in formally accredited Laboratory Science Program Previous job experiences as a MLT/MLS Must be eligible for certification PHYSICAL REQUIREMENTS: Frequent mobility and/or sitting required for extended periods of time Manual dexterity and use of a calculator or computer keyboard. Varied activities including standing, walking, reaching, bending, lifting Occasionally lifts to 25 pounds Requires corrected vision and hearing to normal ranges Requires working under stressful conditions or working irregular hours Exposure to communicable diseases, toxic substances, ionization radiation, medicinal preparations, and other conditions common to a hospital and/or clinic environment

Full-time Description Compounding Pharmacy TechnicianWe are seeking a detail-oriented Compounding Pharmacy Technician to join our team. This role involves preparing customized medications, ensuring accuracy in calculations, and maintaining compliance with all regulatory standards. The ideal candidate will have: Medication & Compounding Expertise: Knowledge of prescription information, drug identification, generic equivalents, and compounding techniques. (Preferred; Training Offered) Technical & Math Skills: Proficiency in pharmacy information systems, computer operations, and precise mathematical calculations. Basic mathematics skills including adding, subtracting, multiplying, and dividing in all units of measure. Communication & Decision-Making: Strong written and verbal communication skills, with the ability to prioritize and work independently. Effective computer and keyboarding skills. Working knowledge of pharmacy information systems. Strong communication skills, both written and oral. Preferred Qualifications: Current pharmacy technician registration/certification Familiarity with pharmacy equipment and systems Join us and contribute to delivering safe, accurate, and personalized medications to our patients. Curexa is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Schedule: Monday through Friday 3:00PM-11:00PM Work Location: In person. Rate of Pay: $18.50 - $22.25 (Tier based on experience) Benefits: Vision, Dental, Medical, Supplimental, 401k, PTO & PPTO. Requirements Ability to commute: Egg Harbor Township, NJ 08234: Reliably commute or planning to relocate before starting work. Education: High school or equivalent. Must be willing to achieve Pharmacy Technician Certification via NHA,PTCB, or Curexa In-House program. As well as must achieve State Registration. Salary Description $18.50 - $22.25

Laboratory Technicianto Director Business Development-Safety & Toxicology ServicesLab TELab Title: Laboratory Technician Reports to : Laboratory Manager Perdiem Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. 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 laboratory technician performs a variety of laboratory procedures as required by the study protocol. Laboratory technicians are responsible for assisting the Laboratory Manager, Principal Investigator, Clinical Research Coordinators, and other medical professionals in the preparation and handling of specimens, analyzing results, and maintaining laboratory equipment. Laboratory Technicians ensure accuracy, quality control, and adherence to safety protocols, contributing directly to scientific research, development of new products, or medical diagnostics. Roles & Responsibilities: Performs routine laboratory procedures including specimen labeling, collection, processing, and shipping in accordance with established SOPs and/or study protocol under the supervision of the Laboratory Manager, Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. Operate and maintain laboratory equipment such as centrifuges, pipettes, and refrigerators/freezers. Develop a strong working knowledge of the study protocols and flow chart of study procedures and implement study procedures in full compliance with protocol requirements. Maintain accurate and timely documentation in laboratory or study-specific documents, temperature logs, and shipping logs. Perform environmental monitoring and equipment temperature checks to ensure proper specimen storage conditions. Assist with inventory management, restocking supplies, and maintaining organized work areas. Ensure compliance with safety, quality, and regulatory standards (GCP and internal QA procedures). Support weekend and surge workload coverage as needed based on operational demands. Assist Laboratory Manager in any task as needed. Education, Experience & Skills Required: Associate or BS in biology, chemistry, or related area, or completion and certification of Lab Technician course from an accredited or allied health training school. 1 year of experience in clinical research laboratory or related medical field. Proficiency in laboratory techniques and laboratory equipment operation. Good communication skills. Excellent organization and planning skills. 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.

We are seeking a highly motivated and experienced Per Diem Lab Technician for our growing organization! In this role, you will be responsible for performing blood and urinary sample collection and processing. Minimum Associates degree in Medical Laboratory Technician-related science from an accredited program. Minimum 2 years in a Lab Tech role, including blood draw/sample processing, comfort with computers and in-lab information systems, data entry and good people skills required. Experience with Diagnostic Lab such as LabCorp and Quest is preferred. These are per diem positions based primarily in our Fair Lawn, NJ office. We have 4 shifts available. 10% pay differential for overnight shifts. Standard pay rate in the range of $25/hour. 2 OVERNIGHTS: must commit to 1-2 overnights weekly for the next 6 months. 2 FLEXIBLE: 5:30am to 3:30pm; 7:30am to 3:30pm; 3:00pm to 11:00pm...must commit to 1-2 shifts weekly for the next 6 months.

We are seeking a highly motivated and experienced Per Diem Lab Technician for our growing organization! In this role, you will be responsible for performing blood and urinary sample collection and processing. Minimum Associates degree in Medical Laboratory Technician-related science from an accredited program. Minimum 2 years in a Lab Tech role, including blood draw/sample processing, comfort with computers and in-lab information systems, data entry and good people skills required. Experience with Diagnostic Lab such as LabCorp and Quest is preferred. These are per diem positions based primarily in our Fair Lawn, NJ office. We have 4 shifts available. 10% pay differential for overnight shifts. Standard pay rate in the range of $25/hour. 2 OVERNIGHTS: must commit to 1-2 overnights weekly for the next 6 months. 2 FLEXIBLE: 5:30am to 3:30pm; 7:30am to 3:30pm; 3:00pm to 11:00pm...must commit to 1-2 shifts weekly for the next 6 months. We are seeking a highly motivated and experienced Per Diem Lab Technician for our growing organization! In this role, you will be responsible for performing blood and urinary sample collection and processing. Minimum Associates degree in Medical Laboratory Technician-related science from an accredited program. Minimum 2 years in a Lab Tech role, including blood draw/sample processing, comfort with computers and in-lab information systems, data entry and good people skills required. Experience with Diagnostic Lab such as LabCorp and Quest is preferred. These are per diem positions based primarily in our Fair Lawn, NJ office. We have 4 shifts available. 10% pay differential for overnight shifts. Standard pay rate in the range of $25/hour. 2 OVERNIGHTS: must commit to 1-2 overnights weekly for the next 6 months. 2 FLEXIBLE: 5:30am to 3:30pm; 7:30am to 3:30pm; 3:00pm to 11:00pm...must commit to 1-2 shifts weekly for the next 6 months.

As a night-shift Assistant Laboratory Manager, or Assistant Operations Manager; at IDEXX's West Sacramento, CA location, you will be a people leader at one of the largest veterinary diagnostic companies in the world. This will be an exciting opportunity to leverage your leadership abilities to coordinate day to day lab operations - including: planning, people management, and delivering results. The focus on enhancing the lives of people and pets, starts with our own employees and empowering them to achieve their goals, focusing on continuous improvement, and supporting the strong collaboration and inclusiveness that exist in our team. You will be joining an innovative and fast-paced work environment with a strong focus on employee culture and development. This is a full-time role with competitive benefits and performance incentives. 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. Want to learn more about this position? Check out what our employees have to say! * Why Timothy Ives, Lab Supervisor, Chose IDEXX * *************************** * Development Opportunities Labs for Ashley Lemley, Labs Manager * *************************** * The Culture in IDEXX Labs with Lauren Antosia, Labs Supervisor * *************************** In This Role: * You will leverage your passion for coaching and developing leaders and employees, helping them reach business goals and their full potential. * You will organize staff schedules, coordinate workflow, and oversee costs and metrics. * You will problem-solve every day, from trouble-shooting diagnostic analyzers to resolving situational workflow and turnaround time challenges. * You will be a business leader and a people leader for the lab and the line of business. * You will bring your passion and enthusiasm for teamwork, success, innovation, and excellence to your role, every day. What You Will Need to Succeed: * At minimum, you've directly supervised 1-5+ Supervisors and / or 20-30+ employees in a high-volume work environment. * You have experience managing the day to day operations of a clinical diagnostic laboratory, fast-paced production environment, or other operations management experience * You are an inspiring, motivating People Leader with experience directly supervising individual contributors and / or Leadership teams * While not required, experience in a lab setting is a plus, as well as knowledge of human clinical or veterinary testing and procedures. * You love a fast-paced, high - volume, innovative work environment. * You are passionate about people leadership. * You are excited about the opportunity to use your skills and abilities in promoting the health and well-being of animals. * 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. What You Can Expect From Us: * Salary rate targeting $100,000/yr based on experience * Opportunity for annual cash bonus * Opportunity for performance based annual merit increase * Health / Dental / Vision Benefits Day - One * 5% matching 401k * On the job training and career advancement opportunities * Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more! Schedule: * This will be a full-time (40 hr/wk), third shift (night-shift) position with hours Tuesday - Saturday 12:00am - 8:30am * The hours may vary depending on business needs. 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 night-shift Assistant Laboratory Manager position will be based out of our West Sacramento, CA location. Does this sound like the opportunity for you? Apply today! #LI-SM1

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. We are seeking a Bioanalytical Laboratory Technician (PBMC) to join our team. This is an exciting opportunity to work on innovative projects, supporting critical processes within a clinical lab setting. This is a full-time role, working onsite in Lincoln, NE. We are seeking candidates who are local to the Lincoln area. About the Role: As a Bioanalytical Laboratory Technician, you'll play a crucial role in ensuring quality and compliance in our lab operations. Your expertise in sterile working, PBMC isolation techniques, and cell counting will directly contribute to our projects' success. We are committed to maintaining high standards in line with regulatory requirements and Celerion SOPs. We are looking for someone who values precision and integrity in their work.What You'll Do: Maintain contamination-free processes through sterile techniques. Perform PBMC isolation techniques and cell counting to support various analyses. Adhere to regulatory standards and SOPs, ensuring compliance across all tasks. Accurately document all lab activities and results, supporting traceability and quality control. Collaborate with cross-functional teams to meet project timelines and objectives. Cover occasional shift work to meet laboratory and project demands. Who You Are: Experienced in sterile laboratory environments. Experienced with pipetting and working in a biosafety cabinet. Able to learn regulatory standards for a CAP/CLIA, GMP, GLP, or GCP setting. Detail-oriented, with a commitment to maintaining the highest standards of laboratory quality and compliance. Able to work Monday - Friday, during normal business hours and flexible to cover occasional evening or weekend shifts as needed. This could include possible overtime opportunities. Possess a learning mindset and a curiosity for science. Strong organizational and multitasking skills. Preferred Qualifications: Two or Four-year degree in Biological Sciences, Biology, Forensics, or a related field. Familiarity with laboratory information management systems (LIMS). Experience with PBMC isolation and cell counting. What We Offer: Competitive salary and benefits package Growth opportunities in a dynamic laboratory environment Ongoing professional development and training Celerion Values: Integrity Trust Teamwork Respect Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability. Celerion Values: Integrity Trust Teamwork Respect Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Do you have basic knowledge of Chromatography or Ligand-Binding techniques and laboratory experience? If so, this could be the position for you! This is a great opportunity to put your skills to work in clinical research. Our Lincoln, NE location is hiring multiple Lab Technicians / Bioanalytical Associate Analysts to join our team. These roles are Full-time, benefited positions. Salary starts at $19 per hour and is commensurate with experience, with opportunities for an increase at 6 months with successful performance and attendance. This role will begin Jan 26, 2026. We are only considering candidates who currently live in the Lincoln, NE area. Responsibilities:Process/extract biological samples (blood, urine, plasma, feces) both manually and using automation Prepare solutions/reagents Record and document test data in notebooks/binders/electronic notebooks Perform analytical analysis of samples using chromatography (LC-MS/MS and HPLC) or ligand-binding techniques (ELISA, RIA, EIA and PCR) Qualifications: Associate's degree, Bachelor's degree or previous coursework in Microbiology, Chemistry, Biochemistry, Biology or a related field is preferred Exposure to pipetting; will pipet an average of 2-3 hours per day, at times up to 8 hours Experience with GLP's is a plus Basic computer skills; able to read and enter information via computer 50% of the shift Strong attention to detail and self-motivation Shift: Monday - Friday daily, during normal business hours, 8am-5pm, with some flexibility Due to the highly variable nature of our business, we ask you to be available for at least 1 weekend day in a four week period, and when workload allows ability to commit to at least 10% hours above your minimum Celerion Values: Integrity Trust Teamwork Respect Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Do you have a basic understanding of Chromatography or Ligand-Binding techniques and laboratory experience? If so, this could be the position for you! This is a great part-time opportunity to put your skills to work in clinical research and grow your career. Our Lincoln, NE location is seeking a part-time Lab Technician / Associate Analyst to join our team. This role is a part-time, non-benefited position. The starting wage is $19/ hr, with potential increases over time with successful performance. You will work between 20-25 hours per week. Responsibilities:Process/extract biological samples (blood, urine, plasma, feces) both manually and using automation Prepare solutions/reagents Record and document test data in notebooks/binders/electronic notebooks Perform analytical analysis of samples using chromatography (LC-MS/MS and HPLC) or ligand-binding techniques (ELISA, RIA, EIA and PCR) Qualifications: Associate's degree, Bachelor's degree or 2 years of previous coursework in Microbiology, Chemistry, Biochemistry, Biology or a related field Strong exposure to pipetting; will pipette an average of 2-3 hours per day, at times up to 8 hours Experience with GLPs is a plus Basic computer skills; able to read and enter information via computer 50% of the shift Strong attention to detail and self-motivation Shift: Work 3 days per week, 8 hours a day, beginning work between 7am and 10am Days of the week can be selected based on your preference; days should be consistent Ability to work an occasional extra shift, when needed Celerion Values: Integrity Trust Teamwork Respect Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

Job DescriptionDescription: Compounding Pharmacy TechnicianWe are seeking a detail-oriented Compounding Pharmacy Technician to join our team. This role involves preparing customized medications, ensuring accuracy in calculations, and maintaining compliance with all regulatory standards. The ideal candidate will have: Medication & Compounding Expertise: Knowledge of prescription information, drug identification, generic equivalents, and compounding techniques. (Preferred; Training Offered) Technical & Math Skills: Proficiency in pharmacy information systems, computer operations, and precise mathematical calculations. Basic mathematics skills including adding, subtracting, multiplying, and dividing in all units of measure. Communication & Decision-Making: Strong written and verbal communication skills, with the ability to prioritize and work independently. Effective computer and keyboarding skills. Working knowledge of pharmacy information systems. Strong communication skills, both written and oral. Preferred Qualifications: Current pharmacy technician registration/certification Familiarity with pharmacy equipment and systems Join us and contribute to delivering safe, accurate, and personalized medications to our patients. Curexa is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Schedule: Monday through Friday 3:00PM-11:00PM Work Location: In person. Rate of Pay: $18.50 - $22.25 (Tier based on experience) Benefits: Vision, Dental, Medical, Supplimental, 401k, PTO & PPTO. Requirements: Ability to commute: Egg Harbor Township, NJ 08234: Reliably commute or planning to relocate before starting work. Education: High school or equivalent. Must be willing to achieve Pharmacy Technician Certification via NHA,PTCB, or Curexa In-House program. As well as must achieve State Registration.

The Interventional /Cath Lab Scrub technologist specializes in assisting with invasive cardiac procedures and other procedures performed in the Cardiac Cath and Interventional Radiology Labs. The Scrub Tech is a professional caregiver who assumes responsibility and accountability for patients, under the direction of the Interventional Radiologist and /or Interventional Cardiologist, for a designated time frame and provides care to these patients. Performs other related duties incidental to the work described herein. The Cath Tech is a registered or eligible professional primarily specializing in the utilization of cardiovascular ultrasound equipment necessary to find arteries, and performs interventional cardiology examinations under the supervision of cardiologists and radiologists. Qualifications/Experience Education: An associate degree in Radiology Technology from an accredited program in required. Experience: Previous experience in Cath Lab preferred. Certifications: Current ARRT certification in Radiology Technology is require RCIS certification desirable Basic Life Support (BLS) certification required. Advanced Cardiac Life Support Certification preferred. Essential Job Functions To perform this job successfully, an individual must be able to perform each of the following Essential Duties satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the Essential Duties of the position, provided it does not create undue hardship on SARH. Uphold and demonstrate “We Care” values in everyday activities and behavior Interacts in a professional manner with internal and external customers. Adhere to all SARH infection control standards and practices. Identify, report, and respond to all safety hazards appropriately and by SARH standard practices. Assist Physician with Cath Lab procedures based on department-specific competency. Report all concerns to Cath Lab Coordinator in a timely manner. Maintain department and procedural supplies with a goal of reducing waste, using items before expiration, and always having the correct supplies available prior to procedure start. Assist Cath Lab Coordinator in documentation, data capture, and all department-specific performance improvement initiatives. Observes professional ethic in maintaining confidential information. Participation in regulatory survey compliance and preparation. Performs other duties as assigned or requested. This job description is a summary of the typical functions of the job, not an exhaustive or comprehensive list of all the possible job responsibilities, tasks, and duties you may be asked to perform when they are assigned. 

The Interventional /Cath Lab Scrub technologist specializes in assisting with invasive cardiac procedures and other procedures performed in the Cardiac Cath and Interventional Radiology Labs. The Scrub Tech is a professional caregiver who assumes responsibility and accountability for patients, under the direction of the Interventional Radiologist and /or Interventional Cardiologist, for a designated time frame and provides care to these patients. Performs other related duties incidental to the work described herein. The Cath Tech is a registered or eligible professional primarily specializing in the utilization of cardiovascular ultrasound equipment necessary to find arteries, and performs interventional cardiology examinations under the supervision of cardiologists and radiologists. Qualifications/Experience Education: An associate degree in Radiology Technology from an accredited program in required. Experience: Previous experience in Cath Lab preferred. Certifications: Current ARRT certification in Radiology Technology is require RCIS certification desirable Basic Life Support (BLS) certification required. Advanced Cardiac Life Support Certification preferred. Essential Job Functions To perform this job successfully, an individual must be able to perform each of the following Essential Duties satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the Essential Duties of the position, provided it does not create undue hardship on SARH. Uphold and demonstrate “We Care” values in everyday activities and behavior Interacts in a professional manner with internal and external customers. Adhere to all SARH infection control standards and practices. Identify, report, and respond to all safety hazards appropriately and by SARH standard practices. Assist Physician with Cath Lab procedures based on department-specific competency. Report all concerns to Cath Lab Coordinator in a timely manner. Maintain department and procedural supplies with a goal of reducing waste, using items before expiration, and always having the correct supplies available prior to procedure start. Assist Cath Lab Coordinator in documentation, data capture, and all department-specific performance improvement initiatives. Observes professional ethic in maintaining confidential information. Participation in regulatory survey compliance and preparation. Performs other duties as assigned or requested. This job description is a summary of the typical functions of the job, not an exhaustive or comprehensive list of all the possible job responsibilities, tasks, and duties you may be asked to perform when they are assigned.