Technician I - Clinical Pathology, 1st Shift

Charles River Laboratories

Mattawan (MI)

Sur place

USD 23 000 - 32 000

Plein temps

Il y a 5 jours
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Avantages offerts par ce poste

Bonus incentives
401K
Paid time off
Health coverage
Wellbeing programs
Work-life balance

Résumé du poste

Charles River Laboratories in Mattawan, MI is seeking a Technician I for the Clinical Pathology Team. This entry-level role trains on onboarding skills and performs basic study support under close supervision.

Responsibilities include handling samples, labeling, aliquoting, processing, slide preparation, staining, and slide verification while maintaining GLP compliance. Typical schedule is Monday–Friday, 9:00 AM to 5:30 PM with occasional overtime and weekend rotation.

Qualifications

  • High school diploma or GED required; BA/BS in biological science preferred.
  • No prior experience required.
  • Excellent written and verbal communication; knowledge of English.

Responsabilités

  • Learn onboarding skills and procedures; cooperate in a team environment.
  • Handle biological samples: labeling, delivery, aliquoting, processing, verification.
  • Prepare, stain, and consolidate slides; maintain equipment and lab cleanliness.
  • Work under close supervision to gain proficiency; adhere to GLP, SOP, BOP, and IACUC rules.
  • May work extended hours, evenings, weekends, and overtime as needed.

Connaissances

Communication skills
English proficiency
Time management
Microsoft Office

Formation

High school diploma or GED
BA/BS in biological sciences (preferred)

Outils

Microsoft Office

Description du poste

Job Overview

We are seeking a Technician I for our Clinical Pathology Team in Mattawan MI.

A Technician I – Clinical Pathology is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include biological sample management including labeling, delivery, aliquoting, processing, and verification; cleaning of lab and equipment; preparation, staining, and consolidation of slides. The technician is working under close supervision to gain proficiency.

The pay for this position is $20/hr annually USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

The work schedule for this role is: Monday - Friday 9:00AM to 5:30PM with a weekend/holiday rotation and overtime, as necessary.

Minimum Requirements
  • Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
  • Experience: No previous experience required.
  • Certification/Licensure: None, unless required by local government.
  • Excellent written and verbal communication skills. Knowledge of English.
  • Ability to manage multiple tasks and priorities to achieve goals.
  • Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
  • Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
  • Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
  • 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.
  • Must be authorized to work in the United States without a sponsor visa, now or in the future.
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.

For more information, please visit www.criver.com.

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