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Bachelor In Biotechnology Jobs in Reno, NV (NOW HIRING)

IQVIA

Assoc Business Development Director

Reno, NV · On-site

$89K - $250K/yr

To be eligible for this position, you must reside in the same country where the job is located ... Bachelor's degree or higher required * Willing to travel throughout the US, estimated up to 50%

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Bachelor In Biotechnology information

What is a bachelor in biotechnology?

Bachelor in Biotechnology graduates are individuals who have completed an undergraduate degree focused on the application of biological systems, organisms, or derivatives to develop products and technologies for various industries such as healthcare, agriculture, and environmental science. They gain foundational knowledge in subjects like molecular biology, genetics, chemistry, and microbiology, along with practical laboratory skills. Graduates may pursue careers in research, quality control, pharmaceuticals, or further studies in biotechnology or related fields. This degree prepares them to work in both public and private sector organizations, contributing to advancements in science and technology.

What entry-level roles are available to a bachelor in biotechnology, and how do they support career advancement?

Graduates with a Bachelor's in Biotechnology often start in roles such as research assistant, laboratory technician, quality control analyst, or production associate in sectors like pharmaceuticals, agriculture, or environmental science. These positions provide hands-on experience with laboratory techniques, data analysis, and compliance with industry regulations. By collaborating closely with scientists and cross-functional teams, entry-level professionals develop technical expertise and soft skills essential for advancement. Gaining experience in these areas can lead to opportunities in research and development, project management, or quality assurance as you progress in your career.

What skills and qualifications are needed to thrive as a bachelor in biotechnology?

To thrive with a Bachelor in Biotechnology, you need a solid grounding in biology, chemistry, and laboratory techniques, typically acquired through a relevant undergraduate degree. Familiarity with laboratory equipment, PCR, gel electrophoresis, and bioinformatics tools is often expected. Strong analytical thinking, problem-solving skills, and effective teamwork set candidates apart in research and industrial environments. These competencies are crucial for conducting reliable experiments, interpreting data accurately, and driving innovation in biotechnology applications.

What is the difference between Bachelor In Biotechnology vs Laboratory Technician?

AspectBachelor In BiotechnologyLaboratory Technician
Required CredentialsBachelor's degree in Biotechnology or related fieldAssociate's degree or diploma in Laboratory Technology
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsClinical, research, or industrial labs
Employer & Industry UsageBiotech firms, research institutions, pharma companiesHospitals, research labs, manufacturing plants
Common Search & ComparisonYesYes

The main difference between a Bachelor In Biotechnology and a Laboratory Technician lies in education level and scope of work. A Bachelor In Biotechnology typically involves more research, development, and analytical tasks, while a Laboratory Technician focuses on executing experiments and maintaining lab equipment. Both roles are essential in the biotech industry, but the bachelor's degree opens doors to more advanced positions and research opportunities.

Is a bachelor in biotechnology worth it?

A bachelor in biotechnology prepares individuals for roles in research, development, and quality control within biotech and pharmaceutical industries. It provides foundational knowledge in biology, chemistry, and lab techniques, which can lead to employment opportunities or further specialization through advanced degrees. The degree is generally considered valuable for entering the growing biotech sector, though job prospects depend on skills, experience, and industry demand.

What can I do with a Bachelor in Biotechnology?

A Bachelor in Biotechnology prepares graduates for roles such as research technician, quality control analyst, laboratory assistant, or production associate in industries like pharmaceuticals, agriculture, and healthcare. It provides foundational knowledge of molecular biology, microbiology, and lab techniques, often requiring proficiency with tools like PCR and chromatography. Further certifications or advanced degrees can expand career opportunities in research, development, and management.

What jobs can I do with a Bachelor in Biotechnology?

A Bachelor in Biotechnology qualifies graduates for roles such as research technician, quality control analyst, laboratory assistant, or bioprocess technician. These positions often require knowledge of laboratory techniques, data analysis, and familiarity with biotech tools and equipment.

What job categories do people searching Bachelor In Biotechnology jobs in Reno, NV look for?

The top searched job categories for Bachelor In Biotechnology jobs in Reno, NV are:

What cities near Reno, NV are hiring for Bachelor In Biotechnology jobs?

Cities near Reno, NV with the most Bachelor In Biotechnology job openings:

Bachelor In Biotechnology jobs near you
Infographic showing various Bachelor In Biotechnology job openings in Reno, NV as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 9% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Senior Toxicology Study Director (Senior Research Scientist)

Charles River Laboratories, Inc.

Reno, NV • On-site

Full-time

Medical, Retirement, PTO

Posted 19 days ago

Charles River Laboratories rating

8.4

Company rating: 8.4 out of 10

Based on 94 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

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 OVERVIEW

Charles River is seeking a Senior Toxicology Study Director (Senior Research Scientist) to join our Safety Assessment team in Reno, Nevada. This role is designed for an experienced Study Director who has successfully led complex GLP and non-GLP in vivo toxicology studies across multiple species and can provide scientific leadership, study oversight, and client consultation throughout the lifecycle of preclinical safety assessment programs.

This role functions as an independent Study Director responsible for overseeing the design, execution, interpretation, and reporting of toxicology studies. You will collaborate across scientific and operational teams, and apply your expertise to drive scientific excellence, operational success, business growth, and capability development within the organization. This is a senior individual contributor role. While the position may involve mentoring, coaching, and serving as a scientific resource to others, it is not primarily a people-management position and does not include direct reports upon hire.

This opportunity is ideal for a highly experienced toxicology professional who thrives in a client-facing environment, brings deep operational study leadership experience, and is looking to make a meaningful impact within a growing and highly collaborative team.

Essential Duties & Responsibilities

  • Lead studies from proposal through final report, serving as Study Director and/or Principal Investigator/Individual Scientist, as applicable.
  • Oversee protocol development, study execution, data interpretation, reporting, and sponsor communications.
  • Ensure compliance with GLP regulations, SOPs, quality standards, and applicable regulatory requirements.
  • Serve as the primary scientific and client contact for assigned studies.
  • Provide technical leadership, mentorship, and consultation to internal teams and external clients.
  • Support business development through proposal development, client relationship management, and identification of growth opportunities.
  • Drive continuous improvement initiatives and maintain awareness of emerging scientific and industry developments.
  • Study Director:
    • Design and manage study plans, schedules, and amendments.
    • Direct and coordinate study execution across functional groups.
    • Ensure studies are conducted in compliance with GLP and regulatory requirements.
    • Review and approve study reports and communicate study progress and outcomes to clients.
  • Principal Investigator / Individual Scientist:
    • Provide scientific leadership within area(s) of specialization.
    • Develop and review study plans and schedules, amendments, and contributing scientist reports.
    • Oversee and coordinate specialized study activities and ensure scientific quality and integrity of results.
QUALIFICATIONS

Required Qualifications

  • PhD, DVM, PharmD, MD, MS, or BS in Toxicology, Pharmacology, Veterinary Sciences, or a related life sciences discipline.
  • Typically 8+ years of relevant industry experience in toxicology, safety assessment, drug development, or a related scientific field.
  • Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment.
  • Experience leading GLP and non-GLP in vivo toxicology studies.
  • Experience working across multiple animal species and study designs.
  • Proven track record of direct client interaction and scientific communication.
  • Strong scientific writing skills, including protocol, report, and study documentation development.
  • Ability to independently manage multiple studies and competing priorities.

Preferred Qualifications

  • CRO toxicology experience.
  • Multi-species experience, including large animal models (NHP, canine, and minipig experience, preferred).
  • Experience serving as a primary Study Director for regulatory toxicology or safety assessment studies.
  • Expertise in a specialty area such as genetic toxicology, ocular toxicology, safety pharmacology, developmental and reproductive toxicology, or related disciplines.
  • Previous mentoring, leadership, or supervisory experience.
  • Experience driving scientific initiatives, capability development, process improvements, or new service offerings.
  • Experience supporting business development activities, client growth opportunities, or proposal development.

The pay range for this position is $130-$144K annually.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. 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 www.criver.com.

What Charles River Laboratories employees say

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About Charles River

Sourced by ZipRecruiter

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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947

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