Research and Development Supervisor jobs in Elyria, OH

Research and Development Supervisor supervises activities in the research and development department. Oversees personnel who utilize established mathematical and scientific techniques to compile and analyze data and write technical reports detailing procedures, outcomes, and observations. Being a Research and Development Supervisor ensures proper procedure, and helps devise new development techniques. A level I supervisor is considered a working supervisor with little authority for personnel actions. Additionally, Research and Development Supervisor may require a bachelor's degree in area of specialty. Typically reports to a manager or head of a unit/department. Working team member that may validate or coordinate the work of others on a support team. Suggests improvements to process, is a knowledge resource for other team members. Has no authority for staff actions. Generally has a minimum of 2 years experience as an individual contributor. Thorough knowledge of the team processes. (Copyright 2024 Salary.com)

Recently Added Research and Development Supervisor jobs

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Research Scientist II Method Development - Bioanalytical Chemistry
  • Charles River Laboratories
  • Ashland, OH FULL_TIME

  • Req ID #: 222288
    Location: Ashland, OH, US, 44805
    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
    Serve as a scientist in the conduct of assigned nonclinical or clinical research studies of moderate to high complexity, to include study management, interpretation, and reporting of study data, and assuring the regulatory compliance of these projects.

    ESSENTIAL DUTIES AND RESPONSIBILITIES:
    • Efficiently perform and document all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.).
    • Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data.
    • Independently execute the completion of laboratory investigations, assay troubleshooting, quality observations, and problem solving of technical and/or regulatory issues.
    • Independently develop and validate quantitative/qualitative methods/procedures with increased complexity/scope in one operational area.
    • Develop and maintain critical thinking, troubleshooting, and time management skills aligned with needs of operational areas.
    • Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
    • Able to recognize method and/or data issues and communicate them to management to minimize study impact independently.
    • Independently prepare summary of method development data.
    • Independently execute review and approval of data for final scientific/technical decisions within a single operational area.
    • Full understanding of compliance expectations to independently respond to quality assurance audit observations in appropriate software.
    • Responsible for writing and preparing study plans/protocols/amendments/reports independently.
    • Independently participate in sponsor visits/tours.
    • Independently function as liaison, maintaining timely and frequent communication between CRL and sponsor/client/SD.
    • Independently ensure scientific integrity of studies.
    • Independently function as a Principal Investigator, Individual Scientist, and/or Study Director as assigned.
    • Independently write, review, and approve deviations.
    • Full understanding of regulatory and GLP requirements, industry standards, and company SOPs with the ability to mentor others within one operational area.
    • Independently manage a portfolio of projects, including method development and validation studies while ensuring timelines are met in a single operational area.
    • Provide support to staff members as required by operational areas, as needed.
    • Lead internal process improvements, presentations, and harmonization efforts.
    • Attend scientific meetings, conferences, and training courses to enhance job and professional skills.
    • Perform all other related duties as assigned.


    The pay range for this position is 110-115K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
    Job Qualifications
    • Education: Associate’s degree (A.A./A.S.) or equivalent from a two-year college, preferred. Bachelor's degree (B.A./B.S.) or equivalent in a scientific related discipline, recommended. Related Master's degree (M.A./M.S.) or Ph.D./D.V.M., strongly recommended.
    • Experience: Minimum of 11 to 14 years related experience in the contract research, academic, or pharmaceutical industry.
    • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
    • Certification/Licensure: None.
    • Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Demonstrate leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations.

    PHYSICAL DEMANDS:
    • Must be able to lift, move, manipulate and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or supplies.
    • Must be able to perform procedures, standing or sitting, for long periods of time, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
    • Must be able to frequently hold and manipulate work materials while utilizing fine motor skills.
    • Must be able to regularly provide information to and receive information from/through various technologies, media, sources, and contacts. Must be able to accurately exchange information in these situations.
    • Regularly operates a computer and other office productivity machinery, such as a calculator, copy machine, and computer printer.
    • Move about inside the work area to access file cabinets, office machinery, etc.
    • Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

    WORK ENVIRONMENT:
    • General office and lab working conditions, the noise level in the work environment is usually quiet.
    • While performing the duties of this job the employee is regularly required to wear protective clothing (i.e., goggles, face shield, cap, gloves, scrubs, shoe covers), work near toxic or caustic chemicals, and work with biohazards.
    • The employee may occasionally be exposed to live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
    • The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and extreme temperature conditions.
      • The noise level in the work environment ranges from low to moderate depending upon the task being performed.
    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 supported the development of 86% of the drugs approved by the FDA in 2021.

    Equal Employment Opportunity
    Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

    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.


    Nearest Major Market: Cleveland
    Nearest Secondary Market: Mansfield
    Job Segment: Research Scientist, Chemistry, Developer, Scientist, Science, Technology, Research

  • 16 Days Ago
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Data entry
  • Maxion Research
  • Mansfield, OH FULL_TIME
  • Remote Work From Home Data Entry Clerk for Entry Level Position Work at home position for job seekers from virtually any work background who are interested in part-time, side gigs, micro jobs, work fr...
  • 1 Day Ago
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Data Entry Clerk - Work
  • Maxion Research
  • Mansfield, OH FULL_TIME
  • Thank you for checking us out! Work From Home Data Entry Research Panelist Jobs - Part Time, Full Time This is a remote work from home position perfect for those with any type of work background such ...
  • 24 Days Ago
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Supervisor
  • Scene75
  • Brunswick, OH FULL_TIME
  • Summary/Objective The Supervisor position assists the Operations Managers and General Manager with real-time operations that facilitate the maximization of resources (human and automated) to achieve c...
  • 1 Month Ago
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Part-Time Maintenance Technician: Union Lofts
  • TWG Development, Construction, Property Management
  • Ashland, OH PART_TIME
  • DescriptionJob Title: Part-Time Maintenance TechnicianReports to: Property ManagerProperty Details: Union Lofts is a 48-unit multifamily development with Brand new 1,2 & 3 bedroom apartments, Fitness ...
  • 1 Day Ago
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Clinical Research Coordinator
  • ONE GI LLC
  • Brunswick, OH OTHER
  • Job Details Job Location: OH 1299 Industrial Pkwy N, Brunswick 0QW40 - Brunswick, OH Education Level: 2 Year Degree Salary Range: Undisclosed Travel Percentage: None Job Category: Research Description...
  • 5 Days Ago
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0 Research and Development Supervisor jobs found in Elyria, OH area

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Training and Development Coordinator
  • Group Management Services Inc.
  • Richfield, OH
  • GMS, one of the countrys leading PEOs, is looking for an ambitious and driven individual to be our newest Training and D...
  • 4/26/2024 12:00:00 AM
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Front Desk Supervisor
  • Schulte Companies
  • Westlake, OH
  • Job Description Schulte Hospitality Group is seeking a dynamic, service-oriented Front Office Supervisor to join our tea...
  • 4/26/2024 12:00:00 AM
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Customer Service Representative
  • Nippon Paint Holdings Co., Ltd.
  • Cleveland, OH
  • ESSENTIAL DUTIES: Process and track customer orders in SAP, ensuring accuracy and completeness, communicates order statu...
  • 4/26/2024 12:00:00 AM
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PCA/Secretary - Outpatient Infusion Center
  • Bon Secours Mercy Health
  • Lorain, OH
  • At Bon Secours Mercy Health, we are dedicated to continually improving health care quality, safety and cost effectivenes...
  • 4/25/2024 12:00:00 AM
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Business Support Specialist
  • Acuative Corporation
  • Strongsville, OH
  • Job Description Job Description The Benefits of working with Acuative Acuative offers a comprehensive benefits program t...
  • 4/24/2024 12:00:00 AM
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Training & Development Coordinator
  • Employ-Temps Staffing Services
  • Medina, OH
  • At Employ-Temps, we are a team of passionate professionals committed to empowering success for both employers and job se...
  • 4/23/2024 12:00:00 AM
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Business Development Consultant
  • PFES
  • Westlake, OH
  • PFES, part of The Planet Group, is a leader in providing consulting services to the utility industry. Our team has a pro...
  • 4/23/2024 12:00:00 AM
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Environmental Associate II
  • Travelcenters Of America
  • Westlake, OH
  • Theres never been a better time to join TravelCenters of America! For more than 50 years, millions of professional truck...
  • 4/23/2024 12:00:00 AM
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About Elyria, Ohio

Elyria (/əˈlɪəriə/ ə-LEER-ee-ə) is a city in the Greater Cleveland metropolitan statistical area and the county seat of Lorain County, Ohio, United States, located at the forks of the Black River in Northeast Ohio 23 miles southwest of Cleveland. As of the 2010 census, the city had a population of 54,533. The city is home to Lorain County Community College. Elyria, part of the Cleveland–Elyria–Mentor metropolitan area, is located at 41°22′24″N 82°6′6″W / 41.37333°N 82.10167°W / 41.37333; -82.10167 (41.373396, -82.101692). Elyria's primary zip code is 44035 with post office boxes being assi...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Research and Development Supervisor jobs
$64,447 to $91,992
Elyria, Ohio area prices
were up 1.3% from a year ago
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What does a Research and Development Supervisor do?

Research and Development Supervisor in Abilene, TX
Collaborates with the SRL, physicians of the practice, and other research management in the process of study selection for the research program.
January 15, 2021
Requires standing and walking for extensive periods of time.
March 10, 2021
Collaborates in the development of research accountability standards, metrics, and reports and identifies areas for improvement.
April 03, 2021