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Sr. Scientific Product Development Specialist - (Remote)

Charles River Laboratories International Inc (CRL)

Wilmington, MA, US, 01887

Sr. Scientific Product Development Specialist - (Remote) Req ID #:  159154 Location: 

Wilmington, MA, US, 01887 US For 70 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.

IMPORTANT:   In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process.  Please make sure work history and education are added correctly. Job Summary We are seeking a Sr. Scientific Product Development Specialist, for our RMS Scientific and Commercial Development team.   This is a remote opportunity.

 

As a key member of the RMS Scientific and Commercial Development team the incumbent will serve as single point of contact to coordinate development projects and the delivery of new products and services to customers for assigned product portfolio.  

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:   Responsible for coordinating the development of new products in the Scientific Model Portfolio at the direction of senior product management.  Partners with RMS Product Management/Marketing/Sales teams to assure consistency in product performance and messaging.  Works closely across internal Charles River businesses and external partners to deliver prompt, efficient and high-quality products to customers.    Works closely with RMS operations to monitor product availability and ensure sufficient supply to meet market expectations.  Manages product Key Performance Indicators (KPIs), troubleshoots product issues and reports to senior management on assigned product development portfolio performance. 

 

MINIMUM QUALIFICATIONS:  Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences or related discipline.   Minimum 1-3 years related practical life science product development and product management experience.  An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.  Willing to own delivery of assigned product portfolio in a dynamic, multi-user working environment.   Must be able to influence and manage resources/staff without direct reporting relationships.  Ability to multi-task and have great organizational skills.  Must have excellent written and verbal communication skills.  Exceptional presentation skills.  Must possess analytical thinking and problem-solving skills and be able to prioritize and re-evaluate priorities as situations change.  Proficient in Computers (MS Word, MS Excel, MS PowerPoint, SFDC).  Periodic domestic travel required (<10%). 

 

PREFERRED QUALIFICATIONS:  MBA and/or advanced life science degree (MS or PhD).  Formal project management training and certification. 

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. 

Vaccine Mandate

Charles River is a U.S. Federal Contractor.  As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19 by December 8, 2021.  Our main priority is the wellbeing, health, and safety of our people. We will be requiring proof of vaccination from all employees. 

Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.

 

About Research Models & Services 

Fundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition.  As the world’s leader in the production and distribution of the highest quality research animal, with 1 out of 2 animal models produced for preclinical research globally, we understand the importance of this step. With seven decades of experience, our expertise is unmatched, allowing us to provide you with the perfect model, including disease-specific and preconditioned options, for basic research and beyond. 

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 18,000 employees within 100 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 >80% of the drugs approved by the FDA for the past 3 years.

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: Boston

Job Segment: Product Development, Scientific, Biotech, Supply, Research, Engineering, Science, Operations

Job posted: 2022-03-08

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