This job posting may have expired!
Use our `search` to find similar offers.
Similar jobs

Sr. Director, Operations - In-Vivo, Post-Life & Training

Charles River Laboratories International Inc (CRL)

Mattawan, MI, US, 49071

Job Summary

Senior Director of Operations is responsible for: providing oversight of and leadership for applicable operational groups - In-Vivo, Post-Life, Training and Business Optimization. The individual in this role is also responsible, as part of the site leadership team, for guiding the development of the site’s strategic and tactical planning so that a full line of quality products and services is managed in response to customer and industry needs. May be delegated certain test facility management (TFM) responsibilities, as applicable.

Essential Responsibilities: •    Supervisory responsibilities in accordance with the organization’s policies and applicable laws to include interviewing, hiring, training, and developing employees; planning, assigning and directing work; appraising performance and completing annual performance review on or before due date; rewarding and disciplining employees; addressing complaints and resolving problems. •    Assist, as a member of the site leadership team, in the development of strategies and tactics to support the mission, vision, values, and performance objectives of the company. •    Provide leadership for business development, developing and maintaining working relationships with key clients, agencies, and global. •    Provide expertise and resources for study management. •    Verify compliance with regulatory requirements, guidelines and best practices; mentor staff, sharing scientific and operational expertise. •    Provide leadership and support to cross-functional teams that work toward enabling successful investigational new drug (IND) applications or new drug application (NDA) submissions. •    Inform internal and external stakeholders of strategy, plans, and changes as needed to provide quality products and services.  •    May be delegated certain TFM responsibilities applicable (see detailed role and responsibilities of TFM below). •    Other duties as assigned.

Job Qualifications

•    Bachelor’s degree (preferred) with 10 or more years of relevant experience, including at least 5+ years in a leadership role; contract research organization experience preferred. •    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. •    Demonstrated ability to problem solve, make quick decisions, communicate decisions effectively, and lead/manage staff in a growing, changing environment. •    Demonstrated knowledge of GxPs and industry guidance documents. •    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.

 “The pay range for this position is $150K - $210K USD.  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 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 [email protected] This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

Job posted: 2023-06-28

3
Suscribir