Laboratory Director - LC-MS/MS Bioanalytical

Laboratory Director - LC-MS/MS Bioanalytical Req ID #:  65541 Location: 

Mattawan, MI, US, 49071 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. Job Summary

We are seeking a Directorfor our Bioanalytical Groupsite located in Mattawan, MI.

The following are responsibilities related to theDirector of Bioanalytical:

A Director - Bioanalytical is responsible for: managing, mentoring, and providing strategicleadership and direction to a staff of employees; preparing annual budgets and monitoringmonthly forecasts, and implementation of new research activities and techniques; strengtheningthe core services provided to pharmaceutical, biotechnology, agrochemical and industrialclients. The individual in this position is also responsible for client relationship development;using scientific expertise to assist with business development activity; working with businessdevelopment staff to develop and execute a strategic plan identifying areas or growth. Inaddition, the Director - Bioanalytical maintains procedures, systems and processes necessary tocomply with Good Laboratory Practices. This position may be delegated the authority to perform

Test Facility Management functions.

The following are minimum qualifications related to theDirector of Bioanalyticalposition:

PhD in Chemistry or related field with a minimum of 5 years previous experience in amanagement role or a Masters Degree and a minimum of 10 years of experience in amanagement roleProven leadership experience in supervising a diverse group of professional scientificemployees, with strong coaching and staff development skills, preferably in thepharmaceutical or CRO environmentDemonstrated expertise in the application of HPLC/MS/MS to the analysis of smallmolecules pharmaceutical agents in body fluid; thorough understanding of GLP regulationsand other regulatory requirements for analytical support of studies at various stages of drugdevelopment.Superior written and verbal communication skills. Ability to analyze and synthesize scientific data, interpret and prepare reports of results ofchemistry projects and communicate in a timely manner with sponsor representatives, studydirectors, management and laboratory staff to ensure client timelines and needs are met. Ability to communicate verbally and in writing at all levels inside and outside theorganization. Basic familiarity with Microsoft Office Suite. Computer skills, commensurate with Essential Functions, including the ability to learn avalidated system. Ability to work extended hours beyond normal work schedule to include, but not limited toevenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice. Ability to work under specific time constraints.

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 120 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 17,000 employees within 90 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. And in 2019, revenue increased to $2.62 billion.

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 ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity 

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

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Nearest Major Market: Kalamazoo

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