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Resource Scheduling Analyst (m/f/d)

Charles River Laboratories International Inc (CRL)

Erkrath, NW, DE, 40699

Resource Scheduling Analyst (m/f/d) Req ID #:  169003 Location: 

Erkrath, NW, DE, 40699 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. . For our Biologics Testing Solutions site in Erkrath we are seeking asap and unlimited an experienced

 

Resource scheduling analyst (m/f/d) Your duties and responsibilities: Partner with IT, operations, and other stakeholders for the creation and improvement of operational scheduling management tools using programs such as PowerBI, Smartsheet, LIMs, and SFDC Create Capacity planning models and assess for accuracy, gaps and actions needed Lead meetings and facilitation collaboration of team leads and key stakeholders to review capacity planning model Improve capacity planning models for personnel, instrumentation, lab space and long-range forecasting Monitor departmental schedules, identify extended lead times and backlogs in departments and notify internal stakeholders when these begin to develop If unexpected lead times and backlogs develop, work with business optimization team to review processes and determine roadblocks and constraints Provide tentative start dates for proposed studies. Confirm that resources are available to accommodate timelines provided by the Sponsors and business development Play a central role in the resource scheduling-related internal business intelligence infrastructure Work with Lab Directors, lab staff and project management to adjust study schedules based on resource availability

  Your qualifications: Bachelor’s degree (B.A. / B.S.) or equivalent in biotechnology or biological sciences with proven experience with capacity planning and a strong affinity with information computer technology.  A commensurate amount of experience will be accepted in place of a degree Science background with IT affinity or IT background with proven track-record, working in a scientific environment preferred 2 years of related experience in a laboratory or research environment  Strong project management skills Preferred: Experience in a GMP environment Experience with LIM Systems and laboratory scheduling tools Experience with software implementation Experience with business optimization and change management Programming skills such as python, C++ are a plus Language: German fluent, English fluent, other languages are a plus

  What we offer:

•  an unlimited full-time position with varied, demanding activities

•  a future-oriented global industries and company

•  flexible working hours

•  an active participation in shaping your field of activity in a motivated team 

  Are you interested?

Please apply under job ID 169003 via our career portal https://jobs.criver.com/ with your application documents in English and your earliest possible starting date.

We look forward to receiving your application!

 

Charles River Laboratories Germany GmbH

Human Resources

Max-Planck-Str. 15a

40699 Erkrath

Phone: 0211 9255-356 (Michaela Klein), 0211 9255-407 (Jan Limbach)

 

About Biologics Testing Solutions

With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs.  Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

 

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 - 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.

Job Segment: Biotech, Scheduler, Pharmaceutical, Implementation Manager, Science, Administrative, Technology, Research

Job posted: 2022-03-28

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