Job Description
BECOME YOUR MOST EXTRAORDINARY SELF! OUR TEAM IS INTENSELY PROUD TO BE A MAJOR PROVIDER OF SERVICES AND PRODUCTS TO THE DRUG DISCOVERY RESEARCH INDUSTRY. JOIN EUROFINS DISCOVERX CORPORATION PART OF THE EUROFINS DISCOVERY ™ GROUP OF COMPANIES SERVING GLOBAL CLIENTS IN THE PHARMA AND BIOTECH INDUSTRIES. WORK ALONGSIDE INDUSTRY EXPERTS AND COLLABORATE WITH TEAM MEMBERS TO DIRECTLY AND POSITIVELY IMPACT HUMAN HEALTH WORLDWIDE!
WE HAVE A PHILOSOPHY TO SUPPORT WORK LIFE BALANCE, CAREER PROGRESSION OPPORTUNITIES AND OFFER MANY BENEFITS SUCH AS FORMAL MENTORING PROGRAMS, TUITION REIMBURSEMENT, EXTENSIVE CAREER TRAINING PROGRAMS, COMPETITIVE HEALTH BENEFITS, PAID TIME OFF AND 10 ANNUAL PAID HOLIDAYS*.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Responsible for scheduling and execution of the technology platform cell-based screens to ensure timely delivery of data.
Direct supervision of junior staff including coordinating, training, and mentoring.
Co-ordinate multiple projects simultaneously. This includes oversight of the efforts for a bi-weekly large-scale safety pharmacology panel, routinely scheduled screens, HTS campaigns and ad-hoc requests.
Ability to maintain all (50+) cell lines needed for the operation and providing screening plates or assay ready cells according to the business needs. Maintain inventory of bulk vials to sustain the business continuity.
Support compound management through open communication and coordinating efforts.
Function as a technical lead for innovation projects or improvement efforts. Take ownership of presentations as necessary to internal stakeholders, collaborators, and clients. Collaborate with vendors on beta testing and promoting new services and equipment.
Go-to person for external partnerships and provide feedback to customers. This endeavor includes taking on a tech support role for screening data and coordination of study implementation.
Support poster presentation at scientific meetings; provide promotional material and webinars to represent the company.
In charge of optimizing screening assays to improve TAT.
Coordinate cross-site screening facility efforts or sister-site harmonization
Set up on boarding and training for new employees, establish and curate SOPs and routine QC.
Heavily involved in data management. Optimize workflow and remedy error prone steps. Understand data management in CBIS.
Independently analyze screening results, provide initial data QC using Spotfire or other data visualization tools. Perform large-scale data analysis and generate customer reports.
Take charge of report writing and delivery. Be able to analyze and send out screening data, as necessary.
Demonstrates and promotes the company vision.
Conducts all activities in a safe and efficient manner.
Performs other duties as assigned.
Owns the accountability and responsibility of delivering to client needs and timeliness.
Provides cross-functional support to other departments as required.
Adjusts work hours as needed to meet client deadlines.
Adheres to site employee health and safety (EHS) requirements.
Qualifications
Additional Information
EUROFINS IS A M/F, DISABLED, AND VETERAN EQUAL EMPLOYMENT OPPORTUNITY AND AFFIRMATIVE ACTION EMPLOYER.