AbbVie Pharmacyclics Senior Clinical Supply Chain Associate in Sunnyvale, California
Senior Clinical Supply Chain Associate
Location: Sunnyvale, CA
# of Openings: 1
Pharmacyclics is committed to the development and commercialization of novel therapies intended to improve the quality and duration of life and to resolve serious unmet medical needs for cancer patients. Pharmacyclics is a wholly-owned subsidiary of AbbVie (NYSE:ABBV), a global, research-based biopharmaceutical company. Oncology is a key therapeutic area for AbbVie, with a portfolio consisting of three marketed products and a pipeline containing multiple promising new molecules that are being studied in more than 200 clinical trials for over 20 different types of cancer.
More than 1,200 Pharmacyclics and AbbVie research scientists, clinicians, marketing, operations and corporate professionals work in the San Francisco Bay Area. They combine their expertise in immuno-oncology, stem cells, and cell-signaling with their knowledge of bispecific antibodies, antibody-drug conjugates (ADCs), and covalent-inhibitor technologies to discover and develop novel cancer treatments. Together, we are striving to outsmart cancer.
General Position Summary/Purpose:
The Sr Clinical Drug Supply Associate will support clinical drug supply activities to ensure clinical products are released and available at distribution sites and depots when required.
Communicating clinical drug supply updates to internal departments and external partners and vendors
Track and follow-up on key milestone activities
Coordination of supply activities with third party contractors
Technical batch record review
Packaging and labeling coordination
Label translation coordination
Monitoring drug supply levels in IXRS systems
Clinical drug distribution coordination
Temperature excursion follow-up
Coordination of clinical drug returns and product destruction
Retest date monitoring
Training on required SOP’s
Education and Qualifications:
Bachelor’s degree or 3 years of experience in business or biological sciences
Minimum of 2 years Clinical Supply Chain experience preferred.
Previous Quality Assurance experience preferred.
Knowledge of cGMP’s and pharmaceutical industry procedures and regulations.
Ability to multi-task and adapt to changing priorities.
Strong communication skills (verbal and written, organizational and time management skills.
Project management skills and computer proficiency.
Experience with the following software is desirable: Microsoft Excel, Word and Project.
Equal Opportunity Employer Minorities/Women/Veterans/Disabled