Clinical Supply Chain Planner
- Employer
- Precision BioSciences, Inc.
- Location
- Durham, NC, United States
- Start date
- Aug 22, 2020
View more
- Discipline
- Clinical, Clinical Research, Manufacturing & Production
- Required Education
- Bachelors Degree
- Position Type
- Full time
- Hotbed
- Bio NC
Job Details
Essential Duties and Responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
- Support Precision BioSciences supply chain planning function from early clinical stages through commercial launch
- Track raw materials from time of purchase to time of receipt and assist the receiving location with any incoming receipt issues/discrepancies
- Identify and communicate any supply delays that may impact manufacturing and/or clinical dosing; proactively resolve/escalate delays
- Collect supply chain data to enable and refine forecasting
- Implement logistic and buying strategies
- Coordinate supply for internal and outsourced activities to ensure timely procurement and distribution of material, including CMO produced drug product intermediates
- Implement restock and re-order levels for critical inputs; monitor inventory levels to avoid excess inventory, inventory shortages and/or inventory expirations
Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
- Bachelor's degree in business, engineering or life sciences with a preference for a multi-faceted business-science or engineering background; or equivalent combination of training and experience
- Minimum of 2 years of experience in operational roles in the Biopharmaceutical industry
- Skilled in data analytics
- Strong understanding of Quality Systems & conceptual, strategic & analytical problem solving
- Excellent communication skills, both verbal and written, and the ability to interface effectively with all level of the organization, as well as with outside contract organizations
- Working knowledge of cGMP's and pharmaceutical industry procedures and regulations
- Strong personal alignment with Precision BioSciences values, mission and vision
Travel Requirements
- No travel is required for this position
Location
- This is an office-based position located at the main headquarters in downtown Durham, NC and/or manufacturing facility in Research Triangle Park, NC.
Precision BioSciences is dedicated to improving life through its proprietary genome editing platform, ARCUS. Precision BioSciences leverages ARCUS in the development of its product candidates which are designed to treat human diseases and create healthy and sustainable food and agriculture solutions. Precision BioSciences is actively developing product candidates in three innovative areas: allogeneic CAR T immunotherapy, in vivo gene correction, and food.
Precision BioSciences provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws. Precision BioSciences complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Company
Precision BioSciences, Inc. (Nasdaq: DTIL) is a clinical stage gene editing company developing in vivo gene editing and ex vivo allogeneic CAR T therapies with its highly precise and versatile ARCUS genome editing platform. ARCUS uses sequence-specific DNA-cutting enzymes, or nucleases designed for gene knock out, as well as highly sophisticated edits for gene insertion and/or gene repair. Precision’s in vivo gene editing pipeline consists of wholly-owned preclinical candidates for primary hyperoxaluria type 1 (PBGENE-PH1), familial hypercholesteremia (PBGENE-PCSK9) and chronic hepatitis B (PBGENE-HBV). It has also partnered with Lilly to develop candidates for Duchenne muscular dystrophy and two other programs targeting the liver and CNS. Precision’s allogeneic CAR T pipeline consists of multiple investigational candidates in early-stage clinical trials, including its first and second generation CD19 targeting candidates PBCAR0191 and PBCAR19B for relapsed and/or refractory (R/R) non-Hodgkin and B-cell lymphoma patients. Precision has also prioritized development of PBCAR269A, its BCMA targeted candidate in combination with a gamma secretase inhibitor for R/R patients with multiple myeloma. Precision BioSciences and its in-house manufacturing facility for AAV, mRNA, and CAR T cells is based in Durham, North Carolina. For more information about Precision BioSciences please visit www.precisionbiosciences.com
Stock Symbol: DTIL
Stock Exchange: NASDAQ
- Website
- http://www.precisionbiosciences.com/
- Phone
- 919-314-5512
- Location
-
302 East Pettigrew Street
Durham
North Carolina
27701
US
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