- Expiry Date: 18 December 2021
Work independently to assist in investigation of process deviations, data trending, change controls and other documentation. Perform manual or automated process performance data extraction, reporting and analysis.
Coordinate the execution of process validation protocols, including scheduling, communication, coordination of sample delivery and data collection.
Coordinate activities between Manufacturing Technology, Manufacturing operating groups, Supply Chain, and QA/QC to meet project timelines.
Achieve high customer satisfaction through effective communication of both technical and non-technical topics with all levels of the organization both verbally and in writing.
BS degree in science or engineering related to biopharmaceutical process technology with minimum of 3-5 years biopharmaceutical or equivalent industry experience. Advanced degree is preferred.
Experience with lyophilization development, filter validation, electronic database systems and statistical analytical packages is highly desirable.
Excellent verbal & written communications skills. Interpersonal / facilitation skills necessary to interface with and influence all levels of the organization.
Broad knowledge of biopharmaceutical facility design and manufacturing operations is highly desirable.
Experience with biopharmaceutical regulatory submissions and interaction with regulatory agency inspectors is desirable
About ASK:ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities
ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.