Quality Associate

Aquestive Therapeutics•Portage, IN

About The Position

This position is responsible for supporting compliance with pharmaceutical industry regulations and standards as well as Company policies and procedures. This position supports ongoing quality programs across development and commercialization of products manufactured by the Company.

Requirements

BS degree in chemistry, biochemistry, pharmacy or related science field preferred.
Minimum 2+ years experience in pharmaceutical or biotechnology industry required.
Previous experience in providing pharmaceutical Drug Product review and release.
Demonstrated knowledge of GMPs and other regulatory requirements for the manufacture, testing, and release of pharmaceutical
Knowledge and understanding of CFR 210, 211 regulations and ability to apply
Ability to make sound, independent quality decisions.
Demonstrates high levels of values and integrity.
Ability to easily multi-task, prioritize and adapt to changing business needs, as well as recognize opportunities for continuous improvement and be a champion of change.
Excellent verbal and written communication skills both internally and externally.

Nice To Haves

ASQ Certification preferred.

Responsibilities

Support management of Events/Deviations and CAPAs.
Author, review and approve Product Complaints and Averse event investigations.
Responsible for verifying all batches manufactured are compliant with Good Manufacturing Practices 21 CFR 210 and 211, product registration/marketing authorization and all other requirements by reviewing manufacturing and laboratory testing records, investigations, non-conformances and out-of-specifications and analyzing cumulatively.
Provides Quality leadership a summary of findings for any batch that does not meet standard requirements for final disposition.
Provide batch disposition and subsequent release to market and/or marketing authorization holder, and issuance of Certificate of Analysis/Conformance according to country specific requirements
Support management of internal process for batch release, working closely with Quality Control, Manufacturing and Supply Chain.
Responsible for communicating batch release status externally to partners, triaging questions and organizing the provision of, and providing responses in a timely manner.
Coordinate activities associated with batch release, ensuring corrections are completed and associated batch documentation and investigations and events are closed out.
Compiles and documents monthly metrics, quarterly reports, and ad-hoc reports and data analysis of reports.
Provide inputs to process validation activities and process risk decisions (PVMP/PFMEA)
Review, consult, and approve validations and equipment/instrument qualifications (IQ, OQ, PQ, etc.)
Author, review and approve risk assessments.
Act as a quality representative on internal product teams, including development of products.
Support quality system functional processes, such as Change Control.
Will be assigned duties and responsibilities within the Quality System/Unit; specific duties will depend on the assignment and experience of the individual and may include any of the following: coordination/evaluation for Change Control, reviewing Annual Product Reviews, review and approval of validation documents, Labeling, Supplier Quality, authoring review and/or approval of standard Quality System documentation (SOPs, Forms, reports, etc.), conducting risk assessments, providing agency and partner audit support, etc.