Quality - QA Associate

---

Job description

• Provides support to manufacturing including quality approval of investigations, participation in change control and area walkthroughs.


• Monitors and trends batch record errors and provides Quality Assurance management with quality indicator data.


• Monitors various stages of processing along with the appropriate paperwork in compliance with specifications.


• Performs general and/or more complex manufacturing formulation batch production record reviews and approval in support of product release in accordance with specifications and SOPs.


• Maintains shop floor quality presence; releases raw materials, in-process materials, and finished product; investigates and resolves deviations and complaints; conducts annual product reviews. Assures the quality of manufactured products are in compliance with all applicable regulations and guidelines. May assist in preparing for a hosting of regulatory and customer audits.


• Samples, inspects and releases consumable and raw materials per specifications.


• Drafts and reviews specifications and SOPs. Reviews and approves discrepancy reporting, investigations and CAPAs associated with incoming, in-process and production batch processing.


• May provide guidance to less experienced staff.


• Provides QC support including lab inspections, method qualification, method technology transfer, LIMS and Smart Lab support, etc.

Requirements:

• Strong communication skills and demonstrated ability to influence stakeholders is required.


• Knowledge of biotech bulk and finished product manufacturing, analytical testing is preferred.


• B.S., in Chemistry, Chemical Engineering, Biochemistry or related discipline, or its equivalent is preferred.


• 5+ years of relevant experience in a regulated environment with at least 2 years focused on product quality.


• Knowledge of US and EU cGMP regulations and guidance.


• Knowledge of SAP, LIMS, Delta V, Maximo, Syncade are a plus

<!– job description page –>