Quality Assurance Associate

This role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing. This role works collaboratively with Manufacturing Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. The responsibilities of the employee is based on the assigned QA organization as outlined below.

What Youll Do:

• Review executed Manufacturing Batch Records.

• Participate in compliance walkthrough of the Manufacturing floor and other assigned areas.

• Partner with Manufacturing to ensure compliance in Manufacturing operations.

• Review and approve Master Batch Records and other supporting documents.

• Execute process performance and product quality monitoring programs.

• Alert senior management of potential deviations or compliance risks.

• Initiate and review all quality events of eQMS (Deviations Change Control CAPA Risk Assessment Management Review Complaint Investigation Product Quality Review etc.) to assure compliance with regulatory and Just-Evotec Global Quality Management Systems (G-QMS) requirements.

• Provide input on communication as to the status of deliverables to customers management and stakeholders.

• Assist with developing training regarding QMS process or system changes.

• Support QA QMS in internal and external client audits and regulatory inspections (including but not limited to SME for QMS processes and individual records).

• Monitor effectiveness for QMS through trending analysis and metrics; report to top management and G-QMS on the performance of the KPIs and identify opportunities for continuous improvement.

• Lifecycle management of the stability program for clinical and commercial products

• Act as the QA representative on cross-functional product teams to integrate stability activities with project milestones.

• Support the design of stability protocols to ensure that they are aligned with program strategy and regulatory requirements.

• Ensure that stability studies are executed according to protocol.

• Review verification disposition and archival of stability study data for assigned programs.

• Escalate unexpected data trends OOS events and risks appropriately and drive/support resolution.

• Interpretate stability results to support expiry trending and conditions of products.

• Support product stability related content in regulatory submission including responses to questions and post-marketing.

Who You Are:

• Bachelors Degree biological sciences chemistry biochemistry engineering or related life science field and 1 year of relevantquality experience OR Associates degree and 3 years of relevant quality experience OR High school diploma / GED and 6 years of relevantquality experience.

• Strong attention to detail

• Ability to collaborate and communicate cross-functionally

Why Join Us:

• Growth Opportunities: Were a company that believes in continuous learning and development. Whether its professional courses mentorship or new projects well help you grow.

• Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life (hybrid model).

• Inclusive Culture: Were committed to building a diverse and inclusive environment where everyones voice is valued and curiosity is encouraged.

• Innovative Projects: Youll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.

• A Place for Big Ideas: We dont just talk about thinking outside the box we throw the box away. If youve got ideas we want to hear them.

Are You Still Curious

If youve read this far then chances are youve got a curious mind just like us. So what are you waiting for Take the leap and apply today. We cant wait to see where your curiosity leads you and how it will shape the future of Just-Evotec.

Let your curiosity guide your career #BeCurious and explore the endless possibilities at Evotec!

The base pay range for this position at commencement of employment is expected to be $65000 to $90000;Base salary offered may vary depending on the individuals skills experience and competitive market value. Additional total rewards include discretionary annual bonus comprehensive benefits to include Medical Dental and Vision short-term and long-term disability company paid basic life insurance 401k company match flexible work generous paid time off and paid holiday wellness and transportation benefits.

Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race gender age disability genetic information gender expression gender identity national origin religion sexual orientation or veteran status.