QA Specialist II

Evonik; Birmingham (AL); On-site; USD 70,000 - 100,000; Full time

Job summary

Evonik is seeking a Quality Assurance professional to support manufacturing campaigns and ensure cGMP compliance across the production line.

The role focuses on reviewing documentation, supporting validation activities, and driving quality improvements through data-driven analysis and investigations.

Qualifications

• Bachelor's degree in STEM required or equivalent experience.
• 2–5 years of pharma or medical device manufacturing experience, including QA.
• Working knowledge of FDA cGMP and QSR; experience supporting validation activities.

Responsibilities

• Perform room clearance before and during manufacturing campaigns to ensure cGMP compliance.
• Review manufacturing documentation; finalize disposition of raw materials, fill/finish components, and batch records.
• Review room cleaning logs and supporting documentation for GMP compliance.

Skills

Analytical skills

Problem-solving

Communication

Attention to detail

Microsoft Excel

Microsoft Word

Quality investigations

Education

Bachelor's degree in Chemistry, Biology, Engineering, or STEM

Tools

Microsoft Office

Job description

What we offer

Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us.

Want to know what it’s like to work at Evonik? To Support Increase production on PDS Products and PDS services Job Descrip

RESPONSIBILITIES

• Perform room clearance activities before and during manufacturing campaigns to ensure cGMP compliance.
• Review manufacturing documentation and perform final disposition of raw materials, fill/finish components, and batch records.
• Review room cleaning logs and supporting documentation for GMP compliance.
• Review analytical data supporting site utilities, including WFI, clean steam, nitrogen, and other critical systems.
• Review environmental monitoring data to ensure cleanroom compliance and product quality.
• Review and approve change control documentation in accordance with quality system requirements.
• Provide on-the-floor QA support during manufacturing campaigns for PDS Products, PDS Services, and MDS operations.
• Provide on-call quality support to address manufacturing issues and maintain production continuity.
• Lead product quality and quality system improvement initiatives using data-driven analysis.
• Analyze quality metrics, identify improvement opportunities, and support continuous improvement projects while assisting with additional business-critical activities as needed.

REQUIREMENTS

• Bachelor's degree in Chemistry, Biology, Engineering, or another STEM field preferred; equivalent relevant experience may be substituted.
• 2-5 years of experience in pharmaceutical or medical device manufacturing, including at least 1 year in a Quality Assurance role.
• Working knowledge of FDA cGMP and/or Quality System Regulations (QSR), with experience supporting validation activities, including process validation.
• Strong technical, analytical, and problem-solving skills, including experience with applied statistics and quality investigations.
• Proficient in Microsoft Office (Word, Excel, Access) with excellent attention to detail, organizational, communication, and interpersonal skills.

The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations.

This is your opportunity to join a thriving global organization that combines cutting-edge science, technology and engineering with world-class business services to create solutions that answer real-world problems. If you join us, we’ll expect you to take ownership of your work, team up with other great minds, and add your name to creations that make a positive difference for generations. As one of the world leaders in specialty chemicals operating in more than 100 countries with over 32,000 employees, we need your diversity of thought to make us better. In return for your passion, initiative and creativity, you’ll enjoy opportunities to improve and to be respected for your contribution.