GMP QA Analyst

Posted 19 Days Ago
Lafayette, IN
Mid level
3D Printing • Chemical
The Role
As a QA Analyst, you will address production issues, ensure compliance with GMP regulations, approve quality events, review validation documents, and support production activities. You'll collaborate with the operations team, manage quality control processes, and provide mentorship to junior staff while contributing to continuous improvement initiatives.
Summary Generated by Built In

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.

Click on the link below to learn what our employees have to say about Evonik:
https://careers.evonik.com/en/about/meet-the-team/

RESPONSIBILITIES

  • First point of contact for production issues and compliance questions 
  • Provide or approve the initial assessments for all quality events 
  • Collaborate with Operations, then review and approve minor deviations and change controls 
  • Review validation documents 
  • Disposition all GMP API and final intermediate batches produced in the production area and support auto-disposition of non-final intermediates (includes resolution of issues) 
  • Ensure adherence to site cleaning program 
  • Approve Master Production Records 
  • Review and approve all process start up activities provide oversight for audit related activities such as equipment use logs, quarterly housekeeping, etc. 
  • Contribute to continuous improvement via membership on project teams (eg., efficiency projects and implementation of new standards). 
  • Provide backup room support for customer audits and inspections by regulatory agencies 

REQUIREMENTS

  • BS in chemistry, engineering, science, or equivalent experience 
  • Must have at least 3-5 years industrial experience in a GMP environment with good technical understanding of the GMP regulations and applications.
  • Application of GMPs have been demonstrated with experience in many aspects of the quality systems, such as change controls, deviation investigations, and validation documentation
  • Able to apply compliance standards to daily production situations 
  • Good communication skills (written and verbal) 
  • Computer skills; experience with Microsoft Office programs required, SAP and TrackWise experience is a plus
  • Strong decision making and problem solving skills 
  • Must provide 24/7 coverage for areas supported, willing to work nights and weekends as needed 
  • Proven ability to work in a team environment
  • This position is responsible to ensure that daily manufacturing operations remain compliant with cGMP and ISO 9001 requirements. The person in this role is expected to ensure compliance in the areas that they support through understanding of the compliance requirements of the products produced. The position will provide mentorship to the Assistant QA representative position. 

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.

Your Application
 

To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at https://careers.evonik.com.

Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations.

Your Talent Acquisition Manager:

Sean Levine [C]

Company is

Evonik Corporation

The Company
HQ: Essen
13,812 Employees
On-site Workplace
Year Founded: 2007

What We Do

Evonik is one of the world’s leading specialty chemicals companies. While we don’t produce electric cars, aircraft, medications or 3D printers, Evonik is part and parcel of these and many other end products. That’s because we contribute the small things that make a big difference. We make electric car batteries perform better, aircraft greener, medications more effective and 3D printers more efficient. In short: We think beyond the bounds of chemistry to make the world a better place. Today and tomorrow. We are an international group with a workforce of over 32,000 people spread across more than one hundred locations. Our daily work is shaped by global concerns, such as sustainability, diversity and digitalization. In all our business decisions, we take the present and future generations into consideration. After all, being ready for tomorrow is our business.

Interested in joining our global team? Our wide range of opportunities extends from creative and innovative research through international management all the way to production. Whether you’re studying, starting out in your career or a seasoned professional, come help us make the world a better place. For more information about careers at Evonik, go to:
www.careers.evonik.com. #HumanChemistry

Find our netiquette on: www.evonik.com/netiquette

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