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Salary
≈ $81k – $153k per year (Estimated)
Location
In office (Birmingham)
Seniority
Senior · 10+ years exp
Employment
Full-Time

First seen by Alion on Oct 16, 2026.

Overview
Company
Impact
Profile match
Evonik Industries is a specialty chemicals company headquartered in Essen, Germany, producing additives, high-performance polymers, animal nutrition ingredients, pharmaceutical lipids, silica, membranes and care ingredients for industrial and consumer markets. Formed in 2007 from the restructuring of RAG and majority-owned by the RAG Foundation, it is active in more than 100 countries with about 31,000 employees and reported sales of 14.1 billion euros in 2025. It hires process and polymer engineers, chemists, production operators, instrument technicians, AI engineers, procurement managers and interns across Germany, the US and Asia.

What we offer

At Evonik, you’re part of a global chemical company working in many sectors that go beyond chemistry. From lipids for tomorrow’s medicines, biosurfactants for green detergents, additives for plastics recycling or membranes to help drive forward the energy transition, you’ll play an essential part in helping the world’s most essential industries succeed.

Our success hinges on a diversity of ideas powered by people, not egos. Whether you’re a scientist or engineer, new to the team or established, in business, production, or anything in between - we cheer each other on. Because we believe we can do anything. Explore everything. And Be Part of Something Special!

Find out more about the many benefits we offer:

https://www.evonik.com/en/careers/why.html

Meet the team and get to know the people behind Evonik:

https://www.evonik.com/en/news/meet-the-team.html

This position is responsible for the performance of biomaterial research and development activities for medical devices; experimental trials; organizing and driving biomaterial process development and design; participation in and supporting GMP manufacturing and processing activities; provide direct input into quality and regulatory compliance activities using databases such as trackwise.

RESPONSIBILITIES

  • Conduct polymer characterization, testing and data interpretation and evaluate results from biomaterial synthesis/processing experiments and research programs in order to meet project goals and objectives. Project activities include synthetic and analytical method development and scale up, Quality and Regulatory documentation, equipment or process validation.
  • Serve as resident Polymer processing expert and utilize structure property, Know-how of polymers, polymer testing methods to support research teams to develop biomaterials for medical device applications in Innovation projects.
  • Follow SOP’s, GMP, and GLP regulations and procedures; generate and maintain thorough and accurate documentation in support of SOP, GMP, and GLP regulated activities.
  • Follow safety practices and procedures; use personal protection equipment (PPE) appropriate to the type of hazard and exposure potential. Actively participate in identifying and resolving safety issues.
  • Interact and communicate effectively with project managers, managers on technical and operational aspects during project realization.
  • Author and review development, production, investigation, and quality reports and summaries for projects or topics of appropriate scope and complicity.
  • Recognize and Encourage opportunities to promote occupational safety and health and ensure quality, especially during process design, hazard analysis, and risk and impact assessments.
  • Design, execute, and review research, development, and operational activities associated with the transfer of technology or manufacturing processes. Prepare, monitor, and report on transfer projects.

REQUIREMENTS

  • MS degree in a relevant scientific discipline plus 10 or more years of relevant experience is preferred; or a PHD in a relevant scientific field plus 5 years is preferred; a demonstrated level of performance and capability as determined by management.
  • Preferably have led projects from concept to commercialization under minimal supervision. Demonstrated use of experience, scientific knowledge, and technical creativity/intuition to independently determine and propose scientific methods and approaches to meet project goals and objectives. Demonstrated resolution of technical challenges.
  • Ability to work on multiple activities in parallel and on multi-faceted research with minimal supervision. Managed research tasks of appropriate scope and complexity. Propose, develop, and implement new methods, assays, and processes of appropriate scope and complexity.
  • Thorough knowledge of relevant scientific principles and theories as well as the capability to use and apply standard scientific procedures and techniques. (Ordinary skills in the art).

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 www.evonik.com/en/careers.html.

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

Your Talent Acquisition Manager:

Kelvin Seals [C]

Company is

Evonik Corporation
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