What we offer
You will work on exciting and challenging topics together with a team in an ultra-modern, innovative and creative environment. Intensive on-the-job training with expert colleagues guarantees you will quickly become familiar with your duties and perform them independently. Performance related pay and the opportunity for personal and professional development are of course part of the package. Since 2009 Evonik Industries AG has been certified as a family-friendly company by the German Hertie Foundation.
Click on the link to learn more about Evonik from our employees:
https://careers.evonik.com/en/about/meet-the-team/
Support existing qualification and Validation programs. Adhere to quality and regulatory compliance policies in support of GMP operations efforts.
RESPONSIBILITIES
- Support and adhere to Qualification & Validation Plans, Procedures and Projects.
- Coordinate and Execute Validation and / or Qualification projects, ensuring activities are on time, within budget, and meet cGMP requirements.
- Ddemonstrates quality practices, ensure projects are compliant with inspection agencies’ (FDA, EU) requirements and Evonik practices.
- Drafts technical documents such as white papers.
- Owns Deviations, CAPA’s, Change Controls and other deliverables to the Quality System.
- Prepare, execute protocols such as but not limited to, Performance Qualification (PQ), scheduled requalifications and test scripts.
- Summarize / analyze data generated from validation or qualification protocols and prepare final summary report on Timely manner.
- Adhere to Plans and SOP’s ensuring ongoing regulatory compliance (FDA/EU) with industry standards, practices and trends.
- Support Continuous Improvement (CI) opportunities related to Facility equipment, materials management, yield and procedures. Support improvements implementations.
- Maintain training on Evonik Quality and Compliance systems.
- When required for assigned projects; support clients audits in providing applicable documentation relevant to validation or qualification activities.
- Maintain current Validation knowledge through review of current Pharmaceutical, Engineering, Scientific literature, and by participating in Professional events, i.e. ISPE, ASQ, PDA, etc.
- Establishes safety as the number one priority through training, actions and behaviors.
- Adhere to all company safety, health and environmental policies, procedures and directives.
- Conduct assigned tasks / validation tests in a safe manner by use of MSDS to establish chemical hazards; observe the appropriate laboratory procedures; and report all incidents that could threaten the safety of personnel.
REQUIREMENTS
- Bachelor’s degree preferably in Science or Engineering discipline. Other disciplines and/or equivalent job experience will be considered.
- 1 to 3 experience in validation of aseptic pharmaceutical processes and / or equipment qualification.
- Strong understanding of Regulatory Guidance Framework FDA/EU, Industry Best Practices and cGMPs.
- Strong problem-solving and critical thinking skills with demonstrated ability to conduct technical programs and to achieve program goals; strong organization skills to handle and delegate multiple projects at differing levels of complexity.
- Excellent interpersonal skills.
- Effective written and verbal communication skills; ability to clearly and effectively communicate observations and outcomes to all levels of employee within the company.
- Comprehensive knowledge of pharmaceutical manufacturing equipment and processes.
- Ability to work closely and effectively with other workgroups in order to successfully complete projects on time and thoroughly.
- Knowledge of the use of personal protective equipment and safety practices related to working with or exposure to hazardous materials that may potentially affect the health of the employee.
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Ability to:
- Work independently or within a team environment;
- Perform work utilizing a computer for extended periods of time;
- Sit for extended periods of time without being able to leave the work area;
- Stand for extended periods of time without being able to leave the work area;
- Grasp objects utilizing the fingers (fine motor manipulation);
- Reach for objects above the head or below the waist;
- Stoop or crouch by bending at the waist or by bending the legs;
- Determine colors
- Lift 50 lbs
- Proficient in the use of word processing, spreadsheet and presentation software programs. Statistical software proficiency, a bonus.
- A thorough understanding and application of relevant scientific theories, principles, and methods.
- Capable of performing and applying standard scientific tests, procedures and techniques.
- Knowledge of a variety of formulation, processing, analytical, and manufacturing equipment and instruments
- Ability to train personnel and supervise technical activities.
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:
Kelvin Seals [C]
Company is
Evonik Corporation
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