At a Glance
- Tasks: Ensure quality compliance in manufacturing and support continuous improvement initiatives.
- Company: Join Evonik, a leader in sustainable solutions with a vibrant team of 33,000.
- Benefits: Enjoy hybrid work, competitive pay, health benefits, and career development opportunities.
- Other info: Embrace a culture of innovation and growth with equal opportunity for all.
- Why this job: Make a real impact on product quality and sustainability in a dynamic environment.
- Qualifications: Degree in STEM and 2-5 years in pharmaceutical or medical device QA roles.
The predicted salary is between 34650 - 42350 £ per year.
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 #Smart Work.
Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us.
- Job Descrip
- To Support Increase production on PDS Products and PDS services
Responsibilities
- Perform room clearance activities before and during manufacturing campaigns to ensure c GMP 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 c GMP 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.
- Company is Evonik Corporation
- #J-18808-Ljbffr
QA Specialist II in Birmingham employer: Evonik
At Evonik, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and sustainability. With access to extensive career development programs and a commitment to employee well-being through flexible working arrangements, our team of 33,000 colleagues thrives in an environment that encourages personal growth and collaboration. Join us in shaping a healthier, more vibrant future while enjoying the benefits of a supportive workplace that values your unique contributions.
StudySmarter Expert Advice🤫
We think this is how you could land QA Specialist II in Birmingham
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Evonik. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Evonik.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Evonik. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Evonik is looking for. A tailored application can really make you stand out!
We think you need these skills to ace QA Specialist II in Birmingham
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Evonik!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Evonik that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Evonik!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Evonik, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Evonik
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Evonik that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Evonik’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
