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For Companies At a Glance
- Tasks: Join our compliance team to enhance quality and drive improvements in manufacturing processes.
- Company: Kindeva is dedicated to creating life-saving products for better health worldwide.
- Benefits: Enjoy a collaborative work environment with opportunities for growth and development.
- Why this job: Make a real impact on patient health while developing your skills in a dynamic industry.
- Qualifications: Production experience in regulated environments; a degree in Science or Engineering is preferred.
- Other info: Be part of a team that values innovation and compliance in the pharmaceutical sector.
The predicted salary is between 36000 - 60000 £ per year.
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
The compliance team is responsible for quality compliance improvement within the value stream. The Compliance Engineer will provide technical support to the Inhalation value stream focusing on driving compliance and improving processes.
Role Responsibilities
- Documentation management for manufacturing including reviews of completed batch records and procedure authoring and updates.
- Management of change control process as a subject matter expert supporting other functions.
- Support of internal and external audits for the manufacturing team.
- Collaboration across site teams to ensure quality including site metrics and improvements.
- Support of planned and unplanned deviations, including root cause investigations and CAPAs.
- Support or complaint investigation processes where appropriate.
- Coaching and mentoring others to improve compliance across departments.
- Provide day-to-day support and problem-solving knowledge to the value stream when an issue arises.
Basic Qualifications
- Production experience in a regulated environment.
- Attention to detail for reviewing and updating documentation.
- Excellent written and verbal communication skills and confidence to communicate effectively with people at all levels.
- Ability to investigate quality incidents and root cause analysis.
Preferred Qualifications
- Degree in a Science or Engineering discipline.
- Pharmaceutical product knowledge and experience, preferably inhalers
- Knowledge of pharmaceutical quality management systems.
- Understanding of GMP, Regulatory and ISO standards.
- Knowledge of D365 and Master Control.
- Knowledge of Six Sigma and Lean Manufacturing.
- Job Family C – Documentation – Document Compliance
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Compliance Engineer employer: Kindeva Drug Delivery
Contact Detail:
Kindeva Drug Delivery Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Compliance Engineer
✨Tip Number 1
Familiarise yourself with the specific regulations and standards relevant to the pharmaceutical industry, such as GMP and ISO. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance.
✨Tip Number 2
Network with professionals in the compliance field, especially those who work in the pharmaceutical sector. Attend industry events or join online forums to gain insights and potentially get referrals for the Compliance Engineer role.
✨Tip Number 3
Prepare to discuss specific examples of how you've improved compliance or quality processes in previous roles. Use the STAR method (Situation, Task, Action, Result) to structure your responses effectively during interviews.
✨Tip Number 4
Showcase your problem-solving skills by discussing any experience you have with root cause analysis and CAPAs. Highlighting these experiences can set you apart as a candidate who is proactive and detail-oriented.
We think you need these skills to ace Compliance Engineer
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and qualifications required for the Compliance Engineer position. Tailor your application to highlight relevant experiences that align with these requirements.
Highlight Relevant Experience: Emphasise your production experience in a regulated environment and any specific knowledge of pharmaceutical quality management systems. Use concrete examples to demonstrate your attention to detail and problem-solving skills.
Showcase Communication Skills: Since excellent written and verbal communication skills are essential, ensure your CV and cover letter are well-structured and free of errors. Consider including examples where you effectively communicated with various stakeholders.
Tailor Your Documents: Customise your CV and cover letter to reflect the specific qualifications mentioned in the job description, such as knowledge of GMP, Regulatory and ISO standards. This shows that you have taken the time to understand what Kindeva is looking for.
How to prepare for a job interview at Kindeva Drug Delivery
✨Know Your Compliance Standards
Familiarise yourself with GMP, Regulatory, and ISO standards relevant to the pharmaceutical industry. Being able to discuss these standards confidently will show your understanding of the compliance landscape.
✨Demonstrate Attention to Detail
Prepare examples from your past experience where your attention to detail made a significant impact, especially in documentation management or quality compliance. This will highlight your suitability for the role.
✨Showcase Your Problem-Solving Skills
Be ready to discuss specific instances where you successfully investigated quality incidents or conducted root cause analysis. This will demonstrate your analytical skills and ability to handle compliance issues effectively.
✨Communicate Effectively
Practice articulating your thoughts clearly and confidently. Since the role requires collaboration across teams, showcasing your excellent written and verbal communication skills during the interview is crucial.
