At a Glance
- Tasks: Lead validation activities in a dynamic Quality Department, ensuring compliance and product quality.
- Company: Join dsm-firmenich, a global leader in nutrition, health, and beauty, dedicated to sustainability.
- Benefits: Enjoy a supportive environment, opportunities for growth, and recognition for your contributions.
- Why this job: Be part of a mission-driven team making a positive impact on communities and the planet.
- Qualifications: Degree in science or engineering with 5+ years in cGMP validation; strong communication skills required.
- Other info: Embrace diversity and inclusion in a workplace where everyone can thrive.
The predicted salary is between 43200 - 72000 £ per year.
Location – Dalry, UK
Job model – On Site
At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work to not only benefit our People, Customers & Communities but also drive business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated.
Your Key Responsibilities
- Leadership role within the Quality Department responsible for the management and co-ordination of the site cGMP validation activities.
- Support validation activity during design, installation & commissioning of new equipment, processes, packaging lines & facilities and utilities.
- Ensure the validated status of site facilities, i.e., equipment, processes, CSV and utilities is complete and compliant with internal local and corporate procedures, relevant regulatory requirements and industry guidance.
- Authoring, reviewing, executing and maintaining validation documentation including site Validation Master Plan and Site Validation Strategy.
- Support Production departments in validation activities for processes and equipment.
- Preparation and management of validation plans, protocols and reports.
- Support and coordinate with corporate validation team.
- Supporting external audits including customer and regulatory inspections, presenting and explaining relevant validation information to inspectors/auditors.
- Execute validation protocols and drive to completion any CAPA associated with non-conformances raised.
- Use quality risk management tools (e.g., FMEA, System Impact Assessments) to ensure that risks are appropriately identified, documented and managed.
- Ensure product quality through robust testing and process monitoring including the use of statistical techniques.
- Support Cleaning, Utilities and Computer System Validation.
We bring
- Empowerment to make meaningful contributions while upholding ethical standards.
- Recognition and celebration of your efforts and accomplishments.
- Being a part of an agile local team at the site.
- Opportunities for growth and advancement for those who embrace innovation and take initiative.
- Opportunity to build a career in a company supplying sustainable products.
- Dedication to creating better futures for customers, communities, people, and the planet.
- Responsibility and accountability in living company values and driving sustainable solutions.
- Supportive environment where individuals are empowered to progress and contribute to meaningful change.
You bring
- Successful candidates should have a degree in a relevant science or engineering discipline.
- Minimum 5 years of validation and qualification experience in a cGMP regulated life science industry, i.e., Pharmaceutical, API or Bio-tech.
- Other essential behaviors are excellent communication and organizational skills, and the ability to work independently & within cross functional teams.
The application process
Interested in this position? Please apply on-line by uploading your resume in English via our career portal.
Equal Opportunities Commitment
dsm-firmenich is fully dedicated to inclusion because when people feel engaged and empowered, their creativity and innovation drives unprecedented progress. We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate there’s a place for everyone at dsm-firmenich.
As a committed equal opportunity employer, we ensure our recruitment practices are inclusive and fair. We encourage the recruitment of a diverse workforce, representative of the communities in which we work, by using inclusive language, diverse interview panels, diversified sourcing strategies. Selection is based on qualifications, competency, experience, performance history and fit with the team to advance fair and equitable opportunity.
Employment decisions are based upon job-related reasons regardless of an applicant's race, color, ethnicity, national origin, religion, gender, gender identity or expression, sexual orientation, age, disability, backgrounds, genetic information, protected veteran status, or any other status protected by law.
We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know.
About Dsm-firmenich
As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world’s growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet.
dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than €12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people.
Pease note this is a direct search led by dsm-firmenich. We only accept applications from candidates, not from agencies nor subject to agency’s fees, percentages or similar.
Lead Expert Validation, Dalry employer: dsm-firmenich
Contact Detail:
dsm-firmenich Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead Expert Validation, Dalry
✨Tip Number 1
Familiarise yourself with the specific cGMP regulations and guidelines relevant to the life sciences industry. Understanding these will not only help you in interviews but also demonstrate your commitment to compliance and quality assurance.
✨Tip Number 2
Network with professionals in the validation field, especially those who have experience in cGMP environments. Attend industry events or join relevant online forums to connect with potential colleagues and learn about the latest trends and challenges in validation.
✨Tip Number 3
Prepare to discuss your previous experiences in leading validation projects. Be ready to share specific examples of how you've managed validation activities, dealt with non-conformances, and collaborated with cross-functional teams to ensure compliance.
✨Tip Number 4
Research dsm-firmenich's values and recent initiatives related to sustainability and innovation. Being able to articulate how your personal values align with theirs can set you apart as a candidate who is not only qualified but also a good cultural fit.
We think you need these skills to ace Lead Expert Validation, Dalry
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in validation and qualification within a cGMP regulated environment. Emphasise your leadership skills and any specific projects that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that not only showcases your qualifications but also reflects your understanding of dsm-firmenich's commitment to diversity, equity, and inclusion. Mention how your values align with theirs and express your enthusiasm for contributing to their mission.
Highlight Key Skills: In your application, make sure to highlight essential skills such as excellent communication, organisational abilities, and experience working in cross-functional teams. Use specific examples to demonstrate these skills in action.
Proofread Your Application: Before submitting, thoroughly proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial for a role in quality management.
How to prepare for a job interview at dsm-firmenich
✨Understand the Role
Make sure you thoroughly understand the responsibilities of the Lead Expert Validation position. Familiarise yourself with cGMP regulations and validation processes, as well as the specific requirements mentioned in the job description.
✨Prepare for Technical Questions
Expect to be asked about your experience with validation documentation, risk management tools, and compliance with regulatory standards. Brush up on your knowledge of FMEA and System Impact Assessments to demonstrate your expertise.
✨Showcase Leadership Skills
As this is a leadership role, be prepared to discuss your previous experiences managing teams or projects. Highlight your ability to coordinate cross-functional teams and support production departments effectively.
✨Emphasise Communication Abilities
Excellent communication skills are essential for this role. Be ready to provide examples of how you've successfully communicated complex validation information to various stakeholders, including during audits and inspections.