Médecin du Travail H / F

ACTIVA CONSEIL; Paris; Sur place; EUR 40 000 - 80 000; Plein temps

Résumé du poste

Join a dynamic organization focused on enhancing health and wellness through innovative solutions. This role involves representing Quality Assurance in critical computer system validation projects, ensuring compliance with stringent regulations such as FDA CFR Part 11 and EU GMP Annex 11. You'll be instrumental in maintaining quality systems, conducting training, and driving improvements in QA processes. With a hybrid working model and a commitment to professional growth, this is an exciting opportunity to advance your career in a supportive and collaborative environment. If you're passionate about quality assurance and regulatory compliance, this position offers a pathway to make a significant impact in the health sector.

Prestations

Career development opportunities

Competitive compensation package

Hybrid working model

Training and coaching support

Qualifications

• 2-5 years experience in Computer System Validation in Pharma/Medical Devices.
• Deep knowledge of FDA regulations and EU GMP standards.

Responsabilités

• Represent QA in computer system validation projects and audits.
• Support maintenance of Quality Management System and training.

Connaissances

Computer System Validation

Quality Assurance

Regulatory Compliance

Training and Development

Data Integrity

Formation

Bachelor's degree in IT, Engineering, Biochemistry, or Chemistry

Outils

Trackwise

LMS

Description du poste

Perrigo is a leading global provider of over-the-counter (OTC) health products and wellness solutions that enhance individual overall well-being.

Originating from the former Omega Pharma, the European branch is today present in 30 countries with a strong local anchorage.

You know us from brands like Physiomer, NiQuitin, XLS Medical, Zaffranax, Arterin, Dermalex, Biover, Galenco, Davitamon, Ymea, Lactacyd.

Perrigo is an organization with a dynamic, transparent and fast-paced atmosphere, characterized by an entrepreneurial and cooperative culture.

Location: Ghent, Belgium or Chatillon, France

We offer a Hybrid working schedule, a mix of onsite and remote working each week.

Scope of the Role

• Represent QA in computer system validation projects including change controls, deviations and periodic reviews and Data integrity for CSCI.
• Provide support with guidelines and regulations such as GAMP 5, EU GMP Annex 11, and FDA CFR Part 11.
• Act according to the Quality Assurance (QA) vision, strategy and standards for the integrated Perrigo CSCI group.
• Keep going awareness of new and developing regulations (different ISO regulations, GMP, GDP, MDR, MDD).
• Support in the maintenance of Quality Systems, including electronic systems (Trackwise, LMS,…).
• Provide QA training to the entire group (European branch of the Perrigo Company) regarding computer system validation and Data Integrity and evaluate training effectiveness, including the creation of PowerPoint presentations, online recorded trainings, etc.
• Ensure adherence to critical procedures and compliance to requirements for record retention.
• Be part of third-party qualification and regular third-party auditing for all topics related to Computer System Validation and Data integrity.
• Assist in performing internal QA audits.
• Support in the maintenance of the Quality Management System by creating and updating Standard Operating Procedures, Best Practices and Working Instructions related to Computer Systems and Data Integrity.
• Provide support in establishing and maintaining the ISO 9001 and ISO 13485 Quality Management System related to Computer Systems and Data Integrity.
• Identify gaps and areas for improvement in QA processes related to Computer system and handling and lead remedial actions and initiatives.

Experience Required

• Bachelor degree in IT, engineering, biochemistry, chemistry or equivalent through experience.
• You are fluent in spoken and written English; other languages are a benefit.
• At least 2-5 years relevant experience in Computer system validation in Pharmaceutical and/or Medical Devices industry.
• Deep knowledge of FDA regulations (especially CFR Part 11), EU GMP Annex 11 and GAMP 5.
• Knowledge of the relevant European regulations for pharmaceutical products (GMP specifically Annex 11, GDP), Medical Devices (MDR, MDD, ISO13485, ISO14971), Food, Food Supplements (HACCP, ISO 22000); Cosmetics (ISO 22716) is an asset.

What we can offer you

• Perrigo offers you a challenging position within a strong and dynamic company.
• A professional environment offering you the opportunity to boost your career through training, coaching & support, learning on the job.
• A competitive compensations and benefits package for the required level and experience.
• The opportunity to work in a hybrid working model as part of our self-care and wellbeing strategy.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. Our full Equal Employment Opportunity and Affirmative Action Policy Statement is available on our main career site in English and Spanish and will be provided in other accessible forms for persons with disabilities.