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Job Location drjobs

Paris - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

For our client we are looking for an experienced GxP Consultant.

Contract: Freelance/Independent Contractor

Location: Paris France



Our client is a company a familyowned French pharmaceutical and dermatological laboratory with a centurylong history of growth and innovation. With a focus across various fields including Gastroenterology Rheumatology ENT General Medicine Dermocosmetics and Medical Devices it operates internationally with subsidiaries across the globe. Upholding values of Responsibility Pragmatism and Caring the company aims to provide the best healthcare solutions and has a strong commitment to patient wellbeing. The companys expertise lies in manufacturing environmental sustainability and renowned brands. Over the years it has expanded its portfolio through acquisitions and launches emphasizing Consumer Healthcare.

Key Responsibilities:

Formulating documentation for cleaning validations analytical methods and procedural processes.
Conducting risk assessments across various GxP domains.
Performing internal and external audits on both national and international scales.
Contributing to the creation of Product Quality Reviews (PQR).
Crafting and assessing technical papers such as Standard Operating Procedures (SOPs) protocols and technical reports.
Drafting documents and executing qualification and validation procedures for equipment and services.
Collaborating with clients on project management activities.
Overseeing the pharmaceutical quality systems document management system.
Managing and drafting deviations and change controls including thorough investigations.
Supervising Corrective and Preventive Action (CAPA) plans and tracking their implementation.
Providing Quality Assurance support for computerized system validation.
Reviewing and assisting in the drafting of User Requirement Specifications (URS) from a Quality Assurance standpoint.
Contributing to the supplier approval process. Ensuring suppliers and clients maintain GxP certification standards.

Requirements

Desired Qualifications:

Bachelors degree in Pharmacy Biology Chemistry Engineering or related disciplines with a keen interest in specializing in the GxP domain.
A Masters degree in Pharmaceutical Industry or equivalent is advantageous.
Prior experience in a Good Manufacturing Practice (GMP) environment with knowledge of best documentation practices.
Proactive individuals with strong analytical and problemsolving capabilities.
Excellent communication and teamwork abilities.
Availability for onsite work at our facilities.
Training in project management is preferred.
Nativelevel of French language
Proficiency in English with highlevel comprehension and writing skills.
Knowledge of additional languages is beneficial.
Seniorlevel experience: >3 years




Benefits

Global Reach: The opportunity to work on projects with international impact spanning over 100 countries.

Stability: Joining a reputable and stable organization with over a century of experience in the pharmaceutical and dermatological industries.

FamilyOwned Environment: Being part of a supportive and familial work environment fostering a sense of community and belonging.

Commitment to Healthcare: Contributing to meaningful work focused on providing effective reliable and accessible healthcare solutions.

Independence and LongTerm Vision: Engaging in projects with a forwardthinking approach and a focus on longterm development plans.

Manufacturing Expertise: Collaborating with a company known for its highquality products and processes with manufacturing expertise dating back to 1909.

International Development Opportunities: Opportunities to work across diverse markets and regions gaining valuable international experience.

Collaborative Work Culture: Joining a collaborative culture where teamwork is emphasized working alongside passionate and committed individuals united in promoting everyday health and wellbeing.




Desired Qualifications: Bachelor's degree in Pharmacy, Biology, Chemistry, Engineering, or related disciplines, with a keen interest in specializing in the GxP domain. A Master's degree in Pharmaceutical Industry or equivalent is advantageous. Prior experience in a Good Manufacturing Practice (GMP) environment with knowledge of best documentation practices. Proactive individuals with strong analytical and problem-solving capabilities. Excellent communication and teamwork abilities. Availability for on-site work at our facilities. Training in project management is preferred. Native-level of French language Proficiency in English with high-level comprehension and writing skills. Knowledge of additional languages is beneficial. Senior-level experience: >3 years

Employment Type

Full Time

Company Industry

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