Quality Auditor - Cosmetics

Sqa Services; Paris; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

An established industry player is seeking a meticulous Quality Auditor to join its global quality auditing team. This role offers the opportunity to work closely with prestigious clients in the pharmaceutical and cosmetics sectors, ensuring quality and compliance in supply chains. You will conduct supplier audits, applying your expertise in GMP regulations and related manufacturing processes. If you are passionate about quality assurance and have a strong background in auditing, this position could be your next career step. Join a dynamic team dedicated to maintaining high standards in regulated environments.

Qualifications

• 4+ years of experience in quality auditing within life sciences.
• Expert knowledge of GMP regulations and auditing standards.

Responsabilités

• Perform quality audits at suppliers for various clients.
• Collaborate with operations to ensure compliance with audit guidelines.

Connaissances

Auditing APIs

GMP regulations knowledge

ISO 22716 familiarity

Strong English communication

Description du poste

Are you passionate about quality in the cosmetics area?

Do you want to work with the most prestigious names in pharma, biologics, animal health, cosmetics, and similar regulated environments? If you have an eye for detail and want to help assure quality of life, then this is the role for you!

What to expect:

You will be part of a global quality auditing team responsible for assuring quality in the supply chains of our clients in the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries. Covering your local region, you will work closely with SQA’s operations center to coordinate, prepare, execute, and deliver supplier quality audits based on client audit schedules. You will collaborate with SQA’s production team to align your findings with each client’s audit program guidelines.

What you’ll do:

You will perform quality audits at suppliers for our clients. Each client has unique program needs, which you will be oriented to during onboarding. You will apply your skills within each program’s parameters to ensure consistent results and seamless integration into each client’s supplier risk management framework.

What you’ll need:

You should have a proven track record in auditing APIs, Excipients, Packaging, or related manufacturing processes, with thorough knowledge of GMP regulations for the life sciences industry. Familiarity with ISO 22716 and/or strong GMP audit experience is preferred.

As an SQA Quality Auditor, you will typically have at least four years of experience and will be deployed based on your expertise in the manufacturing environment. You should possess expert knowledge related to specific commodities and tools. Depending on the program, experience with standards such as 21CFR 210/211, 21 CFR 820, ICH guidelines, 21 CFR 58, 21 CFR 11, or specific activities like API, raw materials, sterilization, components, laboratories, distribution, or CROs is required.

Strong English speaking, reading, and writing skills are necessary, and willingness to travel regionally is desired.

Compensation:

$3,300 - $3,500 one-time

SQA is an Equal Opportunity Employer. Employment is based on merit and qualifications, and is not influenced by race, color, religion, gender, national origin, veteran status, disability, age, sexual orientation, gender identity, marital status, or any other legally protected status.

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