Quality Auditor - Cosmetics

SQA Services; Lyon; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading quality audit firm seeks a Quality Auditor to ensure high standards in the pharmaceuticals and cosmetics industries. Candidates must have a proven audit record and in-depth knowledge of GMP and ISO regulations, along with strong communication skills. If you are detail-oriented and willing to engage with client needs across various programs, this role offers a chance to contribute significantly to supplier quality assurance.

Qualifications

• At least four years' experience in quality audits of APIs, Excipients, or related processes.
• Familiarity with GMP regulations and ISO 22716.
• Strong knowledge of relevant regulations (e.g., 21CFR 210/211, ICH guidelines).

Responsabilités

• Perform quality audits at suppliers for various industries.
• Coordinate with operations to execute audit schedules.
• Produce consistent audit results integrated into management frameworks.

Connaissances

Attention to Detail

Auditing

GMP Knowledge

ISO 22716 Familiarity

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 work with SQA’s world-class production team to align your expert findings to the individual structure and guidelines of each client’s managed audit program.

What you’ll do:

You will be performing quality audits at suppliers to SQA’s clients. Each client has unique program needs to which you will be oriented as part of your on-boarding for each program. You will apply your skills and experience within the parameters of each program to produce the consistent results needed for seamless integration of audit results into each client’s supplier risk management framework.

What you’ll need:

You will need to have a proven track record in performing audits of APIs, Excipients, Packaging or related manufacturing processes and be thoroughly familiar with GMP regulations for the life sciences industry. We are currently looking for someone with familiarity to ISO 22716 and/or strong GMP audit experience.

As a SQA Quality Auditor, you will have at least four year's experience and will be deployed based upon your subject matter expertise relative to the manufacturing environment. You will possess expert knowledge relating to specific commodities and tools. Depending on the requirements of the program, (e.g., 21CFR 210/211, 21 CFR 820, ICH guidelines, 21 CFR 58, 21 CFR 11), you shall be experienced in the commodity or activity of the auditee (e.g., API, raw materials, sterilization, components, laboratories, distribution, CROs).

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

$3,300 - $3,400 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.