Senior Quality Gmp Auditor
2 semanas atrás
Are you passionate about quality in the life sciences area? Do you want to work with the most prestigious names in pharma, bio, animal health 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**:
**What you'll need**:
You will need to have expertise in performing GMP audits in the life sciences industries. Direct audit experience to 21 CFR part 11, ICH Q7, PIC/S GMP Part 1, WHO Guidelines, Eudralex Vol 4, and 21 CFR part 210/211 standards is preferred.
Strong English speaking, reading and writing skills are necessary and willingness to travel regionally is desired. Must speak both English and Spanish.
**Pay Range**:
$1200-1400 USD for a 1-day audit. Includes: Time spent preparing for the audit, traveling, performing the audit, writing the report, and responding to questions from our Content team of editors and the client until the report is finalized. Does not include: Following up on CAPA for any findings or reimbursement for travel expenses - expenses are reimbursed at cost with receipts per SQA travel policy. Note that SQA helps with the preparation of the audit and proofreads all audit reports.
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