Full-Time

Quality Auditor

Pharmaceutical

Posted on 4/18/2024

SQA Services

201-500 employees

Global supplier quality services and data

Data & Analytics

Industrial & Manufacturing

Expert

Baton Rouge, LA, USA

Requirements

Proven track record in performing audits of APIs, Excipients, Packaging, or related manufacturing processes
Thorough familiarity with GMP regulations for the life sciences industry
Audit experience in ICH Q7 and ISO 9001
At least four years of experience as an SQA Quality Auditor
Expert knowledge of specific commodities and tools
Experience with 21CFR 210/211, 21 CFR 820, ICH guidelines, 21 CFR 58, 21 CFR 11
Strong English speaking, reading, and writing skills
Willingness to travel regionally

Responsibilities

Performing quality audits at suppliers to SQA’s clients
Applying skills and experience within the parameters of each program to produce consistent results
Coordinating, preparing, executing, and delivering supplier quality audits based on client audit schedules
Aligning expert findings to the individual structure and guidelines of each client’s managed audit program

Job Description

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:

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 people with audit experience in ICH Q7 and ISO 9001.

As an SQA Quality Auditor, you will have at least four years 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.

Pay Range:

$1000-1200 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 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.

SQA Services

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At SQA Services, Inc., employees are at the forefront of the supplier quality services industry, engaging with the patented STEPQ technology to provide crucial, real-time quality data for quality-critical industries. This role offers a unique opportunity to work within a vast network of experienced professionals in over 50 countries, fostering a rich environment of learning and innovation. The company is committed to maintaining high standards of quality assurance and streamlining global operations, making it an ideal workplace for those passionate about impacting various industries positively through superior quality management systems.

Company Stage

M&A

Total Funding

$282M

Headquarters

Palos Verdes Estates, California

Founded

1995

Growth & Insights

Headcount

6 month growth

↑ 3%

1 year growth

↑ 5%

2 year growth

↑ 11%