Quality Assurance Auditor

6 months ago

Clydebank, United Kingdom SGS Full time

**Company Description**
- ** Job Title**:Quality Assurance Auditor
- ** Job Type**:Permanent
- ** Hours**:35 hours per week (Monday to Friday, 9am - 5pm)
- ** Salary**: Starting from £23,000 per annum depending on experience level
- ** Job Location**:Clydebank - Office based

At SGS, we believe in rewarding our employees for their hard work and commitment. As part of our team, you would be eligible for:

- Competitive pension scheme + Life Assurance
- Generous Annual Leave allowance (increasing with service) plus bank holidays.
- An additional day off for your birthday
- Discounted Gym Membership
- Retailer Discounts
- Enhanced maternity/paternity and adoption pay.
- Length of Service Awards
- Christmas Vouchers
- Health & Wellbeing initiatives

SGS are the world’s leading testing, inspection and certification company.

We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.

We deliver services that touch every part of human activity and improve millions of lives - from ensuring the safety of food, clothing, transportation, and medicine to better testing in the nuclear industry. Whatever your role, you will make an important contribution to delivering safer products, better services and keeping society connected.

As a Quality Assurance Auditor, your role includes reviewing final reports to ensure that the laboratory staff's methods, procedures, and observations are accurately and completely documented, and that the results reported are consistent with the raw data.

You are responsible for promptly communicating any findings from raw data inspections to the Study Director/Scientist, Principal Investigator, and relevant management as necessary.

Your duties also encompass preparing, managing, and maintaining all quality documentation systems, keeping copies of all approved study documents and standard operating procedures currently in use, and verifying that study documentation meets the requirements for compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards.

You will manage your workload to ensure that tasks are adequately resourced and scheduled efficiently and effectively, with all work audited and carried out in line with GLP and GMP principles. You will provide compliance advice and guidance to staff when needed and support Study Directors in resolving issues and discussing projects with clients. Additionally, you will engage with clients regarding any deviations, investigations, or out-of-specification events to ensure that any resulting corrective and preventative actions (CAPAs) are executed properly.
**Qualifications**

You'll also demonstrate;
- Strong attention to detail to uphold excellent auditing standards
- Proficiency in reviewing data and drawing conclusions
- Experience with database management
- Robust IT skills, including proficiency in Word, Excel, and PowerPoint
- Familiarity with adhering to business and regulatory guidelines
- Effective communication abilities
- Solid analytical reasoning and math skills

**Additional Information**
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, colour, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.

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