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:
- Performance related bonus (discretionary and subject to eligibility criteria)
- Private medical cover (subject to eligibility criteria)
- 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
- Access to electric vehicle leasing scheme (subject to eligibility criteria)
- 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.
Job Description
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
The ideal candidate will be educated to degree level in Biomedical or Life Sciences related discipline. Practical experience or job placement in the industry will be highly beneficial.
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.
APPLY NOW for full consideration, you can be sure that your application will be treated confidentially and impartially, and you will always receive an update within 10 business days.