Company Description
As a global leader in sustainability, quality, and integrity, our 99,600-strong workforce across 2,600 offices and labs is dedicated to fostering a safer, more connected world. Our services impact every facet of daily life, enhancing the safety of food, consumer products, transport, and healthcare, to advancing nuclear industry testing. Your role is crucial in providing safer products, superior services, and maintaining societal connectivity.
At SGS, We're committed to recognising the dedication and effort of our team. By joining us, you'll have access to a range of benefits including performance-related bonuses, private medical cover, a competitive pension scheme with life assurance, and a generous annual leave allowance that grows with your service. Enjoy extra perks like a day off for your birthday, discounted gym memberships, retail discounts, an electric vehicle leasing scheme, enhanced parental leave, service awards, Christmas vouchers, and health & wellbeing initiatives.
Job Description
- Job Title : Quality Assurance Auditor
- Job Type: Permanent
- Hours : 35 hours per week
- Salary: Starting from £23,400 per annum depending on experience level
- Job Location : Clydebank - Office based
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.