At a Glance
- Tasks: Ensure compliance with international pharmaceutical standards and support quality management systems.
- Company: Leading pharmaceutical development organisation with a focus on quality and compliance.
- Benefits: Enhanced pension, healthcare, flexi-time, and opportunities for professional development.
- Other info: On-site role in central Scotland with strong career growth potential.
- Why this job: Play a vital role in maintaining regulatory compliance and improving quality systems.
- Qualifications: Degree in a relevant field and 2 years' QA experience in a GMP environment.
The predicted salary is between 29700 - 36300 £ per year.
Sector: CTO, CRO, & CDMO, PharmaceuticalsReference: BBBH187453_1791304264About the RoleA leading pharmaceutical development and manufacturing organisation is seeking a QA Compliance Officer to support the governance and compliance of its Pharmaceutical Quality Management System (PQS).
Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully.
This role plays a key part in maintaining regulatory compliance across international standards including UK/EU/US GMP/GDP and ICH guidelines.
Please note, this is a site based role in central Scotland so you must be comfortable with on site working.
Key ResponsibilitiesSupport quality system elements such as QMS monitoring, supplier qualification, and audits.
Assist in maintaining and updating regulatory registrations, licences, and certifications.
Track site compliance commitments and regulatory trends.
Collaborate with site functions to reduce compliance issues and implement improvements.
Review QMS documentation in line with global regulatory guidance.
Lead Quality Management Review meetings.
Support investigations and develop effective CAPA.Prepare for regulatory and customer audits and support follow-up. Escalate significant compliance concerns to Quality Management.
Build strong working relationships with stakeholders.
Essential Qualifications & ExperienceDegree or relevant qualification in a scientific, business, or engineering discipline.
Minimum 2 years' experience in QA within a GMP environment. Experience conducting internal or supplier audits.
Experience with QMS documentation (SOPs, deviations, investigations, CAPA).
Desirable
ExperienceCertified Auditor training.
Supplier/vendor/material approval experience.
Experience supporting regulatory audits.
Key CompetenciesStrong attention to detailProblem-solving skillsExcellent communicationProficiency in Microsoft Office applicationsWhat is on OfferExcellent benefits package including enhanced pension, healthcare and flexi-time.
Development and learning opportunities. xohmjla Guidant, Carbon60, Lorien & SRG
- The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
QA Compliance Officer in California employer: SRG Talent
As a leading pharmaceutical development and manufacturing organisation based in central Scotland, we pride ourselves on fostering a collaborative work culture that prioritises compliance and quality. Our employees benefit from an excellent package that includes enhanced pension, healthcare, and flexible working hours, alongside ample opportunities for professional development and growth within the industry. Join us to be part of a team that values your contributions and supports your career aspirations in a meaningful way.
StudySmarter Expert Advice🤫
We think this is how you could land QA Compliance Officer in California
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We think you need these skills to ace QA Compliance Officer in California
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at SRG Talent!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show SRG Talent that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at SRG Talent!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At SRG Talent, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at SRG Talent
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at SRG Talent that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with SRG Talent’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
