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- Tasks: Join us as a QA Officer, ensuring top-notch quality in project activities and documentation.
- Company: SRG is a leading recruitment agency connecting talent with exciting opportunities in the pharmaceutical industry.
- Benefits: Enjoy competitive pay, career growth, and the chance to work in a dynamic environment.
- Why this job: Make a real impact on product quality while collaborating with diverse teams in a fast-paced setting.
- Qualifications: A degree in science or engineering plus several years of GMP QA experience is required.
- Other info: Be part of audits and regulatory preparations, enhancing your skills in a supportive team.
The predicted salary is between 28800 - 43200 £ per year.
SRG are working on several opportunities for QA Officers.
If you have Quality Assurance (QA) experience from a GMP environment then we could have a great next step for your career.
The Role:
- Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures and Analytical Procedures.
- Participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues.
- Identify and escalate any identified cGMP areas of concern.
- Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures
- Participate in the audits of suppliers, production and support functions as required.
- Be involved in the preparation for MHRA/FDA and other regulatory body audits.
- Review the relevant documentation relating to incoming raw materials and perform the disposition activities as required.
- Reviewing manufacturing, laboratory and associated documentation prior to performing the relevant disposition of final products. Where potential issues exist, these are to be highlighted to the QA manager.
Requirements:
- Degree in a relevant scientific, engineering or business discipline and/or relevant industry experience
- Several years’ experience within Quality Assurance working to GMP guidelines
- Experience of working within a Quality Management System e.g. completing or reviewing QMS documentation (SOPs/Deviations /Investigations /CAPA)
- Experience of preparing and assisting in external audits with regulatory bodies such as FDA and MHRA
- Organised and attention to detail
- Strong communication skills across all levels
Quality Assurance Officer employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Officer
✨Tip Number 1
Make sure to familiarize yourself with the latest GMP guidelines and regulations. This knowledge will not only help you in interviews but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the QA field, especially those who have experience with regulatory bodies like the FDA and MHRA. They can provide valuable insights and may even refer you to opportunities at StudySmarter.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios related to CAPA and quality investigations. Being able to discuss your past experiences in these areas will set you apart from other candidates.
✨Tip Number 4
Stay updated on industry trends and advancements in quality management systems. Showing that you are proactive about your professional development can impress hiring managers at StudySmarter.
We think you need these skills to ace Quality Assurance Officer
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Assurance Officer position. Highlight key responsibilities and requirements that align with your experience, especially those related to GMP environments.
Tailor Your CV: Customize your CV to emphasize your relevant QA experience, particularly in GMP settings. Include specific examples of your involvement in quality-related investigations, CAPA development, and any audits you've participated in.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the job requirements. Mention your degree, years of experience in Quality Assurance, and your familiarity with regulatory bodies like FDA and MHRA.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no grammatical errors and that all information is clear and concise. Attention to detail is crucial in QA roles.
How to prepare for a job interview at SRG
✨Showcase Your GMP Experience
Make sure to highlight your experience in a GMP environment during the interview. Discuss specific projects or tasks where you applied QA principles and how they contributed to compliance and quality.
✨Prepare for Regulatory Questions
Since the role involves preparing for audits by regulatory bodies like the FDA and MHRA, be ready to discuss your experience with these audits. Share examples of how you've contributed to successful audit outcomes.
✨Demonstrate Attention to Detail
Quality Assurance requires a keen eye for detail. Prepare to provide examples of how your attention to detail has helped identify issues or improve processes in previous roles.
✨Communicate Effectively
Strong communication skills are essential for this role. Practice articulating your thoughts clearly and concisely, especially when discussing complex QA concepts or procedures.
