At a Glance
- Tasks: Review batch records and ensure compliance with GMP standards.
- Company: Leading manufacturing business in Hampshire with a focus on quality.
- Benefits: Flexible working hours, potential for contract extension, and a collaborative team environment.
- Other info: Opportunity to work in a dynamic, regulated manufacturing environment.
- Why this job: Join a vital role in ensuring high-quality product release and continuous improvement.
- Qualifications: Experience in Quality Assurance and strong attention to detail required.
The predicted salary is between 30000 - 40000 £ per year.
Are you an experienced QA Batch Record Reviewer? Do you have experience working within a GMP-regulated manufacturing environment? If so, this could be the role for you!
We are partnered with a leading manufacturing business in Hampshire who are looking to hire a QA Batch Record Reviewer to support their Quality Assurance team.
This role is essential in ensuring manufacturing documentation is accurate, complete and fully compliant with GMP and regulatory standards, helping to support the timely release of high-quality products.
This role is offered for 6 months initially, with the potential to extend. You will be able to work either 06:00-14:00, or 07:00-15:00 Mon-Fri.
Key Responsibilities
- Review batch records, production documentation, cleaning logs and associated GMP records.
- Ensure documentation is complete and compliant to support product release.
- Work closely with Production, Compounding and Quality teams to resolve documentation queries.
- Investigate batch record discrepancies and elevate observations where appropriate.
- Support the implementation and continuous improvement of batch record review procedures.
- Perform SAP transactions and maintain accurate quality records.
- Assist with deviations, investigations and CAPA activities.
- Collect and analyse quality KPI data to support continuous improvement initiatives.
Qualifications
- Previous experience within Quality Assurance, GMP Compliance or other pharmaceutical or FMCG manufacturing.
- Experience working in a regulated manufacturing environment.
- Strong attention to detail and documentation review skills.
- SAP knowledge is advantageous.
- Excellent written and verbal communication skills.
- Ability to work independently and collaboratively across multiple departments.
- Experience in a GMP manufacturing environment; relevant professional certification is beneficial.
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Contact Details:
Advanced Resource Managers Ltd Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Quality Batch Record Reviewer
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like Advanced Resource Managers Ltd.
We think you need these skills to ace Quality Batch Record Reviewer
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at Advanced Resource Managers Ltd.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at Advanced Resource Managers Ltd. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at Advanced Resource Managers Ltd
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with Advanced Resource Managers Ltd.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help Advanced Resource Managers Ltd achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
