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- Tasks: Analyze and ensure quality of packaging materials for production.
- Company: Join GSK, a leading British pharmaceutical and biotechnology company.
- Benefits: Competitive PAYE hourly rate and hands-on experience in a dynamic environment.
- Why this job: Be part of a team that values safety, quality, and continuous improvement.
- Qualifications: No specific qualifications required; just bring your motivation and willingness to learn.
- Other info: Contract role until October 2025, located on-site in Barnard Castle, Durham.
*Contract role*
Contract duration: until end of Oct 2025
PAYE hourly rate
On-site, Barnard Castle, Durham
British multinational pharmaceutical and biotechnology company
Job purpose:
To perform analysis, investigations and decision making to support the operation of the PMQC function and to meet the needs of GSK following relevant site systems and standards.
Responsibilities applicable to all roles at Barnard Castle site:
- To work as a flexible and motivated member of the team.
- To follow all Standard Operating Procedures (SOPs) and/or Standard Work Instructions (SWI) applicable, and in which the individual has been trained.
- To act, at all times, in compliance with Good Manufacturing Practices (GMP) and to report any quality issues.
- To act in a safe manner, always (in compliance with the Health & Safety at Work Act, and all other relevant legislation) and to use safety reporting systems to highlight potential hazards.
- To remain up to date with all training requirements (both ‘classroom’ courses and computer- based training through the ‘My Learning’ internal platform).
- To take part in Continuous Improvement (CI) activities to highlight improvements to equipment and processes.
- To take part in Root Cause Analysis (RCA) and Corrective and Preventative Action (CAPA) processes.
Job Specific Responsibilities:
- Testing and performing batch usage decisions on incoming deliveries prior to production use.
- Writing and checking of methods and SOPs.
- Schedule activities and workload within the department.
- To give support to other team members.
- Vendor rejections
- Document deviations from procedures and processes (DI/VI/SDA)
- Artwork discrepancies.
- Performance monitoring and reporting.
- Performing inspections.
- Validation.
- Support NPI project activity
- Reviewing maintenance routines and LEFs.
- Arrange external testing for 3rd party labs
- Working with Logistics and production areas to ensure the components are in line with the production requirements.
- Filing and archiving of documentation.
Packaging Materials Quality Control Analyst employer: Allegis Global Solutions
Contact Detail:
Allegis Global Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Packaging Materials Quality Control Analyst
✨Tip Number 1
Familiarize yourself with Good Manufacturing Practices (GMP) and the specific Standard Operating Procedures (SOPs) relevant to the role. This knowledge will not only help you in interviews but also demonstrate your commitment to quality control.
✨Tip Number 2
Highlight any experience you have with Root Cause Analysis (RCA) and Corrective and Preventative Action (CAPA) processes. Being able to discuss real-life examples of how you've contributed to continuous improvement can set you apart from other candidates.
✨Tip Number 3
Network with professionals in the pharmaceutical and biotechnology industry, especially those who work in quality control. Engaging with them on platforms like LinkedIn can provide insights into the company culture and expectations at GSK.
✨Tip Number 4
Prepare to discuss your ability to work flexibly within a team. GSK values motivated team members, so be ready to share examples of how you've successfully collaborated with others in past roles.
We think you need these skills to ace Packaging Materials Quality Control Analyst
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Packaging Materials Quality Control Analyst position. Understand the key responsibilities and required skills, especially those related to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs).
Tailor Your CV: Customize your CV to highlight relevant experience in quality control, analysis, and compliance with industry standards. Include specific examples of your work with batch testing, documentation, and any Continuous Improvement (CI) activities you've participated in.
Craft a Strong Cover Letter: Write a cover letter that reflects your motivation for applying to this role at GSK. Mention your understanding of the importance of safety and quality in pharmaceutical manufacturing, and how your background aligns with the company's values and needs.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. Ensure that your application is clear, concise, and professional, as attention to detail is crucial in quality control roles.
How to prepare for a job interview at Allegis Global Solutions
✨Understand GMP and SOPs
Make sure you have a solid understanding of Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). Be prepared to discuss how you've applied these in previous roles, as this will show your commitment to quality and compliance.
✨Show Your Team Spirit
This role emphasizes being a flexible and motivated team member. Think of examples from your past experiences where you collaborated effectively with others or contributed to team success. Highlighting your teamwork skills can set you apart.
✨Prepare for Technical Questions
Expect technical questions related to quality control processes, batch testing, and documentation. Brush up on your knowledge of testing methods and how to document deviations. Being able to speak confidently about these topics will demonstrate your expertise.
✨Continuous Improvement Mindset
Be ready to discuss any Continuous Improvement (CI) initiatives you've been involved in. Companies value candidates who can identify areas for improvement and contribute to enhancing processes. Share specific examples of how you've made a positive impact in previous roles.
