At a Glance
- Tasks: Lead global labelling programmes and ensure compliance across multiple regions.
- Company: Global life sciences organisation undergoing transformation.
- Benefits: Competitive salary, potential for contract extension, and impactful work.
- Other info: Opportunity to drive change in a complex, multi-functional setting.
- Why this job: Join a critical role that shapes labelling strategies in a dynamic environment.
- Qualifications: Experience in labelling, regulatory requirements, and stakeholder management.
The predicted salary is between 56160 - 56160 £ per year.
Salary: £56,160 - 56,160 per year
Requirements:
- Strong exposure to labelling, artwork lifecycle, or product information management.
- Solid understanding of global regulatory requirements, including FDA, EU MDR/IVDR, GMP, and UDI.
- Experience working across multiple functions, particularly Regulatory, QA, and Manufacturing.
- Confidence in influencing senior stakeholders and driving alignment across regions.
- Experience with labelling or artwork systems is helpful but not essential.
- Exposure to transformation or large-scale change programmes is helpful but not essential.
Responsibilities:
- Act as the central programme lead for labelling across the business.
- Own end-to-end delivery of global labelling programmes, including remediation, harmonisation, and compliance uplift.
- Drive execution of artwork updates, IFU updates, UDI implementation, and market-specific labelling requirements.
- Lead programme governance, including timelines, budgets, risk tracking, and stakeholder alignment.
- Align senior stakeholders across regions to deliver consistent labelling strategies.
- Act as the point of escalation for labelling-related risks, compliance gaps, and operational challenges.
- Support audit and inspection readiness, particularly around labelling controls and documentation.
- Improve how labelling is managed across the business, including systems, processes, and ways of working.
Technologies: Support LESS
More: We are a global life sciences organisation undergoing significant transformation across our Quality and Regulatory landscape. This is a highly visible, strategically important contract role sitting at the intersection of Quality, Regulatory, Supply Chain, and commercial delivery. You will join a programme-critical environment where you will bring order and direction to a complex global labelling programme spanning multiple regions, product lines, and manufacturing sites. The initial contract is for 9 months, with strong forward planning in place and a high likelihood of extension into a longer-term programme of around 18 to 24 months.
Labelling Engineer in Basingstoke employer: Sivara GmbH
As a leading global life sciences organisation, we pride ourselves on fostering a dynamic work culture that encourages innovation and collaboration. Our Labelling Engineer role offers competitive remuneration and the opportunity to lead transformative projects that have a significant impact on global compliance and quality standards. With a strong focus on employee development and a commitment to creating a supportive environment, we empower our team members to thrive and grow within the organisation.
StudySmarter Expert Advice🤫
We think this is how you could land Labelling Engineer in Basingstoke
✨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 Sivara GmbH.
We think you need these skills to ace Labelling Engineer in Basingstoke
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 Sivara GmbH.
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 Sivara GmbH. 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 Sivara GmbH
✨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 Sivara GmbH.
✨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 Sivara GmbH 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.
