At a Glance
- Tasks: Ensure laboratory data meets strict regulatory and quality standards in a dynamic environment.
- Company: Leading pharmaceutical manufacturer focused on innovation and employee wellbeing.
- Benefits: Competitive salary, enhanced leave, healthcare initiatives, and career development opportunities.
- Other info: Flexible working environment with strong focus on personal and professional growth.
- Why this job: Join a team dedicated to quality and compliance while making a real impact in pharmaceuticals.
- Qualifications: Degree in Chemistry or related field with experience in a regulated environment.
The predicted salary is between 30000 - 40000 € per year.
Are you detail-driven with a passion for quality and compliance? We're recruiting for a Data Reviewer to join a leading pharmaceutical manufacturing environment where precision, collaboration, and continuous improvement are at the heart of everything they do. This is an excellent opportunity for someone with laboratory or pharmaceutical quality experience who enjoys working in a highly regulated environment and wants to be part of a business known for innovation, employee wellbeing and career development.
Why apply?
- Alongside a competitive, negotiable salary, employees benefit from a strong package designed to support both professional growth and personal wellbeing, including:
- Enhanced annual leave entitlement
- Healthcare and wellbeing initiatives
- Pension scheme
- Life assurance
- Training and career development opportunities
- Employee assistance programme
- Modern working environment
- Health & wellbeing activities
- Recognition and reward initiatives
The Role
- Working within the Quality Control Laboratory, you will play a key role in ensuring all laboratory data, testing, and documentation meet strict regulatory and GMP standards.
- Reviewing analytical data for products, materials, validation, and stability studies
- Reviewing equipment calibration and verification records
- Compiling and reviewing laboratory testing instructions, specifications, and SOPs
- Preparing validation protocols and reviewing associated reports
- Coordinating calibration schedules for laboratory equipment
- Preparing and reviewing technical reports and regulatory submission documentation
- Supporting qualification activities for facilities and equipment when required
- Maintaining compliance with cGMP, FDA, MHRA, and internal quality standards
- Supporting a safe working environment through adherence to EHS procedures and participation in inspections and risk assessments
- Working flexibly to support departmental and business objectives
Criteria:
- Degree in Chemistry or a related scientific discipline
- Experience working within a GLP/GMP regulated environment
- Knowledge of pharmaceutical regulatory requirements, particularly FDA or MHRA standards
- Strong attention to detail and organisational skills
- Comfortable working independently and collaboratively within strict regulatory frameworks
- Proficient in Microsoft Office and computer-based systems
- Self-motivated with a proactive approach to problem solving
If this sounds like the next step in your career, we'd love to hear from you! Even if you don't meet every listed requirement, we encourage you to apply; we may have other suitable roles for you.
Riada Resourcing is an equal opportunities employer.
Data Analyst (Pharmaceutical) TLNT1_NI in Coleraine employer: IrishJobs
Join a leading pharmaceutical manufacturer in Coleraine, where precision and collaboration drive our success. We prioritise employee wellbeing and career development, offering a competitive salary, enhanced annual leave, and comprehensive healthcare initiatives. Our modern working environment fosters continuous improvement and recognition, making us an excellent employer for those passionate about quality and compliance.
StudySmarter Expert Advice🤫
We think this is how you could land Data Analyst (Pharmaceutical) TLNT1_NI in Coleraine
✨Tip Number 1
Network like a pro! Reach out to people in the pharmaceutical industry, especially those working in quality control. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP and FDA standards. Show them you’re not just detail-driven but also passionate about compliance and quality in the pharmaceutical world.
✨Tip Number 3
Don’t forget to showcase your problem-solving skills! Be ready to discuss how you've tackled challenges in previous roles, especially in regulated environments. We love hearing about real-life examples!
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, we might have other roles that fit your skills, so don’t hesitate to throw your hat in the ring!
We think you need these skills to ace Data Analyst (Pharmaceutical) TLNT1_NI in Coleraine
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Data Analyst role. Highlight any relevant laboratory or pharmaceutical quality experience, and don’t forget to mention your attention to detail and compliance knowledge!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about working in a regulated environment and how your background aligns with our values at StudySmarter. Keep it concise but impactful!
Showcase Your Problem-Solving Skills:In your application, give examples of how you've tackled challenges in previous roles. We love self-motivated individuals who can think on their feet, especially in a fast-paced environment like pharmaceuticals.
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be one step closer to joining our innovative team at StudySmarter!
How to prepare for a job interview at IrishJobs
✨Know Your Regulations
Familiarise yourself with the key regulatory standards like cGMP, FDA, and MHRA. Being able to discuss these in detail will show your understanding of the pharmaceutical environment and demonstrate that you’re serious about compliance.
✨Showcase Your Attention to Detail
Prepare examples from your past experiences where your attention to detail made a significant impact. Whether it’s catching an error in data or ensuring compliance with SOPs, concrete examples will help illustrate your skills.
✨Be Ready for Technical Questions
Expect questions related to laboratory practices and data analysis. Brush up on your knowledge of analytical methods and be prepared to discuss how you’ve applied them in a regulated setting. This will highlight your technical expertise.
✨Demonstrate Team Collaboration
Since the role involves working collaboratively, think of instances where you’ve successfully worked in a team. Be ready to discuss how you contribute to a positive team dynamic while maintaining compliance and quality standards.
