Pharmaceutical Development Senior Analyst in Newry

Pharmaceutical Development Senior Analyst in Newry

Newry Full-Time 31500 - 38500 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Join our R&D team to oversee analytical testing for new product launches.
  • Company: CPL, a leading veterinary pharmaceutical company with a focus on innovation.
  • Benefits: Excellent salary, 34 days annual leave, enhanced pension, and annual bonus.
  • Other info: Collaborative culture with opportunities for professional development.
  • Why this job: Make a real impact in veterinary pharmaceuticals while growing your career.
  • Qualifications: Degree in science and two years' experience in a cGMP environment required.

The predicted salary is between 31500 - 38500 £ per year.

CPL is proud to collaborate with one of the leading veterinary pharmaceutical companies globally as they continue to expand their operations across Europe, with a specific focus on Northern Ireland. We are currently seeking a highly skilled Pharmaceutical Development Senior Analyst for a full-time, permanent position based in Newry, County Down.

Why Choose Us:

At CPL, we are guided by our core values, which include Customer Value, One Team, Results Driven, Excellence, Innovation, and Quality. We are committed to fostering a culture that encourages our employees to embody these values, as our ongoing success relies on the expertise, knowledge, and innovation of our team members.

In return for your dedication and skills, we offer:

  • An excellent salary package
  • 34 days of annual leave
  • Enhanced pension contributions
  • Annual bonus

Key Responsibilities:

The successful candidate will be an integral part of our R&D team, working alongside a diverse group of analysts. The role will involve overseeing all aspects of analytical testing to support new product launches within R&D, as well as providing support for existing finished product methods. This includes developing, validating, and transferring finished product analysis methods, conducting process validation testing during batch manufacture, and managing the stability program for pre-approval batches.

The Senior Analyst will be responsible for scheduling daily work for analysts and team leaders to meet project timelines, as well as evaluating and reporting results in a timely and accurate manner. Additionally, there will be close collaboration with the Quality Assurance team to ensure a high standard of data output.

Qualifications and Requirements:

  • A degree (or equivalent) in a science-related discipline.
  • A minimum of two years’ experience working in a cGMP environment.
  • Proficiency in HPLC, UPLC, GC, and practical wet chemistry.
  • Experience in GMP data review.
  • Knowledge of VICH guidance for Method Validation of Finished Product methods, process validation, and stability studies.

Next Steps:

If this opportunity aligns with your career goals, please reach out to Seamus Moore by applying to this advertisement or giving him a call.

Key Skills: analytical chemist, Development Chemist, R&D

Pharmaceutical Development Senior Analyst in Newry employer: jobs pharmaguidelines

Join NHS Jobs as a Foundation Pharmacist in the beautiful coastal town of Torquay, where you will embark on a rewarding two-year rotation programme designed to enhance your clinical skills and professional development. Our supportive work culture fosters collaboration within a multidisciplinary healthcare team, ensuring that you play a vital role in optimizing patient care while enjoying opportunities for continuous learning and growth. With a commitment to quality improvement and a focus on evidence-based practices, NHS Jobs offers a fulfilling environment for those passionate about making a difference in healthcare.

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Contact Details:

jobs pharmaguidelines Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Pharmaceutical Development Senior Analyst in Newry

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We think you need these skills to ace Pharmaceutical Development Senior Analyst in Newry

Analytical Testing
Method Development
Method Validation
Process Validation
Stability Studies
HPLC
UPLC

Some tips for your application 🫡

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