Pharmaceutical Development Senior Analyst

  • Newry

Website CPL

Job Title: Pharmaceutical Development Senior Analyst

Company: CPL

Location: Newry, County Down

Salary: Not Disclosed

Job Type: Permanent

Posted: Recently

CPL (View profile)

Job Description:

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

Contact: Seamus Moore

Reference: NIJobs/JO-2308-521893

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