Method Development & Validation Specialist
Method Development & Validation Specialist

Method Development & Validation Specialist

Full-Time 58000 Β£ / year No home office possible
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At a Glance

  • Tasks: Lead method development and validation in a dynamic pharmaceutical environment.
  • Company: Join a top-tier pharmaceutical client in Cork, focused on innovation and quality.
  • Benefits: Enjoy a supportive team culture with opportunities for professional growth and exposure to advanced technologies.
  • Why this job: Work collaboratively in a GMP-regulated setting, making a real impact in the pharmaceutical industry.
  • Qualifications: Degree in Chemistry and 5 years' experience in an analytical lab, preferably in GMP.
  • Other info: Mentorship opportunities available for junior analysts.

Method Development & Validation Specialist – Analytical Development (Pharmaceutical Services)

Interested in this role You can find all the relevant information in the description below.

Location: Cork, Ireland | Full-Time | On-Site with Client

Are you an experienced analytical scientist ready to take the next step in your career? We are seeking a Method Development & Validation Specialist to join a dynamic Professional Scientific Services (PSS) team supporting a leading pharmaceutical client in Cork. This is a fantastic opportunity to work in a collaborative, GMP-regulated environment where innovation, quality, and scientific excellence are at the forefront.

Key Responsibilities
β€’ Lead and support method development, validation, and transfer activities in line with regulatory guidelines.
β€’ Provide technical expertise for the introduction of new products, including troubleshooting analytical challenges.
β€’ Interpret and document analytical data, ensuring compliance with ALCOA+ and GMP standards.
β€’ Act as a subject matter expert in analytical techniques such as HPLC, GC, IR, LC-MS, and ICP-OES.
β€’ Mentor and train junior analysts, review technical documentation, and contribute to continuous improvement initiatives.
β€’ Communicate effectively with client stakeholders, ensuring project timelines and quality metrics are met.

About You
β€’ Degree in Chemistry or a related scientific discipline.
β€’ Minimum 5 years’ experience in an analytical laboratory, ideally within a GMP environment.
β€’ Strong background in method development and validation for APIs, raw materials, and excipients.
β€’ Proficient in troubleshooting analytical instrumentation and methodologies.
β€’ Excellent communication, documentation, and problem-solving skills.
β€’ Passionate about quality, customer service, and continuous improvement.

Why Join Us?
β€’ Be part of a high-performing team embedded within a global pharmaceutical leader.
β€’ Gain exposure to cutting-edge analytical technologies and diverse product portfolios.
β€’ Enjoy a supportive environment that values professional development and scientific integrity

Method Development & Validation Specialist employer: Kenton Black

Join a leading pharmaceutical client in Cork as a Method Development & Validation Specialist, where you will thrive in a collaborative and GMP-regulated environment that prioritises innovation and scientific excellence. Our supportive work culture fosters professional growth, offering opportunities to mentor junior analysts and engage with cutting-edge analytical technologies, ensuring your career development is both meaningful and rewarding.
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Contact Detail:

Kenton Black Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Method Development & Validation Specialist

✨Tip Number 1

Network with professionals in the pharmaceutical industry, especially those who work in analytical development. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends in method development and validation.

✨Tip Number 2

Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC and LC-MS. Consider reaching out to current employees on platforms like LinkedIn to gain insights into their experiences and the skills that are most valued in the role.

✨Tip Number 3

Prepare to discuss your experience with regulatory guidelines and GMP compliance during interviews. Think of specific examples where you successfully led method development or validation projects, as this will demonstrate your expertise and fit for the role.

✨Tip Number 4

Showcase your passion for continuous improvement by researching recent advancements in analytical methodologies. Be ready to share how you have implemented innovative solutions in past roles, as this aligns with the company's focus on quality and scientific excellence.

We think you need these skills to ace Method Development & Validation Specialist

Method Development
Method Validation
Analytical Techniques (HPLC, GC, IR, LC-MS, ICP-OES)
GMP Compliance
ALCOA+ Standards
Troubleshooting Analytical Instrumentation
Technical Documentation
Data Interpretation
Mentoring and Training
Continuous Improvement Initiatives
Communication Skills
Problem-Solving Skills
Project Management
Collaboration Skills
Attention to Detail

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience in method development and validation, particularly in a GMP environment. Use specific examples that demonstrate your expertise with analytical techniques like HPLC, GC, and LC-MS.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality and customer service. Mention your relevant experience and how it aligns with the responsibilities of the Method Development & Validation Specialist role.

Highlight Technical Skills: In your application, emphasise your technical skills and problem-solving abilities. Provide examples of how you've successfully tackled analytical challenges in previous roles.

Showcase Communication Skills: Since effective communication is key in this role, include examples of how you've successfully communicated with stakeholders or mentored junior analysts in your past positions.

How to prepare for a job interview at Kenton Black

✨Showcase Your Technical Expertise

Be prepared to discuss your experience with analytical techniques such as HPLC, GC, and LC-MS. Highlight specific projects where you led method development or validation, and be ready to explain the challenges you faced and how you overcame them.

✨Demonstrate Your Understanding of GMP Standards

Since the role is in a GMP-regulated environment, it's crucial to show your knowledge of ALCOA+ principles and how they apply to analytical data. Prepare examples of how you've ensured compliance in previous roles.

✨Emphasise Your Mentoring Skills

As a Method Development & Validation Specialist, you'll likely mentor junior analysts. Share experiences where you've trained others or contributed to team development, showcasing your leadership and communication skills.

✨Prepare for Problem-Solving Scenarios

Expect questions that assess your troubleshooting abilities. Think of specific instances where you identified and resolved analytical challenges, and be ready to walk the interviewer through your thought process.

Method Development & Validation Specialist
Kenton Black
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