Senior Analytical Development Chemist

As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

SENIOR ANALYTICAL DEVELOPMENT CHEMIST

Job Description

About the site

Operating for over 40 years, the Cork site is proud to manufacture and supply Active Pharmaceutical Ingredients (API) to our customers for use in clinical trials and approved medicines for commercial supply - medicines to treat Cancer, Parkinson’s Disease, Depression, HIV, Congestive Heart Failure, Diabetes and Respiratory diseases, along with raw material for consumer healthcare products.

The site is welcoming exciting growth and new expansions to support much-needed capacity for APIs currently in development and the growing needs of customers and the patients we serve.

Discover Impactful Work:

The Senior Analytical Development (AD) Chemist will function as a key member of the AD Team and will report to the AD Manager. You will be key to the introduction of new products to the Cork site. You will promote and monitor laboratory GMP / Safety within the AD group.

A day in the Life:

• Provide analytical expertise and support for the introduction of new products to the Site, including method assessment, method development, validation/qualification and transfer.

• Be the lead analyst on projects. Plan the execution of the projects and mentor/lead the support analysts.

• Project/people management for technology transfer projects.

• Lead troubleshooting activities during the development, validation/qualification and transfer of methods. Plan, complete and evaluate fate of impurities studies in collaboration with colleagues and client through interpretation of analytical data and adhering to current and emerging regulatory strategies (quality by design, GMP, ICH’s guidelines) for API.

• Communicate regularly with the clients and internal partners, providing updates on projects progress, hosting clients visits, addressing technical queries and delivering client project requirements to the defined timelines.

• Responsible for managing employees and resources to ensure the delivery of projects in the required timeframe and ensure that the site’s technical, quality and safety metrics are all achieved.

• Prepare, review and approve change controls, protocols, project status report, final reports and other internal documentation relevant to the role.

• Present training sessions to QC and provide technical support during method familiarisation period.

• Work with due care and attention, perform all quality, regulatory and safety duties in a compliant manner whilst acting always in accordance with the Dignity at Work Policy, Code of Business Conduct and Ethics and our values of Integrity, Intensity, Innovation and Involvement.

• Develop/Expand scientific, technical knowledge by reading the peer reviewed scientific literature, attending scientific conferences via relevant training.

Education/Experience required

• BSc; Masters or PhD in relevant scientific field with significant experience in industry or academia.

• Experience in analytical method development, validation and analytical technology transfer within the pharmaceutical industry.

• Project/people management experience for technology transfer projects.

• Experience with HPLC, UHPLC, GC, LC/MS, GC/Headspace, GC/MS, UV, IR, KF, ion chromatography and ICP.

• Empower experience.

• An up to date knowledge of Quality guidelines e.g. ICH, FDA, EMA and GMP

• Excellent written and verbal communication skills.

What’s in it for you?

• Competitive base salary

• Annual bonus

• Contributory Pension

• Private medical insurance

• Life Assurance

• 25 days holiday, plus Bank Holidays, with the option to purchase additional days

• Free onsite parking

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 90,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.