For the Ardena Business Unit based in Somerset (US), we are looking for aAnalytical Development Scientist.

As an Analytical Development Scientist at Ardena, you will contribute to pharmaceutical development projects by performing scientific, technical, or operational activities within the [Department]. You will work in a regulated pharmaceutical environment, ensuring that all work meets GMP, GxP, and applicable ISO standards.

You will collaborate with cross-functional teams including Quality Assurance, Regulatory Affairs, Project Management, Production, and other departments across Ardena's European and US sites.

Summary of Essential Functions:

The primary responsibilities of this position are to provide analytical support for the Analytical Development team in the evaluation, development and validation of analytical methods, with limited supervision. The Scientist will also perform routine analysis of APIs and finished product using laboratory techniques and instrumentation.

Specific Duties, Activities, and Responsibilities:
• Hands-on method development, method improvement, and validation, including but not limited to HPLC, GC, Dissolution, UV-Vis Spectroscopy, FTIR, KF, Microscopy, PSD etc.
• Assists in complex experiments and tasks such as unknown impurity identification and excipient compatibility studies.
• Prioritizes activities to provide timely analytical support to product development.
• Anticipates analytical issues early in the R&D development process and provides long term planning for analytical method development and improvement.
• Supports formulation development and transfer activities for assigned projects.
• Supports the investigations of method performance, reliability and conducts optimizations studies, as needed.
• Participates in the preparation of technical documents, including validation protocols and reports, stability protocols and reports and analytical test procedures

Position Requirements:

Education and Experience:
• BS, MS in Chemistry, Biochemistry or related discipline with 6 - 8 years (BS), 4+ years (MS) of experience in the pharmaceutical industry.

Knowledge/Skills:
• Working knowledge of GXP, regulatory (ICH) and compendial (USP/EP/JP) requirements during generic development.
• An Ability to multi-task and demonstrate diplomatic skills.
• Proficient (excellent) in English verbal and written communication skills to convey and receive ideas and instructions to/from others within and outside the organization.
• Strong organizational skills.
• Proficient skills in Microsoft Office applications (Word, Excel, PowerPoint).
• Ability to work effectively under pressure to meet deadlines.

Physical Requirements:
• Individual may be required to sit, stand, walk regularly
• Occasionally lift 0-15 pounds
• Be accessible to manufacturing floor and office staff and to use required office equipment
• Specific vision requirements include reading of written documents and frequent use of computer monitor

Work Environment/Safety Conditions:

Individual's primary workstation is in an office and laboratory area, where the noise level is low.

Benefits and perks at Ardena include:
• Competitive salary and tailored benefits package (adjusted per role and location)
• Flexible working arrangements and paid annual leave (where applicable, depending on role and site)
• International and collaborative work environment across European and US sites
• Access to professional development and training programs
• Meaningful work on pharmaceutical development projects that advance patient health
• A values-driven culture guided by Ardena's CARE principles: Communicative, Accountable, Reliable, and Excellent

Salary Range $80,000 -$90,000 DOE

How to Apply

Ready to advance your career in pharmaceutical development? Apply now through the Ardena Careers website at careers.ardena.com.