FSP Senior Research Scientist-Dissolution Method Development

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Description:

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Location/Division Specific Information

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our clients to make the world healthier, safer, and cleaner.

Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

This is an onsite position located in Collegeville, PA.

Discover Impactful Work

The Senior Research Scientist independently performs, oversees, and directs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical compounds for Long-Acting Injectables. Responsible for strategic planning, review, and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol, and product specifications. Provides strategic technical guidance and mentorship to the analytical team. Leads the development and implementation of new analytical methods and procedures. Acts as a primary point of contact for high-level client interactions and strategic project updates.

A Day in the Life

• Independently plans the best scientific approach to develop analytical methods and/or other specialty technologies studies that meet client requirements.

• Acts as on-site Subject Matter Expert (SME) for instrumentation / technique / technology.

• Evaluates available technical options to obtain desired quality of analytical results, economics, ease of introduction into a production environment, and robustness in analytical applications.

• Demonstrates viability of in-house developed methods by designing experiments or other appropriate aspects of specialty methodology or technology.

• Ability to lead client discussions regarding project definitions, technical information exchanges and discussions of project status. Provides recommendations to clients on technical and regulatory issues.

• Leads in developing innovative technology and in evaluating and implementing new capabilities.

• Completes all laboratory documentation in clear and accurate language and according to SOP and GLPs.  Leads advanced troubleshooting for various equipment & instruments.

• Reviews protocols, compiles results from assignments and makes determination on acceptability per SOP acceptance criteria. Reviews overall study results and other project related technical documents.

Keys to Success

• Previous experience in or non-GMP development phase laboratory
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 10+ years).

Knowledge, Skills, Abilities

• Demonstrated knowledge of multiple analytical techniques with an emphasis on dissolution testing, Apparatus 1, 2, & 4 dissolution, non-compendial or novel dissolution
• 2-5 years' experience doing method development on dissolution
• Experience leading or contributing to dissolution method development
• Knowledge of pH, pKa, buffer systems, surfactants, solubility
• Performs and interprets analyses using techniques such as RP‑HPLC, SEC, UV‑Vis, DLS, and SCISSor,
• Knowledgeable about the drug formulation and development process
• Experienced in HPLC method development and und