Scientist, Vaccine Analytical R&D
Merck · West Point, PA · 1 wk ago
Analyst$87k–$137k/yrFull-time
About the role
The Scientist position is open for a laboratory-based, scientific role within our Vaccine Analytical Research and Development team in West Point, PA. The role involves developing state-of-the-art analytical techniques to support vaccine process development, formulation development, vaccine investigations, vaccine characterization, method qualifications and transfers.
Responsibilities
- Develop and apply advanced analytical techniques including separations of small molecules, polymers, proteins, conjugates and nanoparticles (FPLC, HPLC, CE)
- Conduct research projects, troubleshoot technical issues related to analytical methods
- Collaborate with a multidisciplinary team to solve complex analytical problems
- Document experiments in a detailed and organized manner following ALCOA principles
- Apply knowledge of analytical techniques and molecular structure characterization to support vaccine development
- Work independently and as part of a team, demonstrating integrity, precision, accomplishment, motivation, respect, and inclusion
Requirements
- Bachelor's or Master's degree in analytical chemistry, chemistry, biochemistry, biomedical engineering or related field with relevant industry experience
- Minimum 2 years of biotech/pharmaceutical industry experience or relevant academic work with publications
- Experience with cGMP or cGLP practices, electronic lab notebooks, assay robustness evaluation, method qualifications, validations and transfers, and familiarity with relevant compendial guidelines
- Strong organizational, oral/written communication, scientific leadership, and problem-solving skills
- Knowledge of protein chemistry, structural biology, and biochemistry with applications to biomolecules such as viruses, virus-like particles, proteins, and DNA/RNA
- Ability to prioritize tasks and work in a fast-paced, integrated, multidisciplinary team environment
Preferred Experience and Skills
- Experience with cGMP or cGLP practices and using electronic lab notebooks
- Experience with assay robustness evaluation and method qualifications, validations and transfers and familiar with relevant compendial guidelines (e.g., USP1220, ICH Q2/Q14)
- Authoring and reviewing internal technical reports, and external scientific publications
- Current employees apply HERE
- Contingent workers apply HERE
Benefits
- Comprehensive benefits package including medical, dental, vision healthcare, retirement benefits, paid holidays, vacation, and compassionate and sick days
- Annual bonus and long-term incentive, if applicable
- Flexible work arrangements available
- Relocation: No relocation