Senior Scientist - Analytical Commercialization Technology (ACT)

Merck

Shift: Full time

Job Description We aspire to be the premier research-intensive biopharmaceutical company. Our company is at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. The Analytical Commercialization Technology (ACT) group is seeking applicants for a Senior Scientist position available at the Rahway, NJ and West Point, PA sites. ACT is an R D group responsible for analytical development of late-stage pharmaceutical products. The successful candidate will utilize innovative analytical characterization technologies to drive pharmaceutical drug product development and commercialization. The Senior Scientist responsibilities include, but not limited to problem solving with the use of advanced analytical tools, data analysis with the use of statistical tools to drive product development and characterization, development and validation of robust analytical methods, drug product testing and analytical investigations in a cGMP environment, drug product and manufacturing process characterization, drug product stability studies, specification development, manufacturing process scale-up and validation support, preparation of Chemistry, Manufacturing, and Controls (CMC) documents for global regulatory submissions, and technology transfer for commercial manufacture. The successful candidate must be able to collaborate in a dynamic, integrated, and multidisciplinary team environment. Responsibilities Utilize advanced analytical tools for problem-solving Analyze data for technical insights and trending Develop and validate robust analytical methods Conduct drug product testing and analytical investigations in a cGMP environment Characterize drug products and manufacturing processes Perform drug product stability studies Develop specifications and support manufacturing process scale-up and validation Prepare Chemistry, Manufacturing, and Controls (CMC) documents for global regulatory submissions Facilitate technology transfer for commercial manufacture Collaborate in a dynamic, integrated, and multidisciplinary team environment Qualifications Required PhD in Chemistry or related discipline with no experience required OR Master of Science (MS) in Analytical Chemistry or related discipline with at least five (5) years of relevant pharmaceutical development experience. Strong knowledge and hands-on experience in chemistry and common analytical techniques Demonstrated problem-solving ability Excellent verbal and written communication skills Demonstrated creativity and strong interpersonal skills Ability to work in a team environment with cross-functional interactions Preferred Strong background and extensive hands-on experience with common analytical techniques such as Ultrahigh/High-Performance Liquid Chromatography (UHPLC/HPLC), Gas Chromatography, Ultraviolet (UV) and Infrared (IR) spectroscopy, Karl Fischer titration, and dissolution testing . Required Skills: Analytical Method Development, Chemical Proteomics, Chemical Synthesis, Chemometrics, Chromatography, Data-Driven Decision Making, Mass Spectrometry Based Proteomics, Method Validation, Motivation Management, Process Analytical Technology (PAT), Protein Chromatography, Spectroscopy, Synthetic Biology Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The primary location for this posting is: USA - New Jersey - Rahway Where required by law, the compensation range for this role is provided below. The salary range for the primary location of this role is: