Senior Scientist - Analytical Commercialization Technology (ACT)
About The Position
The Analytical Commercialization Technology (ACT) group is an R&D organization responsible for the analytical development of late-stage pharmaceutical products. The Senior Scientist will use innovative analytical characterization technologies to support pharmaceutical drug product development and commercialization. The role is available at the Rahway, New Jersey and West Point, Pennsylvania sites, with Rahway listed as the primary location. The successful candidate will work in a dynamic, integrated, multidisciplinary team and contribute to analytical development, product and process characterization, testing, stability studies, regulatory documentation, and technology transfer for commercial manufacture. The position is a regular role with a first-shift schedule and 10% travel. Domestic relocation is indicated, and visa sponsorship is not available.
Requirements
- PhD in Chemistry or a related discipline; no experience is required for candidates with a PhD, OR a Master of Science (MS) in Analytical Chemistry or a related discipline and at least five years of relevant pharmaceutical development experience.
- Strong knowledge of 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.
Nice To Haves
- Strong background and extensive hands-on experience with common analytical techniques, including UHPLC/HPLC, gas chromatography, UV and IR spectroscopy, Karl Fischer titration, and dissolution testing.
Responsibilities
- Utilize advanced analytical tools for problem-solving.
- Analyze data to identify technical insights and trends.
- 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.
Benefits
- Medical, dental, and vision healthcare and other insurance benefits for employees and family.
- Retirement benefits, including 401(k).
- Paid holidays.
- Vacation.
- Compassionate and sick days.
- Eligible for annual bonus and long-term incentive, if applicable.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
Ph.D. or professional degree
