Job Description: Analytical R&D group at Merck is looking for a qualified scientist. • Conducts release and stability testing of drug products following SOPs and cGMPs. • Plans and executes validation of analytical methods. • May develop and/or adapt methods. • Solves more complex problems with some guidance from senior scientists. • Troubleshoots instrumentation. • May investigate new technologies. • Documents results in ELN and RLIMS and performs second chemist review. • May author analytical reports and SOPs. • Receives mentorship from scientific supervisor. • Carries out all assignments to the standards of efficiency, innovation, accuracy, and safety in accordance with Company and regulatory requirements. • Provides analytical support to development projects and research activities within Analytical Sciences.

Responsibilities: Analytical R&D group at Merck is looking for a qualified scientist. • Conducts release and stability testing of drug products following SOPs and cGMPs. • Plans and executes validation of analytical methods. • May develop and/or adapt methods. • Solves more complex problems with some guidance from senior scientists. • Troubleshoots instrumentation. • May investigate new technologies. • Documents results in ELN and RLIMS and performs second chemist review. • May author analytical reports and SOPs. • Receives mentorship from scientific supervisor. • Carries out all assignments to the standards of efficiency, innovation, accuracy, and safety in accordance with Company and regulatory requirements. • Provides analytical support to development projects and research activities within Analytical Sciences.

Qualifications: Qualifications • BS Degree in Chemistry, Pharmaceutical Sciences, other Life Sciences, or equivalent with 2-5 years of experience; or similar MS degree with 1-2 years of experience; or PHD with 0-1 years of experience. Required Skills and Experience • Experience with chromatographic analysis using various UPLC and HPLC techniques. • Experience with Empower chromatographic data program and with analysis of oral solid dosage forms. • A proven record of technical problem-solving experience with standard operating procedures and cGMP analytical testing; most tasks will be non-GMP. • Excellent communication (oral and written) and attention to detail. • Excellent organization to multi-task and manage multiple projects. • Ability to work as part of a team, self-motivation, adaptability, and a positive attitude. Desired Skills and Experience • Experience with dissolution, water activity, Karl Fischer titration preferred. Note: 6 months assignment. Need someone to start ASAP. 100% onsite lab based role at Rahway,NJ.