Specialist, Research (2nd Shift Specialist: In-Process Controls)

Job Description The Pharmaceutical Analytical Sciences group has an opening for a second shift Specialist based in Rahway, NJ. Join us and experience our culture first‑hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Responsibilities Coordinate and analyze real‑time analytical support for critical manufacturing samples during second shift (3 PM to 11 PM) operations. Support the execution of Good Manufacturing Practices (GMP) activities such as release of raw materials, solvents, excipients for use in the Rahway manufacturing areas. Provide analytical support to our pilot plants for cleanout samples pre‑batch and post‑batch. Transfer analytical methods to support manufacturing scale‑up batches under GMP settings. Perform data entry, data review/approval, and author analytical reports or data summaries. Troubleshoot and lead any investigations associated with GMP testing through active collaboration with cross‑functional project teams and/or Quality stakeholders. Identify appropriate corrective and preventative actions. Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA principles. Contribute expertise and creativity to collective knowledge and aid in solving complex problems. Directly contribute to experimental design, execution and data interpretation for GMP project support. Strong collaboration with internal stakeholders and partners such as Chemical Engineering, Process Chemistry, Pharmaceutical Operations, and Quality Assurance. Support internal and external compliance audit activities. Manage incoming and outgoing flow of samples, ensuring samples are properly disposed of. Minimum Education Requirements Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree. 1 year of relevant industry experience for applicants with a Master of Science degree. Degree in Chemistry, Pharmaceutical Sciences, or other Life Sciences. Required Experience and Skills A proven record of executing a myriad of analytical techniques. Methodologies, instrumentation, and strong technical problem‑solving skills. Excellent written and oral communication skills. Interpersonal skills necessary for this role. Preferred Experience and Skills Hands‑on experience in GMP operations. Real‑time analytical support for a manufacturing facility. Experience with LIMS, Empower, and SAP. Compensation Salary range: $96,200.00 – $151,400.00. This range reflects the expected compensation for this role as of the posting date and may be adjusted based on qualifications, location and business needs. Eligible candidates may also receive annual bonus and long‑term incentive opportunities. Benefits We offer a comprehensive package that includes medical, dental, vision, healthcare and other insurance benefits (for employee and family), retirement benefits including 401(k), paid holidays, vacation, and compassionate and sick days. For more details, refer to Shift & Location Location: Rahway, NJ. Shift: 2nd – Evening (3 PM to 11:30 PM). This role is fully onsite. Equal Employment Opportunity 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. We comply with affirmative action requirements for protected veterans and individuals with disabilities. #J-18808-Ljbffr Merck