Senior Scientist, Quality Control

Merck & Co.; Piscataway Township (NJ); On-site; USD 115,000 - 120,000; Full time

Job summary

Merck & Co. is seeking a Senior Scientist for Quality Control based in Piscataway, NJ. This role is responsible for testing raw materials, finished products, and ensuring compliance with regulatory standards. Ideal candidates will possess a Bachelor's degree in Pharmacy or Chemistry with 5 years of experience in quality control.

You will conduct physical and chemical analyses using advanced techniques, troubleshoot instrument-related issues, and participate in method transfers. The position offers an annual salary of $115K - $120K.

Qualifications

• In-depth knowledge of analytical chemistry techniques.
• Ability to follow compendial procedures for analysis.
• Experience applying cGMP requirements.

Responsibilities

• Perform testing of raw materials and finished products.
• Document analysis steps and report results.
• Assist with non-routine special projects.

Skills

Analytical chemistry techniques

Chromatographic techniques

cGMP compliance

Trend analysis

Troubleshooting instruments

Education

Bachelor's degree in Pharmacy or Chemistry

Tools

HPLC

UV-Vis spectrophotometer

Karl Fischer titrator

Job description

Senior Scientist, Quality Control

Responsible for performing testing of raw materials, in‑process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents, participate in method transfer activities within departments or between facilities or organizations. This role will also provide feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. Perform physical and chemical analysis of raw materials, in‑process, and finished pharmaceutical products, including products on stability, according to written methods, material specification, and company policies as identified in standard operating procedures (SOPs). Comply with cGMps, SOPs, and STPs to avoid out‑of‑specification situation. Assure compliance with state and federal regulations. Actively participate in any project work as and when assigned. Perform process validation and cleaning validation/verification testing on various drugs. Assist other scientists with analytical, instrument and software related problems as required. Use sonic sifter, laser diffraction, Karl Fischer, UV‑Vis spectrophotometer, Infra‑red spectrophotometer, HPLC with UV detection as well as with conductivity detection, TLC, pH meter, and dissolution. Calibrate HPLC, Dissolution apparatus equipped with auto‑sampler and /or in‑line UV, pH meters, analytical balances, and Karl‑Fischer titrator. Document steps followed during analysis execution, calculate and report results. Actively participate in investigation of laboratory results. Review laboratory analysis data for completeness, specification compliance, and compliance with company's written policies. Report any abnormal findings to the Supervisor. As assigned, perform in‑depth review of analytical records/reports to assure that calculations and other data are technically correct and compliant to relevant specifications. Assist the laboratory supervisor with handling non‑routine special projects requiring activities such as out‑of‑specification investigations and out‑of‑alert limit investigations in the laboratory. Ensure that expired chemicals and reference standards are removed from laboratory area. Perform calibration of HPLC, GC, and other equipment as assigned by the supervisor. Assist with hands‑on training of newly hired Technicians or Scientists 1 and 2 levels.

Job Location: Piscataway, NJ
Salary: $115K - $120K per annum
Hours: 40 hrs/wk 8:30am - 5:30pm
Location: Piscataway

• Must possess in‑depth knowledge of analytical chemistry techniques, such as spectrophotometric, dissolution and drug release, chromatographic techniques (standalone or hyphenated) and measuring physical parameters (viscosity, particle size or droplet size by laser diffraction, melting point by DSC, water content by TGA, identification by XRPD, and other techniques).
• Must be able to follow compendial (USP/EP/BP/JP) procedures for analysis.
• Must understand and apply cGMP requirements applicable to quality control laboratory.
• Must have ability to apply advanced technical skills to troubleshoot and resolve complex analytical and instrument‑related problems effectively and in a timely manner and report actions to the laboratory management in a timely manner.
• Must be able to identify trends in analytical data.
• Must have at least a Bachelor's degree in Pharmacy or Chemistry or Pharmaceutical Manufacturing.
• Must have 60 months of experience in the position or in a related position.

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at [e-mail] . Requests will be handled confidentially and in accordance with applicable laws.