Job Description Primary Responsibilities (but not limited to): Review and approve batch records; perform product release in the SAP system. Manage product status (block/unblock) and coordinate status changes in SAP. Process owner for Change Control process at the maunfacturing site. Ensure the process is met company’s requirement and all change actions met expectation timeline. Manage and update product BOMs, ensuring accuracy and timeliness for both domestic and export markets. Draft quality-related documents such as notification letters and commitment letters. Plan and implement periodic Product Quality Review (PQR) activities. Review and update SOPs/Tools as assigned. Perform Quality Oversight activities as required by the quality system. Member of the self-inspection team, responsible for conducting assessments and monitoring the completion of CAPA (Corrective and Preventive Actions). Desired Experience/Education/Skills: Graduated with a major in Pharmacy/Veterinary Medicines/Aquaculture/Chemical Technology/Biochemistry or Biotechnology Knowledge in GMP, PIC/S, ISO, HACCP Minimum of 03 years of experiences in QA departments of Phamaceutical/veterinary medicine/feed processing manufacturing facilities. Basic English proficiency (listening & writing) Experience in SAP system is a plus Work effectively in a team, perform under pressure, and adhere to committed deadlines Flexible and adaptable to a dynamic work environment with frequent changes. Office package proficiency: Word, Excel & Power Point Required Skills: Analytical Chemistry, Compliance Testing, Corrective Action Management, Good Manufacturing Practices (GMP), High-Performance Liquid Chromatography (HPLC) Systems, Microbiology Laboratory, Mycoplasma Testing, Pharmaceutical Quality Assurance, Quality Control Management, Quality Improvement Programs, Quality Inspections, Quality Mindset, Raw Material Testing, Regulatory Experience, Test Lab Management Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Not Applicable Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 12/1/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.