MSD Malaysia
Quality Officer- Manufacturing ( Dong Nai) page is loaded## Quality Officer- Manufacturing ( Dong Nai)remote type:
Not Applicablelocations:
VNM - Dong Nai - Loc Antime type:
Full timeposted on:
Posted Todaytime left to apply:
End Date: December 1, 2025 (30+ days left to apply)job requisition id:
R369626Job 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 applyCurrent Contingent Workers apply**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.** #J-18808-Ljbffr
Not Applicablelocations:
VNM - Dong Nai - Loc Antime type:
Full timeposted on:
Posted Todaytime left to apply:
End Date: December 1, 2025 (30+ days left to apply)job requisition id:
R369626Job 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 applyCurrent Contingent Workers apply**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.** #J-18808-Ljbffr