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[Factory 1] R&D Quality Compliance Officer (Pharmacy/ Organic Chemistry Fresher)

Nơi làm việc:Bình Dương
Số lượng: 2
Ngày hết hạn:4/7/2026

MÔ TẢ CÔNG VIỆC:

1. Compliance Implementation

  • Implement assigned compliance activities to ensure adherence to applicable standards.
  • Follow established procedures to support compliance with Good Practices (e.g., GLP, GMP).
  • Ensure data integrity (ALCOA+) principles are applied in daily R&D activities.
  • Keep updated with relevant regulatory requirements and internal procedures.

2. Change Control & Risk Assessment

  • Support to ensure proper documentation and timely submission for change control process.
  • Participate in risk assessments related to product development and process changes as assigned.
  • Assist in the investigation and documentation of deviations and non-conformances.

3. Documentation & Process Support

  • Prepare, review, and maintain R&D documentation to ensure compliance with good practices provisions.
  • Support process harmonization activities by following standardized procedures and templates.

4. Cross-functional Coordination

  • Coordinate with internal teams including Formulation Development, QA, QC, RA, and other departments for compliance-related activities.
  • Support communication and alignment of R&D documentation and requirements across functions.

5. Technical & Operational Support

  • Provide support during product registration, validation, and troubleshooting activities when required.
  • Participate in analytical method development or related laboratory activities as assigned.

6. Audit & Inspection Support

  • Support internal and external audits by preparing required documents and records.
  • Assist in tracking and following up audit findings and CAPA actions.

7. Equipment & GLP Compliance

  • Ensure proper use and maintenance of R&D equipment in accordance with GLP provisions
  • Maintain accurate and complete records related to equipment usage.

8. Training and Awareness

  • Conduct regular training sessions for staff on compliance management practices.
  • Promote a quality culture within the R&D department.

YÊU CẦU CÔNG VIỆC:

Official Education: Bachelor’s degree or master’s degree – Major should be related to pharmacy or organic chemistry

 

Work/ Skills/ Experiences

  • 1-2 years in the quality field is preferred
  • Have good attention to detail and ability to thoroughly cross check self and others.
  • Have a structured and organised approach to document and record management.
  • Basic knowledge of regulatory requirements and industry standards.
  • Good attention to detail and organizational skills.
  • Effective communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Good organizational and time management skills with the ability to prioritize and manage multiple projects and deadlines. 
  • Flexibility to adapt to frequent project changes.

Supplementary Certificate

  • Proficient in MS Office (Word, Excel, PowerPoint)
  • Good command of English (speaking, reading, writing); TOEIC, etc

THÔNG TIN KHÁC:

  • Thử việc: 2 months of probation with full salary
  • Thời gian làm việc: 44 hours/week
  • Cơ hội huấn luyện:

    A2E skill training
    Pre-mortems
    Prioritization
    Problem solving
    Owner’s mindset
    Idea generation
    Coaching
    Influencing
    Courageous conversations
    Effective communication
    Presenting with impact
    Closed-loop conversations
    Creating business value
    Effective meetings
    Effective emailing
    Organizational health

  • Đồng nghiệp: Friendly, supportive
  • Ngày nghỉ:

    - 15 working days: from full 1 year to less than 3 years;
    - 16 working days: from full 3 years to less than 7 years;
    - 22 working days: from full 7 years or more to less than 37 years.

  • Phúc lợi:

    Japanese Health Insurance for Staffs over 2 years contribution
    Company trip, Team building activities
    Holiday events

  • Phụ cấp khác :

    Company bus from HCMC to Factory
    Parking fee
    Meal allowance