[Factory 1] Chief of Dedicated Quality Compliance

CÔNG TY TNHH ROHTO-MENTHOLATUM (VIỆT NAM)

Bình Dương

Thỏa thuận

30/09/2026

Toàn thời gian

Ứng tuyển

Ngành nghề:

Nghệ thuật - Điện ảnh, QA-QC/ Thẩm định/ Giám định

MÔ TẢ CÔNG VIỆC:

1. Operational Management of DQCT

Day-to-Day Oversight:

Manage and coordinate the daily operations of all DQCO Officers across shifts.
Review all deviation reports, observation logs, and escalation notifications produced by officers.
Ensure DQCT shift coverage is maintained across all production schedules.
Conduct daily/weekly briefings with officers to review findings, escalations, and priorities.

Performance Management:

Monitor individual officer performance against KPIs and compliance targets.
Identify skill gaps and coordinate targeted training and development activities.
Conduct regular one-to-one reviews and formal performance assessments.

2. Compliance Oversight & Escalation

Review all critical deviation reports and ensure timely escalation to the Head of DQCT and relevant management.
Participate in root cause analysis (RCA) for significant compliance findings.
Review and monitor CAPA plans for DQCT-identified deviations and track implementation effectiveness.
Approve final observation reports before submission to QA and management.

3. Inspection Readiness & Regulatory Support

Ensure all DQCT records, observation forms, and reports are maintained in a continuously audit-ready state.
Serve as the primary DQCT point of contact during internal and external regulatory inspections.
Coordinate DQCT contributions to regulatory inspection preparation and response activities.

4. Reporting & Trend Analysis

Review compliance trend reports, KPI dashboards, and management review inputs produced by the DQC-REA Officer.
Present DQCT performance summaries to the Head of DQCT and site senior management.
Identify systemic issues and drive targeted improvement initiatives across DQCT functions.

5. Cross-Functional Coordination

Act as the primary operational interface between DQCT and site QA, QC, Production, Engineering, and Microbiology teams.
Coordinate cross-functional investigations, CAPA implementation, and compliance improvement projects.
Facilitate effective communication between DQCT officers and department heads.

YÊU CẦU CÔNG VIỆC:

Education

Bachelor's degree in Pharmacy, Microbiology, Chemistry, Biotechnology, Chemical Engineering, or a related science discipline.
Advanced degree or specialized GMP management qualification is preferred.

Work Experience

Minimum 3 years of experience in a GMP-regulated pharmaceutical environment, with at least 1 years in a team leadership or management role.
Proven experience managing compliance oversight teams in sterile or aseptic manufacturing is strongly preferred.
Demonstrated experience managing regulatory inspections (FDA, EMA, WHO, or local authority).

Technical Knowledge

Comprehensive knowledge of cGMP: 21 CFR Part 210/211, EU GMP, WHO GMP.
Strong expertise in Data Integrity (ALCOA+), Contamination Control Strategy, aseptic processing, and Environmental Monitoring.
Proficiency in LIMS and GMP electronic systemsis preferred.
Knowledge of ICH Q9 (Quality Risk Management) and RCA methodologies.

Skills

Strong leadership, team management, and people development skills.
Advanced analytical, report writing, and communication skills in Vietnamese and English.
Proficient in Microsoft Office; Power BI / advanced Excel is an advantage.
Audit management and inspection coordination skills.

Personal Attributes

High integrity, independent judgment, unwavering under production schedule pressure.
Strong organizational skills with ability to manage multiple priorities under pressure.
Willing to work shift-based schedules including nights and weekends as required.

THÔNG :

Thử việc: 2 months of probation with full salary
Thời gian làm việc: 44 hours/week
Cơ hội huấn luyện: A2E skill training
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

Thông tin chung

Thu nhập: Thỏa thuận

Ứng tuyển

Báo cáo tin tuyển dụng

Việc làm tương tự

Kỹ Thuật Trộn Nấu Keo Sản Xuất Gỗ

Công ty TNHH Tập đoàn Rita Võ

Thỏa thuận

Hồ Chí Minh, Bình Dương

12/09/2026

Nhân viên Business Analyst

Công ty TNHH CÔNG NGHỆ EMPOS

Từ 10-20 triệu VND

Hà Nội, Hồ Chí Minh, Đà Nẵng, Hải Phòng, Bình Dương

11/09/2026

Nhân Viên Quản Lý Chất Lượng (Tiếng Nhật, Điện Tử)

Công ty Cổ phần Giải Pháp Nhân sự Việt Nam - HRchannels Group

10 - 12 triệu VNĐ

Hồ Chí Minh, Bình Dương, Đồng Nai

03/09/2026

Nhân Viên Phòng Lab

CÔNG TY CỔ PHẦN CHẾ BIẾN THỰC PHẨM HOÀNG SƠN

10 triệu - 12 triệu

Bình Dương

14/09/2026

Nhân Viên Kho

CÔNG TY CỔ PHẦN CHẾ BIẾN THỰC PHẨM HOÀNG SƠN

Cạnh tranh

Bình Dương

17/09/2026

Nhân Viên Chạm Khắc- Điêu Khắc

Gốm Sứ Minh Long - Công ty TNHH Minh Long I

10 - 14 triệu

Bình Dương

25/09/2026

Nhân viên kiểm soát chất lượng

Công ty TNHH Thực phẩm An Phước

6-10 triệu VND

Bình Dương, Trà Vinh

08/09/2026

QC Data Analysis Specialist

CÔNG TY TNHH PERFETTI VAN MELLE (VIỆT NAM)

Thoả thuận

Bình Dương

31/08/2026

QA Staff (Machinery, work in Ben Cat - Binh Duong)

Công ty Cổ phần Giải Pháp Nhân sự Việt Nam - HRchannels Group

14 Tr - 16 Tr VND

Hồ Chí Minh, Bình Dương, Đồng Nai

16/09/2026

[Bình Dương] Kỹ sư QC - Dự án Green City

Tổng Công ty Cổ phần Công trình Viettel - Viettel Construction

Cạnh tranh

Bình Dương

20/09/2026

Vị trí [Factory 1] Chief of Dedicated Quality Compliance do công ty CÔNG TY TNHH ROHTO-MENTHOLATUM (VIỆT NAM) tuyển dụng tại Bình Dương, Joboko tự động tổng hợp mức lương Thỏa thuận, tìm thêm việc làm về [Factory 1] Chief of Dedicated Quality Compliance hoặc công ty CÔNG TY TNHH ROHTO-MENTHOLATUM (VIỆT NAM) ở các link phía trên

Giới thiệu công ty