Dụng Head of Quality Control- QC Director

Công ty Cổ Phần Pymepharco

Địa điểm làm việc: Phú Yên

Hết hạn: 25/12/2022

Chi tiết công việc
Giới thiệu công ty

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Tuyển Dụng Head of Quality Control- QC Director

Job Description

ESSENTIAL DUTIES

Manages and provides leadership for the Quality Control's development, direction, and effectiveness, adhering to organizational policies and processes and supporting overall business and corporate objectives.
Develops and maintains policies, programs, and strategies to ensure continuous full compliance with relevant EU-GMP, US FDA, Pharmacopeias, and ISO requirements.
Effectively plans and execute QC capacity strategy to accommodate and excel in company's compliance and business targets.
Communicates performance expectations and business and corporate policies to section staff and others. Ensures accurate and complete associate records are maintained within the section. Coaches and develops local QC team to ensure business continuity and sustainable people development.
Develops and justifies Capital Expenditure Requests and Corporate policies to support goals and mission objectives.
Provides continuous oversight and guidance, and systematically monitors the optimization projects within QC to ensure successful continuous improvements
Ensures QC Tech Transfer projects are appropriately managed and resourced;
Working with local leadership, develops preliminary section budgets, goals, objectives, and operations that will be integrated into the full department budget.
Responsible for the QC department KPIs and addresses unmet targets appropriately.
Interprets, monitors regulatory requirements in Chemical, physical, and microbial testing.
Manages the team's workload, projects arrangement, QC activities relevant to product transfer and testing support for validations and others.
Develops strategies to assess and mitigate cross-contamination risks within QC responsibilities.
Actively works to identify new and expanding areas of contribution for the lean processes and utilization of technologies
Routinely updates and reports to Site Quality Head on emerging issues, changes relevant to overall strategic direction.

OTHER DUTIES AND RESPONSIBILITIES

Will be responsible for all technical assessment on microbial aspects of production and control necessary to ensure the sterility of relevant manufactured products.
May contribute as a member of the business regulatory compliance team.
Reviews physical and equipment requirements for the laboratory. Regularly assesses short and long term needs and prioritizes equipment acquisition.

MINIMUM QUALIFICATION REQUIREMENTS

Education

Bachelor's degree in Pharmacy, Biology, Chemistry or equivalent education and experience sufficient to successfully perform the essential functions of the job.
A Master's degree in Pharmacology or related discipline is preferred.

Experience

Minimum 12 years progressive management experience in pharmaceutical QC Lab at a globally recognized organization
Proven track record in managing large team with completing priorities and developing sustainable and growing QC team.

Skills

Demonstrated effective leadership and managerial skills.
Ability to manage complexity of QC projects and compliance responsibilities
Demonstrated knowledge in applicable regulations affecting areas of responsibility.
Comprehensive knowledge of the principal chemical, physical and microbial testing
Strong leadership skills and demonstrated successes in managing a medium to big-sized team (50-70).
Excellent and effective verbal and written communication skills in English
Success with working with multifunctional teams: Global and local
Comprehensive knowledge of EU-GMP, US FDA, and international regulations relevant to pharmaceutical industry and to Quality Control and Quality Assurance.
Ability to succeed in a team-oriented atmosphere and lead team activities.
Working knowledge of Lean methodologies such as 6-sigma, OpEx.
Understanding of applications and limitations of testing methodologies.
Knowledge and use of relevant PC software, Lab software applications and skills to apply them effectively.

All contact information:
+ Candidates please apply directly at the address: 166-170 Nguyen Hue, Ward 7, City. Tuy Hoa, Phu Yen
+ Either by post to the Human Resources Department, or by email: [protected info]
+ For more information please call: [protected info] (Linh Nhu/ HR Dept.)

Thông tin chung

Ngày hết hạn: 25/12/2022
Thu nhập: Thỏa thuận

Giới thiệu công ty Xem trang công ty

PYMEPHARCO được thành lập vào năm 1989 với nhiệm vụ sản xuất dược phẩm, kinh doanh thuốc & vật tư thiết bị y tế.

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Quy mô công ty

Từ 5000 - 10000 nhân viên

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