三桁成長達成　外資スペシャリティ製薬メーカー / QA Manager 品質保証

Company Overview
希少疾患を対象とした、画期的なバイオ医薬品を開発・販売している同社。
2023年にはAPAC Regionから独立し、Japan単独Regionとしてさらなる事業拡大フェーズです

Job Description
SUMMARY
This position reports to the Director of Drug Product Market Release within the External Quality organization and will maintain responsibility, oversight, and management of quality-related activities for drug product releases to Japan and APAC region as required.

As part of the External Quality team, the responsibilities consist of maintaining the compliance profile and quality mindset including planning, implementation, project management and management of applicable Quality Systems and oversight of partners. The manager will work closely with peers in a team-matrix environment to have proper oversight of all the partner(s).

The Quality Manager is responsible for the support of Quality Assurance (QA) and Quality Control (QC) activities specifically to Japan as required by GQP ordinances and the APAC region. The Quality Manager interacts with partners that act as Marketing Authorization Holders of our products to accomplish Quality Technical Agreement (QTA) activities and provide QA support to Supply chain Management (SCM) related activities.

This position will be based in Tokyo, Japan and will require travel.

RESPONSIBILITIES:
Specifically to Japan, the Quality Manager is responsible for all QA duties required at the Japan entity in accordance with Good Quality Practice (GQP) and Good Manufacturing Practice (GMP) for QC, secondary packaging and visual inspection.

A) Perform the duties of the Quality Manager to ensure company products, procedures and policies are in compliance with Japanese regulations, Good Quality Practices (GQP), Good Manufacturing Practices (GMP) and the company's Global procedures.
These duties include, but are not limited to:
- Supervise all in-country (Japan) quality assurance duties
- Establish a quality standard code for each product
- Ensure all required quality assurance duty procedures are in place and approved to conform to the standards for quality assurance
- Establish GQP agreements with all ex-country manufacturers
- Ensure drug product releases conform to Japanese regulations and the Japan marketing authorization (MA)
- Promptly report to the Marketing Supervisor General and Corporate Quality Director any manufacturing, quality control, or product quality defects identified during product release evaluation
- Closely collaborate with and maintain a timely and open communication channel with other departments such as drug safety control /BPV, Regulatory Affairs and other departments to ensure product safety and quality
- Periodically verify the manufacturing and quality control of the Manufacturer’s of the drug product
- Change Management, to include ensuring that any proposed manufacturing, testing or specification change does not seriously impact the quality of the product
- Notify the Manufacturers in the event that any improvements to the manufacturing or quality control are required
- Ensure appropriate investigations are performed in the event of any product complaint or other reported product quality or safety concern
- Ensure appropriate procedures are in place for handling product recalls
- Perform self-inspections, including internal audits
- Ensure drug product shipment and storage maintains drug product quality and safety throughout the in-country supply chain
- Ensure controlled documents are approved, distributed and maintained in accordance with GQP and established quality assurance duty procedures.

B) Other duties include:
- Review and report results of all in-country product testing results, visual inspection and secondary packaging to the corporate quality department, as requested
- Work closely with the Regulatory Affairs department in Japan and in Global on the strategy for the region and for Japan
- Perform temperature data review during transportation from foreign manufacturing site to Japan
- Work with chemistry manufacturing and controls (CMC) to inspect for consistency between Marketing Approval Document and Manufacturing Practice
- Ensure all required documents are prepared for new product launching and work with a CRO to ensure GMP compliance inspection after the submission of regulatory application to the authority

*10% traveling required to partners

Requirements
SKILLS and KNOWLEDGE
The ideal candidate will have the following skills:
- Partner Oversight – Understand risk management and able to assess health of a partner and work with multiple partners. Experience with collaborating with partners to mitigate and improve control strategy for clinical and commercial products.
- Decision Making/Problem Solving – Identifies problems and be able to lead and handle complex situations (e.g. major investigations). Collect input from key stakeholders in making sound and effective decisions and ensure the solutions and approach are aligned within and across teams. Be decisive and move to action in the absence of clear information. - - Be proactive in implementing process improvements.
- Influence and Collaboration – Success in working in a matrixed organization and work with different time zones. Demonstrates effective communication and interpersonal skills that brings cross functional teams together to reach a shared goal. Possesses strong verbal and written communication skills and the ability to influence at all levels.
- Agility – Ability to pivot quickly and recover constructively from setbacks, while continually learning and modifying approach.
- Leadership – Ability to interact with and provide leaders with guidance and recommendations to assist with decision making. Ability to facilitate meetings, influence stakeholders, and manage teams effectively in projects and goals.
- Quality Systems/GMP/Regulations - Working knowledge of GMP Quality Systems and cGMP Regulations (e.g., deviations, change controls, lot release, annexes).

SCOPE
- Quantify the scope or impact of the job in terms of revenue, expenses, capital investment, headcount, etc.

This position is needed to assure continuity business of Marketing Authorization Holders of Drug Product in the region that have responsibilities to follow local/APAC requirements, regardless of the responsibilities of Distribution partner.

EDUCATION
- Degree in the microbiology, biotechnology, chemistry or equivalent, in a technical discipline is required
- Technical knowledge of Biologics CMC, GQP, GMP and pharmaceutical-related laws and regulations in Japan
- Knowledge of GMP compliance inspection for JNDA
- General technical knowledge of GMP compliance inspection for the APAC region

EXPERIENCE
- Overall knowledge for SCM related activities, especially cold chain products
- Knowledge of US and EU GMP and ICH guidelines
- Minimum 10+ years of biopharmaceutical experience in a Quality, Compliance, and/or Regulatory setting
- Previous experience working with or liaising with the pharmaceutical and medical device agencies (PMDA and APAC region Health Authorities) and other administrative agencies preferred
- Partner oversight, risk and project management
- Demonstrated conversational English language skills
- Strong written and verbal English language skills preferred

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