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【EN】Regional Quality Management,Assistant Manager,Tokyo

BASF

BASF

Quality Assurance
Tokyo, Japan
Posted on Oct 10, 2024

【Main Areas of Responsibilities and Key Activities】

■Quality support:

  • Act as QA in BJL-GMP organization and maintain local GMP warehouse for import pharma goods.

  • Monitoring and understanding relevant laws and regulations related GMP/Quality management.

  • Support / Lead customer communication for quality related topics based on Quality Agreement in accordance with Japan Good Quality Practice (GQP) ministerial ordinance).

  • Working closely with country sales, regulatory, and Supply Chain Management to ensure quality issue is adequately manage and address.

  • Work together with governmental / provincial authorities or Industry associations when applying, interpreting and implementing regulations

  • Act as key responsible for Customer audit request on local GMP warehouse.

  • Conduct and support quality audits according to internal and external guidelines

  • Customer on-site audit include coordinate global on-site audit as a coordinator between functional unit(s), in setting up timeline, process and accompany with customer etc.

  • Provide quality compliance related to computer systems implementation and upgrade projects.

  • Provide Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) support, in Quality related topics for Asia-Pacific region.

Quality Guidelines:

  • Responsible for the regional rollout, adaption & implementation of quality guideline

  • Develop and maintain Quality Agreements (customers) and Service Level Agreements (“SLA”) with BASF sites and 3rd party contract manufacturers, Distributors, e.g. draft SLA and Quality Agreements with legal (“ICHQ7”)

  • To handle Non Conformance Management (“NCM”). To be engaging in EN NC community and conducting joint reviews of NCM performance (cases & response time) and counter-measures

  • To coordinate ENP/ ENN/ ENF non-conformances to ensure effective root cause analysis and the implementation of corrective actions (“CAPA”) to minimize customer impact by the reduction of repetitive complaints. Analyse NC trends and work with business partners (external & internal) to recommend / implement changes to EN business processes where required.

■Material Data & Label Management:

  • Take on the role as regional contact person for SAP material master data and label topics

■Quality Community:

  • Actively participate in relevant EN (such as Pharma / Nutrition Health / Aroma etc.) trade organizations to keep abreast of industry guidelines and best practices

  • Support Global EN community for qualification of regional suppliers according to the EN guidelines

  • Create communication matrix among the EN quality teams in Asia-Pacific

  • Represent BASF at governmental organizations for the quality part

  • Ensure timely and accurate completion of customer questionnaires, surveys and other information requests in coordination with global teams

【Job Requirements】

Education

  • Bachelor or Master’s degree in science, Pharmacy or related education

Working Experience

  • Minimum of 4-5 years with hands-on experience in excipient testing, strong analytical and GMP background in pharma industry.

  • Good knowledge of Pharmacopeia requirements such as JP, USP, EP etc.

Technical & Professional Knowledge, Skills

  • Knowledge of, QM-systems, standards & processes, good understanding of laboratory operations & methods

  • Demonstrate cross-functional leadership skills, communication, interpersonal and influence management skills

  • Ability to multi-task, and must be able to organize and direct diverse activities in a changing environment

  • Establish longer term priorities and contingencies, utilizing strong project management skills in order to guarantee successful project completion

  • Willing to travel when required

  • Ability to converse fluently in Japanese and English