仕事内容

You will be responsible for:

 Overseeing onsite construction activities to ensure compliance with quality standards, regulatory
requirements, and specifications for CSA (Civil, Structural, Architectural) and MEP (Mechanical, Electrical, Plumbing) trades.
 Developing and implementing effective quality control processes and procedures for all phases of construction.
 Conducting regular inspections, audits, and reviews to identify and address quality issues promptly.
 Acting as the primary liaison for quality matters, ensuring alignment between project teams, contractors, and stakeholders.
 Collaborating with the construction team to resolve quality-related issues in real-time and ensure adherence to STA compliance standards.
 Preparing and maintaining comprehensive quality documentation and reports to support project transparency and accountability.
 Management and coordination of complex projects, with a focus on engineering, planning and design activities.
 Coordinate and supervise all phases of the construction of pharmaceutical construction sites, including civil and mechanical aspects.
 Manage multidisciplinary teams of technicians, suppliers and subcontractors, ensuring compliance with time and budget.
 Monitor work progress and ensure compliance with quality, safety and GMP standards.
 Interface with customers and stakeholders for project updates and alignments.
 Analyze any critical issues and propose effective solutions to achieve objectives.
 Evaluation and management of project risks, with particular attention to technical feasibility and construction sequences.
 Monitoring the progress of the project, ensuring compliance with budget and timing.
 Supervision on the field to ensure that implementation activities are in line with the engineering project.

応募資格

About you:

 A minimum of 7-10 years of experience in construction quality management, preferably in pharmaceutical or industrial construction projects

 In-depth knowledge of CSA and MEP standards, regulatory requirements, and industry best practices.

 Strong understanding of regulatory requirements and industry guidelines (e.g., GMP, FDA, EMA).

 Strong leadership and problem-solving skills, with the ability to drive quality improvements across all phases of construction

 Hands-on experience with onsite inspections and contractor supervision.

 Excellent communication and interpersonal skills, with the ability to manage multiple stakeholders and resolve conflicts effectively.

給与情報

面談時にご説明いたします。

労働時間

休暇休日

福利厚生・待遇

PR内容

私たちについて:
私たちは1998年に設立された、医薬品および医療機器分野のサービスプロバイダー企業です。世界中（ヨーロッパ、アジア、アメリカ大陸）で1,500人以上の従業員を抱え、30の子会社を展開しています。PQEに加わることで、国際的なプロジェクトに携わるだけでなく、世界中の同僚と関わる機会を得られる、文化的で挑戦に満ちた企業に参加することになります。

現在の成長に伴い、PQEでは日本の大阪にあるチームに加わる新しいC&Q/CQVエンジニアを募集しています。

担当コンサルタント

担当

Krubally Ali

興味のある求人があれば転職相談からお問い合わせください

Construction Manager

仕事内容

応募資格