As a Pharmaceutical Engineering Project Interface Manager, you will be the key liaison ensuring seamless collaboration between internal teams (engineering, quality, validation, procurement, EHS) and external stakeholders (design institutes, contractors, equipment vendors, and regulatory agencies). You will develop and execute the interface management strategy, resolve conflicts, and maintain clear communication channels to enable the successful delivery of complex pharmaceutical projects in compliance with GMP and global standards. You will gain vast industry experience that will open doors for you, extend your skillset and expand your perspective. We will empower, support, and enable you to take real responsibility in your role so that you can take charge of your career progression with us. For us lasting trusted relationships are everything, both with our teams and our clients.​

In this role your responsibilities are:​

• Interface Management & Planning

  • Develop and maintain the Interface Management Plan, including interface matrix, communication protocols, and resolution processes.
  • Identify and track all critical internal and external interface points across the project lifecycle.
  • Maintain the Interface Register and monitor status of all interface matters.

• Coordination & Communication

  • Facilitate effective collaboration between cross-functional teams and external partners.
  • Break down information silos and ensure timely information flow across engineering, QA/QC, validation, and EHS.

• Issue Resolution & Risk Management

  • Proactively identify and mitigate risks related to unclear interfaces.
  • Drive resolution of technical, commercial, and schedule conflicts.
  • Manage interface-related changes in line with Change Control processes.

• Documentation & Compliance

  • Ensure proper documentation of interface agreements, meeting minutes, and key decisions.
  • Monitor timely submission of interface deliverables (datasheets, drawings, etc.).
  • Ensure compliance with GMP, GEP, and internal quality systems; support audits.

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We would love to hear from you if you have:​

• 5+ years of experience in pharmaceutical construction projects

• Proficiency in interface management principles and methodologies with practical application experience 
• Bachelor's Degree or higher in Engineering (Process, Piping, Mechanical)

• Familiarity with GMP/GEP, China's "Good Manufacturing Practice for Drugs", and major international pharmaceutical regulatory guidelines, Performance/Process Qualification (PQ), Cleaning Validation, Computerized System Validation(CSV), and Analytical Method Validation, etc

• Ideally have experience with multinational projects or collaboration with international engineering companies, and ability to understand both technical and commercial aspects, assessing the impact of technical solutions on project cost and schedule
• Fluency in Mandarin and English (often required for interaction with international suppliers and standards)

• Detail-oriented, quality-focused, and comfortable managing competing priorities in a dynamic environment

• Willingness to be based in Tianjin for the duration of the project.

All CVs need to be submitted in English. 

All interviews are conducted either in person or virtually with video required.

Linesight is a highly successful global project and cost management consultancy that keeps clients coming back. And for that we have our people to thank. You see we’re not like the others. We’re different. Unique. It’s our fresh thinking and focus on what matters that has led to our evolving. We are on a journey working in some of the most exciting innovative sectors with some of the world’s most prestigious companies delivering major projects that deliver a more sustainable built environment. We have an open culture and a flat structure where you can expect to be treated with genuine care, respect, and empathy. With Linesight, you can truly discover the power of team!

Diversity, inclusion and accessibility  

Linesight is committed to transparent, equal opportunity employment practices. We are building a diverse and inclusive organisation, accessible to all, based on having a safe culture which enables all our people to be their true selves. We are a people business, and we understand that the more inclusive we are, the happier our people and better our work will be. We will ensure that individuals with disability are provided reasonable accommodation to participate in the application or recruitment process and are accommodated in the workplace. If you require assistance or accommodation of any kind, please mention this in your application, we would love to hear from you!