Full Time

Senior Project Engineer / Project Engineer

Posted 1 month ago
Application ends: November 9, 2021
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Job Description

Be part of something altogether life-changing

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

What You’ll Do

  • The Senior Project Engineer position reports to the China/Asia Region Program Manager, part of Life Sciences, CYTIVA.
  • The Senior Project Engineer is responsible for assisting the assigned Enterprise Solutions Project Manager with project activities per company policies and procedures and work instructions, ensuring project design and execution are completed according to the project plans.
  • The Senior Project Engineer is responsible for site activities schedule preparation, pre-planning and resource allocation for site execution and other technical activities relating to the execution project. The Senior Project Engineer will oversee the performance of engineering subcontractors, during both the design and site execution phases reviewing design deliverables and execution activities for accuracy, quality and on-time completion.
  • Support design and construction discussions/issues between CYTIVA, Customer and EPCMV organization representatives
  • Oversee and coordinate facility design development
  • Oversee and coordinate technical deliverables for CYTIVA review, approval, distribution, tracking and control
  • Oversee and coordinate additional CYTIVA Engineers/Staff, P&ID and AutoCAD support
  • Generate Change Control estimates and secure cross functional input, review and approval
  • Update Project Plan and associated documents (schedules, cost estimates, resource needs, etc.)
  • Liaise with Site Implementation Leaders regarding Site installation, commissioning and testing requirements and planning
  • Ensure compliance with country and local regulations
  • Work with local governmental agencies as required (example, in China, interact with LDI and ACC as needed to streamline design compliance and approvals)
  • Assist the ES Project Manager with the following:
  • Stand-in as ES Project Manager whenever required
  • Maintenance of project schedule by monitoring project progress; coordinating activities; recommending and expediting when necessary, resolving schedule issues
  • Control of project plan by reviewing design, specifications, and plan and schedule changes; recommending actions
  • Oversee project costs by reviewing and administering contractor contracts
  • Support project costs by maintaining project budgets per the approved scope. Ensure change requests (internal/external) have been approved for work to continue within CYTIVA project team.
  • Prepares project status reports by collecting, analysing, and summarizing information and trends; recommending actions

Quality Specific Goals:

  • Aware of and comply with the CYTIVA Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
  • Aware of and comply with the CYTIVA ES Project Management Manual, applicable laws and regulations as they apply to this job type/position
  • Complete all planned EHS & Compliance training within the defined deadlines
  • Identify and report any compliance concerns and take immediate corrective action as required

Who You Are

  • Having obtained a BSc degree in Chemical, Mechanical, Manufacturing Engineering or equivalent (defined as a BSc degree and 5-8 years relevant work experience)
  • Min 5 years relevant project engineering or project management experience. Worked in a cGMP manufacturing or engineering environment is a plus. Good Analytical, Design Skills, Project Management.
  • Good Safety Management, Supervision.
  • Good understanding of Bioprocess Manufacturing Methods and Procedures, Bioprocess Technical Understanding, Process Improvement methods. Proficient in Microsoft Office and Microsoft Project required.
  • Good understanding of Good Documentation Practices, cGMP and FDA guidelines required. Good command of the English, Mandarin language, both oral and written.
  • Able to work in a fast-paced, dynamic environment and enjoys teamwork. Experience with problem solving, conflict resolution and risk management. Working experience with construction projects in China, securing permits, working with LDI, and ACC Expected to be out stationed 50% of the time.

When you join us, you’ll also be joining Danaher’s global organization, where 68,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we’ll empower you to push the boundaries of what’s possible.

If you’ve ever wondered what’s within you, there’s no better time to find out.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.

When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

If you’ve ever wondered what’s within you, there’s no better time to find out.