Senior Project Manager, Tech Ops

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27 Locations
Remote
Senior level
Biotech
The Role
Provides operational oversight and project management for Process Science and Technical Operations activities. Coordinates continuous improvement projects, cross-functional technical issue resolution, workload prioritization, timelines, resources, risks, budgets, and stakeholder communications. Supports the Process Science Lead with accountability, operational meetings, and departmental execution across Manufacturing Operations, Quality Assurance, Regulatory Affairs, and Supply Chain. Requires pharmaceutical manufacturing or development experience, project leadership, GMP knowledge, and strong stakeholder management.
Summary Generated by Built In
Senior Project Manager

The Senior Project Manager within Process Science department of the IPT (Integrated Product Team) Iron and Small Molecules serves as an operational partner focused on ensuring efficient execution of the department's day-to-day activities, project delivery, and supporting prioritization of such activities and continuous improvements according to the strategic product roadmaps.

The role emphasizes business-as-usual oversight, operational coordination and leadership support across Process Science activities. It thereby enables the Process Science and Technical Operations Lead to focus on scientific and people leadership, strategic decisions, and stakeholder engagement.

Key Responsibilities

Business Operations and Project Oversight

  • Maintain oversight of the Continuous Improvement (CI) projects and tasks and the respective departmental workload.
  • Coordinate resolution of cross-functional technical issues impacting product delivery for commercial supply.
  • Track CI project progress against timelines, deliverables, and resources and proactively identify execution risks.
  • Ensure alignment of CI project priorities with organizational objectives.
  • Support CI project teams in maintaining focus on commitments and deadlines.
  • Escalate critical issues requiring management intervention.

Cross-Functional Coordination

  • Facilitate collaboration on CI projects and tasks between the IPT and partner functions such as:
    • Manufacturing Operations
    • Quality Assurance
    • Regulatory Affairs CMC
    • Supply Chain
  • Coordinate communication on CI project status, priorities, and risks via existing systems and tools

Leadership Support

  • Serve as an advisor to the Process Science Lead on operational matters.
  • Support budget tracking and expenditure monitoring.
  • Coordinate departmental communications and organizational updates.
  • Drive follow-up and accountability for key departmental commitments.
  • Act as representative of Process Science in designated operational meetings, as assigned.

Minimum Requirements

  • Bachelor's or Master's degree (or equivalent) in Pharmaceutical Sciences, Chemistry, Life Sciences, Chemical Engineering or a related discipline.
  • >5 years of experience in pharmaceutical manufacturing or development organizations.
  • Project management principles.
  • Experience working with external manufacturing organizations (CMOs/CDMOs).
  • Demonstrated experience managing technical projects and cross-functional teams.
  • Highly organized and capable of managing multiple interconnected topics at the same time, ensuring effective collaboration and alignment across a broad stakeholder community.
  • Self-driven, proactive, and able to take ownership in a dynamic environment.
  • Excellent communication, and stakeholder management skills.

Preferred Requirements

  • Experience in operational management, project management, or business operations roles
  • Operational Leadership: execution excellence, prioritization and clear accountability
  • Solid understanding of Pharmaceutical quality systems and GMP environment
  • Strong analytical thinking, problem-solving, and decision-making capabilities combined with expertise in Operational Excellence methodologies.
  • Demonstrated ability to influence stakeholders and navigate complex matrix organizations.
  • Experience working in an international, multicultural environment.
  • Fluent in English; German is considered an advantage.


About CSL Vifor

CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in iron deficiency and nephrology. We specialize in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision healthcare, aiming to help patients around the world lead better, healthier lives. Headquartered in St. Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

 

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.


You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

 To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

 

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.


Skills Required

  • Bachelor's or Master's degree, or equivalent, in Pharmaceutical Sciences, Chemistry, Life Sciences, Chemical Engineering, or a related discipline
  • More than 5 years of experience in pharmaceutical manufacturing or development organizations
  • Knowledge of project management principles
  • Experience working with external manufacturing organizations, including CMOs or CDMOs
  • Demonstrated experience managing technical projects and cross-functional teams
  • Ability to manage multiple interconnected topics while ensuring collaboration and stakeholder alignment
  • Self-driven, proactive, and able to take ownership in a dynamic environment
  • Excellent communication and stakeholder management skills
  • Experience in operational management, project management, or business operations roles
  • Operational leadership experience, including execution excellence, prioritization, and accountability
  • Understanding of pharmaceutical quality systems and GMP environments
  • Analytical thinking, problem-solving, decision-making, and Operational Excellence expertise
  • Ability to influence stakeholders and navigate complex matrix organizations
  • Experience in an international, multicultural environment
  • Fluency in English
  • German language skills

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The Company
HQ: Melbourne, Victoria
20,401 Employees

What We Do

CSL is a leading global biotechnology company with a dynamic portfolio of lifesaving medicines, including those that treat haemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency, dialysis and nephrology. Since our start in 1916, we have been driven by our promise to save lives using the latest technologies. Today, CSL – including our businesses, CSL Behring, CSL Seqirus, CSL Plasma and CSL Vifor – provides lifesaving products to patients in more than 100 countries and employs 32,000 people. Our unique combination of commercial strength, R&D focus and operational excellence enables us to identify, develop and deliver innovations so our patients can live life to the fullest. See our community guidelines: https://bit.ly/3Bs17Ra

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