Technical Project Manager – CMC

This is a fully remote position, open to applicants in Ireland.

📋 Description

• Deliver consulting services for Sia/LBG’s clients, which includes providing tactical support for daily project operations such as documenting meeting minutes, tracking actions, and monitoring decisions.

• Contribute proactively to project management outputs (such as reports and dashboards) and regular updates (including schedule, budget, and risk), typically by preparing initial drafts.

• Develop and sustain comprehensive predecessor-driven project schedules (Gantt charts, integrated timelines) using scheduling tools/software (e.g., MS Project, Smartsheet, Planisware, Primavera, or similar).

• Offer timely and clear schedule updates, variance analyses, and risk evaluations to project leaders and stakeholders to ensure that project timelines align with project strategy, portfolio priorities, and critical decision points (e.g., regulatory submissions, health authority interactions).

• Coordinate among project functional areas and personnel as needed to ensure the advancement of project activities.

• Assist in building and managing a diverse team across various functions and sites, including overseeing multiple projects and teams in different locations.

• Exhibit and promote exceptional teamwork while effectively engaging within multidisciplinary teams.

• Manage project demands to ensure alignment or realignment of Budget, Quality, Timeline, and Scope as necessary.

• Support product development meetings and ensure that all Project Leaders and/or subteam leaders have the necessary information and resources to implement the project.

• Prioritize customer service with agility and effective communication.

• Comply with Sia/LBG quality standards for client deliverables.

⛳️ Requirements

• A minimum of 2 years of experience in the biopharmaceutical sector, including at least 1 year in project management roles.

• BS, MS, or PhD in a scientific or engineering field (e.g., Chemistry, Biochemistry, Chemical or Biomedical Engineering, Pharmaceutical Sciences).

• Experience collaborating with CDMOs to facilitate outsourced development and manufacturing processes, including oversight of deliverables and timelines.

• Capability to engage in technical and scientific discussions.

• Strong communication and interpersonal skills.

• Proficiency in Planisware.

• Fluent and articulate in English, both written and spoken.

• Effective written and verbal communication, presentation, problem-solving, and negotiation skills.

• Ability to function independently as well as collaboratively with others.

• Flexibility and adaptability to ambiguity, along with a strong sense of personal responsibility for deliverables and outcomes.

• Ability to work effectively within teams that may comprise multiple disciplines.

🏝️ Benefits

• Employee Wellbeing

• Continuous learning & development opportunities