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Project Manager (Biotechnology)

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Onsite

Project Manager (Biotechnology)

CK Life Sciences

Project Manager (Biotechnology)

Skills

Google Cloud PlatformTesting & QARJiraAsanaComplianceRisk Management

19 days ago

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Important information


Contract type:

Permanent

Work mode:

Onsite

Published on:

5 October 2026

What they need


Key Responsibilities:

  • Develop and manage detailed project plans, timelines, budgets, and resource allocations for our biotechnology projects.

  • Define project scope, objectives, and deliverables in alignment with company strategy.

  • Track project progress and proactively manage risks, dependencies, and changes.

  • Facilitate collaboration between scientific, clinical, regulatory, and business teams.

  • Lead regular project meetings with project updates, dashboards & presentation, ensuring clear communication and alignment.

  • Serve as the primary point of contact for project stakeholders.

  • Coordinate with RA & QA team to ensure projects adhere to relevant regulatory standards (e.g., FDA, EMA, GMP, GCP) and compliance requirement.

  • Identify potential risks early and develop mitigation strategies.

  • Resolve project issues efficiently while minimizing disruption.

  • Maintain accurate project documentation, including timelines, reports, and decisions.

  • Drive efficiency and scalability as the organization grows.

Requirements:

  • Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Bioengineering or a related field.

  • PMP, PRINCE2, or equivalent project management certification is a plus.

  • Minimum 5 years of project management experience, preferably in biotech, pharma, or life sciences.

  • Experience managing R&D, clinical development or product development projects.

  • Startup or high-growth environment experience is highly desirable.

  • Strong understanding of the drug development lifecycle or biotech product development.

  • Familiarity with project management tools (e.g., MS Project, Asana, Jira, Smartsheet).

  • Ability to translate complex scientific concepts into actionable plans.

  • Experience with regulatory submissions or clinical trial management.

  • Knowledge of quality systems (GMP, GLP, GCP).

  • Exposure to fundraising milestones, investor reporting, or partnership projects.

Thank you for your interest in a career with CK Life Sciences. Competitive compensation and benefits package will be offered to the right candidate. We operate a 5-day workweek. Regular shuttle bus service is also provided with pick-ups and drop-offs at designated and convenient locations.

To apply for our position, please click the QUICK APPLY button. For more company information, please visit www.ck-lifesciences.com.

We are an equal opportunity employer and welcome applications from all qualified candidates. Personal data collected will be treated in strictest confidence and handled confidentially by authorized personnel for recruitment-related purposes within the Group.

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