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 Apply now 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.