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Project Manager – Laboratory (Contract/Full-Time)
Location: [Competitive Salary/Global Opportunities] Employment Type: Contract or Full-Time
About the Role
The ideal candidate is a highly organised, detail-oriented professional who thrives in a fast-paced, client-facing environment. You must excel in managing multiple priorities, building strong stakeholder relationships, and ensuring consistently high service delivery.
A scientific background with strong communication and project coordination skills is essential, along with the ability to translate complex technical information into clear, client-friendly insights.
Key requirements include:
- Expertise in cGMP regulations and pharmacopoeia standards
- Proactive problem-solving and customer service orientation
- Passion for continuous learning in a dynamic industry
About You
Key Requirements
- Education: Higher education qualification in a relevant scientific discipline (e.g., Chemistry or related fields), with laboratory experience
- Experience:
- Proven expertise in laboratory/project coordination
- Project management experience with multitasking abilities
- Strong track record in analytical chemistry environments (e.g., HPLC / LCMS)
- Prioritisation of inhaled drugs/biologics projects is desirable
- Technical Proficiency:
- cGMP compliance and pharmacopeia knowledge
- Microsoft Office (advanced organisational tools)
- Excellent attention to detail with a proactive mindset
- Soft Skills:
- Exceptional communication and presentation abilities
- Relationship-building skills with all levels of stakeholders
- Adaptable, those seeking growth and learning opportunities
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About the Opportunity
As the Project Manager for a global quality assurance company, you will:
Role Overview
- Lead end-to-end project delivery across the scientific process, ensuring timeliness, quality, and client satisfaction
- Serve as primary client liaison, guiding projects from quotation phase through to final delivery
Responsibilities
- Project Organisation & Admin:
- Act as the single point of contact for assigned projects, handling documentation, protocol writing, and client communication
- Define project scope and deliverables while ensuring alignment with clinical and scientific objectives
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Risk & Quality Management:
- Monitor key performance metrics (e.g., turnaround times, on-time delivery)
- Proactively identify, manage risks, and resolve issues
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Stakeholder Coordination:
- Translate technical scientific updates into clear, actionable communication
- Lead and document project meetings (slides, action logs)
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Deduction & Compliance:
- Ensure adherence to scientific standards and client-specific requirements -managing equipment, consumables, and operational workflows
What We Offer
- A supportive, diverse, and inclusive work environment driven by precision, pace, and passion
- Career development and global opportunities
Benefits
✅ Competitive salaries & performance bonuses ✅ Training and upskilling programs ✅ **Collaborative, adaptive high-performance team culture
Commitments
- Equal opportunities: Free from bias unrelated to qualifications or potential (Age, disability, gender, sexuality, etc.)
- Fair pay: Real Living Wage Employer
- Inclusive recruitment: Reasonable adjustments for federal support needs
“Intertek – helping industries and consumers achieve innovation ever better.”
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