We are looking to speak with an experienced Project Engineer to join a Pharmaceutical client of ours. This role will be responsible for support project scoping, commissioning, qualification, validation and start-up operations. This is a 12 month contract, fully onsite.
Key Responsibilities:
- Lead and deliver engineering projects on time, within budget, and in compliance with safety and quality standards.
- Coordinate project interfaces with internal teams (Operations, Maintenance, Quality, etc.) and third parties (suppliers, service providers).
- Lead and participate in commissioning, qualification, and risk management activities associated with the project.
- Manage project documentation, cost estimation, scheduling, and reporting.
- Ensure compliance with GMP/EHS regulatory requirements and procedures.
- Facilitate cross-functional project teams and continuous improvement initiatives.
- Organize and lead project meetings, training sessions, and post-project performance reviews.
- Lead investigations and contribute to high standards of teamwork and open communication.
Qualifications & Requirements:
- Degree in Engineering, Microbiology, Biochemistry, Biotechnology, or related field.
- Experience in delivering engineering projects in a GMP-regulated environment.
- Qualification in Project Management.
- Proficiency in Microsoft Office Suite (Word, Excel, Outlook) and business systems like SAP.
- Experience with problem-solving methodologies like 6-Sigma or Kepner-Tregoe.
- Strong interpersonal and communication skills, both written and verbal.
- Ability to work effectively as part of a team in a multinational corporate environment.
- Detail-oriented, adaptable, and focused on results and performance.
