The company is a well-established, mid-sized organization operating in the healthcare sector. It is committed to delivering high-quality products and services, supported by a professional and dedicated workforce.
Qualifications
Deep knowledge on GMP pharmaceutical manufacturing equipment and facilities
Growing company in the healthcare industry
Responsibilities
Lead a team of engineers to ensure projects are delivered on schedule, within budget, and in full compliance with industry regulations and safety standards.
Equipment and facilities oversight: manage the installation, calibration, maintenance, and early qualification stages (FAT, SAT, IQ) of manufacturing equipment, HVAC systems, cleanrooms, and other critical infrastructure. Ensure all assets meet regulatory and industry requirements.
Review and approve FAT and SAT documentation, and evaluate IQ documentation for accuracy and completeness.
Capital projects: direct the planning, budgeting, and execution of major capital initiatives, including new facility construction, site expansions, and equipment acquisitions. Collaborate with cross-functional teams, contractors, and regulatory agencies to ensure projects are completed on time and within budget.
Team leadership: provide technical guidance, mentorship, and support to engineers and technical personnel, establishing clear objectives, fostering collaboration, and maintaining a positive and productive work environment.
Project management: oversee the planning, organization, and coordination of engineering projects from concept through completion, including budgeting, resource management, scheduling, and risk assessment.
Ensure effective lifecycle management of equipment and facilities, utilizing reliability metrics to inform leadership and drive continuous improvement.
Supervise the planning and execution of preventive maintenance and calibration programs.
Manage external contractors for equipment validation, servicing, and maintenance activities.
Technical expertise: apply knowledge of chemical engineering principles and pharmaceutical manufacturing processes to provide technical direction and ensure successful project delivery.
Compliance and safety: maintain adherence to all relevant regulations, quality standards, and safety requirements. Stay current with industry best practices and implement strategies to mitigate operational risks.
Cross-functional collaboration: work closely with R&D, manufacturing, quality assurance, and CMC teams to support product development and production activities.
Develop and track key performance indicators (KPIs), including schedule adherence, project execution, and equipment reliability.
Benefits
Opportunity to work in the healthcare industry.
Permanent contract offering stability and career growth.
Professional development opportunities in a supportive environment.
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