Consultants/Engineers for Pharma Industry




Detalhe da Oferta:

Scope:
We are looking for to be incorporated in our office in Lisbon (Portugal). The candidates will integrate the local consultancy team. The Consultant Engineer will play a key role in providing technical expertise and innovative solutions to address complex challenges in healthcare and life sciences environments. This team operates mostly for clients in the Portuguese pharmaceutical industry, providing services through projects associated to GMP compliance, Equipment Qualification, Facility Design, Validation, QA support and advisory.

What we offer:
• Incorporation in a company that provides global solutions for Life Sciences industry with worldwide presence.
• Integration in a skilled and experienced pharma/GMP consultancy team, market leader in its field of activity.
• Opportunity to work for reference clients of pharmaceutical industry.
• Possibility to integrate multinational and multi skilled teams in international projects.
• Compensation package in line with qualifications and market value of the selected candidate.

Functions:
• Join, develop, and lead consultancy projects at pharma industry clients.
• Manage projects according to client needs, regulatory demands, and best practices (GMP).
• Write and review project documentation, such as Mater Plans, Risk Analysis, Protocols and Reports.
• Execute project activities.
• Present and discuss project solutions to clients and within internal team.


Requirements:
• University Degree such as Engineering, IT, Chemical, Biotechnology, Pharmaceutical Sciences or similar.
• Fluent in English (written and spoken).
• Strong analytical skills, proactive approach, and dynamic attitude.
• Excellent communication and interpersonal skills.
• Availability to travel.

Non-essential requirements that will be valued:
• Experience in working in Quality Assurance, Equipment Commissioning and Qualification or Computer System Validation for Pharma Industry.
• Understanding of Industrial Pharmaceutical Processes (Planning, Manufacturing, Quality Control, Logistics, Quality Assurance, Maintenance, …).
• Awareness regarding GMP regulations and best practices applicable to pharmaceutical industry.

Applications
• Applications shall be sent to

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