Mowlid Petersen

Freelance Project Manager and CQV specialist with 7+ years of experience delivering GMP-regulated projects across pharma and life science. Strong track record in commissioning, qualification, validation, clean utilities, facility design, process equipment, and cross-functional project execution in highly regulated environments. Available for freelance and contract assignments as Project Manager, CQV Lead, Validation Lead, or Engineering Project Manager.

I bring a structured, stakeholder-focused delivery approach and can support projects from design and risk assessment through execution, verification, and operational handover.

Senior Consultant (Owner) at Engipharm Consulting (Present)

Project Manager, Clean Utility at Engipharm Consulting (2025-07 – Present)

Global Pharma Company

• Act as primary client-vendor interface, driving alignment, progress, and delivery quality across the clean utility scope.
• Drive Package Owner delivery against schedule, scope, and GMP expectations.
• Lead technical clarification and stakeholder alignment between internal teams and external engineering partners.
• Coordinate clean utility risk assessments and support compliant decisions and timely approvals.
• Manage vendor documentation and turnover packages to support efficient handover to validation and operations.

Senior Consultant at Alten

Production Supporter (Fermentation & Recovery) at Alten (2024-09 – 2025-05)

• Managed minor and major deviations using structured A3 problem-solving.
• Partnered with QA, production, and technical teams to secure compliant and timely deviation closure.

Engineer / Consultant at Ramboll (2022 – 2024)

Project Manager, Air Separation Unit (Medicinal Oxygen API) at Ramboll (2022 – 2024)

• Developed and maintained the master schedule in Microsoft Project, securing delivery of key milestones.
• Directed project execution and resource planning across the full project lifecycle.
• Led verification activities and CAPA management to support compliance and inspection readiness.
• Authored and reviewed key project documentation, including VMP, VPL, and URS.
• Facilitated PFMECA-based risk assessments to identify and mitigate critical design and delivery risks early.

CQV Lead / Project Manager, GMP Facility at Ramboll (2022 – 2024)

• Coordinated cross-functional work packages and engineering disciplines to maintain scope, interface, and priority alignment.
• Led Basic and Detailed Design for utilities and process equipment with strong focus on GMP compliance and technical robustness.
• Owned CQV delivery from DQ through SAT, line walks, vendor coordination, verification execution, and final handover.

Team Lead, Lean Implementation at Ramboll (2022 – 2024)

• Implemented Lean tools and visual management systems to strengthen engagement and operational performance.

Quality Engineer at Prent Corporation (2021 – 2022)

• Prepared and executed OQ and PQ protocols in close collaboration with customers.
• Performed statistical analysis of validation data (Cpk/Ppk).
• Managed validation activities across multiple projects to ensure compliant and timely delivery.
• Served as liaison between Sales, Production, and QA to align validation requirements and stakeholder expectations.

GMP Supporter at Novo Nordisk (DFP) (2019 – 2021)

• Conducted root cause analyses of deviations and improved production SOPs to support compliant operations.
• Supported daily GMP operations across production and QA.

Project Management Programme – Mannaz (2026-05)

B.Eng. in Chemical Engineering – Technical University of Denmark (DTU) (2019)