Senior Commissioning, Qualification and Validation Engineer — Biopharmaceutical

Job overview

The Senior Commissioning, Qualification and Validation Engineer works onsite at client facilities in Portland, OR. Compensation is not specified. MMR Consulting provides engineering, project management, and validation services to pharmaceutical and biotechnology industries. The role leads or performs commissioning and qualification work for sterile and aseptic filling and packaging operations. It contributes to reliable equipment and processes through design support, troubleshooting, validation, and coordination with client teams and vendors.

What you'll do

• Lead or participate in design and operation of pharmaceutical fill/finish and packaging systems
• develop user, design, and functional specifications with production groups and vendors
• assess packaging operations and identify troubleshooting and improvement opportunities
• conduct reliability and optimization studies
• support or execute factory and site acceptance testing, commissioning, and qualification
• coordinate cross-functional project meetings
• provide occasional support during shutdowns or extended hours as project phases require.

What we're looking for

Skills & competencies

senior cqv engineer

biopharmaceutical

pharmaceutical packaging

sterile manufacturing

aseptic operations

commissioning

qualification

validation

portland or

mmr consulting

gxp

leadership

Work arrangement

• Weekend coverage required

Benefits & perks

• Relocation packages or travel packages are available.

Why this role

Previous pharmaceutical or biotechnology experience is mandatory; the posting specifies 8+ years in a GxP environment and an engineering degree or diploma. Relocation or travel packages are available.

About the employer

MMR Consulting is hiring for this role. Industry: Engineering Services. Sector: 54.