Senior CSV / CQV Project Lead - Sweden at Advanced Manufacturing Tech Solutions (AMTSOL)

Stockholm, , Sweden -

Full Time

Start Date

Immediate

Expiry Date

11 May, 26

Salary

0.0

Posted On

10 Feb, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

CSV, CQV, DeltaV, OQ, Commissioning, GxP, GAMP 5, Validation, Automation, Engineering, Quality, Pharmaceutical, Biotech, Risk Management, Project Management, Technical Advisory

Industry

Pharmaceutical Manufacturing

Description

Advanced Manufacturing Tech Solutions (AMTSOL) www.amtsol.com A Leader in Life science Manufacturing Technology solutions, we are looking for top talent to be part of the dynamic team and drive the growth of the business. Role: Senior CSV / CQV Project Lead - Sweden Industry: Pharmaceutical / Life Sciences Start: ASAP Full time : Onsite in Sweden Project Phase: DeltaV Upgrade – (OQ) Role Overview This role is focused on advising, guiding, and stabilizing CQV execution, ensuring the project can progress through OQ and into commissioning readiness. The successful candidate will work closely with site teams, automation, engineering, and quality to bring proven DeltaV CQV experience and best-practice execution to the project. Onsite presence is preferred to maximize impact, though a hybrid model may be considered for the right candidate. Immediate availability is highly desirable. Key Responsibilities Provide senior leadership and hands-on guidance for CSV / CQV activities during the OQ phase Review current validation status, execution approach, and documentation Advise and support the existing CQV team to improve execution quality and pace Lead and guide DeltaV OQ planning, execution, deviation handling, and closure Identify critical risks, gaps, and recovery actions impacting project timelines Support commissioning readiness and transition from OQ to operational handover Act as a trusted technical advisor to site leadership and project stakeholders Ensure compliance with GxP, GAMP 5, and site validation standards Interface effectively with Automation, Engineering, QA, and Operations teams Qualifications & Experience 15+ years experience in CSV / CQV within regulated pharmaceutical or biotech environments Proven experience leading DeltaV CQV activities, particularly OQ and commissioning readiness Strong understanding of DeltaV systems, automation lifecycle, and GMP validation requirements Demonstrated experience supporting challenged or recovery-phase projects Ability to work effectively in high-pressure, fast-moving project environments Hands-on, delivery-focused mindset rather than purely governance or oversight

Responsibilities

Provide senior leadership and hands-on guidance for CSV / CQV activities during the OQ phase. Act as a trusted technical advisor to site leadership and project stakeholders.