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Quality Integrator
Quality Integration, GMP / GxP, Process Harmonization,
Job
CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences.For our client Johnson & Johnson MedTech - Vision we are searching for a Quality Integrator.
Keywords
- Quality Integration
- GMP / GxP
- Process Harmonization
- Change Management
- Stakeholder Management
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Acting as a trusted advisor to Site Quality Heads and Senior Quality Leadership, you guide integration strategies, support centralization initiatives, and ensure that quality transformations deliver measurable and sustainable outcomes. This is a highly visible role in which you combine deep quality expertise with strong stakeholder management and change leadership.
Responsibilities
You are responsible for aligning and harmonizing quality processes such as CAPA, Change Control, Deviations, Document Control, and Validation across sites. You identify opportunities for collaboration and standardization, reducing duplication and improving cycle times.
You provide governance for multiple site-level quality initiatives, ensuring risks are managed and execution remains on track. You advise senior stakeholders on priority setting, sequencing, and integration strategies, and actively support centralization efforts such as shared standards, templates, and services.
In addition, you prepare executive-level reports and dashboards, highlighting progress, risks, decisions, and realized benefits. You proactively anticipate compliance risks related to integration decisions and ensure appropriate mitigations, including updates to SOPs in line with GMP, GxP, and ISO requirements.
Change management is a key component of the role: you lead stakeholder engagement, training, and adoption to ensure long-term success. Regular travel (25–50%) is required to support on-site workshops, alignment sessions, and problem-solving activities.
Profile
You bring 8–12+ years of experience in Quality leadership or integration roles within regulated GMP environments, with a proven track record in multi-site harmonization or centralization initiatives. Experience within Medical Devices is highly relevant; experience in Pharma is also considered.You have strong project and program management capabilities and are comfortable working with large, global, cross-functional teams. You are data-driven, analytically strong, and experienced in translating complex information into clear recommendations for senior leadership.
A Bachelor’s or Master’s degree in Quality, Engineering, Life Sciences, or a related field is preferred, as are certifications such as Lean Six Sigma (Green/Black Belt) or PMP/Prince2. You excel in stakeholder management, influencing at senior levels, and applying a “global where possible, local where necessary” mindset to process integration.
Benefits
- This contract will run for a 6 - 9 month period.- Travel is required: Approximately 25–50% travel for site visits Uppsala, Sweden for workshops, and integration activities
- Hybrid working style: 2-3 days on site required in NL. Full time on-site while in Sweden
Company profile
Johnson & Johnson Vision combines science, technology, and people to help preserve and restore sight worldwide. Partnering with eye care professionals, the organization delivers a broad portfolio of solutions including ACUVUE® contact lenses, consumer eye health products, dry eye treatments, refractive (LASIK), and cataract solutions. Working at Johnson & Johnson Vision means contributing to meaningful healthcare innovation and being part of a global organization driven by purpose and impact.
