Manager Quality (Gcp) - Fixed Term Contract

Moonlake; Porto; Hybrid; EUR 70,000 - 100,000; Full time

Benefits offered by this job

Learning Environment

Flexibility and Balance

Career Growth

Job summary

MoonLake Immunotherapeutics in Porto, Portugal seeks a Manager Quality (GCP) on a fixed-term contract to lead GCP quality oversight across clinical programmes and support audits, CAPAs and inspections readiness. You will collaborate with CROs and internal teams to ensure trials meet regulatory standards.

Key responsibilities include maintaining the QMS, monitoring quality metrics, and providing guidance on risk management and quality issues to study teams.

Qualifications

• Experience managing quality issues and CAPAs in biotech/biopharma.
• Proven track record monitoring GCP compliance within biotech/biopharma companies.
• Experience conducting GCP clinical audits as lead or support auditor (investigator site audits, GCP vendor audits, process/system audits).
• Experience quality oversight of clinical trials from protocol development to clinical study reporting.

Responsibilities

• Provide GCP quality oversight and support for clinical trials and vendors.
• Lead CAPA processes and ensure CAPA effectiveness.
• Conduct internal and external GCP and GCLP audits as lead or support auditor.
• Support inspection readiness activities and regulatory inspections.
• Maintain and monitor the QMS to ensure regulatory compliance.
• Develop and report quality metrics and dashboards to senior management.

Skills

GCP knowledge

Audit processes

Regulatory guidelines

Communication skills

Risk management

Analytical thinking

Organisational skills

Collaborative work

Education

Bachelor’s degree in life science or healthcare

Tools

GxP Quality Management System

Quality management software

Audit tools

Job description

Manager Quality (GCP) - Fixed Term Contract

Empresa : Moonlake Tipo de Emprego : Periodo Integral Porto, Portugal

Job Purpose

The Manager Quality (GCP) ensures robust GCP compliance and quality oversight across MoonLake´s clinical development programmes by serving as a quality expert, leading and supporting audits, managing quality risks, and supporting inspections readiness. The role provides operational quality support to clinical teams and vendors to ensure trials are conducted to the highest regulatory standards.

Key Accountabilities

• GCP Quality Oversight & Clinical Trial Support: Support implementation and delivery of GCP Quality oversight requirements within MoonLake and our vendors. Provide quality guidance to assigned clinical trial teams (acting as sponsor Study GCP Quality Lead). Attend internal clinical meetings and provide Quality representation on assigned clinical trials. Collaborate and share information within GCP team to ensure ongoing oversight of all GCP activities within and subcontracted by Moonlake. Ensure proactive oversight of quality risk management processes in assigned clinical programme/trials, including quality risk assessments and management to ensure clinical programmes are always complying and inspection ready.
• Quality Issues, CAPA & Risk Management: Act as Study GCP Quality lead for Quality issues, CAPAs, and CAPA effectiveness checks for assigned clinical programmes/trials and working with Owners and counterpart CRO leads to resolution.
• Audits, Inspections & Vendor Oversight: Conduct (as Lead or Support auditor depending on areas of expertise) assigned internal and external (vendor) GCP and/or GCLP audits. Conduct vendor qualifications and QA assessments. Support GCP inspection readiness activities and management of regulatory inspections of MoonLake (e.g. mock inspection activities and backroom activities, etc.).
• Quality Systems & Documentation: As a member of the MoonLake Quality Team, maintain and monitor the GxP Quality Management System (QMS). Ensuring that the QMS meets all necessary regulatory requirements, including good practice guidelines and standards, with specific emphasis on GCP compliance. To maintain awareness of, and ensure compliance with, policies and procedures relating to quality standards within the Company.
• Performance Monitoring & Quality Metrics: Maintain agreed quality metrics and dashboards to enable clear communication to senior management and clinical study teams of compliance performance and any risks or issues identified. To provide support and advice to clinical study teams with regards to management of quality issues, CAPAs and changes.
• Reporting & Governance: Ensure that Director, GCP is kept informed of progress, highlighting successes as well as potential issues on clinical programmes or Moonlake Quality management system activities.

Your profile

Education: Bachelor´s degree in life science or healthcare field is preferred.

Experience:

• Experience of managing quality issues and CAPAs in a biotechnology or biopharma setting.
• Proven track record in monitoring GCP compliance within biotechnology or biopharma companies.
• Conducting GCP clinical audits as lead or support auditor (investigator site audits, GCP vendor audits, process/system audits during end-to-end clinical lifecycle).
• Experience of quality oversight of clinical trials, from protocol development to clinical study reporting is preferred.

Skills/knowledge/behavioural competencies:

• Demonstrable knowledge of GCP and related industry/regulatory guidelines.
• Working knowledge of audit processes and audit conduct.
• Confident communicator, both verbally and written.
• Critical thinking, risk management and risk-based mindset.
• Ability to work in a flexible, collaborative style with colleagues and teams within the company and with external entities including CROs and consultants.
• Highly organised self-motivator, able to prioritise activities, work well under pressure and meet deadlines.
• The ability to interrogate and analyse systems to identify new ways of working.

Work Location:

• 2 days a week in our brand new Porto office.

Why us?

An exciting job opportunity awaits you! MoonLake is a dynamic and innovative company pushing the boundaries of possibility, and we are looking for passionate individuals to join our stellar team.

What we offer

• Learning Environment: An opportunity to learn and grow alongside experienced professionals in a supportive and innovative biotech environment.
• Impactful Work: Contribute to ground-breaking projects that have the potential to transform global healthcare.
• Flexibility and Balance: Work remotely/hybrid, enjoying a healthy work-life balance while making meaningful contributions to our team.
• Career Growth: A clear path for career progression, with the chance to take on more responsibilities as you develop your skills.

Our Core Values

We look for potential MoonLakers that embody our three core values that drive our pursuit of excellence:

• We do Stellar Science: We aspire to create novel therapies that elevate treatment horizons, with innovative science, and high quality, always.
• We go beyond: We aspire to be positively disruptive in our field, and bold in the way we challenge the norms and each other.
• We unlock value: We aspire to create long-term value for investors and communities.

About us

MoonLake Immunotherapeuticsis a clinical-stage biopharmaceutical company unlocking the potential of sonelokimab, a novel investigational Nanobody® for the treatment of the inflammatory disease, to revolutionize outcomes for patients.

We continue to make significant progress in our Global Clinical Development Programs. The company’s focus is on inflammatory diseases with a major unmet need, including hidradenitis suppurativa and psoriatic arthritis – conditions affecting millions of people worldwide with a large need for improved treatment options. MoonLake was founded in 2021 and is headquarted in Zug, with hubs in Cambridge & Porto.

Further information is available at www.moonlaketx.com