Hays (Schweiz) AG

Technical Project Manager (m/f/d) Freelance/temporary employment for a project Visp Start date: asap Reference number: 845362/1 Responsibilities Lead technical projects to expand manufacturing capacity and support production scale-up Provide expert input into project design, ensuring alignment with operational and regulatory requirements Coordinate cross-functional teams and external vendors, manage project governance, and ensure timely delivery Develop and implement best-practice processes in line with industry and regulatory trends Manage change controls, troubleshoot technical issues, and handle deviations related to equipment and processes Collaborate with manufacturing and quality teams to establish and update operational procedures Profile Experience in GMP manufacturing (Drug Product experience preferred) Proven track record in project coordination or management within pharmaceutical production Experience with CAPEX projects and equipment qualification is a strong advantage Solid understanding of cGMP and EU Annex 1 requirements Fluent in English; German is advantageous Strong interpersonal and communication skills, with a collaborative and results-driven mindset Agile and adaptable, able to deliver under pressure and shifting priorities Benefits A dynamic and impactful role in a growing pharmaceutical environment Opportunity to shape technical projects that directly support strategic growth Collaborative team culture with clear ownership and accountability

QA Project Manager (m/f/d) Freelance/temporary employment for a project Visp Start date: asap Reference number: 842508/1 Responsibilities Lead and manage a team of QA Project Managers, ensuring alignment with internal and external customer expectations Oversee quality deliverables during tech transfer, process validation, and production phases Act as escalation point for QA-related issues, ensuring timely resolution and compliance Support and guide the team in handling deviations, change controls, CAPAs, and regulatory matters Drive risk assessment and resolution processes, ensuring efficient and compliant outcomes Provide training, mentoring, and development in quality principles and regulatory standards Step in as QA Project Manager for client projects when needed Monitor and report on key performance indicators (KPIs) and implement continuous improvement initiatives Represent QA in cross-functional meetings and support audits (regulatory and customer) Collaborate with departments such as MSAT, Engineering, QC, Validation, Supply Chain, and Manufacturing Profile Bachelor-s or Master-s degree in Biotechnology, Life Sciences, or a related field Solid experience in Quality Assurance within the life sciences industry Proven leadership experience managing direct reports Strong knowledge of GMP, regulatory compliance, and quality systems Experience in managing complex projects and customer-facing roles Excellent communication, decision-making, and problem-solving skills Ability to manage multiple priorities and deliver under pressure Proficiency in QA tools, documentation systems, and data analysis Fluent in English (written and spoken); additional languages are advantageous Experience in audit preparation and regulatory inspections is preferred Benefits Strategic leadership role in a global, innovation-driven organization Opportunity to shape quality standards and processes across key projects Collaborative work environment with cross-functional and international teams Professional development and training programs