At
Albedis
, we open doors to opportunities where your skills and ambitions can truly thrive.
Deputy QA Site Lead and Senior Quality Assurance Officer will
strengthen our client's QA team at GMP and ISO 9001 certified chemical production site in Staad. The role combines operational QA responsibilities with leadership duties, acting as deputy to the QA Lead and support global cross-site projects.
This position requires a strong grasp of GMP and ISO standards in a vibrant CDMO
environment, the ability to manage complex quality matters independently, and the
leadership to drive audits, compliance, plant qualification projects, and continuous
improvement initiatives.
Key Responsibilities
• Act as Deputy QA Site Lead, supporting and substituting for the QA Lead in day-to-day
operations and decision-making.
• Ensure compliance with GMP and ISO 9001 requirements across all QA activities at
the Staad site.
• Lead, coordinate, and support internal and external audits, including customer audits
and authority inspections.
• Manage QA oversight of production, laboratory, and supply chain operations in a
CDMO environment.
• Drive qualification, validation, and compliance projects, including plant and
equipment qualification.
• Collaborate with global QA and cross-site teams to align processes, implement best
practices, and contribute to strategic initiatives.
• Provide guidance and training to QA team members and other departments on quality
matters.
• Identify, implement, and monitor continuous improvement initiatives within the QA
system.
• Prepare, review, and approve QA documentation such as SOPs, CAPAs, deviations,
and change controls.
• Serve as key contact for quality-related questions, risk assessments, and decisionmaking on complex issues.
Requirements
• University degree in chemistry, pharmacy, biology, or related natural sciences, or
equivalent qualification.
• Several years of professional experience in QA within a GMP-regulated environment,
ideally in chemical production or a CDMO setting.
• In-depth knowledge of GMP and ISO 9001 requirements and proven ability to apply
them pragmatically.
• Strong track record in audits, inspections, and compliance oversight.
• Experience in qualification/validation projects and knowledge of computerized
system validation is an advantage.
• Leadership experience or strong leadership potential, with the ability to motivate and
develop team members.
• Excellent communication skills in English and German.
• Analytical and structured working style with strong problem-solving abilities.
• High level of independence, reliability, and resilience in a dynamic environment.
Are you interested and would you like to seize this opportunity? Then we should definitely get to know each other Simply click on "Apply now" and we look forward to receiving your complete application documents.