Quality Assurance Associate in Pharmaceutical Compliance and Validation

Launch your career in quality assurance as an Associate focusing on compliance and validation. Support vital processes that ensure high standards are met in pharmaceutical production. This role offers the opportunity to provide technical quality oversight across various operations within pharmaceutical manufacturing.

You'll collaborate closely with engineering and validation teams to ensure adherence to best practices and regulatory standards. Your analytical skills will shape the development of validation documents and support continuous improvement initiatives, enhancing overall quality. Key Responsibilities:

• Provide QA oversight for validation activities
• Collaborate on development of quality assurance documents
• Approve validation project plans based on risk assessments
• Participate in key cross-functional operational meetings
• Conduct audits and assist in CAPA execution Requirements:
• 5 years’ hands-on experience in pharmaceuticals
• Degree in Science or Engineering is required
• Knowledge of cGMP and validation lifecycle
• Familiarity with validation tools and systems
• Excellent communication and teamwork skills Become an essential part of a quality-driven environment in the pharmaceutical sector.