Key Responsibilities
We are seeking a highly skilled Validation Specialist to create and execute validation documentation and coordinate validation activities for moulding, assembly, testing equipment, computerised systems and facilities within the quality management system.
1. Write comprehensive validation plans protocols reports & amendments ensuring compliance with Regulatory Agency directives within Medical Device Pharma Sector.
2. Generate high-quality quality documentation in conjunction with validation activities.
3. Liaise effectively within cross-functional team to provide drive valuable insights into operational activities.
4. Liaise with external vendors for precise requirements of validations plans.
5. Development of robust master validation plans support implementation Company Policies GMP safety programs initiatives ensuring ongoing compliance. - Ensure adherence to regulatory standards by maintaining accurate records processes learnings training events Perform generate risk assessment documents regulated processes QMS participate drive audits Knowledge LEAN sigma tools problem solutions Interested applicants have Degree Engineering/Science discipline At least 3-5 years experience Validation Quality Engineering role Strong working knowledge process capability method characterization advantage Experience ISO13485 ISO14644 FDA regulations Ability work cross-functional environment initiative decision-making results Excellent technical report writing time management presentation interpersonal communication skills Note passport holder country vacancy might need work permit Check Blog more information Bank payment details should provided when applying job Eurojobs.com not responsible any website content All applications made via Apply now button