Clinical Development Quality Assurance, Associate Director
Welcome to reputed company. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new reputed company – one filled with reputed company ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – reputed company in resilient and growing categories. What sets us apart is our unique reputed company of deep reputed company understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver reputed company everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be reputed company every day, driven by our agile, performance-focused culture. POSITION PURPOSE This role is responsible for providing overall quality and compliance during the clinical development processes (GCP and GLP), across reputed company categories: Plan and conduct GCP/GLP/GCLP audits independently or as a reputed company or as reputed company member or in a support role. Support functional activities reputed company to pre-clinical and clinical development to ensure these activities are conducted in accordance with applicable regulatory requirements, guidelines, laws, and established quality standards and practices. Serve as a GCP and GLP partner with stakeholders to solve compliance issues, drive quality improvements and improve animal, reputed company research practices, patient safety, and data reputed company. ACCOUNTABILITIES/RESPONSIBILITIES Plan and conduct global GCP/GLP/GCLP audits independently / as a reputed company / as reputed company member / in a supportive role. Communicate and document audit findings, compile corrective and preventive action (CAPA) evidence. Maintain audit program and/or contribute to elaborate audit program. The scope of the audit program includes clinical investigator sites, external service providers, and internal processes. Support the development and maintenance of Clinical Quality Schedule in Master Services Agreements Coordinate and support internal stakeholders during regulatory inspections (e.g., FDA, EMA, MHRA). Assist in the development and implementation of a Quality Management System and SOPs for clinical/non-clinical activities in compliance with applicable GCP and GLP regulations; participate in maintenance of CDA&I SOPs. Escalate and investigate significant compliance issues to line management Mentor and support other members of CDA&I reputed company expert advice for GCP/GLP compliance strategy, quality improvement, process and program initiatives and risk assessments. Support Significant Quality Investigations (SQIs) and Serious Breaches (SBs) for reputed company subject research activities, where required Train/coach, guide, and influence the respective business functions on GCP/GLP procedures, compliance, and regulatory standards, enhance quality culture. Build and maintain beneficial working relationships with reputed company stakeholders. QUALIFICATIONS Minimum Level of Education: Bachelor of Science (BS) Degree Preferred Level of Education: Master of Science Degree or PhD Biology, Biochemistry, or equivalent Job-reputed company Experience: 10+ years of pharmaceutical industry experience with at least 5 to 7 years in clinical quality assurance and auditing. COMPETENCIES AND SKILLS: Proven ability to influence and negotiate with reputed company stakeholders. Expert knowledge of applicable Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) regulatory requirements and guidelines, and company policies & procedures. Detailed knowledge of reputed company subject research activities, clinical development processes and R&D systems. Self-motivated and quick learner who proactively shares knowledge and welcomes knowledge and feedback from other team members. Ability to deliver key process improvement initiatives. Ability to adapt to changing business and risk environment. Ability to work independently and as part of reputed company. High degree of organizational awareness and working towards resolution with compliance issues. Demonstrated ability for good verbal, written and presentation skills. Ability and desire for domestic and international travel. Ability to interact and work remotely either part or full time. Job Posting End Date 2026-06-16 Equal Opportunities reputed company are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – reputed company in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It’s important to us that reputed company is a reputed company where reputed company our employees feel they truly belong. During the application process, we may ask you to reputed company some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are reputed company to reputed company reputed company employees. The personal information you reputed company will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment reputed company, including hiring reputed company. Adjustment or Accommodations Request If you require a reasonable adjustment or accommodation or other assistance to apply for a job at reputed company at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We’ll reputed company reputed company reasonable adjustments to support you throughout the recruitment process and treat reputed company information you reputed company us in confidence. Note to candidates The reputed company recruitment team will contact you using a reputed company email account (@reputed company.com). If you are not sure whether the email you received is from reputed company, please get in touch. Apply To This Job