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Lilly Sr. Principal Associate Quality Auditor GQAAC (m/f/d) in Basingstoke Lilly House, United Kingdom

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Position Brand Description:

The Sr. Principal Associate Quality Auditor GQAAC is part of the Global Quality Auditing and Compliance (GQAAC) division and provides quality assurance through the execution of internal and external audits in support of pharmaceutical development, non-clinical and clinical research, product commercialization, pharmacovigilance and consumer information quality (CIQ) for Lilly. Through auditing, the Sr. Principal Associate Quality Auditor assures that GXP operations conducted and sponsored by Lilly are performed in accordance with company standards, policies, procedures and practices and are compliant with current regulatory requirements and expectations and applicable guidelines and industry standards.

GQAAC has adopted a proactive approach to ensure the effective implementation of a continuous quality assurance program. This program has the objectives of guaranteeing compliance with regulations in all geographies where Lilly operate and of further enhancing the quality of operations of Lilly and their contracted parties. The Sr. Principal Associate Quality Auditor is an expert quality professional, acting as a key contributor to the development and execution of the GQAAC audit program within the GXP area(s) of responsibility.

Applicants from Germany, but also from other EU locations (e.g., UK, Netherlands, France, Spain, Austria, Germany, Italy, Ireland, Denmark, Poland and Finland) are welcome to apply.

Key Objectives/Deliverables

The following activities will be performed according to current GQAAC procedures, guidelines and tools. These responsibilities are not intended to be all-inclusive:

Auditing

  • Scheduling, preparing, conducting and reporting Global Quality audits and assessments of research and commercial operations, both internally and externally (contracted) to assess the level of compliance with company standards, policies, practices and procedures and current regulations and guidelines. This includes leadership of audit teams –including GXP- and ability to successfully execute a portfolio of complex audits as lead or solo auditor, as appropriate (e.g.: for cause, process and system audits, affiliates, large TPOs and pre-inspection audits). Performance of this work requires limited supervision.

  • Participate in mock-inspections, as appropriate.

  • Participate in or lead the risk assessment of research and commercial operations. Integrate the information obtained through auditing and risk assessment and influence actions within and across GQAAC and the business areas involved/impacted.

  • Drive the escalation of any compliance issues or significant risks identified during audits or when conducting risk assessment.

  • Meet the requirements outlined in quality standards, quality manuals, policies, procedures, and tools.

This implies establishment and maintenance of a comprehensive knowledge of all applicable regulations, technical knowledge, and training to meet these responsibilities.

Global Quality – Business Related Responsibilities

  • Identify the need and drive the revision of GQAAC quality system documents when appropriate. Participate in or lead the preparation and/or review of standards, policies, procedures and guidelines that are used to establish quality requirements, when needed.

  • Participate in or lead the preparation of organizational metrics and trending of audit findings, when required.

  • Provide advice to research and manufacturing operations on the interpretation of corporate and regulatory GXP requirements, when required.

  • Establish and maintain relationships with relevant regulatory authorities, including supporting or facilitation of regulatory inspections, when required.

  • Provide technical expertise in identifying, formulating, assembling and delivering quality and compliance education to customers, as required.

  • Influence internal and external customers and partners when improvement needs are identified.

Personal Development

  • Maintain good interpersonal and communication skills with auditees and business areas with particular emphasis on verbal and technical writing skills.

  • Complete required training identified in the Individual Learning Plan

  • Be continually aware of current industry trends and regulatory agency interpretation of GXP requirements.

  • Seek self-development in GxP areas (e.g., grand rounds, attend training courses, conferences or association meetings) and share such information and knowledge with other members of the group or company to increase internal intelligence.

  • Mentor others in the implementation of GXP requirements.

  • Participate or lead divisional improvement efforts, including Six Sigma projects and departmental teams.

  • Act as a proactive coach for others within the organization: focused on systematic execution under highest standards of quality. The Sr. Principal Associate Quality Auditor is considered a person of reference within the function / team for technical and general auditing advice.

Minimum Requirements

  • Relevant experience(s) (minimum of 7 years) within the relevant GXP area at Lilly or within the pharmaceutical environment.

  • Experienced in working with Third Party Organizations.

  • Ability to analyze detailed technical scientific information, while understanding the bigger picture. The senior auditor should be able to clearly identify and assess risk and impact associated with specific and overall findings and situation for an auditable unit, event or case, and to articulate such risk and impact when communicating to the business (including senior management) and the quality organizations.

  • Ability to interpret and apply regulations, regulatory guidance, codes and public expectations, and identify and recommend compliance changes as appropriate.

  • Excellent interpersonal skills, ability to remain constructive and civil in difficult situations.

  • Ability to deliver timely and professional communications (oral and written) with precision and clarity to all levels of the organization.

  • Experienced in working on a global team and sharing knowledge.

  • Experience with computers, entering and managing data in databases.

  • Good analytical/problem-solving skills.

  • Ability to successfully handle several complex projects in parallel.

  • Systematic approach to ensure self-safety and that of the audit team.

Additional Preferences

  • Work under pressure on multiple tasks concurrently and meet deadlines in a fast-paced work environment with frequent interruptions and changing priorities.

  • Proven ability to think and analyze from a process perspective. Project management skills.

  • Process information to identify linkages and trends and apply findings to compliance strategies as well as to individual assignments.

  • Work independently as well as collaboratively within a global team environment.

  • Deliver constructive feedback to customers while providing a high level of customer service.

  • Ability to influence and manage change/conflict.

  • Establish and maintain effective working relationships at all levels internal and external to Lilly.

  • Ability to think on your feet and be pragmatic in decision making.

Education Requirements

Bachelors Degree (or equivalent work experience) in physical or biological sciences, Engineering or other technical area.

Other Information

Domestic and international travel is required to fulfill these job responsibilities. Must be able to travel up to 40% (duration 1-2 weeks), sometimes on short notice.

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( LillyRecruitingCompliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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