New job Top Pharmaceutical Company-voted one of the best companies to work for in the world! Associate Quality Consultant

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Group: Job Openings, Job Leads and Job Connections! Subject: Top Pharmaceutical Company-voted one of the best companies to work for in the world! Associate Quality Consultant Tracy Clinger CIR, CDR, CSSR, ACIR, PRC posted a job: Top Pharmaceutical Company-voted one of the best companies to work for in the world! Associate Quality Consultant "I am a recruiter working with Fortune 500 companies. I am working to fill an Associate Quality Consultant position for a leading Pharmaceutical Company. My company has been consistently ranked as one of the best companies in the world to work for. The Associate Quality Consultant role is part of the Global Quality Auditing and Compliance (GQAAC) division and represents the Corporate quality auditing interface for Lilly supporting Elanco (global commercial animal health and warehouse/distribution operations). Elanco is the animal health division of Eli Lilly and Company focusing on enriching lives through food and companionship. Through auditing, the Quality Consultant assures that global commercial operations conducted and sponsored by the Company are performed in accordance with company standards, policies, practices and procedures and are compliant with current regulations and guidelines. This position involves the auditing of Elanco commercial operations as well as third party contract manufacturing partners. KEY OBJECTIVES/DELIVERABLES: Auditing: Scheduling, preparing, conducting, communicating and reporting GQAAC audits and assessments of 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. Participate or lead the due diligence assessments of commercial contract operations, as assigned. Appropriately escalate any compliance issues. Meet the requirements defined 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 Participate or lead the preparation and/or review of standards, policies, procedures and guidelines that are used to establish quality requirements, when needed. Participate or lead the preparation of organizational metrics and trending of audit findings, when required. Establish and maintain relationships with relevant regulatory authorities, including facilitation of regulatory inspections, when required and as assigned. Personnel Development: Maintain good interpersonal and communication skills with peers, auditees and business areas with particular emphasis on verbal and technical writing skills. Complete required training for the roles identified in the Individual Training Plan (ITP)Be continually aware of current industry trends and regulatory agency interpretation of cGMP requirements. Attend training courses, conferences or association meetings to continue to gain knowledge in GMPs and to share such information with other members of the group or company to increase their awareness, as assigned. Participate or lead divisional improvement efforts, including Six Sigma projects and departmental teams, as assigned. MINIMUM REQUIREMENTS: Bachelors Degree (or 7 or more years of work experience) preferred in Microbiology or Veterinary Biological or Pharmaceutical Sciences, however chemistry, physical or biological sciences, Engineering or other technical areas are acceptable. Relevant experience(s) (5 or more years) with Quality and Veterinary Vaccine Manufacturing or Development environments. Previous experience with biotech manufacturing. 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. HOW TO APPLY: If you are interested in this position, please send your resume and salary requirements to tracy.clinger@rightthinginc.com. If you have any questions, please feel free to contact me at 866-203-8227 x5007."

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