BrightOwl Loader Loading

Senior Specialist Quality and Compliance- GMP Lucerne Switzerland,  

MSD (company)


Posted on : 22 April 2017

Project Description


Description
  • Our company  is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. 
  • Today, we are building a new kind of healthcare company  one that is ready to help create a healthier future for all of us.
  • Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you.  
  • To this end, we strive to create an environment of mutual respect, encouragement and teamwork.  
  • As part of our global team, you ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career
  • Responsible to achieve and maintain qualification / certification status through robust training and continuing education programs to enable conducting audits of Human Health, Animal Health and Consumer Care Sites, Contracted facilities, Distribution Centers, Business Partners and Suppliers. 
  • Responsible for accepting audit assignments, performing audit pre-work, conducting audits and ensuring post audit activities are completed within defined time frames. 
  • The position requires negotiating with external firms to attain acceptable corrective actions and independent generation of extensive, high quality, GMP documentation as well as extensive communication and partnership with divisional oversight groups and commercial sites.


Responsibilities
  • Schedule and perform assigned audits and ensure timelines for audit steps (prework, conducting audit, issuance of audit report, CAPA receipt) meet established expectations. 
  • This requires approximately 50% worldwide travel.
  •  Review and approve audit reports.
  •  Maintain a broad based expertise of cGMP's, company Policies, Procedures and Guidelines, regulatory requirements, etc. that are pertinent to the pharmaceutical industry including, but not limited to Biologics, Medical Devices, Vaccines, Small Molecules, Combination Products, APIs and Controlled Substances.
  •  Obtain and maintain cutting-edge knowledge, application, and certification status for various technical/Quality auditing topics
  •  Maintain awareness of evolving industry and regulatory trends/regulations. Support New Business opportunities through Due Diligence (electronic due diligence as well as on-site visits) and Pre-Contract Audits, issuance of reports, and evaluation of corrective and preventive actions.
  •  Assist with preparation of annual audit schedule, using risk based approaches for auditor assignment
  •  Lead & Coordinate with Procurement and impacted Site Quality leads on critical audit findings and or audit refusals. 
  • Generate comprehensive presentations/summary of issues for effective communication to all levels, ensuring required assessments are performed.
  •  Provide regulatory inspection support to company Sites as it relates to the Divisional Audit program, status of audits, and specific audit results.
  •  Provides support and administrative functions for the electronic Supplier Tracking and Repository System, and assists in data maintenance.
  •  Leads initiatives / drive results in various projects, as assigned, to maintain the effectiveness and efficiency of the audit program, and to ensure the audit program continues to meet using site, management and regulatory expectations.
  • Mentor new auditors to ensure comprehensive training and full understanding of auditor roles and responsibilities and associated strategic/tactical thinking.



Qualifications
Education Minimum Requirement:
  • Bachelor Degree in Engineering, Biology, Chemistry or related field
  • Required Experience and Skills:
  •  Minimum of 5 years of manufacturing, technology, and/or quality experience within an FDA, and/or EU API, Drug Product, Medical Device or equivalent environment.
  •  Experience performing audits of external and internal manufacturers and testing laboratories. 
  • Must have a working knowledge of processes to support the manufacturing of APIs and Drug Products.
  •  Strong compliance knowledge and proficiency in interpreting and applying regulatory requirements and guidelines.
  •  Ability to travel globally approximately 50% of the time.
  •  Ability to work independently with limited supervision in a virtual-management environment
  •  Excellent/accomplished communication, negotiation, and facilitation skills.
  • Preferred Experience and Skills:
  •  Demonstrated ability to establish and maintain collaborative relationships with key stakeholders.
  •  Demonstrated ability to lead and drive results/impact for critical business / compliance initiatives
  •  Demonstrated ability for process improvement and to create/implement simple, compliant systems in a diversity of areas
  •  Lean six-sigma belt / demonstrated process improvement experience
  •  Experience with development, implementation and optimization of IT tools to deliver business outcomes/impact.



Offer:
  • Our employees are the key to our company s success.  
  • We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. 
  • Our Company s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

  
    
Job Segment:  Engineer, Medical, CAPA, Compliance, Lean Six Sigma, Engineering, Healthcare, Management, Legal                       

Locations

Luzern CH

Find a Job Find Candidates

Similar Jobs

More jobs from MSD

Other jobs in Switzerland

Other jobs in Lucerne

Other jobs from MSD in Lucerne

Other Jobs

Most Recent Searches

Most Famous Searches

You might also like