Commercial Quality Manager SAGEA
We are IMETA
ROPU IMETA is a Regional Operating Unit consisting of 6 mid-sized Operating Units: India, Turkey, Southern Africa (South Africa & Sub Sahara Africa) Northeast & West Africa, Near East & UAE, Saudi Arabia, Gulf & East Africa (SAGEA).
IMETA is home to more than 47 nationalities. We are a myriad of color and culture and embracing this diversity is one of our greatest opportunities.
We are a powerhouse of talent, and we work together to ensure that we grow, nurture, and retain our talent. Uniting and working together is the key to our success.
The Opportunity
We are looking for a Commercial Quality Manager for SAGEA based in Riyadh. This position will proactively create, establish and maintain the Human Pharma & Animal Health division Quality Management System and in turn will be responsible for GDP (Good Distribution Practice) towards authorities, maintaining and ensuring compliance, product supply support and managing external service providers.
Tasks & Responsibilities:
• Ensure Good Distribution Practice (GDP) towards authorities and manage audits and inspections are performed at appropriate intervals and necessary corrective measures are put in place
• Coordinate and promptly perform any recall operations for medicinal products
• Ensure proper escalation of major and critical product/quality defects and relevant customer complaints are handled effectively in a timely manner
• Carry out appropriate measure for testing and usability checks on import and batch release as per local regulation
• Establish and maintain the Quality Management System and align with key functions for continuous improvement
• Manage and maintain the documentation system and ensure accuracy and quality of records
• Manage external service providers in all quality relevant aspects during the life cycle of a contract until termination to ensure supply and manufacture of products or services with acceptable quality.
Requirements:
• Bachelors degree
• 6-8 years experience in pharmaceutical industry or a similar regulated industry with clear focus on quality
• 3-5 years experience into a management position
• Experience in performing Quality Audits
• Strong knowledge of international regulations/guidelines concerning GDP/GMP and Quality Assurance
• Regional experience is preferred
• Proficiency in English & Arabic, in its written and oral form
• Extensive experience in using electronic systems as SAP, GO Track, VEEVA Vault is a must
• Effective communication with ability to build and maintain relationships
• Interdisciplinary thinking, problem solving and open communication
• Excellent interpersonal skills, assertiveness and decision-making ability
• Capable of organizing, planning, and prioritizing tasks
• Must be a Saudi national
Make millions of lives better. A career with purpose. Yours for the taking.
What happens Next?
We are looking forward to receiving your application! We will then have a look at your CV. If we see a match, we will invite you for a screening interview.
SPL Screening:
In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (“SPL”). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.