Quality assurance abroad pharma job vacancies by piramal pharma solutions
PIRAMAL PHARMA SOLUTIONS – GRANGEMOUTH, SCOTLAND
OVERVIEW:
At Piramal, we believe that Quality is a collective responsibility, and is woven into the fabric of our organization. If you are passionate about a similar career path, design your next career move with us.
ROLES:
QA Officer – Quality Assurance
QUALIFICATION & EXPERIENCE:
â–¸ A minimum of 3 years of experience within a GMP environment manufacturing drug products or biological drug substances / intermediates is required.
Must also have 2 years of Quality Assurance experience.
Qualification : A College/University qualification in a scientific subject is essential.
Key Roles/Responsibilities:
QA primary point of contact (internal and external) for designated projects.
Collaborate with internal and external stakeholders to ensure quality of all product related activities.
Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures, Analytical Procedures and associated documentation.
Participate in quality related investigations, assist in the development, approval and implementation of effective CAPA in order to resolve production, audit and customer issues.
Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures
Participate in the audits of suppliers and self-inspection of internal production and support functions as required.
Be involved in preparation for and successful completion of MHRA/FDA and other regulatory body audits.
Coordinate quality disposition activities associated with designated materials and products.
Verify manufacturing, laboratory and associated documentation prior to performing the relevant disposition of products. Where potential issues exist, these are to be highlighted to the QA manager.
Promote and work to ensure compliance with all relevant GMP/GxP requirements.
Support and lead as required, quality process improvements and quality management system improvements within the department and on site.
Escalate any identified GMP / GxP areas of concern to Quality Management and QP.
JOB LOCATION: Grangemouth, Scotland
To apply: Click on the link in the caption.
FOR QUERIES: [email protected]
