This position will provide support for and be directly responsible for a range of Quality Assurance/Qualified Person functions. This position will contribute to ensure that performance of manufacturing packaging operations and drug product contract manufacturing organizations (CMOs) and product quality conforms to established cGMPs to ensure lasting customer satisfaction. This individual will demonstrate a high level of involvement in continuous improvement of the quality assurance philosophy and practice to ensure the right standards are implemented.
MAIN DUTIES:
Review of batch records for accuracy and completeness
Review and approve all Master Batch Records used in manufacturing and packaging operations
Disposition and release of product manufactured and/or packaged on site or by 3rd Party Manufacturers & New Product Introduction Products
Collaborate in the execution of cGMP-training program.
Prepare and Participate in the GMP audit program (internal and supplier audits)
Perform Quality Assurance activities associated with: Change control Deviations CAPA and Customer Complaints
Support the preparation/approval of the Product Quality Review reports
Provide support to operational and functional groups to handle all situations that may adversely impact quality
The successful candidate will have knowledge skills & experience gained in a pharmaceutical industry.
University degree in Pharmacy and further knowledge in GMP regulation
Experience as Qualified Person
Minimum of 3 years experience in the pharmaceutical/biotech industry and with a thorough knowledge of quality systems GMP and regulatory requirements.
Previous experience using SAP and ability with IT tools and experience in Microsoft office
Fluid in the communications (both written and spoken) in English
Strong interpersonal and leadership skills in dealing with a variety of cultures on non-routine matters in stressful situations can deal organisational complexity and ambiguity
Quality mindset ability to detect errors and propose improvements.
Required Experience:
IC
JOB PURPOSE:This position will provide support for and be directly responsible for a range of Quality Assurance/Qualified Person functions. This position will contribute to ensure that performance of manufacturing packaging operations and drug product contract manufacturing organizations (CMOs) and ...
JOB PURPOSE:
This position will provide support for and be directly responsible for a range of Quality Assurance/Qualified Person functions. This position will contribute to ensure that performance of manufacturing packaging operations and drug product contract manufacturing organizations (CMOs) and product quality conforms to established cGMPs to ensure lasting customer satisfaction. This individual will demonstrate a high level of involvement in continuous improvement of the quality assurance philosophy and practice to ensure the right standards are implemented.
MAIN DUTIES:
Review of batch records for accuracy and completeness
Review and approve all Master Batch Records used in manufacturing and packaging operations
Disposition and release of product manufactured and/or packaged on site or by 3rd Party Manufacturers & New Product Introduction Products
Collaborate in the execution of cGMP-training program.
Prepare and Participate in the GMP audit program (internal and supplier audits)
Perform Quality Assurance activities associated with: Change control Deviations CAPA and Customer Complaints
Support the preparation/approval of the Product Quality Review reports
Provide support to operational and functional groups to handle all situations that may adversely impact quality
The successful candidate will have knowledge skills & experience gained in a pharmaceutical industry.
University degree in Pharmacy and further knowledge in GMP regulation
Experience as Qualified Person
Minimum of 3 years experience in the pharmaceutical/biotech industry and with a thorough knowledge of quality systems GMP and regulatory requirements.
Previous experience using SAP and ability with IT tools and experience in Microsoft office
Fluid in the communications (both written and spoken) in English
Strong interpersonal and leadership skills in dealing with a variety of cultures on non-routine matters in stressful situations can deal organisational complexity and ambiguity
Quality mindset ability to detect errors and propose improvements.