There is an exciting opportunity for a Quality Assurance Manager for a boutique Clinical Trial sourcing Pharmaceutical company based in New Jersey!
The successful candidate must have a strong background in secondary Pharmaceutical packaging & labelling.
Experience within clinical trial sourcing would also be advantageous!
QA Manager – Key Responsibilities & Experience:
Initiate and handle EQMS reports (i.e. Deviation, CAPA, Change Control, etc.) reports as required
Qualify GMP Equipment/Systems/Facilities
Ensure all regulatory and quality-related documentation is maintained in accordance with relevant SOPs and regulatory requirements
Provide support for customer and regulatory inspections
Conduct supplier and customer verification/qualification and approval
5 or more years in a QA role in clinical trial packaging and labelling, pharma packaging or pharma distribution
A degree in a related discipline
This is an urgent position so please apply if you wish to be considered