Vacancy expired!
- 0-4 years of pharmaceutical industry experience required.
- Preferred to have a B.A./B.S. degree (preferably in Science or Engineering) but it is not required.
- 1 year of experience in a similar position is acceptable.
- Preferred experience using SAP, but not required. // Ability to perform routine assignments and develops competence by performing structured work assignments.
- Requires knowledge and exposure to fundamental theories, principles, and concepts.
- Receives instruction, guidance, and direction from others and also seeks advice/information from others when addressing serious business issues that may impact other functions.
- Verification that prints is correct for components like inserts, circulars, etc.
- Performs component verification review and release in SAP of printed material for packaging. Responsible for defect resolution and the control of printed material throughout the plant. Completes routine printed component packaging investigations and recommends disposition of affected material.
- Facilitates/participates in internal/external and joint venture GMP audits.
- Participates/facilitates audits of vendors, tollers, or other Client’s sites/operations.
- Performs the following responsibilities as required: Supplies Inspection statistical sampling and testing per Quality Standard, primary packaging component and print inspection and release, and Copy reading pre/post press items.
- Interprets Client’s Quality policies, GMP's and other agency regulations for application to Wilson Operations.
- Provides Quality Assurance review and approval of all GMP-related SOPs. Develops programs/procedures to improve compliance status of Wilson operations, including special investigations and GMP audits.
- Ensures investigations, batch release, vendor investigations, complaint investigations, etc. are completed on time.
- Identifies and implements continuous improvement activities.
- Maintains 5S organization and identifies improvement opportunities.
- Demonstrates leadership by maintaining a safe workplace and identifying actions to prevent safety incidents.
- Promotes an environment conducive with the 12 inclusive behaviors, actively promotes an inclusive culture and leads by example.
- Participates and leads internal/external and joint venture GMP audits. Participates/facilitates audits of vendors, tollers, or other Client sites/operations. Participates in regulatory inspections.
- Interprets Client Quality policies, GMP's and other agency regulations for application to Wilson Operations.
- Provides Quality Control review of all GMP-related SOPs. Develops procedures to improve compliance status of Wilson operations.
- Trends a variety of compliance performance indicators and works to drive compliance improvement. Participates in the implementation of new programs/regulations/divisional processes at the site. Identifies continuous improvement (business and compliance excellence) opportunities and through collaboration and engagement with other functional groups, implements changes to processes.
Vacancy expired!