Grifols
Manager, Quality / Sr. Manager, Quality (QA)
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Manager, Quality / Sr. Manager, Quality (QA)
role at
Grifols
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Shift: Day Shift
Summary
Responsible for managing all aspects (i.e. quality systems, release, documentation, laboratory operations, compliance, training, staffing and budgetary needs, etc.) of the Quality Assurance Packaging/Warehouse Business Unit.
Primary Responsibilities
Manage all aspects of the QA Packaging/Warehouse Business Unit (quality systems, overall compliance, oversee department budget, employee relations, etc.).
Follow cGMP and department safety practices.
Provide guidance and consult with manufacturing, maintenance, logistics, and internal regulatory departments on GXP matters.
Use expertise and sound judgment to make independent decisions within defined areas of responsibility.
Plan and analyze workflow, delegate and prioritize to ensure that assignments and projects are completed in a timely manner and within projected budget.
Participate in regulatory inspections/customer audits including providing written responses as applicable for area of responsibility.
Practice high level of facilitation skills to reach consensus and work toward solutions.
Review and revise Standard Operating Procedures and generate reports.
Investigate and initiate corrective actions for quality related issues.
Collaborate and efficiently communicate to internal and external customers.
Apply quality risk‑based processes to seek continuous improvement of systems, processes, and facilities.
Provide effective leadership to employees in the Quality Assurance Packaging/Warehouse Business Unit.
Demonstrate high levels of value and integrity.
Demonstrate skills in managing projects to bring in on budget, on schedule, and technically correct (Sr. Manager level).
Provide Quality support, reviews and approvals of regulatory labeling and submissions.
In addition to the duties described above the QA Manager provides support of manufacturing packaging, label control and warehouse operations as needed. Responsibilities may include roles such as document author/reviewer or approver in the administration of quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Record Review, Documentation, SAP Master Data, and Annual Product Reviews as well as provide Quality input for validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. Manage and facilitate Quality support for packaging and batch release schedules. Responsible for representing Quality Packaging at manufacturing business unit meetings, and project meetings.
Excellent communication skills (written and verbal) and extensive working knowledge of applicable regulations (i.e. U.S. Food and Drug Administration, Eudralex, and Health Canada) and other applicable regulatory agency requirements/guidelines. Ability to perform methodical, risk‑based analysis of situations and propose improvements. Good organizational skills are a must and ability to follow up on items to completion.
Minimum Requirements
Manager, Quality – Ph.D. in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 6 years relevant experience. MS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 8 years relevant experience. BS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 10 years relevant experience. At least 2 years of previous supervisory experience is also required. Previous experience with packaging, label control, warehouse and quarantine operations is a plus.
Sr. Manager, Quality – Ph.D. in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 6 years relevant experience. MS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 8 years relevant experience. BS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 10 years relevant experience. At least 2 years of previous supervisory experience is also required. Previous experience with packaging, label control, warehouse and quarantine operations is a plus.
Third Party Agency And Recruiter Notice
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location:
NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
#J-18808-Ljbffr
Manager, Quality / Sr. Manager, Quality (QA)
role at
Grifols
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Shift: Day Shift
Summary
Responsible for managing all aspects (i.e. quality systems, release, documentation, laboratory operations, compliance, training, staffing and budgetary needs, etc.) of the Quality Assurance Packaging/Warehouse Business Unit.
Primary Responsibilities
Manage all aspects of the QA Packaging/Warehouse Business Unit (quality systems, overall compliance, oversee department budget, employee relations, etc.).
Follow cGMP and department safety practices.
Provide guidance and consult with manufacturing, maintenance, logistics, and internal regulatory departments on GXP matters.
Use expertise and sound judgment to make independent decisions within defined areas of responsibility.
Plan and analyze workflow, delegate and prioritize to ensure that assignments and projects are completed in a timely manner and within projected budget.
Participate in regulatory inspections/customer audits including providing written responses as applicable for area of responsibility.
Practice high level of facilitation skills to reach consensus and work toward solutions.
Review and revise Standard Operating Procedures and generate reports.
Investigate and initiate corrective actions for quality related issues.
Collaborate and efficiently communicate to internal and external customers.
Apply quality risk‑based processes to seek continuous improvement of systems, processes, and facilities.
Provide effective leadership to employees in the Quality Assurance Packaging/Warehouse Business Unit.
Demonstrate high levels of value and integrity.
Demonstrate skills in managing projects to bring in on budget, on schedule, and technically correct (Sr. Manager level).
Provide Quality support, reviews and approvals of regulatory labeling and submissions.
In addition to the duties described above the QA Manager provides support of manufacturing packaging, label control and warehouse operations as needed. Responsibilities may include roles such as document author/reviewer or approver in the administration of quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Record Review, Documentation, SAP Master Data, and Annual Product Reviews as well as provide Quality input for validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. Manage and facilitate Quality support for packaging and batch release schedules. Responsible for representing Quality Packaging at manufacturing business unit meetings, and project meetings.
Excellent communication skills (written and verbal) and extensive working knowledge of applicable regulations (i.e. U.S. Food and Drug Administration, Eudralex, and Health Canada) and other applicable regulatory agency requirements/guidelines. Ability to perform methodical, risk‑based analysis of situations and propose improvements. Good organizational skills are a must and ability to follow up on items to completion.
Minimum Requirements
Manager, Quality – Ph.D. in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 6 years relevant experience. MS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 8 years relevant experience. BS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 10 years relevant experience. At least 2 years of previous supervisory experience is also required. Previous experience with packaging, label control, warehouse and quarantine operations is a plus.
Sr. Manager, Quality – Ph.D. in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 6 years relevant experience. MS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 8 years relevant experience. BS in a Life Sciences, Chemical Sciences, or relevant degree (STEM degree preferred) with minimum of 10 years relevant experience. At least 2 years of previous supervisory experience is also required. Previous experience with packaging, label control, warehouse and quarantine operations is a plus.
Third Party Agency And Recruiter Notice
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location:
NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
#J-18808-Ljbffr