Quality Control Supervisor is responsible to oversee the Environmental Monitoring (EM) Program, testing, reports, and release of results. Supervise EM Data Review and Archiving while routinely performing, tracking, and trending EM data. In addition, manage and supervise direct reports daily activities including establishing priorities and coordinating activities.
What You’ll Do
As a hand-on Working Supervisor, work side-by-side with the team, roll up the sleeves and pitch in to support EM and the lab. In addition, perform EM as required and monitoring during bulk fill operations.
Assist in assuring the EM program is in compliance with appropriate regulatory requirements and understands Corporate and Divisional policies related to documentation and ensure compliance.
Coordinate projects as directed by department or manager to implement efficiencies in document/system automation and business process improvements.
Write and revise investigations and procedures as needed.
Assist in troubleshooting assays and provide support for the department.
Develop and maintain trend, backlog, and document error reports supporting performance.
Monitor production schedule and prepare EM schedule on a weekly basis.
Support Quality Control Microbiology department/Production on area releases as needed and review the data in a timely manner.
May be responsible for one or more shifts. Facilitate department or shift communication meetings.
Part-take in hiring, promotion/placement, and termination process.
Provide direct reports coaching and training including annual performance review and merit increase.
What You’ll Have
Bachelor’s Degree, preferably in science related field.
- Minimum 2+ years of supervisory/leadership experience, preferably in Microbiology, Environment Monitoring, and/or Aseptic Manufacturing/Contamination Control Practices.
- Willingness to perform any task that is asked of others to accomplish. Someone who can still roll up their sleeves.
- Knowledge in Microbiology- Environmental Monitoring, Quality Control Lab Operation and Regulatory related requirements.
Skilled working independently, and in a team setting to meet operational and business goals.
Ability to plan, execute, and make operational and business decisions.
Must have knowledge and skill in personnel management.
Strong building and fostering relationships with internal and external stakeholders.
Broad knowledge and understanding of the issues and trends relevant to science, technology, and business.
What You’ll Receive
Comprehensive Healthcare: Medical, Vision, Dental, FSA, HSA
Financial Well-being, Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan
AbbVie Vitality: Health & Wellness programs including Employee Assistance Program (EAP), Health Advocate, Global Well-Being Programs
Generous Paid Time Off include, Company Holidays, Vacation, Parental and Caregiver Leave
Community Outreach Programs and company match of charitable contributions
Perks include AbbVie Product Shop, Employee Loyalty Program, Tuition Assistance, Adoption and Surrogacy Assistance, Mothers at Work and Milk Stork to list a few
Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Job Type: Experienced