Senior Analyst, Manufacturing Process
AbbVie
August 31, 2026
On-site
Waco, TX
$78,500 - $141,000 USD yearly
Operations
Job Description
Responsible for management of Production projects that improve manufacturing efficiency and safety, decrease costs, decrease opportunity for human error, or increase compliance. Works with peers in other departments to meet project timelines. Tracks transfer, implementation, and monitoring of projects. Uses SAP, LIMS, PI, and other systems/databases to input, verify, monitor, and analyze data. Identifies opportunities for improvement of manufacturing and business processes; proposes, plans, and facilitates implementation of solutions. Responsible for inventory maintenance and production tracking.
Responsibilities
- Support Production objectives; execute systems/procedures efficiently and compliantly; improve inter-group consistency and GMP compliance.
- Schedule tasks to support project/campaign timelines; manage document review/approval.
- Apply judgment to determine appropriate action; track problems, analyze data, propose solutions, and create implementation plans.
- Assist with validation activities, provide technical assistance, and troubleshoot manufacturing equipment.
- Establish requirements and implement changes to the Process Control System.
- Investigate production events with quality/compliance impact; lead/participate in RCPS or FMEA and document outcomes.
- Transfer methods into Production instructions and provide training for rollout.
- Inventory maintenance and production tracking; SAP SME for inventory/production; track/report bulk usages; interface with Planning for process order numbers and batch numbers; initiate/track blanket POs; track weekly/monthly yield and report to supervision/Finance.
- Present technical information and collaborate with functional peer groups.
- Comply with AbbVie policies/procedures, Engineering Standards, Plant procedures, and regulatory requirements.
Qualifications
- Bachelor’s degree or equivalent (preferably engineering or related).
- 5+ years’ manufacturing/production process experience; strong writing skills.
- Working knowledge of safety, quality systems, and GMP; familiarity with regulatory filings; tech transfer and equipment/facilities validation.
- Flexibility; professional under pressure; team-oriented; build working relationships.
- Intermediate to high computer and MS Office skills.
Responsible for management of Production projects that improve manufacturing efficiency and safety, decrease costs, decrease opportunity for human error, or increase compliance. Works with peers in other departments to meet project timelines. Tracks transfer, implementation, and monitoring of projects. Uses SAP, LIMS, PI, and other systems/databases to input, verify, monitor, and analyze data. Identifies opportunities for improvement of manufacturing and business processes; proposes, plans, and facilitates implementation of solutions. Responsible for inventory maintenance and production tracking.
Responsibilities
- Support Production objectives; execute systems/procedures efficiently and compliantly; improve inter-group consistency and GMP compliance.
- Schedule tasks to support project/campaign timelines; manage document review/approval.
- Apply judgment to determine appropriate action; track problems, analyze data, propose solutions, and create implementation plans.
- Assist with validation activities, provide technical assistance, and troubleshoot manufacturing equipment.
- Establish requirements and implement changes to the Process Control System.
- Investigate production events with quality/compliance impact; lead/participate in RCPS or FMEA and document outcomes.
- Transfer methods into Production instructions and provide training for rollout.
- Inventory maintenance and production tracking; SAP SME for inventory/production; track/report bulk usages; interface with Planning for process order numbers and batch numbers; initiate/track blanket POs; track weekly/monthly yield and report to supervision/Finance.
- Present technical information and collaborate with functional peer groups.
- Comply with AbbVie policies/procedures, Engineering Standards, Plant procedures, and regulatory requirements.
Qualifications
- Bachelor’s degree or equivalent (preferably engineering or related).
- 5+ years’ manufacturing/production process experience; strong writing skills.
- Working knowledge of safety, quality systems, and GMP; familiarity with regulatory filings; tech transfer and equipment/facilities validation.
- Flexibility; professional under pressure; team-oriented; build working relationships.
- Intermediate to high computer and MS Office skills.