Manufacturing Technician I, UD Fill, A2 (7PM-7:30AM)
AbbVie
Manufacturing Technician I, UD Fill, A2 (7PM-7:30AM)
Job Description
Manage production lines to meet the established production schedule in accordance with Standard Operating Procedures (SOP’s) and Good Manufacturing Principles (GMP’s) while monitoring product to ensure quality standards are maintained. This is an A2 Shift 7PM-7:30AM Sunday/Monday/Tuesday & every other SaturdayResponsibilitiesComply with all safety regulations and conduct all activities in a safe, efficient manner.Apply 5S and cGMPs in all areas of responsibility.Operate high-speed equipment for the manual or automated assembly, filling, packaging and labeling of pharmaceutical products: ensuring adherence to specifications.Perform tasks that may be verified by an independent individual; or perform inspection/verifications of work performed by others.Clean packaging rooms and machinery in accordance with SOPs and cGMPs.Conduct Set-Ups, in-process actions, data entry, and other computer-related tasks.Complete batch records accurately and documents production volumes in accordance with SOP’s and cGMP’s.Accept or reject products according to acceptability standards determined by cGMP’s, customer requirements, and SOP’s.Complete Line Clearances and Change Overs on production lines in accordance with SOP’s and cGMP’s.Conduct in-process inspections and reconcile incoming and completed components and products to ensure accuracy and accountability.Perform other duties as assigned.
Locations
- Waco, TX
Salary
18 - 32 USD / yearly
Estimated Salary Rangemedium confidence
45,000 - 65,000 USD / yearly
Source: AI estimated from job description
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Knowledge of SOPs and GMPsintermediate
- Operation of high-speed pharmaceutical equipmentintermediate
- Quality control and inspectionintermediate
- Data entry and batch record managementintermediate
- Safety compliance and 5S methodologyintermediate
- Line setup, clearance, and changeover proceduresintermediate
Responsibilities
- Manage production lines to meet the established production schedule in accordance with Standard Operating Procedures (SOP’s) and Good Manufacturing Principles (GMP’s) while monitoring product to ensure quality standards are maintained.
- Comply with all safety regulations and conduct all activities in a safe, efficient manner.
- Apply 5S and cGMPs in all areas of responsibility.
- Operate high-speed equipment for the manual or automated assembly, filling, packaging and labeling of pharmaceutical products: ensuring adherence to specifications.
- Perform tasks that may be verified by an independent individual; or perform inspection/verifications of work performed by others.
- Clean packaging rooms and machinery in accordance with SOPs and cGMPs.
- Conduct Set-Ups, in-process actions, data entry, and other computer-related tasks.
- Complete batch records accurately and documents production volumes in accordance with SOP’s and cGMP’s.
- Accept or reject products according to acceptability standards determined by cGMP’s, customer requirements, and SOP’s.
- Complete Line Clearances and Change Overs on production lines in accordance with SOP’s and cGMP’s.
- Conduct in-process inspections and reconcile incoming and completed components and products to ensure accuracy and accountability.
- Perform other duties as assigned.
Tags & Categories
Manufacturing Technician I, UD Fill, A2 (7PM-7:30AM)
AbbVie
Manufacturing Technician I, UD Fill, A2 (7PM-7:30AM)
Job Description
Manage production lines to meet the established production schedule in accordance with Standard Operating Procedures (SOP’s) and Good Manufacturing Principles (GMP’s) while monitoring product to ensure quality standards are maintained. This is an A2 Shift 7PM-7:30AM Sunday/Monday/Tuesday & every other SaturdayResponsibilitiesComply with all safety regulations and conduct all activities in a safe, efficient manner.Apply 5S and cGMPs in all areas of responsibility.Operate high-speed equipment for the manual or automated assembly, filling, packaging and labeling of pharmaceutical products: ensuring adherence to specifications.Perform tasks that may be verified by an independent individual; or perform inspection/verifications of work performed by others.Clean packaging rooms and machinery in accordance with SOPs and cGMPs.Conduct Set-Ups, in-process actions, data entry, and other computer-related tasks.Complete batch records accurately and documents production volumes in accordance with SOP’s and cGMP’s.Accept or reject products according to acceptability standards determined by cGMP’s, customer requirements, and SOP’s.Complete Line Clearances and Change Overs on production lines in accordance with SOP’s and cGMP’s.Conduct in-process inspections and reconcile incoming and completed components and products to ensure accuracy and accountability.Perform other duties as assigned.
Locations
- Waco, TX
Salary
18 - 32 USD / yearly
Estimated Salary Rangemedium confidence
45,000 - 65,000 USD / yearly
Source: AI estimated from job description
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Knowledge of SOPs and GMPsintermediate
- Operation of high-speed pharmaceutical equipmentintermediate
- Quality control and inspectionintermediate
- Data entry and batch record managementintermediate
- Safety compliance and 5S methodologyintermediate
- Line setup, clearance, and changeover proceduresintermediate
Responsibilities
- Manage production lines to meet the established production schedule in accordance with Standard Operating Procedures (SOP’s) and Good Manufacturing Principles (GMP’s) while monitoring product to ensure quality standards are maintained.
- Comply with all safety regulations and conduct all activities in a safe, efficient manner.
- Apply 5S and cGMPs in all areas of responsibility.
- Operate high-speed equipment for the manual or automated assembly, filling, packaging and labeling of pharmaceutical products: ensuring adherence to specifications.
- Perform tasks that may be verified by an independent individual; or perform inspection/verifications of work performed by others.
- Clean packaging rooms and machinery in accordance with SOPs and cGMPs.
- Conduct Set-Ups, in-process actions, data entry, and other computer-related tasks.
- Complete batch records accurately and documents production volumes in accordance with SOP’s and cGMP’s.
- Accept or reject products according to acceptability standards determined by cGMP’s, customer requirements, and SOP’s.
- Complete Line Clearances and Change Overs on production lines in accordance with SOP’s and cGMP’s.
- Conduct in-process inspections and reconcile incoming and completed components and products to ensure accuracy and accountability.
- Perform other duties as assigned.
Tags & Categories