Manufacturing Technician ( Multidose)
AbbVie
Manufacturing Technician ( Multidose)
Job Description
We are looking for a Manufacturing Technician at our site Westport in the mulitdose department. ( Weekend shift role 39 hours)ResponsibilitiesCarry out daily tasks as assigned by the Production Manager according to GMP and the quality system.Active involvement and management of batch related CAPA’s as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigation is completed and timely resolution and closure is met.Accurately completing documentation in a timely manner, accurately and legibly.Responsible for maintaining & monitoring grade A conditions inside isolator, including end of batch EM and utilizing the FMS system for data collection and completing glove testing for integrity of RAB units.Adhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies.Competent in surface sanitization and use of qualified Disinfectants/Detergents/Biocide cleans, competent in both SIP sterilization & bespoke autoclave counter pressure training.Manage requirements in order to deliver the KPIs as they relate to the Product Flow function with a specific emphasis on the 32 day release cycleAdhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies.Follow gowning procedures on entry to areas and donning additional garbing for specific tasks within the compounding area.Adhere to and support all EHS & E standards, procedures, and policies.
Locations
- Westport, MO
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
40,000 - 55,000 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
- GMP complianceintermediate
- CAPA management and root cause analysisintermediate
- Documentation and data collectionintermediate
- Isolator maintenance and environmental monitoringintermediate
- Surface sanitization and sterilization techniquesintermediate
- Gowning and garbing proceduresintermediate
- EHS standards adherenceintermediate
Required Qualifications
- Competent in surface sanitization and use of qualified Disinfectants/Detergents/Biocide cleans (experience)
- Competent in both SIP sterilization & bespoke autoclave counter pressure training (experience)
- Follow gowning procedures on entry to areas and donning additional garbing for specific tasks within the compounding area (experience)
Responsibilities
- Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
- Active involvement and management of batch related CAPA’s as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigation is completed and timely resolution and closure is met
- Accurately completing documentation in a timely manner, accurately and legibly
- Responsible for maintaining & monitoring grade A conditions inside isolator, including end of batch EM and utilizing the FMS system for data collection and completing glove testing for integrity of RAB units
- Adhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies
- Manage requirements in order to deliver the KPIs as they relate to the Product Flow function with a specific emphasis on the 32 day release cycle
- Adhere to and support all EHS & E standards, procedures, and policies
Tags & Categories
Manufacturing Technician ( Multidose)
AbbVie
Manufacturing Technician ( Multidose)
Job Description
We are looking for a Manufacturing Technician at our site Westport in the mulitdose department. ( Weekend shift role 39 hours)ResponsibilitiesCarry out daily tasks as assigned by the Production Manager according to GMP and the quality system.Active involvement and management of batch related CAPA’s as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigation is completed and timely resolution and closure is met.Accurately completing documentation in a timely manner, accurately and legibly.Responsible for maintaining & monitoring grade A conditions inside isolator, including end of batch EM and utilizing the FMS system for data collection and completing glove testing for integrity of RAB units.Adhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies.Competent in surface sanitization and use of qualified Disinfectants/Detergents/Biocide cleans, competent in both SIP sterilization & bespoke autoclave counter pressure training.Manage requirements in order to deliver the KPIs as they relate to the Product Flow function with a specific emphasis on the 32 day release cycleAdhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies.Follow gowning procedures on entry to areas and donning additional garbing for specific tasks within the compounding area.Adhere to and support all EHS & E standards, procedures, and policies.
Locations
- Westport, MO
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
40,000 - 55,000 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
- GMP complianceintermediate
- CAPA management and root cause analysisintermediate
- Documentation and data collectionintermediate
- Isolator maintenance and environmental monitoringintermediate
- Surface sanitization and sterilization techniquesintermediate
- Gowning and garbing proceduresintermediate
- EHS standards adherenceintermediate
Required Qualifications
- Competent in surface sanitization and use of qualified Disinfectants/Detergents/Biocide cleans (experience)
- Competent in both SIP sterilization & bespoke autoclave counter pressure training (experience)
- Follow gowning procedures on entry to areas and donning additional garbing for specific tasks within the compounding area (experience)
Responsibilities
- Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
- Active involvement and management of batch related CAPA’s as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigation is completed and timely resolution and closure is met
- Accurately completing documentation in a timely manner, accurately and legibly
- Responsible for maintaining & monitoring grade A conditions inside isolator, including end of batch EM and utilizing the FMS system for data collection and completing glove testing for integrity of RAB units
- Adhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies
- Manage requirements in order to deliver the KPIs as they relate to the Product Flow function with a specific emphasis on the 32 day release cycle
- Adhere to and support all EHS & E standards, procedures, and policies
Tags & Categories