Associate, Manufacturing I

Purpose

Performs cGMP manufacturing operations within a biologics production environment with primary responsibility for upstream processing and buffer preparation activities. Executes routine and non-routine manufacturing operations in accordance with approved batch records SOPs safety requirements and current Good Manufacturing Practices. Operates monitors and supports the setup and calibration of process equipment and associated systems in collaboration with technical support personnel. Prepares buffers solutions and process materials; performs material transfers sampling in-process checks and related quality activities to support manufacturing execution. Uses systems such as LIMS SAP and automated control platforms to document work collect and evaluate operating data and verify compliance with procedural and batch requirements. Makes routine adjustments to equipment materials or process parameters within defined limits to maintain process control product quality and operational efficiency. Supports troubleshooting of equipment and process issues investigates deviations as assigned and escalates unusual conditions appropriately. Maintains accurate and complete documentation including batch records logs and electronic entries. Contributes to continuous improvement efforts by identifying opportunities to enhance upstream and buffer preparation processes strengthen compliance and improve executional consistency.

Responsibilities

• Perform cGMP manufacturing activities in a biologics production environment with primary focus on upstream processing and buffer preparation.
• Execute routine manufacturing tasks in accordance with approved batch records SOPs safety requirements and current Good Manufacturing Practices.
• Prepare buffers solutions and process materials; perform material transfers sampling and in-process checks to support campaign execution.
• Operate monitor and support process equipment including setup and calibration activities with engineering and technical support personnel.
• Use systems such as LIMS SAP LabX Pi SAIS and automated control platforms to document work review data and support compliant execution.
• Make routine adjustments to equipment materials or process parameters within defined limits to maintain process control and product quality.
• Transfer methods into Production instructions to support successful execution of scheduled campaigns.
• Draft moderate-scope documents manage review cycles and support timely completion of deliverables.
• Track issues gather information analyze moderate-complexity problems and work with management and senior staff to determine appropriate actions.
• Coordinate with other groups provide status updates and maintain accurate documentation to support compliance and operational consistency.

Qualifications :

• Bachelors Degree or equivalent required.
• At least 2-5 years relevant experience with good writing skills.
• Working knowledge of media/buffer preparation cell culture or purification of biological drugs is required.
• Computer proficiency. A working knowledge of safety quality systems and current Good Manufacturing Practices is required. Familiarity with tech transfer processes.
• Must be flexible to handle multiple tasks including ability to handle pressure in a professional manner. Effectively work in a team environment. Maintain a high level of energy and professionalism on the job. Build effective working relationships with customers co-workers cross-functioned groups and management.
• Basic understanding of current Good Manufacturing Practices as applied to equipment and process steps in area of responsibility.

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: 

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at  the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors  including  geographic location and we may ultimately  pay more or less than the posted range. This range may be  modified in the future. 

• We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.

• This job is eligible to  participate in our short-term incentive programs.  Note: No amount of pay is  considered to be wages or compensation until such amount is earned  vested  and determinable. The amount and availability of  any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a   particular employee  remains in the Companys sole and absolute discretion unless and until paid and may be  modified at the Companys sole and absolute discretion  consistent with applicable law. 

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

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Work :

No

Employment Type :

Full-time