Lead Pharmaceutical Technologist

Main Responsibilities

• Leads and executes daily activities in Central Services (API) in order to assure materials are available on-time in-full and right first time.
• Handles materials sampling and tank farm activities to ensure materials are available on-time in-full and right first time.
• Ensures compliance to SOPs EHS guidelines GDP or ALCOA principles and lead junior Pharmaceutical Technologists by examples.
• Communicates on-going activities and issues with Supervisor/Manufacturing Lead for all task being executed and communicates any anomalies/exceptions and suggest possible solutions (5S/Root Cause Analysis).
• Independently verifies and support other Pharmaceutical Technologists to ensure all activities in Central Services are carried out smoothly.  
• Primary contact for troubleshooting on-floor issue resolution and escalations of Central Services activities.
• Assists Supervisor/Manufacturing Lead in planning and leading Central Services activities.
• In the absence of supervisor deputize the supervisor while on the shopfloor.
• Performs reviews of executed batch records and worksheets. Work with QA to resolve potential compliance issues.
• Support the team to ensure housekeeping facilities fitness to achieve audit readiness. 

Safety

• Anticipate or communicate any irregularities or risks that could affect safety quality or production schedule
• Leads safety risks assessments or participates in process hazard analysis as an operations representative (PHA)
• Works on safety related assignments that are moderately difficult requiring judgement in resolving issues or in making recommendations
• Exercises good judgment when handling process safety related issues
• Had the ability to recognize when accepted practices and deviated from.

Quality

• Perform routine housekeeping and facilities fitness checks by ensuring all areas are always in an audit ready state
• Sufficient know-how in Central Services routine tasks and system for regulatory audits and inspections support.
• Partakes in quality risks assessments and walkdowns with Quality Operations team. Resolves exceptions under minimum supervision or independently.
• Possesses an excellent understanding of material handling systems (e.g. DeltaV POMSnet etc.)

Schedule

• Plans daily shift deliverables ahead anticipate complexities and prevent potential delays
• Ensures processes are running as per planned schedule with minimal delays. Highlights effectively to supervisor if delays are expected.
• Clear ghost inventory regularly to ensure inventory accuracy.
• Familiar with INFOR and able to perform Central Services daily task planning.

People and Culture

• Sets a positive team environment and exemplifies the AbbVie Ways We Work behaviors.
• Highlight potential engagement risks to Production Support Supervisor.
• Act as Trainer for other Pharmaceutical Technologists
• Assists in developing JSTM training materials

Qualifications :

• Bachelors degree in an Engineering field or equivalent is required with at least 2 years of experience as a team leader in Manufacturing.
• GMP and GDP knowledge required.
• Good interpersonal and communication skills required.
• Experience as trainer for operations procedures required.
• Excellent team player with experience in shift work preferred.
• Leadership experience in leading a small team preferred.
• Agile and able to work in a fast-paced environment preferred.

Additional Information :

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. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time