Lead Pharmaceutical Technologist

Allergan; Singapore; On-site; SGD 61,000 - 95,000; Full time

Job summary

AbbVie in Singapore seeks a Pharmaceutical Technologist to lead daily Central Services (API) activities, ensuring materials are available on-time, in-full and right first time. You will manage sampling, tank farm tasks and maintain strict compliance with GMP, GDP and EHS guidelines while coaching junior team members.

You will plan shift deliverables, support QA with batch review, and drive audit readiness through rigorous housekeeping and facility fitness checks.

Qualifications

• Diploma in Engineering or equivalent; 2+ years as a team leader in Manufacturing.
• GMP and GDP knowledge required.
• Excellent interpersonal and communication skills; experience as a trainer.

Responsibilities

• Lead daily Central Services activities to ensure materials are available on-time, in-full and right first time.
• Coach and mentor Pharmaceutical Technologists; escalate issues as needed.
• Plan daily shift deliverables and ensure audit-ready housekeeping and facilities.
• Work with QA to review batch records and resolve potential compliance issues.
• Maintain inventory accuracy and use INFOR for Central Services planning.

Skills

Leadership

Communication

Trainer experience

Agile

Team player

Education

Diploma in Engineering

Degree in relevant field

Tools

DeltaV

POMSnet

Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

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

• Diploma in Engineering field or equivalent required with at least 2 years' experience as a team leader in Manufacturing required.
• Degree in relevant field preferred.
• 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html