Senior Biotechnologist (Central Services)

AbbVie Pte Ltd; Singapore; On-site; SGD 78,000 - 106,000; Full time

Job summary

AbbVie Pte Ltd in Singapore seeks a skilled Biologics Production Specialist to perform cGMP manufacturing operations in the biologics facility, ensure accurate batch documentation, and support process improvements.

You will operate upstream and downstream steps, maintain clean room standards, and troubleshoot with senior staff during shifts, while coaching junior biotechnologists and upholding safety and quality.

Qualifications

• Bachelor Degree education with at least 5 years of experience working in Biologics Production facility or equivalent.
• Minimally 3+ years prior experience in large scale GMP purification manufacturing.
• Completes complex tasks in creative and effective ways.
• Consistently works on complex assignments requiring independent action and a high degree of initiative to resolve issues.
• Comfortable working in clean room environments.
• Acts independently to determine methods and procedures on new assignments with high learning agility.
• Rotating shift work is required.

Responsibilities

• Executes upstream/downstream manufacturing operations as part of the production process.
• Operates equipment cleaning and setup for stream-specific tasks.
• Uses DeltaV, SAP and MES for process control and data entry.
• Adheres to SHE safety requirements and reports incidents.
• Coaches and trains junior biotechnologists in area of expertise.
• Assists lead in planning production schedule and leading area activities.

Skills

Biologics production

GMP manufacturing

Clean room

Shift work

Troubleshooting

Training others

Education

Bachelor's degree in related field

Tools

DeltaV

SAP

MES

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 on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Purpose Statement

• Performs functions associated with cGMP manufacturing operations within the biologics production facility.
• Completes batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner.
• Serves as a highly skilled subject matter expert within the manufacturing area, contributing to the development of concepts, techniques, and process improvements.
• Supports and drives troubleshooting efforts during course of shiftwork to ensure adherence to schedule and production plan.

Major Responsibilities

• Executes manufacturing operations to perform operations including but not limited to equipment cleaning and set up as well as stream specific operations like:

  • Upstream: Vial Thaw, Inoculation, Cell Culture and Recovery
  • Downstream: Chromatography, Filtration, Ultrafiltration, Final Filling
  • Central Service: Buffer/ Media Preparation, Autoclave, Glasswashand cleaning processes, Sampling of raw materials.
• Execute on computerized systems (such as Delta V, SAP and MES) for process control and data entry
• Adhere to safety requirements in all tasks, report incidents and near misses promptly, and assist with Safety, Health, and Environmental (SHE) incident investigations.
• Participates in resolution of anomalous processing events
• Assists lead in planning production schedule and leading area activities
• Performs advance process and equipment troubleshooting
• Coach and train junior biotechnologists in area of expertise
• Sets a positive team environment and inculcates a nurturing AbbVie culture

Qualifications

• Bachelor Degree education with at least 5 years of experience working in Biologics Production facility or equivalent
• Minimally 3+ years prior experience in large scale GMP purification manufacturing
• Completes complex tasks in creative and effective ways
• Consistently works on complex assignments requiring independent action and a high degree of initiative to resolve issues
• Comfortable working in clean room environments
• Acts independently to determine methods and procedures on new assignments with high learning agility
• Rotating shift work is required

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