Career Progression Program (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals

We are pleased to announce the Career Progression Program (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals, a distinguished talent development initiative aimed at cultivating the next generation of skilled professionals for Singapore's biopharmaceutical manufacturing industry.

Program Overview:

Program Type: Fresh/Mid-Career Change

Duration: 15 months

Attachment: Local attachment to Pfizer Inc.

Eligibility:

Singapore Citizens or Singapore Permanent Residents

Have no prior working experience in the biopharmaceutical sector

Fresh graduates are welcome to apply

Mid-Career Candidate: Graduated for at least 2 years prior to point of application

Training Allowances: CPF exempted

This comprehensive program is meticulously designed to provide participants with the requisite skills and experience to meet the anticipated hiring demand within the biopharmaceutical manufacturing sector.

We invite eligible candidates to apply for this exceptional opportunity to advance their careers with one of the industry's leading organizations.

Use Your Power for Purpose

Pfizer’s Environmental Health and Safety team plays a crucial role in upholding the highest safety standards for both our patients and colleagues. As a member of this innovative community, you will contribute to delivering excellence, ensuring that Pfizer's medicines reach those who need it. Your dedication to maintaining these standards is essential in enabling Pfizer to provide life-saving treatments to patients around the world, fostering a safer and more effective healthcare environment.

What You Will Achieve

In this role, you will:

1. Continuous Improvement (CI)

Identify, analyze, and implement continuous improvement initiatives within warehouse operations aligned with GMP/cGMP requirements.

Support Lean, Six Sigma, or similar CI methodologies to reduce waste, improve process efficiency, and enhance compliance.

Track improvement metrics and warehouse dashboard according to IMEX performance.

2. GMP / cGMP Compliance

Ensure warehouse processes, activities, and records comply with GMP and cGMP standards, internal quality systems, and regulatory requirements.

Create, review, and maintain cGMP documentation including SOPs, Work Instructions, Forms, and Logbooks related to warehouse activities.

Ensure documents are accurate, current, and compliant with document control procedures.

3. Change Control

Initiate, assess, and support change control requests related to warehouse processes, systems, layouts, equipment, and master data.

Perform impact assessments to determine potential effects on GMP compliance, data integrity, and operations.

Coordinate with Quality, IT, Supply Chain, and other stakeholders to ensure timely and compliant change implementation.

4. SOP Updates & Process Standardization

Review and update SOPs to reflect process changes, continuous improvement initiatives, and regulatory requirements.

Ensure SOPs are aligned with actual warehouse practices and systems.

Support training and user understanding of updated procedures.

5. Master Data & Analytics

Support governance, maintenance, and quality of warehouse-related master data (e.g., material master, storage locations, batch attributes).

Perform master data analysis to identify inconsistencies, errors, and improvement opportunities.

Develop reports and dashboards to support data-driven decision-making for warehouse and supply chain operations.

Here Is What You Need

Bachelor’s degree in Supply Chain, Logistics, Industrial Engineering, Life Sciences, Business, or a related field.

  
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.