QC Chemist Testing (PCP) - 15 months training programme

Pfizer; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

Pfizer announces a 15-month Career Progression Program for fresh graduates as QC Chemists. This training program is designed to equip participants with necessary skills for the biopharmaceutical manufacturing sector, focusing on quality control and compliance within a supportive team environment.

Qualifications

• Degree in Science (Chemistry) is essential.
• Ability to work in shifts and effective problem-solving skills are important.
• Knowledge of cGMPs and ALCOA principles is preferred.

Responsibilities

• Perform and document analytical testing and results.
• Support laboratory investigations and troubleshoot equipment.
• Author SOPs and comply with safety procedures.

Skills

Effective problem-solving skills

Teamwork

Knowledge of cGMPs

ALCOA principles

Digital technology use

Education

Degree in Science (Chemistry)

Job description

QC Chemist Testing (PCP) - 15 months training programme page is loaded

QC Chemist Testing (PCP) - 15 months training programme

Apply locations Singapore - Tuas time type Full time posted on Posted 5 Days Ago job requisition id 4933620 Job Description

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 Graduates
• 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
• 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

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.

What You Will Achieve

The incumbent is a member of the Quality Control (QC) Laboratory team. Under the supervision of the QC Manager /Supervisor, the key responsibilities are:

• Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
• Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
• Assist / troubleshoot laboratory technical problems.
• Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).
• Use Imex "way of working" for day-to-day operations, problem solving, escalation and continuous improvements.

Responsibilities

• Perform / review and document analytical testing (In-Process, Raw Materials, API samples) and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
• Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
• Support laboratory investigations and perform equipment troubleshooting where required.
• Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.
• Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).
• Set up and maintain QC processes (e.g. reference standards and retention sample management), perform investigations as required for any associated deviations.
• Conduct training for fellow colleagues from QC and other departments (e.g. Production).
• Uphold Pfizer's code of conduct and values.
• Collaborate with cross-functional teams to drive flawless execution.
• Play an active and impactful role in Tier processes by updating performance against metrics, highlighting issues, with appropriate escalations. Support development and implementation of solutions.
• Contribute to the continuous improvement activities in QC laboratory or cross functional teams as nominated.

Here Is What You Need (Minimum Requirements)

• Able to work in shift (IPC team)
• Effective problem-solving skills.
• Demonstrated ability to perform in a team.
• Knowledge of cGMPs and ALCOA principles.
• Possess a can-do / pride to succeed attitude.
• Embrace the use of digital technology to scale and speed up every form of interaction and action.
• Degree in Science (Chemistry)

Bonus Points If You Have (Preferred Requirements)

• A minimum of 1 year QC experience in an analytical laboratory is preferred.

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.

Quality Assurance and Control

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Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.