QC Chemist (Testing) - 15 months training programme

Pfizer, S.A. de C.V; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading biopharmaceutical company in Singapore offers the Career Progression Program for Fresh Graduates in Advanced Biopharmaceuticals Manufacturing. As part of the Quality Control Laboratory team, you will perform analytical testing and document results, support laboratory investigations, and assist in troubleshooting. Candidates should possess a Degree in Science (Chemistry) and exhibit strong problem-solving skills. Join us to contribute to patient care and the biopharmaceutical industry.

Benefits

Competitive compensation

Career development opportunities

Qualifications

• Ability to work in shifts
• Demonstrated ability to perform in a team environment
• Knowledge of ALCOA principles

Responsibilities

• Perform and document analytical testing accurately
• Highlight abnormalities during testing
• Assist in troubleshooting laboratory technical problems
• Author SOPs and GMP documentation
• Collaborate with cross-functional teams

Skills

Problem-solving skills

Teamwork

Knowledge of cGMPs

Attention to detail

Education

Degree in Science (Chemistry)

Job description

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

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.
• Singapore Citizens or Singapore Permanent Residents
• Have no prior working experience in the biopharmaceutical sector

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.

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.

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

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