Senior QC System Specialist - CSV (Pharmaceutical)

Private Advertiser; Singapore; On-site; SGD 60,000 - 100,000; Full time

Job summary

An established industry player in pharmaceuticals is seeking a Senior QC Specialist to enhance quality control processes. This role offers an opportunity to work in a dynamic environment, overseeing the setup of a new manufacturing plant and QC lab, while ensuring compliance with industry regulations. As a key player, you'll manage QC equipment, optimize methods, and lead continuous improvement efforts. Join a forward-thinking company that values growth and development, and be part of a team dedicated to maintaining high standards in quality assurance. This is a chance to make a significant impact in a rapidly evolving industry.

Benefits

Competitive salary and benefits package

Opportunities for professional development

Dynamic and collaborative work environment

Qualifications

• 5+ years in quality control within the pharmaceutical industry.
• Strong knowledge of GMP and regulatory requirements.
• Proficiency in QC equipment qualification and method validation.

Responsibilities

• Assist in establishing the new manufacturing plant and QC lab.
• Oversee lifecycle of QC lab equipment and ensure compliance.
• Lead development and maintenance of lab computer systems.

Skills

Quality Control

GMP Knowledge

Analytical Methods

Method Validation

Communication Skills

Leadership Skills

Education

Bachelor's degree in Chemistry

Bachelor's degree in Chemical Engineering

Bachelor's degree in Biotechnology

Bachelor's degree in Pharmaceutical Sciences

Tools

QC Lab Equipment

Job description

Senior QC System Specialist - CSV (Pharmaceutical)

Our client is seeking a Senior QC Specialist - CSV (Pharmaceutical) to join their team!

About Our Client

Our client is a renowned pharmaceutical brand with over six decades of industry expertise. They are currently expanding their global footprint, with Singapore serving as their central hub. This presents an excellent opportunity for growth and development in a rapidly evolving, innovative environment.

What you'll be doing?

1. Plant & Lab Setup: Assist in establishing the new manufacturing plant and QC lab, ensuring smooth integration of equipment and systems.
2. Equipment Management: Oversee the lifecycle of QC lab equipment, from qualification to maintenance, while addressing compliance and capacity needs.
3. Method Optimization: Support method validations, annual reviews, and lead continuous improvement efforts to enhance lab processes.
4. Quality Assurance: Ensure proper documentation, investigate quality issues, and implement remediation actions to maintain high standards.
5. Regulatory Compliance: Support inspections and audits, while fostering a culture of regulatory excellence and safety.
6. System Validation: Lead the development and maintenance of lab computer systems, ensuring compliance with industry regulations.

Who are they looking for?

1. Educational Background: A Bachelor's degree in Chemistry, Chemical Engineering, Biotechnology, Pharmaceutical Sciences, or a related field.
2. Industry Experience: At least 5 years in quality control within the pharmaceutical industry, with strong knowledge of GMP and regulatory requirements.
3. Technical Expertise: Proficiency in QC equipment qualification, method validation, and analytical methods (wet chemistry and instrumental testing).
4. Regulatory Knowledge: In-depth understanding of pharmaceutical regulations, global quality policies, and data integrity requirements.
5. Leadership Skills: Ability to make independent decisions and promote a quality-driven culture within the organization.
6. Communication: Strong interpersonal and communication skills to collaborate effectively across teams and during inspections.

Why you should consider this opportunity?

Our client offers an attractive remuneration package and other benefits, such as:

• Competitive salary and benefits package
• Opportunities for professional development and advancement
• A dynamic and collaborative work environment

How to apply

Ready to join this role? Click Apply now to submit your resume and share your availability and expected salary with us!

We value diversity and encourage applications from candidates of all backgrounds and experiences.

All information received will be kept strictly confidential and will be used only for employment-related purposes.

Low Jia Yi | R25127265

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Your application will include the following questions:

• Which of the following statements best describes your right to work in Singapore?
• What's your expected monthly basic salary?
• Have you worked in a role which requires a sound understanding of Good Manufacturing Practices (GMP)?
• How many years' experience do you have as a Validation Engineer?
• How much notice are you required to give your current employer?