QC Shift Analyst

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A pharmaceutical consultancy company in Singapore is seeking a QC Raw Material Analyst to manage testing and quality control of raw materials, ensuring compliance with GMP standards. Ideal candidates hold a relevant science degree and possess experience in lab settings. This position involves critical responsibilities such as documentation, problem-solving, and lab support. Join us to advance your career and make an impact in the pharmaceutical industry.

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Career advancement opportunities

Qualifications

• Well versed in cGMP regulations.
• Relevant lab-related experience in a biotech or medically related field.
• Relevant experience to dictate final position qualifications.

Responsibilities

• Prioritize and perform testing/analysis timely.
• Documentation of results according to cGMP.
• Problem-solving for analytical methods and troubleshooting.

Skills

Knowledge of cGMP regulations

Problem solving of analytical methods

Effective documentation practices

Technical selection of QC equipment

Education

Degree in a relevant Science field or Equivalent

Job description

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development empowering our team members to grow personally and professionally.

Position Overview

The QC Raw Material Analyst is responsible for sampling, testing, and releasing incoming raw materials in accordance with GMP, pharmacopeial standards, and company procedures. The role ensures that only materials meeting defined specifications are used in manufacturing, thereby safeguarding product quality and patient safety.

Key Responsibilities

• To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements.
• Analysis of bulk product according to Standard Operating Procedures and Test Methods.
• Documentation of results in accordance with current Good Manufacturing Practices (cGMP).
• Problem solving of analytical methods as well as troubleshooting of equipment.
• Involvement in method transfers and validation.
• Involved in equipment qualification and technical selection of QC equipment and/or standards and reagents.
• Assay trend analysis, document revision and update.
• General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc.
• Any other duties as assigned by your Supervisor/Manager.

Required Qualifications

• Degree in a relevant Science field or Equivalent.
• Relevant Lab related experience in a biotech or medically related field.
• Relevant experience and accomplishment to dictate final position for which the candidate may qualify.
• Well versed in cGMP regulations.
• Knowledge of area specific responsibilities.

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.