Quality Assurance Specialist (3 months Contract)

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A leading pharmaceutical solutions company in Singapore seeks a motivated Junior Quality Assurance Specialist. This role is crucial for ensuring compliance with Good Manufacturing Practices and internal quality standards. The ideal candidate will have a diploma or degree in Life Sciences and 1-3 years of relevant experience. Join our team and contribute to impactful projects in an inclusive culture that values innovation and collaboration.

Benefits

Inclusive culture

Career advancement opportunities

Qualifications

• 1 to 3 years of relevant experience in pharmaceutical/biotech manufacturing or quality assurance.
• Ability to follow procedures accurately.

Responsibilities

• Review and approve batch records and SOPs.
• Support timely documentation and adherence to Good Documentation Practices.
• Participate in internal audits and support regulatory inspection.
• Provide QA oversight on manufacturing activities for GMP compliance.
• Assist in investigating deviations and complaints.

Skills

Attention to detail

Communication skills

Interpersonal skills

Education

Diploma or Bachelor's degree in Life Sciences

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

We are seeking a motivated and detail-oriented Junior Quality Assurance (QA) Specialist to support our manufacturing operations. This role ensures that products are manufactured in compliance with Good Manufacturing Practices (GMP), internal quality standards, and regulatory requirements. The successful candidate will collaborate closely with production, engineering, and quality teams to maintain a culture of quality and continuous improvement.

Key Responsibilities

• Review and approve batch records, standard operating procedures (SOPs), and deviations related to manufacturing operation.
• Support timely documentation and ensure adherence to GDP (Good Documentation Practices).
• Participate in internal audits and support regulatory inspection.
• Provide on-the-floor QA presence to oversee manufacturing activities and ensure compliance with GMP.
• Assist in the investigation of deviations, non-conformances, and complaints.

Required Qualifications

• Diploma or Bachelors degree in Life Sciences, Pharmaceutical Science, Chemistry, Biotechnology, or a related discipline.
• 1 to 3 years of relevant experience in pharmaceutical/biotech manufacturing or quality assurance.
• Strong attention to detail and ability to follow procedures accurately
• Good communication and interpersonal skills to work effectively with cross-functional teams

Why join us?

• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• 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.