Medical Writer Job at Thermo Fisher Scientific | Apply Now
QA Specialist Job opportunities at Thermo Fisher Scientific offer an excellent career path for candidates seeking to build expertise in quality assurance, GMP compliance, and regulatory operations within the life sciences industry. This role is based in Auckland, New Zealand, and provides the chance to work with a global leader dedicated to making the world healthier, cleaner, and safer. If you are looking for Thermo Fisher careers, a freshers job, or a job in New Zealand, this opportunity could be the perfect fit.
- Job Position: Quality Assurance Specialist (Quality Specialist I)
- Job ID: R-01356592
- Category: Quality & Regulatory
- Location: Auckland, New Zealand
About the Company
QA Specialist Job opportunities at Thermo Fisher Scientific allow professionals to join one of the world’s leading scientific organizations. Thermo Fisher Scientific is committed to enabling customers to make the world healthier, cleaner, and safer. With more than 125,000 colleagues worldwide, the company supports scientific research, technological innovation, environmental protection, food safety, and healthcare advancements. As part of leading Thermo Fisher careers, employees gain access to world-class learning, development, and career growth opportunities.
QA Specialist Job Description
QA Specialist Job responsibilities focus on ensuring quality compliance across manufacturing operations while maintaining Good Manufacturing Practices (GMP). The Quality Specialist I will provide quality oversight through documentation review, process monitoring, product release activities, and collaboration with cross-functional teams. This role offers an excellent freshers job opportunity for candidates looking to develop expertise in quality assurance within a regulated life sciences environment.
Qualifications
QA Specialist Job applicants should possess the following educational qualifications:
Education
- Bachelor’s degree in Biology, Life Sciences, or a related field.
- ISO Auditor, Six Sigma, or similar certifications are advantageous.
- No prior experience required; GMP manufacturing experience preferred.
Experience
- Experience in a biological manufacturing environment is advantageous.
- Thorough knowledge of FDA, EMA, ISO, and international GMP regulations.
- Ability to review and approve GMP documentation, batch records, and quality records.
QA Specialist Job – Key Responsibilities
QA Specialist Job duties include supporting and maintaining quality systems to ensure compliance with GMP requirements.
- Manage and maintain quality system documentation, including SOPs and BMRs.
- Review and approve manufacturing records, quality documents, and product releases.
- Process deviations, CAPAs, and non-conformance records using quality management software.
- Ensure compliance with Quality Management System and GMP requirements.
- Conduct internal audits and support continuous improvement initiatives.
- Train employees on quality systems and documentation practices.
- Support change management activities across regional sites.
- Maintain quality system operations and regulatory compliance.
- Follow safety procedures, PPE requirements, and report workplace hazards or incidents.
QA Specialist Job opportunities at Thermo Fisher Scientific offer an excellent platform for graduates and early-career professionals to build expertise in quality assurance, GMP compliance, and regulatory operations. With comprehensive training, career development programs, and the chance to work for a global leader in life sciences, this role is ideal for candidates seeking Thermo Fisher careers, a rewarding freshers job, or a long-term job in New Zealand.
