Senior Quality Assurance Analyst

Neogen Corporation

Pindamonhangaba

On-site

BRL 90,000 - 130,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Neogen Corporation is seeking a Quality Assurance professional to lead and sustain the Quality Management System in Brazil. The role covers document control, change control, nonconformity investigations, and customer complaints within ISO 9001 and GMP standards.

You will train staff and audit processes to ensure traceability and regulatory compliance. Required are a Bachelor’s degree in a related field, ISO 19011 auditor training, and 3+ years in QA/QMS.

Qualifications

  • Bachelor's degree in Chemistry, Chemical Engineering, Pharmacy, or related field.
  • Internal Auditor training or certification per NBR ISO 19011.
  • Experience applying QMS tools to investigations, deviations and CAPAs.
  • Knowledge of GMP and regulatory requirements for veterinary/household products (MAPA/ANVISA).

Responsibilities

  • Execute, maintain, and improve the QMS in compliance with ISO 9001 and regulatory requirements.
  • Monitor processes for QMS, GMP, and internal procedures compliance.
  • Prepare and control QMS documentation with traceability and record retention.
  • Onboard and train employees on QMS requirements and quality culture.
  • Develop KPIs, track trends, and report quality performance.
  • Deliver ISO 9001 and GMP training and participate in internal audits.
  • Conduct supplier audits and manage customer complaint handling.
  • Manage change control, root cause investigations, and CAPA closures.
  • Oversee nonconformities, deviations, and waste management aligned with QMS.

Skills

MS Office
ISO 9001 knowledge
NBR ISO 19011 internal audit
Quality tools

Education

Bachelor's degree in Chemistry/Engineering/Pharmacy
Postgraduate QM cert (preferred)

Tools

Microsoft Office

Job description

It’s fun to work in a company where people truly believe in what they are doing!

Responsible for executing, maintaining, and supporting the continuous improvement of the Quality Management System (QMS) in compliance with NBR ISO 9001 and applicable regulatory requirements. Works independently in document control, change control, nonconformity investigations, customer complaint handling, internal audits, and continuous improvement activities, contributing to process compliance, risk mitigation, and a strong quality culture.

Key Responsibilities
  • Execute, support, and drive the implementation, maintenance, and continuous improvement of the Quality Management System (QMS) in compliance with NBR ISO 9001 requirements.
  • Monitor organizational processes to ensure compliance with QMS requirements, Good Manufacturing Practices (GMP), and internal procedures.
  • Prepare, review, control, and maintain QMS documentation, ensuring proper traceability, version control, and record retention.
  • Support the onboarding and training of new employees regarding QMS requirements and the organization’s quality culture.
  • Develop, monitor, and report quality performance indicators (KPIs), identifying trends, risks, and opportunities for improvement.
  • Deliver and support training related to ISO 9001, QMS procedures, and Good Manufacturing Practices.
  • Plan, conduct, and participate in internal audits in accordance with ISO 9001 and ISO 19011 guidelines, and support external audits.
  • Perform supplier audits to assess compliance with quality standards, regulatory requirements, and internal supplier qualification processes.
  • Manage the customer complaint process, ensuring proper documentation, root cause investigation, and implementation of corrective actions.
  • Execute and monitor change control activities, assessing risks and potential impacts on the Quality Management System.
  • Investigate process deviations, nonconformities, product issues, raw material concerns, packaging material issues, and operational deviations using quality management tools.
  • Define, monitor, and verify the effectiveness of corrective and preventive actions, ensuring timely closure.
  • Oversee the handling of customer-returned products from receipt through final disposition in accordance with internal procedures.
  • Ensure appropriate communication regarding waste management activities in compliance with QMS requirements and applicable regulations.
  • Support follow‑up activities and action plans resulting from Management Review meetings, maintaining accurate records and meeting minutes.
  • Actively contribute to continuous improvement initiatives across the Quality Management System.
  • Perform other duties and responsibilities as assigned by the immediate supervisor.
Education, Experience, and Language Requirements
Education

Required:

  • Bachelor’s degree in Chemistry, Chemical Engineering, Pharmacy, or a related field.

Preferred:

  • Postgraduate degree, specialization, or certification in Quality Management, Management Systems, or a related discipline.
Knowledge, Skills, and Qualifications

Required:

  • Proficiency in Microsoft Office and corporate digital tools.
  • Knowledge and interpretation of NBR ISO 9001 requirements.
  • Internal Auditor certification/training based on NBR ISO 19011.
  • Experience with quality tools applied to investigations of deviations, nonconformities, and corrective and preventive actions.

Preferred:

  • Validation and Qualification methodologies.
  • Risk and Opportunity Management.
  • Knowledge of regulatory requirements applicable to veterinary products (MAPA) and household/institutional pesticide products (ANVISA).
Experience

Required:

  • Previous experience working with Quality Management Systems (QMS).

Preferred:

  • Minimum of 3 years of experience in Quality Assurance, Quality Management Systems, or related areas.
Languages

Required:

  • Fluent Portuguese.
  • Intermediate English.

Preferred:

  • Advanced English.
  • Intermediate Spanish.
Behavioral Competencies
  • Strong attention to detail and commitment to quality.
  • Analytical thinking and problem-solving skills.
  • Excellent organizational and prioritization abilities.
  • Effective communication and training facilitation skills.
  • Teamwork and cross-functional collaboration.
  • Proactive mindset with a focus on continuous improvement.
  • Ability to work independently and manage multiple priorities in a dynamic environment.

Come Be Part Of A Mission that Matters!

From inside the farm gate to our dinner plates, Neogen protects the world’s food supply. Through a variety of animal healthcare products, to food safety solutions for dangerous bacteria, allergens, toxins, drug residues and much more, Neogen is there — and you can be too.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Quality Control Laboratory Leader
Quality Control Laboratory Leader

Novonesis • Valinhos

On-site
BRL 180,000 - 300,000
Manager, Quality Control
Manager, Quality Control

Baxter Healthcare • São Paulo

On-site
BRL 280,000 - 440,000
Quality Systems and Performance Analyst
Quality Systems and Performance Analyst

Kenvue • São José dos Campos

Hybrid
BRL 90,000 - 130,000
Quality Systems and Performance Analyst
Quality Systems and Performance Analyst

Mcneil Ab • São Paulo

Hybrid
BRL 60,000 - 100,000
Quality & Compliance Audit Senior Analyst
Quality & Compliance Audit Senior Analyst

7600-Johnson& Johnson do Brasil Industria e Comercio de Produtos para Saude Ltda Legal Entity • São José dos Campos

On-site
BRL 180,000 - 240,000
Operador de Produção
Operador de Produção

Neogen • Pindamonhangaba

On-site
BRL 20,000 - 27,000
Técnico de Hardware (Temporário)
Técnico de Hardware (Temporário)

Neogen • Indaiatuba

On-site
BRL 39,000 - 61,000
Technical Service Research Associate
Technical Service Research Associate

Novonesis • Araucária

On-site
BRL 60,000 - 90,000
Mid Level Quality Control Analyst
Mid Level Quality Control Analyst

CEVA SANTE ANIMALE • Paulínia

On-site
BRL 66,960 - 89,280
Assistente de Qualidade (Tratamento de Não Conformidades)
Assistente de Qualidade (Tratamento de Não Conformidades)

Essentia Group • São José

On-site
BRL 36,000 - 60,000