Quality Assurance (QA) Manager to Nanexa AB

QRIOS Life Science & Engineering; Uppsala kommun; On-site; SEK 669,600 - 892,800; Full time

Job summary

QRIOS Life Science & Engineering is seeking a Quality Assurance (QA) Manager for Nanexa AB in Uppsala. The position is full-time, integral to building a quality function in a growing pharmaceutical company.

The QA Manager will develop and implement a Quality Management System, ensuring compliance with GMP requirements and leading audits. Applicants should have a relevant MSc degree, several years of QA experience, and proficiency in Swedish and English.

This is an opportunity to make a significant impact in a small, dynamic team.

Qualifications

• Several years of experience within QA in a GMP-regulated pharmaceutical or biotech environment.
• Experience in development and/or validation of manufacturing or analytical processes.
• Experience in authoring and reviewing GxP-critical documentation including SOPs, deviations, CAPAs and change controls.

Responsibilities

• Develop, implement and continuously improve the Quality Management System.
• Assess and approve batch-related documentation.
• Ensure compliance with GMP requirements for clinical trial materials.
• Lead internal audits and audits of external service providers.
• Provide guidance in quality-related matters.

Skills

Quality Systems

GMP regulations

Problem-solving

Collaboration

Documentation

Education

MSc in Pharmacy, Biology, Chemistry, Engineering, or a related field

Job description

Quality Assurance (QA) Manager to Nanexa AB

QRIOS Life Science & Engineering

Kommun: Uppsala

Nanexa is now recruiting a Quality Assurance (QA) Manager. The position is full-time and based at our headquarters in Uppsala, and we are looking for a new colleague to join our growing organisation.

As a QA Manager at Nanexa, you will play a key role in building and shaping the quality function in a growing pharmaceutical company. This is not a traditional QA role in a large organisation – instead, you will be part of a small, highly skilled team where your contributions will have a direct and visible impact on how we work and grow. You will have the opportunity to develop, implement and continuously improve our Quality Management System while being actively involved in the full product lifecycle – from early development to manufacturing of clinical trial material. The role combines strategic responsibility with hands‑on work and close collaboration across functions.

At Nanexa, you will not work in a silo. You will be involved across the organisation, working closely with colleagues in development, production and analytics, gaining a broad understanding of our technology, products and processes. As a company of approximately 15 employees, we offer an environment where each individual plays an important role, and where you will actively contribute to building something new.

Responsibilities

• Develop, implement and continuously improve the Quality Management System in line with company growth and regulatory requirements
• Assess and approve batch‑related documentation such as specifications, batch records, deviations and change requests
• Ensure that production and testing of clinical trial materials are conducted in accordance with applicable GMP requirements
• Review and approve SOPs, manage periodic reviews and support supplier qualification and re‑evaluation
• Lead and participate in internal audits and audits of external service providers
• Represent QA in cross‑functional project teams and contribute to project execution
• Provide guidance and support to the organisation in quality‑related matters
• Perform internal training within GMP and quality systems
• Contribute to the strategic development of the QA function and quality processes

Your Profile

We are looking for a driven and quality‑minded professional who enjoys working in a dynamic and developing environment.

Key qualifications include:

• MSc in Pharmacy, Biology, Chemistry, Engineering, or a related field
• Several years of experience within QA in a GMP‑regulated pharmaceutical or biotech environment
• Experience in development and/or validation of manufacturing or analytical processes
• Experience in authoring and reviewing GxP‑critical documentation, including SOPs, deviations, CAPAs and change controls
• Strong knowledge of Quality Systems and applicable GMP regulations
• Fluency in Swedish and English

As a person, you are proactive, structured and solution‑oriented, with a strong sense of ownership and accountability. You thrive in a dynamic organisation where processes are still being developed, and where you have the opportunity to make a real impact. You are comfortable taking on multiple responsibilities and enjoy working both independently and in close collaboration with others.

At Nanexa, each employee contributes to the overall success of the company and you will have the opportunity to influence not only your own area of responsibility, but also the development of the company as a whole.