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Quality Assurance Specialist

ID:  1494
Date of Posting:  Apr 25, 2025
Business Area:  Quality
Job Type:  Direct Employee
On site / Remote / Hybrid:  On Site
Location: 

Campoverde Aprilia, IT

Territory: 
Full-Time or Part-Time:  Full Time
Seniority:  Associate

With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn.

We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries.

At Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves.

This drive will never stop. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases.

Recordati. Unlocking the full potential of life.

Job Purpose

We are seeking a Quality Assurance Specialist to work together to ensure the high quality of our operations and services, with the goal of ensuring the long-term success of our business. Your duties include inspecting procedures and products, identifying errors or nonconformity issues in products and related manufacturing processes and analysis.

Establish quality and safety standards and criteria to be met.

Establish procedures for monitoring achievement of standards.

Analyze and supervise business processes from production to marketing of products and draft related documentation. 

Key Responsibilities

  • Batch record review
  • Product quality review
  • Supplier qualifications
  • Process validations
  • SOPs revision
  • Monitoring and tracking closure and timelines of quality system KPI’s (including deviation, change control and CAPA)
  • Other quality system related tasks

Required Education

Bachelor's degree in a scientific discipline

Required Skills and Experience

  • Experience of 2+ years working as a Quality Assurance Specialist or other similar position in a GMP regulated pharmaceutical environment or equivalent.
  • Significant experience using quality assurance methodologies and standards and managing GMP documents and version control.
  • Significant experience in data analysis and statistical methods
  • Good hands-on experience with MS Office and databases
  • Strong numerical skills, great attention to detail, and a results-oriented approach
  • Strong communication, organizational and leadership skillsStrong ability to work on own initiative or in a cross-functional team.
  • Quality control certification, such as ISO 9000, will be a bonus.

Required Languages

English fluent

At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.

If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.

Apply now »