Vacant job

SallyQ is currently recruiting consultants for two separate assignments with a client in the pharmaceutical industry in Uppsala – one within Quality Assurance (QA) and one within Regulatory Affairs CMC. The assignments are initially for approximately 6 months with immediate start and possibilities for extension.

About the role

Examples of responsibilities include:

• Working with quality assurance and regulatory issues within the pharmaceutical industry
• Handling, reviewing, and following up on GMP-related documentation
• Supporting work related to release, deviations, change controls, and CAPA
• Compiling and reviewing CMC documentation and supporting regulatory submissions
• Ensuring compliance with current regulatory requirements and quality standards
• Collaborating cross-functionally with QA, production, and QC

Your profile

• Relevant higher education or university degree in chemistry, biotechnology, pharmacy, or similar
• At least 2 years of experience in QA or Regulatory Affairs CMC within the pharmaceutical industry
• Good knowledge of GMP and regulatory requirements
• Experience with documentation and quality processes
• Strong communication skills with fluent Swedish and English in both speech and writing

About SallyQ

We are a company founded with the ambition to build a competence-based business where customer value and people are at the center. We describe ourselves as a competence provider and offer recruitment services, expert competence for construction and projects, as well as training initiatives within the Life Science industry. Our vision is to help innovative companies and individuals make as large a positive difference as possible in the world. We believe in quality in everything from interactions and communication to delivery and relationships.

Application

Does this sound like a role for you? Send in an application or give us a call. We process applications on an ongoing basis, so send in your application as soon as possible!