Senior Regulatory Affairs Associate - Cmc Biologics/Vaccines (Home Or Office Based)

Parexel; Pescara; Remote; EUR 60,000 - 90,000; Full time

Job summary

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biologics and vaccines. The role supports post-approval activities, variations, renewals, and market expansions, delivering timely regulatory assessments and risk mitigation.

Remote options are available across several European locations, with collaboration across manufacturing, QA, QC, and regulatory teams to drive submissions and global compliance.

Qualifications

• Strong knowledge of post-approval regulatory requirements for CMC.
• Experience writing CMC sections of regulatory documents.
• Experience with regulatory submissions for variations/renewals.

Responsibilities

• Develop post-approval CMC submission strategies for variations and renewals.
• Assess regulatory impact of quality changes in production and QC.
• Coordinate submission preparation with cross-functional teams.
• Write/review submission content aligned with regulatory expectations.

Skills

CMC knowledge

Regulatory submissions

Veeva Vault

Biologics knowledge

Team collaboration

Communication skills

Education

Bachelor's degree in Life Sciences

Tools

Veeva Vault

MS Office (Word/Excel/PowerPoint)

Job description

As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. Your work supports variations, renewals, and market expansions, delivering timely regulatory assessments and risk mitigation. This role offers remote options in several European locations and partners closely with cross-functional teams to make a patient impact.

• Develop post-approval CMC submission strategies for variations, renewals, market expansions, and annual reports
• Assess regulatory impact of quality changes in production and QC
• Review study reports for regulatory compliance with requirements
• Coordinate submission preparation with manufacturing, supply chain, quality control, QA, and local/regulatory teams
• Write/review submission content aligned with regulatory expectations, including health authority inquiries
• Manage Regulatory Information Management systems to maintain worldwide submissions
• Identify, escalated, and mitigate regulatory risks
• Prepare regulatory documentation for registration files or variations (CMC/technical)
• University-level education, preferably Life Sciences, or equivalent by experience
• Experience in regulatory affairs related to technical/CMC/quality in pharma
• Strong understanding of CMC and post-approval regulatory requirements
• Experience writing CMC sections of regulatory documents
• Knowledge of biological or vaccine processes
• Background in validation/Quality Assurance/production with regulatory documentation experience
• Understanding of qualification/validation principles
• Proficiency with Word, PowerPoint, Excel; experience with Veeva Vault valued
• Team spirit
• Flexibility
• Accountability
• CMC knowledge
• Post-approval regulatory requirements
• Regulatory submissions for variations/renewals

Senior Regulatory Affairs Associate - CMC biologics/vaccines (home or office based) pescara, abruzzo, it