• Creative linguists with a proven track record in the beauty/cosmetics industry. • Focus on brand voice, tone, and engaging consumer-facing content. • This is a highly technical role requiring subject matter expertise. Candidates must demonstrate: • Regulatory Knowledge: Deep familiarity with EU Cosmetic Regulation (EC) No 1223/2009 and INCI naming conventions. • Compliance Experience: Expertise in claims substantiation (e.g., "hypoallergenic"), ingredient restrictions, and safety documentation. • Technical Precision: Experience with final label reviews (artwork markups) before printing. • Background: Previous experience with regulated brands like P&G or Unilever is a significant plus. Medical experience would also be an advantage.

• Creative linguists with a proven track record in the beauty/cosmetics industry. • Focus on brand voice, tone, and engaging consumer-facing content. • This is a highly technical role requiring subject matter expertise. • Candidates must demonstrate deep familiarity with EU Cosmetic Regulation (EC) No 1223/2009 and INCI naming conventions. • Expertise in claims substantiation (e.g., "hypoallergenic"), ingredient restrictions, and safety documentation. • Experience with final label reviews (artwork markups) before printing. • Previous experience with regulated brands like P&G or Unilever is a significant plus.

Role Description Astrion has an exciting opportunity for a highly reliable and detail-oriented temporary Cyber Compliance Assistant to support our cybersecurity and compliance functions throughout the summer. This fully remote position requires someone who can work independently with minimal supervision and communicate professionally with employees across the organization--both working in-office and remotely. Qualifications - Enrollment in accredited Alabama university - Strong attention to detail and exceptional organization skills - Ability to work independently and produce high-quality work with minimal supervision - Reliable, punctual, and committed to meeting deadlines - Strong written and verbal communication skills with the ability to interact professionally with personnel - Proficiency with Microsoft Office tools (Outlook, Word, Excel, SharePoint, Teams) and Adobe Acrobat - Ability to quickly learn new systems and follow established processes Requirements - Assist with maintaining and organizing cybersecurity compliance documentation. - Support evidence collection for ongoing audits and assessments. - Track progress on compliance remediation items and provide timely status updates. - Review internal policies and procedures for accuracy and alignment with standards. - Perform data entry, quality checks, and file clean-up in compliance platforms or shared repositories. - Collaborate effectively with cybersecurity, IT, and business staff across multiple locations and working arrangements. - Handle sensitive information with discretion and adhere to organizational confidentiality requirements. Benefits - Fully remote role with standard working hours - Fast-paced environment with occasional shifting priorities - Opportunities for hands-on real-world compliance programs - Supportive team available for guidance, but expectations for independent task ownership

• Works closely with functional leaders to 1) create the optimal development path for Iovance product candidates, 2) negotiate optimal development paths within internal cross-functional teams and with health authorities, 3) execute clinical-regulatory development plans on-time and while managing all identified risks. • Collaborates with RA CMC Product Lead to execute CMC Submission and Authoring strategy for assigned project. • Ensures that submission documents and correspondence are of the highest quality in terms of content, organization, clarity of writing, and accuracy. • Ensures that evolving global regulations, guidelines and health authority expectations, especially those related to cell therapies, are incorporated into program decision making. • Ensures writing activities meet quality standards and expectations and adhere to applicable Corporate SOPs, policies, guidelines, and regulation. • Assures that standardized practices are implemented and maintained across regulatory documents. • Collaborates with Regulatory Operations to ensure timely and accurate submissions • Critically review source documents for consistency, completeness, and quality. • Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics • Perform miscellaneous duties as assigned.