Hybrid Labelling Regulatory Affairs Associate

Cycle Pharmaceuticals; Cambridge; Hybrid; GBP 37,000 - 42,000; Full time

Benefits offered by this job

Performance-based bonus

Hybrid working hours

Company pension scheme

Private health insurance

Life and critical illness insurance

Gym membership

Team-building events

Job summary

Cycle Pharmaceuticals Ltd in Cambridge is hiring a Regulatory Affairs Associate, Labelling for a full-time role on a hybrid basis (minimum 3 days in the office). You will support day-to-day labelling activities across Cycle’s product portfolio, preparing, reviewing, maintaining and updating product labelling and artwork for different markets.

You will collaborate with Regulatory Affairs, Quality, Medical Affairs, Compliance, Product Development, Supply Chain, Legal and Project Management, while

Qualifications

• Bachelor’s degree in life sciences or related subject.
• At least 1 year’s experience in regulatory affairs, labelling or artwork creation.
• Familiarity with regulators such as FDA and MHRA; experience with other regulators is helpful.

Responsibilities

• Support the preparation, review and maintenance of product labelling and artwork.
• Coordinate labelling updates across Cycle’s portfolio with focus on US requirements and UK/MHRA considerations.
• Review labelling materials for accuracy and regulatory compliance.
• Assist regulatory submissions by preparing and maintaining labelling-related documentation.
• Manage version control, approvals tracking and record keeping for labelling and artwork.

Skills

Attention to detail

Regulatory affairs

Communication

Team collaboration

Proactive/organized

Labelling

Education

Bachelor’s degree in life sciences

Job description

Cycle Pharmaceuticals Ltd in Cambridge is hiring a Regulatory Affairs Associate, Labelling for a full-time role on a hybrid basis (minimum 3 days in the office). You will support day-to-day labelling activities across Cycle’s product portfolio, preparing, reviewing, maintaining and updating product labelling and artwork for different markets.

You will collaborate with Regulatory Affairs, Quality, Medical Affairs, Compliance, Product Development, Supply Chain, Legal and Project Management, while