Quality Control Reviewer & Regulatory Writer (Pharma)

Bioscript Group; City of Westminster; On-site; GBP 32,000 - 52,000; Full time

Benefits offered by this job

Salary aligned with experience and kit

25 days holiday + bank holidays +冬季休假/

Enhanced sick and compassionate leave

Enhanced maternity, paternity & adopt.

Life Insurance

Private Medical (UK)

Health cash plan

Employee Assistance Program

Job summary

Bioscript Group is seeking a QC Reviewer / Regulatory Writer to join our pharma/agency client support team. The role focuses on QC review, ensuring document accuracy, consistency, and adherence to templates and style guides.

You will collaborate with authors to resolve findings and maintain timelines. Responsibilities include documenting QC findings, supporting publishing processes, and ensuring compliance with client standards.

Qualifications

• Experience as QC Reviewer / Regulatory Writer in pharma or agency setting.
• Attention to detail to ensure accuracy and quality of deliverables.
• Ability to manage multiple tasks independently and communicate clearly.

Responsibilities

• Perform QC review and manage QC projects within agreed timelines.
• Verify accuracy of document content using source regulatory documents.
• Ensure consistency within documents and across related documents.

Skills

Attention to detail

Initiative

Multitasking

Strong communication skills

Job description

Bioscript Group is seeking a QC Reviewer / Regulatory Writer to join our pharma/agency client support team. The role focuses on QC review, ensuring document accuracy, consistency, and adherence to templates and style guides.

You will collaborate with authors to resolve findings and maintain timelines. Responsibilities include documenting QC findings, supporting publishing processes, and ensuring compliance with client standards.