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- Tasks: Join a team to create essential quality documents and SOPs for a leading biotech company.
- Company: Warman O’Brien partners with a top mid-size biotechnology firm focused on global transformation.
- Benefits: Enjoy remote work flexibility and a collaborative environment within the pharmaceutical industry.
- Why this job: Be part of impactful projects that enhance quality assurance in a dynamic biotech setting.
- Qualifications: 3+ years in pharma, knowledge of GxP, and experience in SOP development required.
- Other info: This role is contract-based, inside IR35, and requires UK citizenship or permanent settlement.
The predicted salary is between 36000 - 60000 £ per year.
Technical Writer – Quality Assurance (UK – Remote) Warman O’Brien proud to be partnered with a leading Consulting Firm looking for Technical Writers on behalf of a leading Mid-Size Biotechnology Company. As a part of a global transformation project we’re looking for a team of Technical Writers to support this Biotech’s Quality teams (SMEs) to develop SOPs, quality documents and procedures for the department. If you have the below experience then please click apply! 3+ years direct experience in the pharmaceutical industry Awareness of GxP regulatory requirements Experience with deviations, inspection commitments, corrective/ preventative actions, and other gaps Experience in design/development of SOPs, supporting documents and forms/templates Contract specifics: Inside IR35 (Umbrella) 30-40 hours per week Remote (UK) Must be British Citizen or have UK permanent settlement status
Technical Writer - Quality employer: Warman O'Brien
Contact Detail:
Warman O'Brien Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Writer - Quality
✨Tip Number 1
Familiarize yourself with GxP regulatory requirements and be prepared to discuss how your experience aligns with these standards. This knowledge will demonstrate your expertise and commitment to quality in the pharmaceutical industry.
✨Tip Number 2
Highlight any specific projects where you developed SOPs or quality documents. Be ready to share examples of how your contributions improved processes or compliance within your previous roles.
✨Tip Number 3
Network with professionals in the biotechnology and pharmaceutical sectors. Engaging with industry peers can provide insights into the company culture and expectations, which can be beneficial during interviews.
✨Tip Number 4
Prepare to discuss your experience with deviations and corrective/preventative actions. Being able to articulate your problem-solving skills in these areas will set you apart as a candidate who can contribute effectively to the Quality teams.
We think you need these skills to ace Technical Writer - Quality
Some tips for your application 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Technical Writer in Quality Assurance. Familiarize yourself with GxP regulatory requirements and the specific tasks related to developing SOPs and quality documents.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 3+ years of experience in the pharmaceutical industry. Be specific about your familiarity with deviations, inspection commitments, and corrective/preventative actions.
Tailor Your Application: Customize your application materials to reflect the job description. Use keywords from the listing, such as 'SOPs', 'quality documents', and 'biotechnology', to demonstrate your fit for the role.
Proofread Your Documents: Before submitting your application, carefully proofread your CV and cover letter. Ensure there are no grammatical errors or typos, as attention to detail is crucial for a Technical Writer.
How to prepare for a job interview at Warman O'Brien
✨Showcase Your Industry Knowledge
Make sure to highlight your experience in the pharmaceutical industry, especially your understanding of GxP regulatory requirements. Be prepared to discuss specific examples where you've applied this knowledge in your previous roles.
✨Demonstrate Your Technical Writing Skills
Bring samples of your previous work, such as SOPs or quality documents you've developed. This will not only showcase your writing skills but also your ability to create clear and concise documentation that meets industry standards.
✨Prepare for Scenario-Based Questions
Expect questions related to deviations, inspection commitments, and corrective/preventative actions. Prepare to discuss how you've handled these situations in the past and what processes you followed to ensure compliance and quality.
✨Understand the Company’s Mission
Research the biotechnology company and understand their goals and values. Being able to articulate how your skills and experiences align with their mission will demonstrate your genuine interest in the role and the organization.
