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- Tasks: Create and review GMP Batch Records and documentation for pharmaceutical manufacturing.
- Company: Join Almac Pharma Services, a leader in the pharmaceutical industry.
- Benefits: Enjoy flexible working hours and a competitive salary with excellent perks.
- Why this job: Be part of a dynamic team making a real impact in healthcare.
- Qualifications: Bachelor's degree in a scientific field or relevant experience in pharma.
- Other info: Applications close on 22nd July 2025; apply now!
The predicted salary is between 36000 - 60000 £ per year.
The post holder will be responsible for authoring, editing, reviewing and approving GMP Batch Records for the Technical Operations and Formulation Development department, and will include documents for new product introduction, product transfer and GMP (Clinical and/or Commercial) Manufacturing.
The Technical Specialist will also be required to conduct a variety of tasks pertaining to documentation, including:
- Author, edit and review GMP documents inclusive of, but not limited to, Master Batch Records, SOPs and Forms
- Respond to internal and external comments, working with SMEs to ensure comments are incorporated
- Set priorities to ensure documents are ready when needed per production schedule
- Work with quality and manufacturing to ensure all processes conform to quality requirements
Key Requirements
- Bachelors degree (or equivalent) in a related Scientific/Technical discipline or significant relevant experience working within the Pharmaceutical Manufacturing Industry.
- Experience within a Pharmaceutical / Engineering environment supporting generation of documentation
Desirable Requirements
- Knowledge of cGMP and manufacturing processes of pharmaceutical products
- Experience in problem solving.
- Experience of compiling reports and presentation on technical projects
Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.
Closing Date: We will no longer be accepting applications after 5pm (local time) on Tuesday 22nd of July 2025.
RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Technical Specialist (Documentation) in Loughborough employer: Almac Group (Uk) Ltd
Contact Detail:
Almac Group (Uk) Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Specialist (Documentation) in Loughborough
✨Tip Number 1
Familiarise yourself with GMP documentation standards and practices. Understanding the nuances of Good Manufacturing Practices will not only help you in the role but also impress the hiring team during discussions.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who work in documentation roles. Engaging with them can provide insights into the company culture and expectations, which can be beneficial during interviews.
✨Tip Number 3
Prepare to discuss specific examples of your experience with documentation in a pharmaceutical or engineering environment. Highlighting your problem-solving skills and how you've handled challenges in past roles can set you apart from other candidates.
✨Tip Number 4
Stay updated on the latest trends and technologies in pharmaceutical manufacturing. Showing that you are proactive about learning can demonstrate your commitment to the field and your potential value to the team.
We think you need these skills to ace Technical Specialist (Documentation) in Loughborough
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Technical Specialist position. Highlight key skills and experiences that align with the role.
Tailor Your CV: Customise your CV to reflect how your background in scientific or technical disciplines meets the job criteria. Emphasise your experience in documentation within the pharmaceutical industry, particularly in GMP processes.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your relevant experience and explains why you are a good fit for the Technical Specialist role. Mention specific examples of your work with GMP documents and collaboration with SMEs.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. Ensure that all information is clear and professional, as attention to detail is crucial in this role.
How to prepare for a job interview at Almac Group (Uk) Ltd
✨Know Your GMP Basics
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP). Understanding the principles and regulations surrounding GMP will show that you're serious about the role and can contribute effectively from day one.
✨Showcase Your Documentation Skills
Prepare examples of your previous work with documentation, especially in a pharmaceutical context. Be ready to discuss how you've authored, edited, or reviewed documents like Master Batch Records or SOPs, as this is a key part of the job.
✨Demonstrate Problem-Solving Abilities
Think of specific instances where you've encountered challenges in documentation or project management. Be prepared to explain how you approached these problems and what solutions you implemented, as problem-solving is a desirable skill for this position.
✨Engage with the Interviewers
Don't hesitate to ask questions during the interview. Engaging with the interviewers shows your interest in the role and helps you understand the company culture and expectations better. Prepare thoughtful questions related to the team dynamics and the projects you'll be working on.
