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For Companies At a Glance
- Tasks: Create and review GMP Batch Records and documentation for pharmaceutical manufacturing.
- Company: Join Almac Group, a leader in pharmaceutical services with a commitment to quality.
- Benefits: Enjoy flexible working hours and a competitive salary with an excellent benefits package.
- Why this job: Be part of a dynamic team making a real impact in the pharmaceutical industry.
- Qualifications: Bachelor's degree in a related field or significant experience in pharmaceutical manufacturing required.
- Other info: Applications close on 22nd July 2025; apply now to kickstart your career!
The predicted salary is between 36000 - 60000 £ per year.
Join to apply for the Technical Specialist (Documentation) role at Almac Group
Join to apply for the Technical Specialist (Documentation) role at Almac Group
Location: Loughborough, UK
Hours: 37.5 Hours per week, Monday – Friday, flexible working hours
Salary: Competitive plus excellent benefits package
Business Unit: Almac Pharma Services
Open To: Internal and External applicants welcome to apply
Ref No.: HRJOB10794
The Role
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
- Bachelor’s 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 Now
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.
Seniority level
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Seniority level
Entry level
Employment type
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Employment type
Part-time
Job function
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Job function
Information Technology
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Industries
Pharmaceutical Manufacturing
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Technical Specialist (Documentation) employer: Almac Group
Contact Detail:
Almac Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Specialist (Documentation)
✨Tip Number 1
Familiarise yourself with GMP (Good Manufacturing Practice) guidelines and documentation standards. Understanding these will not only help you in the role but also show your commitment to quality and compliance during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical manufacturing industry, especially those who have experience in documentation roles. Engaging with them can provide insights into the company culture and expectations, which can be beneficial during your application process.
✨Tip Number 3
Prepare to discuss specific examples of how you've handled documentation in previous roles. Highlighting your problem-solving skills and ability to work with subject matter experts (SMEs) will demonstrate your readiness for the Technical Specialist position.
✨Tip Number 4
Stay updated on the latest trends and technologies in pharmaceutical documentation. Showing that you are proactive about learning and adapting can set you apart from other candidates and align with the innovative spirit at Almac Group.
We think you need these skills to ace Technical Specialist (Documentation)
Some tips for your application 🫡
Tailor Your CV: Make sure to customise your CV to highlight your relevant experience in documentation and the pharmaceutical industry. Emphasise your skills in authoring, editing, and reviewing GMP documents, as these are crucial for the role.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your motivation for applying to Almac Group. Mention specific experiences that demonstrate your understanding of cGMP and your ability to work with SMEs to incorporate feedback.
Highlight Relevant Experience: In your application, clearly outline any previous roles or projects where you have worked with GMP Batch Records or similar documentation. Use specific examples to showcase your problem-solving skills and attention to detail.
Proofread Your Application: Before submitting, thoroughly proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your professionalism and attention to detail, which is essential for a Technical Specialist.
How to prepare for a job interview at Almac Group
✨Know Your GMP Basics
Make sure you have a solid understanding of Good Manufacturing Practices (GMP) as they are crucial for the role. Brush up on relevant regulations and how they apply to documentation in pharmaceutical manufacturing.
✨Showcase Your Documentation Skills
Prepare examples of your previous work with documentation, such as Master Batch Records or SOPs. Be ready to discuss how you approached authoring, editing, and reviewing these documents.
✨Familiarise Yourself with the Company
Research Almac Group and their specific operations. Understanding their products and processes will help you tailor your responses and show genuine interest in the role.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving abilities. Think of scenarios where you had to address challenges in documentation or compliance, and be ready to explain your thought process.
