Analytical Development Chemist (Project Analysis - Level 1)

ZipRecruiter; Tredegar; On-site; GBP 33,000; Full time

Job summary

A leading health and beauty provider in Tredegar is seeking an Analytical Development Chemist. This role involves supporting new product introductions through method validation and laboratory testing. The ideal candidate will have a degree in a scientific discipline and practical skills in analytical techniques. This on-site position offers a competitive salary and opportunities for professional development.

Qualifications

• Degree or relevant experience in a scientific discipline is essential.
• Demonstrable practical skills in analytical techniques.

Responsibilities

• Perform sample analysis adhering to Health and Safety and GMP requirements.
• Conduct method development and validation studies.

Skills

Analytical Techniques

Computer Literacy

Attention to Detail

Education

Degree in Scientific Discipline

Chemistry Graduate

Tools

Microsoft Office 365

Q-Pulse

Navision

Job description

Job Description

HBI EuroCaps, part of HBI Health and Beauty Innovations are one of Europe’s leading health and beauty providers and are a world class Soft Gelatin Capsule and Nutritional Gummy Contract Manufacturer, supplying the nutritional supplement and OTC markets across Europe and worldwide. We specialise in the manufacture of complex softgels, Vegetarian softgels and other speciality softgels, simply providing one the highest quality softgel products available. Our mission is to provide a total solution to our customers with superior quality softgels and gummies along with outstanding service.

We were one of the first UK manufacturers to invest in, and offer, nutritional gummies, and the only ones to offer vegetarian softgels, making us one of the world leaders in Vegetarian softgel technology. We are experts in complex paste formulation and have invested heavily to ensure we are at the forefront of this technology.

Our state-of-the-art manufacturing facility based in Tredegar, South Wales, where we currently employ around 300 people, operates as a GMP (Good Manufacturing Practice) facility and is licensed by the UK Medicines and Healthcare products Regulatory Agency (MHRA). We are Europe’s leading contract manufacturer, with capacity to manufacture over 2.5 billion softgel capsules per year (rising to over 5 billion in the next few years) and over 500 million gummies per year (with potential for more). We supply many of the key brands and supplement companies across Europe, whilst maintaining our founding principles which have been key to our growth and success.

We recognise that our people are our greatest asset, and we are committed to fostering an inclusive and respectful workplace where everyone is treated fairly and with dignity and as an equal opportunities employer, we welcome applications from individuals of all backgrounds, regardless of , , , , , , or any other protected characteristic. We are also a Confident Employer, we are dedicated to supporting candidates with disabilities or long-term health conditions, ensuring equal opportunities for success. To reinforce this commitment, we operate a Guaranteed Interview Scheme for applicants who meet the minimum requirements of the role. If you wish to be considered under this scheme, please inform us during the recruitment process.

The Analytical Development Chemist will report directly to the QC Project Team Leader.

This role is an integral part of provided laboratory services that supports new product introduction, offering method validation, method verification and stability services along with project analysis testing.

Key Responsibilities:

The Analytical Development Chemist will report directly to the QC Project Team Leader. This role is an integral part of provided laboratory services that supports new product introduction, offering method validation, method verification and stability services along with project analysis testing.

Responsibilities include (but are not limited to):

• Planning and prioritising own day to day workload with the Project Team Leader and customer requirements and adapt where necessary.
• To perform sample analysis in accordance with documented procedures, adhering to Health and Safety and GMP requirements against defined lead times.
• Perform method development, method validation and method verification studies in accordance with defined protocols and procedures.
• Perform routine laboratory procedures right first time with minimal analyst related out of specification investigations.
• To ensure all Health and Safety procedures are adhered to with respect to personal duties, always conducting work in a safe manner and highlight any safety issues to an appropriate person as soon as possible.
• To attend all training as required.
• To always maintain good standards of housekeeping with in the QC laboratory.
• Communicate and collaborate efficiently and professionally with your colleagues and other departments.
• To provide QC project support to the wider company to ensure that business needs are met. This could include direct liaison with customers and external contract laboratories.
• Assist with the introduction and qualification of new equipment as required.
• All analytical testing to fully comply with data integrity requirements.
• To act as a point of contact for issues encountered during routine analysis work and to assist with finding a speedy resolution by utilising the team's expertise.
• Liaise with the Quality Management team to ensure laboratory resources and testing performance always meet regulatory expectations for continued compliance.
• Assist with preparing relevant documentation as required such as specification, standard test methods, operating procedures and performing risk assessments.
• Identify and support with Continuous Improvement activities to continuously improve laboratory standards.
• To achieve set targets for the delivery of laboratory projects and ongoing commitments.
• Proactively take ownership of your own performance and continual professional development.

Person Specification:

• Degree or relevant experience in a scientific discipline (essential)
• Demonstrable practical skills and good theoretical knowledge in a wide range of analytical techniques (essential)
• Chemistry graduate (desirable)
• Demonstrable experience/knowledge in analytical method validation and laboratory technical transfers (desirable)

Skills and Knowledge

• Good level of computer literacy: Microsoft Office 365 package software (Work/Excel/Outlook), Q-Pulse, Navision and the usage of laboratory chromatographic data systems
• Understanding of the requirements of Good Manufacturing Practice (GMP) within a Quality Control laboratory

Personal Attributes

• Good verbal and written skills
• Good attention to detail
• Team player
• Enthusiasm, personal drive and initiative
• Friendliness and approachability
• Ability to handle pressure and meet deadlines
• Flexibility in adapting to changing circumstances and handling new situations
• Individual project management and organisational skills

Competitive basic salary of £32,462.80

To find out more about us, take a look at our website at www.hbieurocaps.com and if you would like to apply, then please submit a copy of your up-to-date CV.

Closing Date: Friday, 30th May 2025

Please note that we not hold a Sponsor Licence and therefore are unable to recruit individuals who do not already possess full right to work in the United Kingdom.

This is an on-site role and therefore applicants should be willing and able to travel to our site in Tredegar, South Wales NP22 4EF

*NO AGENCIES, THANK YOU