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Manufacturing Engineer- Pharmaceutical/ Medical Device

I am working with a pharmaceutical/ Medical Device manufacturing site based in Liverpool specialising in Single-Use Technology (SUT) manufactured in a sterile environment. Your will be responsible for defining the manufacturing & inspection process, for single use components. Very exciting time to start as the development of the product has now moved into manufacturing.

Key responsibilities for the Manufacturing Engineer- Pharmaceutical/ Medical Device

Design, implement, and validate single-use assemblies and systems for internally manufactured parts.Investigate any issues within the manufacturing process and create and implement corrective and preventive procedures.Author and review technical documentation, including protocols, SOPs, and engineering reports.Work closely with technicians in the clean room, providing technical support for the manufacturing process, this can be daily at times.Ensure compliance is met within manufacturing to ISO standards.

Requirements for the Manufacturing Engineer- Pharmaceutical/ Medical Device

Bachelor's degree in engineering (Mechanical, Chemical, Bioprocess, or related field).Good understanding of ISO programming.Strong understanding of CAD Modelling, CMM Equipment and CAM Programming.Experience in GMP, ISO, validation protocols, and cleanroom practices.Strong expertise in Single-Use Components, such as bags, tubing, filters, and connectors.

Benefits for the Manufacturing Engineer- Pharmaceutical/ Medical Device

25 holidays per year + Bank HolidaysChristmas shutdown.Cycle to work schemeIncome Protection schemeLife Assurance 4x salaryEarly finish on a Friday and flexible working hours.

To apply for the Manufacturing Engineer- Pharmaceutical/ Medical Device or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email me at

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Contract Analyst - Method Validation - Bristol - 4-6 Month Contract

*** Urgent Vacancy to support method validation for a new generic tablet formulation ****

Do you have experience in method validation for HPLC methods for products registered under MHRA/GMP ?

Are you skilled in report writing & protocol generation for HPLC & dissolution testing methods ?

Are you immediately available for a new contract ?

Please apply now or contact Simon Fowler at NGAGE Smart4Sciences on 01925239725 or to process your application

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Role: Lab Technician

Location: Oxfordshire

Salary: Circa £30,000

The role:

Monitoring and maintaining general laboratory stocks.Monitoring and maintaining gas stocks.Ordering specific consumables and reagents Scheduling and organising waste collections.Laboratory cleaning and general maintenance.Overseeing laboratory coat laundering and restocking of clean laboratory coats into the appropriate lockers.Organising stocks and storage to achieve the best usage of the available space.

Experience:

Experience of working in a laboratory environment.Excellent organisation skills.Proactive.Flexible and adaptable, able to prioritise.Quality minded.

If you would like to apply to this position please click the link "apply" or email with your CV!

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Role: Senior Quality Control Analyst

Location: Cardiff

Salary: £30,000 - £40,000

This is an exciting opportunity for a Quality Control Analyst to join an experienced team on the South Coast of Wales.

The role: Senior QC Analyst

As an Analyst you will:

Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verificationSupport the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis.

The successful QC Analyst will have:

A relevant science degree or equivalent qualificationUnderstanding of current GMP, Health and Safety and COSHH regulationsExperience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervisionThe ability to take on a limited supervisory role would be an advantageRelevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation

To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

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Role: Stability Analyst

Location: Derbyshire

Salary: £27,000 - £32,000

Monday - Friday 8:30am - 4pm

The role:

Focused on HPLC Analysis for stability studies and validation of analytical methods. We're looking for degree qualified candidates that are experienced in the following:

HPLC AnalysisStability studiesMethod developmentICH ValidationExperience in GMP environmentStrong Analytical Skills

Responsibilities

Conducting stability studies on raw materialsAnalysing stability dataEnsure compliance with relevant regulatory guidelinesSupport process validation activitiesPreparing stability protocolsMaintaining stability chambers

If you want to apply or require further information please contact Jack Challinor at

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