QA Scientist Analyst
Posted on Jun 15, 2026 by CV-Library
Worthing, West Sussex, United Kingdom
Pharmaceutical
Immediate Start
£15.9 - £16.9 Hourly
Contract/Project
QC Analyst - Temporary
Location - Worthing
Contract - 6 Months
Pay Rate - £16.92 per hour paye
We are currently recruiting a QC Analyst to join our client's Quality Control team at the Worthing Manufacturing site. You'll be working in a motivated, high performing team of eight analysts, sharing knowledge and support on a daily basis. The role requires testing of physical and chemical analytical test methods on oral products for release to market. Also, stability studies on those products using SOPs, and accurately documenting the results as part of the Quality Control process to ensure a batch of products is of satisfactory quality.
Key Responsibilities include:
* To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets.
* Calibrate and maintain analytical equipment.
* Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc).
* To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required.
* To check and verify analytical testing and data generated by other analysts
* To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date.
* Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC.
* Supplying data / reports to Value Stream as requested.
* May be required to communicate with the relevant Value Steam. to progress OOS investigations
About You:
This role would suit a motivated individual who has experience of working in a laboratory environment, as well as suitable qualifications in Chemistry (or scientific discipline). You will be a self-starter with keen attention to detail and compliance at the forefront of your decision-making process. A strong Quality and continuous improvement mind-set, as well as strong communication skills are also needed.
Basic Qualifications:
Relevant scientific qualification (eg; HNC or equivalent level in scientific discipline)
Understanding of laboratory analysisGuidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
Location - Worthing
Contract - 6 Months
Pay Rate - £16.92 per hour paye
We are currently recruiting a QC Analyst to join our client's Quality Control team at the Worthing Manufacturing site. You'll be working in a motivated, high performing team of eight analysts, sharing knowledge and support on a daily basis. The role requires testing of physical and chemical analytical test methods on oral products for release to market. Also, stability studies on those products using SOPs, and accurately documenting the results as part of the Quality Control process to ensure a batch of products is of satisfactory quality.
Key Responsibilities include:
* To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets.
* Calibrate and maintain analytical equipment.
* Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc).
* To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required.
* To check and verify analytical testing and data generated by other analysts
* To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date.
* Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC.
* Supplying data / reports to Value Stream as requested.
* May be required to communicate with the relevant Value Steam. to progress OOS investigations
About You:
This role would suit a motivated individual who has experience of working in a laboratory environment, as well as suitable qualifications in Chemistry (or scientific discipline). You will be a self-starter with keen attention to detail and compliance at the forefront of your decision-making process. A strong Quality and continuous improvement mind-set, as well as strong communication skills are also needed.
Basic Qualifications:
Relevant scientific qualification (eg; HNC or equivalent level in scientific discipline)
Understanding of laboratory analysisGuidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
Reference: 225251474
https://jobs.careeraddict.com/post/113414536
QA Scientist Analyst
Posted on Jun 15, 2026 by CV-Library
Worthing, West Sussex, United Kingdom
Pharmaceutical
Immediate Start
£15.9 - £16.9 Hourly
Contract/Project
QC Analyst - Temporary
Location - Worthing
Contract - 6 Months
Pay Rate - £16.92 per hour paye
We are currently recruiting a QC Analyst to join our client's Quality Control team at the Worthing Manufacturing site. You'll be working in a motivated, high performing team of eight analysts, sharing knowledge and support on a daily basis. The role requires testing of physical and chemical analytical test methods on oral products for release to market. Also, stability studies on those products using SOPs, and accurately documenting the results as part of the Quality Control process to ensure a batch of products is of satisfactory quality.
Key Responsibilities include:
* To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets.
* Calibrate and maintain analytical equipment.
* Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc).
* To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required.
* To check and verify analytical testing and data generated by other analysts
* To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date.
* Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC.
* Supplying data / reports to Value Stream as requested.
* May be required to communicate with the relevant Value Steam. to progress OOS investigations
About You:
This role would suit a motivated individual who has experience of working in a laboratory environment, as well as suitable qualifications in Chemistry (or scientific discipline). You will be a self-starter with keen attention to detail and compliance at the forefront of your decision-making process. A strong Quality and continuous improvement mind-set, as well as strong communication skills are also needed.
Basic Qualifications:
Relevant scientific qualification (eg; HNC or equivalent level in scientific discipline)
Understanding of laboratory analysisGuidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
Location - Worthing
Contract - 6 Months
Pay Rate - £16.92 per hour paye
We are currently recruiting a QC Analyst to join our client's Quality Control team at the Worthing Manufacturing site. You'll be working in a motivated, high performing team of eight analysts, sharing knowledge and support on a daily basis. The role requires testing of physical and chemical analytical test methods on oral products for release to market. Also, stability studies on those products using SOPs, and accurately documenting the results as part of the Quality Control process to ensure a batch of products is of satisfactory quality.
Key Responsibilities include:
* To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets.
* Calibrate and maintain analytical equipment.
* Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc).
* To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required.
* To check and verify analytical testing and data generated by other analysts
* To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date.
* Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC.
* Supplying data / reports to Value Stream as requested.
* May be required to communicate with the relevant Value Steam. to progress OOS investigations
About You:
This role would suit a motivated individual who has experience of working in a laboratory environment, as well as suitable qualifications in Chemistry (or scientific discipline). You will be a self-starter with keen attention to detail and compliance at the forefront of your decision-making process. A strong Quality and continuous improvement mind-set, as well as strong communication skills are also needed.
Basic Qualifications:
Relevant scientific qualification (eg; HNC or equivalent level in scientific discipline)
Understanding of laboratory analysisGuidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
Reference: 225251474
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