Pharmaceutical Quality Control Analyst

Oxfordshire, South East Taylorollinson

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Job Description

permanent

Pharmaceutical Quality Control Analyst

Location: Oxfordshire

Sector: Pharmaceutical

Our client is a leading Pharmaceutical CRO based in Oxfordshire and due to continued expansion, they now have an exciting opportunity for an experienced QC Analyst to join the company

The role:

As a QC Analyst you will be responsible for analysing pharmaceutical samples using a range of analytical techniques and for a variety of projects. All work must be carried to the highest quality standards and in compliance with industry guidelines. You will also be expected to report and provide written documentation for the laboratory work completed.

Experience expectations:

Suitable applicants;

  • Previous Pharmaceutical industry experience working in an analytical or QC role is essential
  • Experienced in the use of analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR
  • Knowledge of Quantitative and Qualitative analysis
  • Good knowledge of GMP, FDA and MHRA guidelines
  • Educated to degree level (or equivalent experience) in Analytical Chemistry, Pharmaceutical Science or Chemistry discipline
  • Any method development or method validation experience would be beneficial
  • Organised and methodical approach to work
  • Good communication skills

The Package:

Our client offers an opportunity to work for a leading Pharmaceutical company on a permanent basis with a competitive annual salary and benefits.

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Pharmaceutical Quality Control Analyst

Oxfordshire, South East Taylorollinson

Posted 3 days ago

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Job Description

permanent

Pharmaceutical Quality Control Analyst

Location: Oxfordshire

Sector: Pharmaceutical

Our client is a leading Pharmaceutical CRO based in Oxfordshire and due to continued expansion, they now have an exciting opportunity for an experienced QC Analyst to join the company

The role:

As a QC Analyst you will be responsible for analysing pharmaceutical samples using a range of analytical techniques and for a variety of projects. All work must be carried to the highest quality standards and in compliance with industry guidelines. You will also be expected to report and provide written documentation for the laboratory work completed.

Experience expectations:

Suitable applicants;

  • Previous Pharmaceutical industry experience working in an analytical or QC role is essential
  • Experienced in the use of analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR
  • Knowledge of Quantitative and Qualitative analysis
  • Good knowledge of GMP, FDA and MHRA guidelines
  • Educated to degree level (or equivalent experience) in Analytical Chemistry, Pharmaceutical Science or Chemistry discipline
  • Any method development or method validation experience would be beneficial
  • Organised and methodical approach to work
  • Good communication skills

The Package:

Our client offers an opportunity to work for a leading Pharmaceutical company on a permanent basis with a competitive annual salary and benefits.

This advertiser has chosen not to accept applicants from your region.

Pharmaceutical Quality Control Analyst - Validation

Oxfordshire, South East £25000 - £35000 Annually Taylorollinson

Posted 3 days ago

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Job Description

permanent

Pharmaceutical Quality Control Analyst - Validation

Location: Oxfordshire

Sector: Pharmaceutical

Our client is a leading Pharmaceutical CRO based in Oxfordshire and due to continued expansion, they now have an exciting opportunity for an experienced QC Analyst to join the company and support in Validation studies within the analytical team.

The role:

As a QC Analyst you will be responsible for analysing pharmaceutical samples using a range of analytical techniques and for a variety of projects.

This role will focus on:

  • Validation and verification of analytical methods for HPLC, GC, NMR, KF etc.
  • Degradation and stability studies for a variety of conditions
  • LCMS analysis for impurity identification
  • Running and reporting on multiple projects simultaneously
  • All work must be carried to the highest quality standards and in compliance with industry guidelines.
  • You will also be expected to interpret and report on the laboratory work completed.

Experience expectations:

Suitable applicants;

  • Previous Pharmaceutical industry experience working in an analytical or QC role is essential
  • Experienced in the use of analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR
  • Knowledge of Quantitative and Qualitative analysis
  • Good knowledge of GMP, FDA and MHRA guidelines
  • Experience with Method Validation and Stability studies
  • Educated to degree level (or equivalent experience) in Analytical Chemistry, Pharmaceutical Science or Chemistry discipline
  • Organised and methodical approach to work
  • Good communication skills

The Package:

Our client offers an opportunity to work for a leading Pharmaceutical company on a permanent basis with a competitive annual salary, benefits and career progression opportunities.

Applicants must be fully eligible to work in the UK. Visa Sponsorship is not available with this position and therefore applicants must not require immediate sponsorship or have Visa sponsorship requirements in the future.

This advertiser has chosen not to accept applicants from your region.

Pharmaceutical Quality Control Analyst - Metrology

Oxfordshire, South East Taylorollinson

Posted 3 days ago

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Job Description

permanent

Pharmaceutical Quality Control Analyst - Metrology

Location: Oxfordshire

Sector: Pharmaceutical

Our client is a leading Pharmaceutical CRO based in Oxfordshire and due to continued expansion, they now have an exciting opportunity for an experienced QC Analyst to join the company and support the team with Metrology projects.

The role:

As a QC Analyst - Metrology you will be responsible for have a more instrument led approach to analytical chemistry and use your experience in Metrology to support the on-going development of analytical projects.

This role will focus on:

  • Maintenance and calibration of analytical instrumentation
  • Carry-out investigations to highlight functional and preventative issues
  • Run analytical testing to ensure accuracy of analytical instrumentation
  • Troubleshoot analytical anomalies and provide solutions.
  • You will also be expected to interpret and report on the laboratory work completed.

Experience expectations:

Suitable applicants;

  • Previous Pharmaceutical industry experience working in an analytical or QC role is essential
  • Experienced in the use of analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR
  • Understanding of Quantitative and Qualitative analysis
  • Interest in laboratory instrumentation and calibration
  • Good knowledge of GMP, FDA and MHRA guidelines
  • Educated to degree level (or equivalent experience) in Analytical Chemistry, Pharmaceutical Science or Chemical Engineering.
  • Organised and methodical approach to work
  • Good communication skills

The Package:

Our client offers an opportunity to work for a leading Pharmaceutical company on a permanent basis with a competitive annual salary, benefits and career progression opportunities.

Applicants must be fully eligible to work in the UK. Visa Sponsorship is not available with this position and therefore applicants must not require immediate sponsorship or have Visa sponsorship requirements in the future.

This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst

Oxford, South East Helio Display Materials

Posted 6 days ago

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Job Description

About us:


At Helio Display Materials, we're crafting the fundamental materials that will shape the future of displays.

Using the power of perovskites, these enabling materials facilitate the creation of displays that are not only brighter and more vibrant but also operate with remarkably low power consumption.

Our team is dedicated to pioneering the future of colour. As we accelerate, we are looking for talented individuals to join us on the next phase of our journey.


Our Values:


  • Knowledge
  • Driven
  • Unity


About the Role:


Join our team as a key contributor to advancing product performance through collaboration with experienced chemists and materials scientists. Your role will involve conducting quality control testing, preparing materials for analysis, and performing non-routine analyses under direction.

You will also investigate deviations and maintain accurate records of laboratory tests.

This position offers a dynamic environment where your contributions will directly impact innovative projects. If you are detail-oriented and passionate about laboratory work, this role provides an excellent opportunity to enhance your career.


Responsibilities:

  • Work closely with experienced chemists and materials scientists to progress our products to the next stage of performance.
  • Strictly follow Standard Operating Procedures to conduct quality control testing for chemical and physical analysis.
  • Prepare substrates, materials and samples for internal or external characterization.
  • Assist in the investigation of deviations, out-of-specification results, and non-conformances.
  • Perform non-routine analyses under direction.
  • Track and monitor stock which include chemicals and consumables.
  • Operate, calibrate, and maintain analytical instruments such as FTIR, UV-Vis, XRF, TGA, Optical Microscope, DLS.
  • Support development and validation of analytical methods to support R&D and quality control initiatives.
  • Maintain detailed and accurate records of all laboratory tests.
  • Follow health, safety, and environmental (HSE) protocols within the laboratory setting and promote laboratory safety amongst peers.


Experience & Attributes:

  • HNC/HND or degree in Chemistry, Materials Science or related disciplines.
  • Passion for working hands-on in the lab, including willingness to perform repetitive work.
  • Excellent attention to detail in performing laboratory practices and in data recording.
  • Strong organizational and time-management skills.
  • Effective communication skills and the ability to work as part of a team and independently.
  • Commitment to maintaining high standards of laboratory safety and quality assurance.
  • Adaptability and eagerness to learn new techniques and technologies.


Advantage:

  • Proven experience in an analytical/materials characterisation laboratory, preferably in a chemical R&D or quality control environment.
This advertiser has chosen not to accept applicants from your region.

Product Quality Control Support

Wanborough, South West £24000 - £27000 Annually Storm Recruitment (Swindon)

Posted 11 days ago

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permanent

Title: Product Quality Control Support - Maternity Cover 

Salary:  £26,193.44 p/annum 

Hours: 37.5 hrs p/week

Location: Swindon

Job Purpose : To carry out quality control functions to ensure product conformity relating to stocked products, customer returns and associated parts.

Duties and Responsibilities:

  • Deal with customer returns
  • li>Stock control inclusive of testing for low OCV CCA
  • Monitoring the shelf life of products
  • Goods in inspection of labels
  • Pre-delivery inspection for OEM and OES customers
  • Data entry

Supplementary Duties and Responsibilities:

This is a summary job description and not an exhaustive list. You should be prepared when required to undertake any work or additional training allocated to you by your manage.

Personal Traits:

  • Self-Motivated
  • Able to work on own initiative as well as part of a team.
  • Excellent Communication Skills
  • Ability to multitask and prioritise tasks
  • Work well under pressure.
  • High attention to detail
  • Good team player

Experience and Qualifications:

  • Previous administration experience preferably in a warehouse background with knowledge of Microsoft applications such as Outlook, Excel, Word and Dynamics 365.
  • Forklift Truck Licences would be an advantage.
This advertiser has chosen not to accept applicants from your region.

Quality and Compliance Analyst

Oxfordshire, South East £40000 Annually Stellar Select

Posted 11 days ago

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Job Description

permanent

Job Title: Quality and Compliance Analyst

Location: Oxfordshire - Hybrid - 2 days WFH

Salary: Up to 40,000, with flexibility to offer a higher salary for the right candidate

Hours: Monday to Friday 9 am to 5.30 pm

Benefits:

  • 23 days holiday plus bank and public holidays
  • Simply Health Cash plan
  • Employee assistance programme
  • Bupa (after qualifying period)
  • Free Legal and Conveyance fees
  • Volunteering days off
  • Enhanced Maternity and Paternity Leave
  • Company sick pay
  • Ongoing learning and development opportunities

About our Client and the role of Quality and Compliance Analyst:

Our client, a well-established and highly regarded firm of solicitors with deep roots in the Oxfordshire and Buckinghamshire area, is looking to appoint a Quality and Compliance Analyst to join their growing team.

This role will be central in ensuring that all conveyancing processes across the property department are fully compliant with legal, regulatory, and lender-specific requirements, while supporting continuous improvements in service delivery and risk management.

It's an excellent opportunity for someone with a strong background in property law and compliance to join a forward-thinking practice focused on quality, client care, and professional development.

Responsibilities for the role of Quality and Compliance Analyst:

  • Conduct regular file reviews across residential, BTL, and bridging property matters to ensure compliance with legal and regulatory frameworks, internal policies, and lender requirements
  • Develop and maintain robust quality assurance procedures to ensure consistent and high standards of service
  • Identify risk areas and non-compliance issues, providing clear recommendations for remediation
  • Investigate and assist with resolving client complaints in a timely and professional manner
  • Deliver training and ongoing guidance to staff on compliance and quality improvement
  • Monitor, analyse, and report on compliance trends and key risks
  • Liaise with stakeholders across the firm to support continuous improvement
  • Keep up to date with changes in legislation, regulation, and lender criteria

Experience required for the role of Quality and Compliance Analyst:

  • In-depth understanding of conveyancing processes, including residential, BTL, and bridging finance
  • Strong working knowledge of legal and regulatory frameworks relevant to property law and compliance
  • Excellent attention to detail, analytical, and problem-solving skills
  • Confident communicator with the ability to engage and advise at all levels
  • Proactive and self-motivated, with the ability to work independently
  • Knowledge of risk and quality assurance best practices
  • High level of personal integrity and professional ethics

For more information regarding the role of Quality and Compliance Analyst please contact us

Stellar Select is acting as an employment agency and is a corporate member of the REC.

Due to a high volume of applications, we will only contact you if your application has been successful. We aim to contact all successful contacts within two business days.

This advertiser has chosen not to accept applicants from your region.
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