QC Analyst

Vantive; Liverpool; On-site; GBP 28,000 - 36,000; Full time

Benefits offered by this job

Competitive salary and benefits

Career development and progression

Collaborative and inclusive culture

Work-life balance and employee well‑be

Job summary

Vantive is seeking a QC Analyst to join our high-performing manufacturing facility in Liverpool. You will support analytical testing throughout the manufacturing lifecycle, ensuring accuracy, efficiency, and compliance with regulatory and site requirements.

The role offers opportunities to contribute to product quality, continuous improvement, and operational excellence within a regulated pharmaceutical environment.

Qualifications

• Degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or related discipline, or significant QC laboratory experience.

Responsibilities

• Perform analytical testing of raw materials, in-process samples, finished products, and stability studies.
• Conduct analytical techniques including SEC-HPLC, AA, pH, Conductivity and TOC testing.
• Manage laboratory samples: receipt, logging, storage and disposal.
• Support laboratory workload planning with QC leadership.
• Follow SOPs and testing methodologies.
• Maintain GLP, GMP and GDP compliance.
• Maintain laboratory housekeeping and 6S standards.
• Assist with investigations, deviations, CAPAs and root-cause analysis.
• Review analytical data and records for accuracy and compliance.
• Support training and development of colleagues in the laboratory.
• Participate in method maintenance and validation activities.
• Periodic review of procedures and documentation.
• Conduct pharmacopeial compliance assessments and support regulatory readiness.
• Drive continuous improvement and digital transformation in QC.

Skills

Attention to detail

Problem solving

Independent worker

Organisational skills

Education

Degree in Chemistry, Pharmaceutical Sciences, Life Sciences or related

Tools

SEC-HPLC

Atomic Absorption (AA)

pH

Conductivity

TOC

Job description

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

We are currently seeking a QC Analyst to join our high-performing manufacturing facility in Liverpool.

As a QC Analyst, you will play a key role in supporting laboratory testing activities throughout the manufacturing lifecycle. Working as part of a collaborative Quality Control team, you will ensure analytical testing is performed accurately, efficiently, and in compliance with regulatory and site requirements. The role offers the opportunity to contribute to product quality, continuous improvement, and operational excellence within a regulated pharmaceutical manufacturing environment.

Working Hours: Monday to Friday, 9:00am to 5:00pm (with flexibility where required).

Key Responsibilities

• Perform analytical testing of raw materials, in-process samples, finished products, and stability studies.
• Conduct complex analytical techniques including SEC-HPLC, Atomic Absorption (AA), pH, Conductivity, and TOC testing.
• Manage laboratory samples, including receipt, logging, storage, and disposal.
• Support laboratory workload planning in collaboration with the QC leadership team.
• Carry out laboratory support activities to ensure efficient day-to-day operations.
• Follow approved Standard Operating Procedures (SOPs) and testing methodologies.
• Maintain compliance with Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and Good Documentation Practice (GDP).
• Maintain laboratory housekeeping standards and support established 6S initiatives.
• Assist with laboratory investigations, deviations, CAPAs, and root cause analysis activities.
• Review analytical data and laboratory records for accuracy and compliance.
• Support the training and development of colleagues within the laboratory.
• Participate in analytical method maintenance and validation activities.
• Perform periodic reviews of laboratory procedures and analytical documentation.
• Conduct pharmacopeial compliance assessments and support regulatory readiness.
• Drive continuous improvement and digital transformation initiatives within the Quality Control function.

Experience & Qualifications

To be successful in this role, you will ideally have:

• A degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related scientific discipline, or significant relevant QC laboratory experience.
• Experience working within a regulated pharmaceutical, medical device, healthcare, or manufacturing environment.
• Knowledge of analytical techniques including SEC-HPLC, AA, pH, Conductivity, and TOC.
• Experience with analytical weighing, sample preparation, and dilution techniques.
• Understanding of GMP, GLP, and GDP requirements.
• Ability to interpret pharmacopeial methods and laboratory procedures.
• Strong problem-solving and troubleshooting skills.
• Excellent attention to detail and organisational skills.
• Ability to work independently while contributing effectively within a team environment.

Why Join Vantive?

At Vantive, our mission is to extend lives and expand possibilities for patients around the world. We are committed to creating an environment where employees can grow, contribute, and make a meaningful impact.

What we offer:

• Competitive salary and benefits package.
• Professional development and career progression opportunities.
• A collaborative and inclusive workplace culture.
• A strong commitment to work-life balance and employee wellbeing.
• The opportunity to work on products that positively impact patients' lives every day.

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

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