Quality control associate Work, Jobs in Grove, Oxf (with Salaries)

Quality Associate II, Quality Assurance
Replimune —Abingdon
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
Quick apply
2d
Associate Software Engineer
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- Full-time
- Azure
- Oracle
- Computer Science
1d
Quality Documentation Technician
Becton Dickinson —Swindon
- Microsoft Office
- SharePoint
- Communication skills
Quick apply
Nursing Associate
Dr Howells & Partners —Hungerford
- Up to £29,095 a year
- Full-time
- Driving
- Computer skills
- In-person
- Free parking
- Employee discount
Quick apply
Associate Engineer, GxP IT Support
Moderna, Inc. —Oxford
- Full-time
- Oracle
- Microsoft Outlook
- Computer Science
- Annual leave
Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays
Moderna, Inc. —Oxford
- Full-time
- Data analysis skills
- Bachelor's degree
- Communication skills
- Annual leave
Onsite Warehouse Support Specialist
ShipBob, Inc. —Abingdon
- Full-time
- English
- IT
- In-person
Quick apply
Associate Quality and Systems Manager – (Asbestos, Fire & Water)
Tetra Tech —Abingdon
- Hybrid work
- Travel
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7d
Senior Support Worker - Mental Health Lead
Homeless Oxfordshire —Oxford
- £30,385 a year
- Weekend availability
- In-person
- Paid training
- Health & wellbeing programme
Quick apply
Associate Analyst, RFP
Invesco —Henley on Thames
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
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System Test Technician
OrganOx —Oxford
- Full-time
- Azure
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Quick apply
7d
Associate Director - Head of Trend & Change
Mace —Reading
- Full-time
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- Microsoft Office
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Quantity Surveyor
Leda Group —Oxford
- £70,000 - £80,000 a year
- Full-time
- Contracts
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- In-person
Quick apply
1d
Senior Surveyor/Associate | Compulsory Purchase & Compensation
Knight Frank —Hendred
- Full-time
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Pensions Administrator
XPS Pensions Group —Reading
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Employee discount
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14d
Senior Production Quality Engineer
Oxford Nanopore Technologies —Oxford
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Senior Machine Learning Scientist
AIOI NISSAY DOWA INSURANCE MANAGEMENT LIMITED (ANDIM) —Oxford
- Azure
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Production Supervisor
Legrand Group —Reading
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
Quick apply
Clinical Practice Educator
Oxford University Hospitals NHS Foundation Trust —Headington
- £39,959 - £48,117 a year
- Full-time
- Mentoring
5d
Associate Dentist
Dentopedia Group —Dorchester
- Part-time
Quick apply

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Quality Associate II, Quality Assurance

Replimune -
Abingdon

Quick apply

Job details

Full-time
2 days ago

Qualifications

Microsoft Office
Master's degree
Bachelor's degree
IT
Root cause analysis
Communication skills
Time management

Full job description

Overview

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it.

At Replimune, we live by our values:

United: We Collaborate for a Common Goal.

Audacious: We Are Bold.

Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other.

People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.

Join us, as we reshape the future.

Summary of job description:

This position will be required to interact with all departments within the company and to proactively support GMP compliance. The role provides an opportunity to enhance quality skills and experience within a GMP environment.

This position is based in our Milton Park location and typically has a 5-day on-site expectation.

Key responsibilities:

Provide support for the day-to-day operation of the Quality Assurance department to ensure the implementation and maintenance of Quality Management System (QMS) in accordance with applicable standards established by MHRA, EMA, FDA and other regulatory bodies.
Assist and perform batch review for GMP lots, in support of Qualified Person release including final Quality Review of associated quality records. Prioritize batch release in support of business needs including maintaining batch release status and communicate release needs throughout the organization.
Assist with the oversight of Replimune GMP compliance and Quality systems: Change control, Deviation, and Corrective and Preventive actions (CAPA).
Assist thorough root cause analysis (RCA) investigations related to quality issues.
Review and approve Standard Operating Procedures (SOPs), Deviations, CAPAs, Validation Protocols/Reports, Testing Records and CoAs, ensuring internal and external standards are met.
Conduct routine compliance oversight activities e.g. facility/laboratory walkarounds.
Assist in tracking and populating QMS metrics.
Interface and provide support to internal customers in Product Development, Quality Control Labs, etc., and, as appropriate, with external vendors to support ongoing compliance with Replimune requirements and quality standards.
Prepare and issue controlled logbooks for internal customers.
Archive and retrieval of documentation.

Other responsibilities

Drafts, reviews, provides oversight to content, and approves controlled documents which may include but is not limited to standard operating procedures, validation documents, material specifications, etc.
Work cross functionally with Quality Assurance, Quality Control, Regulatory and Clinical groups to support Replimune Clinical and Commercial operations.
Other duties as assigned.

Educational requirements:

A minimum of a bachelor’s degree (BSc or equivalent).
Masters preferred.

Experience and skill requirement:

2 years’ experience in relevant Quality Systems in a regulated biotechnology or pharmaceutical industry environment.
High level of attention to details and excellent time management.
Strong written and verbal communication skills to interact with other functions.
IT skills – competent in using Microsoft Office.
An interest in pharmaceutical Quality Assurance.
A level of flexibility is essential to meet varying workloads.

About Replimune

Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.

We are an Equal Opportunity Employer.

Quick apply

Refine Your Search

quality control associate jobs in grove, oxf

Quality Associate II, Quality Assurance

Associate Software Engineer

Quality Documentation Technician

Nursing Associate

Associate Engineer, GxP IT Support

Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

Onsite Warehouse Support Specialist

Associate Quality and Systems Manager – (Asbestos, Fire & Water)

Senior Support Worker - Mental Health Lead

Associate Analyst, RFP

System Test Technician

Associate Director - Head of Trend & Change

Quantity Surveyor

Senior Surveyor/Associate | Compulsory Purchase & Compensation

Pensions Administrator

Senior Production Quality Engineer

Senior Machine Learning Scientist

Production Supervisor

Clinical Practice Educator

Associate Dentist

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