Quality assurance Work, Jobs in Kidlington, Oxf (with Salaries)

Quality Associate II, Quality Assurance
Replimune —Abingdon
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
Quick apply
Quality Assurance Officer I
Replimune —Abingdon
- Full-time
- Master's degree
- Bachelor's degree
- Computer skills
Quick apply
Quality Improvement Officer
OXFORDSHIRE COUNTY COUNCIL —Oxford
- £41,771 - £45,091 a year
- Part-time
- Continuous improvement
- Contracts
- Annual leave
- Employee assistance programme
8d
Quality Assurance Technical Officer
University of Oxford —Oxford
- £39,424 - £51,983 a year
- Full-time
- Laboratory experience
SVP Regulatory Affairs & Quality Assurance
PrecisionLife Ltd —Oxford
- £85,000 - £105,000 a year
- Full-time
- Hybrid work
- Doctoral degree
- Computer Science
- Engineering
- Free parking
- Annual leave
Quick apply
6d
QA Releaser
Baxter —Oxford
- Full-time
- English
- Microsoft Office
- Time management
- Annual leave
Quality Control Chemist
Biosynth Carbosynth —Newbury
- £28,000 - £29,000 a year
- Full-time
- Computer literacy
- Laboratory experience
- Bachelor's degree
- Free parking
- Sick pay
Quick apply
13d
Quality Assurance Engineer
MDA —Didcot
- Full-time
- Hybrid work
- Engineering
- Analysis skills
- Bachelor's degree
- Employee assistance programme
- Life insurance
QA Test Analyst
Bibby Financial Services —Banbury
- £40,000 - £46,000 a year
- Full-time
- Agile
- Gym membership
Quick apply
3d
QA Specialist W&D
ASID BONZ GmbH —Bicester
- Microsoft Word
- Bachelor's degree
- Continuous improvement
- Employee assistance programme
- Life insurance
10d
Senior QA Analyst - Fixed-Term Contract
Rebellion —Oxford
- In-person
- Employee assistance programme
- Employee discount
Quick apply
QA Coordinator (12 months fixed term contract)
Bio-Techne —Abingdon
- £34,400 - £55,120 a year
- Full-time
- English
- Bachelor's degree
- Business
- Employee stock purchase plan
9d
Quality Engineer (Medical Devices)
Amber Therapeutics —Didcot
- Full-time
- Hybrid work
- Engineering
- Quality control
- Communication skills
Quick apply
QA Officer
Vantive —Newbury
- Monday to Friday
- Continuous improvement
Associate Quality and Systems Manager – (Asbestos, Fire & Water)
Tetra Tech —Abingdon
- Hybrid work
- Travel
- Leadership
QA Engineer
GRIFFIN —Oxford
- Maintenance
QA Automation Engineer
RM Education Limited —Abingdon
- Hybrid work
- Contracts
- APIs
- Agile
- Annual leave
Quality Engineer
ALTEN —Banbury
- £35,000 - £50,000 a year
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Employee assistance programme
- Life insurance
Quick apply
1d
Quality Lead
Active Care Group —Thame
- £35,000 - £40,000 a year
- Full-time
- Analysis skills
- Continuous improvement
- Training & development
- Employee assistance programme
- Referral programme
Quick apply
Senior Production Quality Engineer
Oxford Nanopore Technologies —Oxford
- Full-time
- Engineering

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quality assurance jobs near kidlington, oxf

Quality Associate II, Quality Assurance

Replimune -
Abingdon

Quick apply

Job details

Full-time

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 assurance jobs in kidlington, oxf

Quality Associate II, Quality Assurance

Quality Assurance Officer I

Quality Improvement Officer

Quality Assurance Technical Officer

SVP Regulatory Affairs & Quality Assurance

QA Releaser

Quality Control Chemist

Quality Assurance Engineer

QA Test Analyst

QA Specialist W&D

Senior QA Analyst - Fixed-Term Contract

QA Coordinator (12 months fixed term contract)

Quality Engineer (Medical Devices)

QA Officer

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

QA Engineer

QA Automation Engineer

Quality Engineer

Quality Lead

Senior Production Quality Engineer

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