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

Quality Associate II, Quality Assurance
Replimune —Abingdon
- Full-time
- Master's degree
- Bachelor's degree
- Computer skills
Quick apply
Research Associate, Assay Development
OraSure Technologies Inc. —Oxford
- £20,000 - £36,000 a year
- Full-time
- Hybrid work
- Laboratory experience
- Analysis skills
- Bachelor's degree
- Annual leave
- Employee assistance programme
Quick apply
12d
Quality Documentation Technician
Becton Dickinson —Swindon
- SharePoint
- Communication skills
Quick apply
Casual Support Worker
Homeless Oxfordshire —Oxford
- £14.06 an hour
- Weekend availability
- In-person
- Store discount
- Health & wellbeing programme
Quick apply
12d
Quality Control Inspector
ZeroAvia —Kemble
- Full-time
- English
- Bachelor's degree
- Quality control
- Employee assistance programme
Quick apply
Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays
Moderna, Inc. —Oxford
- Full-time
- Bachelor's degree
- Communication skills
- Annual leave
Associate Director, Quality Assurance
Immunocore —Oxford
- Full-time
- Microsoft Word
- Bachelor's degree
- Continuous improvement
4d
Senior Production Quality Engineer
Oxford Nanopore Technologies —Oxford
- Full-time
- Engineering
- Continuous improvement
- Quality control
Senior Machine Learning Scientist
AIOI NISSAY DOWA INSURANCE MANAGEMENT LIMITED (ANDIM) —Oxford
- Doctoral degree
- Computer Science
- Research
- Annual leave
- Employee assistance programme
Onsite Warehouse Support Specialist
ShipBob, Inc. —Abingdon
- Full-time
- English
- Continuous improvement
- In-person
Quick apply
Nursing Associate
Hedena Health (Bury Knowle Health Centre) —Headington
- Part-time
- Employee discount
Quick apply
13d
Test Technician - Systems Engineering
OrganOx —Oxford
- Full-time
- Schematics
- Engineering
- Bachelor's degree
Quick apply
Associate Principal Embedded Software Engineer
Dyson —Malmesbury
- Engineering
- Laboratory experience
- English
- Employee assistance programme
- Employee discount
Associate Software Engineer
Halliburton —Abingdon
- Full-time
- Computer Science
- Engineering
- No experience needed
Specialist in Geriatric Medicine
Great Western Hospitals NHS Foundation Trust —Swindon
- £104,401 - £115,341 a year
- Full-time
- Team management
- Training & development
- Teaching
3d

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Research Associate, Assay Development
OraSure Technologies Inc. —Oxford
Perform assay-development activities such as PCR, RT-PCR, isothermal amplification setup, primer-mix preparation, nucleic acid handling, target addition, serial…
£20,000 - £36,000 a year
Quick apply
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Research Fellow– Preventing mental health issues in ethnically diverse youth: A feasibility pilot study (PRIMA)
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Please note that if not already an employee of the University of Worcester, the appointed candidate will be employed through our subsidiary company Uniworc…
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Quality Associate II, Quality Assurance

Replimune -
Abingdon

Quick apply

Job details

Full-time

Qualifications

Document control
Non-conformance investigation
Stakeholder collaboration
Quality management change control procedures
Internal department liaison
Microsoft Office Suite
Master's degree
Quality assurance
Bachelor's degree
Computer skills
Multidisciplinary collaboration
Root cause analysis
Communication skills
Internal quality assurance
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 watchfield, oxf

Quality Associate II, Quality Assurance

Research Associate, Assay Development

Quality Documentation Technician

Casual Support Worker

Quality Control Inspector

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

Associate Director, Quality Assurance

Senior Production Quality Engineer

Senior Machine Learning Scientist

Onsite Warehouse Support Specialist

Nursing Associate

Test Technician - Systems Engineering

Associate Principal Embedded Software Engineer

Associate Software Engineer

Specialist in Geriatric Medicine

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