Associate director, quality assurance Work, Jobs in Abingdon, Oxf (with Salaries)

Quality Associate II, Quality Assurance
Replimune —Abingdon
- Full-time
- Master's degree
- Bachelor's degree
- Computer skills
Quick apply
Quality Assurance Specialist
Science and Technology Facilities Council —Didcot
- £46,444 a year
- Full-time
- Bachelor's degree
- Travel
- In-person
- Employee discount
- Flexible schedule
Associate Director, Quality Assurance
Immunocore —Oxford
- Full-time
- Microsoft Word
- Bachelor's degree
- Continuous improvement
3d
Quality Improvement Officer
OXFORDSHIRE COUNTY COUNCIL —Oxford
- £41,771 - £45,091 a year
- Part-time
- Continuous improvement
- Contracts
- Annual leave
- Employee assistance programme
Quality Assurance Officer II
Replimune —Abingdon
- Full-time
- Master's degree
- Bachelor's degree
- Computer skills
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
Quality Assurance Engineer
MDA Space —Didcot
- Hybrid work
- Engineering
- Analysis skills
- Bachelor's degree
- Employee assistance programme
- Life insurance
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Associate Director - Environmental, Health and Safety (EHS)
Vantive —Newbury
- Remote
- Engineering
- English
- Master's degree
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Director, Medical Affairs (Europe & International)
Immunocore —Oxford
- Management
- Doctoral degree
- Travel
Associate Director, Facilities and Engineering
Replimune —Abingdon
- Full-time
- Microsoft Word
- Computer literacy
- Engineering
Quick apply
Associate Director of Communications and Engagement
Buckinghamshire Healthcare NHS Trust —Aylesbury
- £79,504 - £91,609 a year
- Full-time
- Annual leave
Quality Assurance Manager
University of Oxford —Oxford
- £39,424 a year
- Full-time
- Bachelor's degree
- Annual leave
3d
Quality Assurance Engineer
MDA —Didcot
- Full-time
- Hybrid work
- Engineering
- Analysis skills
- Bachelor's degree
- Employee assistance programme
- Life insurance
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International plc —Marlow
- £80,000 - £140,000 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
Associate Director
AtkinsRéalis —Oxford
- Full-time
- Hybrid work
- Business development
- Mentoring
- Training & development
Associate Director - Nuclear Safety
Tetra Tech —Abingdon
- Hybrid work
- Engineering
- Business development
- Analysis skills
Head of Global Student Recruitment & Associate Director of Global Engagement
University of Reading —Reading
- £59,966 - £67,468 a year
- Full-time
- Business development
- University
- Recruiting
3d
Senior Quality Assurance Manager (Clinical)
Bio Pharma Resourcing —Thames Valley
- £35,000 - £40,000 a year
- Computer literacy
- Travel
- Computer skills

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associate director, quality assurance jobs near abingdon, oxf

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

associate director, quality assurance jobs in abingdon, oxf

Quality Associate II, Quality Assurance

Quality Assurance Specialist

Associate Director, Quality Assurance

Quality Improvement Officer

Quality Assurance Officer II

QA Coordinator (12 months fixed term contract)

Quality Assurance Engineer

Local Study Associate Director

Associate Director - Environmental, Health and Safety (EHS)

Senior Regulatory Affairs Specialist

Director, Medical Affairs (Europe & International)

Associate Director, Facilities and Engineering

Associate Director of Communications and Engagement

Quality Assurance Manager

Quality Assurance Engineer

Associate Director Global CMC QU – Clinical GMP/GDP

Associate Director

Associate Director - Nuclear Safety

Head of Global Student Recruitment & Associate Director of Global Engagement

Senior Quality Assurance Manager (Clinical)

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