Quality assurance associate Work, Jobs in Curridge, Brk (with Salaries)

Quality Associate II, Quality Assurance
Replimune —Abingdon
- Full-time
- Master's degree
- Bachelor's degree
- Computer skills
Quick apply
Associate Clinical Project Manager - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Leadership
- Work from home
Casual Support Worker
Homeless Oxfordshire —Oxford
- £14.06 an hour
- Weekend availability
- In-person
- Store discount
- Health & wellbeing programme
Quick apply
11d
Internal Operations Auditor Associate (Lettings & Legislation)
LRG —Camberley
- Remote
- Administrative experience
- Communication skills
Quick apply
Quality Assurance Technician - Weekend Days
Rich Products Corporation —Andover
- Weekend availability
- Bakery
- Quality control
- Annual leave
Quality Assurance Technician - Weekend Nights
Rich Products Corporation —Andover
- 12 hour shift
- Bakery
- Quality control
- Annual leave
Quality Analyst (6 months temporary role)
South East Water —Farnborough
- £32,884 a year
- Full-time
- Computer literacy
- Laboratory experience
- Analysis skills
- Annual leave
9d
PLOS One Associate Editor- 12 Month FTC
Public Library of Science —Oxford
- £35,000 - £38,950 a year
- Remote
- Doctoral degree
- Research
- Travel
1d
FS&QA Administrator
Rich Products Corporation —Andover
- Analysis skills
- Bakery
- Annual leave
Pensions Administrator
XPS Pensions Group —Reading
- Full-time
- Quality control
- Mentoring
- Employee discount
- Referral programme
Senior Laboratory Services Analyst
South East Water —Farnborough
- Up to £36,493 a year
- Weekend availability
- Team management
- Mentoring
- Annual leave
Chemistry Technician
South East Water —Farnborough
- £25,948.87 a year
- Full-time
- Computer literacy
- No degree
- Quality control
- Annual leave
8d
(Fixed-Term) Manufacturing Associate I
Moderna, Inc. —Oxford
- 12 hour shift
- Bachelor's degree
- Continuous improvement
- No degree
- Annual leave
13d
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Reading
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Business development
Associate Project Manager
AECOM —Oxford
- Full-time
- Hybrid work
- Management
- Engineering
- Business development
8d
Water Safety Plan Scientist
South East Water —Farnborough
- Up to £41,930 a year
- Full-time
- Hybrid work
- Analysis skills
- Communication skills
- Annual leave
3d
(Fixed Term) Manufacturing Associate I
Moderna, Inc. —Oxford
- 12 hour shift
- Bachelor's degree
- Continuous improvement
- No degree
- Annual leave
13d
Associate Director, Quality Assurance
Immunocore —Oxford
- Full-time
- Microsoft Word
- Bachelor's degree
- Continuous improvement
3d
Associate Director - Nuclear Safety
Tetra tech Ltd. —Basingstoke
- Hybrid work
- Engineering
- Business development
- Analysis skills
Quick apply
4d
Associate Director - Nuclear Safety
Tetra Tech —Abingdon
- Hybrid work
- Engineering
- Business development
- Analysis skills

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quality assurance associate jobs near curridge, brk

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 assurance associate jobs in curridge, brk

Quality Associate II, Quality Assurance

Associate Clinical Project Manager - Sponsor Dedicated

Casual Support Worker

Internal Operations Auditor Associate (Lettings & Legislation)

Quality Assurance Technician - Weekend Days

Quality Assurance Technician - Weekend Nights

Quality Analyst (6 months temporary role)

PLOS One Associate Editor- 12 Month FTC

FS&QA Administrator

Pensions Administrator

Senior Laboratory Services Analyst

Chemistry Technician

(Fixed-Term) Manufacturing Associate I

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Associate Project Manager

Water Safety Plan Scientist

(Fixed Term) Manufacturing Associate I

Associate Director, Quality Assurance

Associate Director - Nuclear Safety

Associate Director - Nuclear Safety

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