Pharmaceutical manufacturing Work, Jobs in Chipping Norton, Oxf (with Salaries)

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Quality Assurance Officer I
Replimune —Abingdon
- Full-time
- Master's degree
- Bachelor's degree
- Computer skills
Quick apply
14d
Quality Assurance Officer II
Replimune —Abingdon
- Full-time
- Master's degree
- Bachelor's degree
- Computer skills
Quick apply
Junior QA Officer (Double Days shift)
Thermo Fisher Scientific —Swindon
- Full-time
- Organisational skills
- Time management
(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position
Moderna, Inc. —Oxford
- Overtime
- Bachelor's degree
- No degree
- Organisational skills
- Annual leave
(Fixed-Term) Manufacturing Associate II - Shift Position
Moderna, Inc. —Oxford
- 12 hour shift
- Bachelor's degree
- No degree
- Organisational skills
- Annual leave
GMP Cleaner
MICRONCLEAN LIMITED —Oxford
- £13.45 - £13.95 an hour
- Part-time
- Computer literacy
- English
- Cleaning
- Profit sharing
- Health & wellbeing programme
13d
Senior Scientist I – Biocompatibility
Abbott Laboratories —Witney
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
Process Engineer - Consumables
Refeyn Ltd —Oxford
- £43,000 - £54,000 a year
- Engineering
- Analysis skills
- Continuous improvement
- Annual leave
- Life insurance
Quick apply
6d
Technician, Production
Baxter —Oxford
- Full-time
- Communication skills
SVP Head of Global EHS (all genders)
Evotec —Abingdon
- Full-time
- Engineering
- English
- Master's degree
Supply Chain Specialist II (12 months Fixed Term)
Thermo Fisher Scientific —Swindon
- Full-time
- Engineering
- Master's degree
- Analysis skills
ESMU Assembly Fitter
Spirax Sarco —Cheltenham
- Computer literacy
- Assembly
- Continuous improvement
- Free parking
- Annual leave
5d
Statistics & Analysis Manager
Abbott Laboratories —Witney
- Full-time
- Team management
- Training & development
- Leadership
4d
Senior Manager, Quality (Sterility Assurance)
Thermo Fisher Scientific —Swindon
- Full-time
- Bachelor's degree
- Continuous improvement
- Communication skills
16h
Account Manager
Equans —Oxford
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
- Employee assistance programme
Vision Systems Engineer
Abbott Laboratories —Witney
- Full-time
- Engineering
- Maintenance
- Programmable logic controllers
Technical Support Engineer - Operations
Thermo Fisher Scientific —Swindon
- Full-time
- Maintenance
- Analysis skills
- Continuous improvement
Production Manager
Voy —Wallingford
- Weekend availability
- Inventory control
- Computer literacy
- Supervising experience
Quick apply
5d
Sourcing and Supply Chain Manager
Matcon Limited —Evesham
- Full-time
- Management
- Up to 50% travel
- Engineering
HSE & Maintenance Manager
BVI Medical —Bidford
- Full-time
- Continuous improvement
- Team management
- Training & development
1d

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pharmaceutical manufacturing jobs near chipping norton, oxf

Quality Assurance Officer I

Replimune -
Abingdon

Quick apply

Job details

Full-time
14 days ago

Qualifications

Document control
Non-conformance investigation
Stakeholder collaboration
Quality management change control procedures
Internal quality management system auditing
Compliance audits
Internal department liaison
Microsoft Office Suite
Master's degree
Quality assurance
Bachelor's degree
Computer skills
Multidisciplinary collaboration
Supplier quality management
Supply chain quality assurance
Root cause analysis
Quality management system (QMS) implementation
Communication skills
Internal quality assurance
Corporate regulatory compliance oversight
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:

The Quality Assurance Officer I provides guidance and coordination in the development, implementation and maintenance of Quality Assurance systems and activities at Replimune. Manages batch review to ensure timely release of drug product for clinical and commercial use. Ensures relevant quality and regulatory requirements are met for manufacturing and testing and ensures site compliance with quality system regulations issued by MHRA, EMA, FDA and other applicable regulatory bodies. Responsible for the evaluation and assurance that appropriate quality systems are in place at approved vendors and suppliers supporting GXP.

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

Key responsibilities:

Work cross functionally with Quality Assurance, Quality Control, Regulatory and Clinical groups to ensure inspection readiness. Provide QA input and approvals to assist in and drive projects as needed.
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.
Drive improvement of Replimune GMP compliance and Quality systems: change control, deviation, and corrective and preventive action (CAPA) systems including support of thorough root cause analysis investigations related to quality issues.
Possess strong writing skills to utilize best practices in documenting deviations in records and associated reports.
Collect and report quality metrics supporting Quality Management Review (QMR) deliverables.
Review and approve Standard Operating Procedures (SOPs), Validation Protocols / Reports, GMP records, Testing Records and other records generated by the site ensuring internal and external standards are met.
Interface and provide support to internal customers.
Lead and participate in Risk assessments.
Conduct trainings as needed (change control, batch release, risk assessment methodology, etc.).
Conduct routine compliance oversight activities e.g. facility/laboratory walkarounds.
Take part in Replimune internal and external audit program. Lead and direct audits of GMP materials and service providers.
Interface with 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.
Ability to prepare slides and provide training to staff in applicable procedures.
Prepare and issue controlled logbooks for internal customers.
Archive and retrieval of documentation.

Other responsibilities

Support Replimune QA activities.
Drafts, reviews, provides oversight to content, and approves controlled documents which may include but are 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:

4 years’ experience in relevant Quality Systems, technology and/or supervision in a regulated biotechnology or pharmaceutical industry environment.
GxP experience, including auditing.
Knowledge of MHRA, EMA and MHRA guidelines regarding GMPs.
Excellent verbal and written communication skills to interact with other functions.
High level of attention to details and excellent time management.
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

pharmaceutical manufacturing jobs in chipping norton, oxf

Quality Assurance Officer I

Quality Assurance Officer II

Junior QA Officer (Double Days shift)

(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position

(Fixed-Term) Manufacturing Associate II - Shift Position

GMP Cleaner

Senior Scientist I – Biocompatibility

Process Engineer - Consumables

Technician, Production

SVP Head of Global EHS (all genders)

Supply Chain Specialist II (12 months Fixed Term)

ESMU Assembly Fitter

Statistics & Analysis Manager

Senior Manager, Quality (Sterility Assurance)

Account Manager

Vision Systems Engineer

Technical Support Engineer - Operations

Production Manager

Sourcing and Supply Chain Manager

HSE & Maintenance Manager

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