Analytical validation manager Work, Jobs in Canary Wharf, Gtl (with Salaries)

QA Executive
Crescent Pharma —Park Royal
- £30,000 - £35,000 a year
- Full-time
- Microsoft Office
- Continuous improvement
- Quality control
- Free parking
- Life insurance
Quick apply
2d
Technology Innovation – Senior Consultant/Associate/Engagement Manager – London
Oliver Wyman —London
- Full-time
- Data analysis skills
- English
- Analysis skills
Senior Technical Project Manager - SDLC - Fintech
Wealth Dynamix —London
- Full-time
- Hybrid work
- Conflict management
- Organisational skills
- Communication skills
Quick apply
Quality Lab Manager
Tropic Skincare —Croydon
- £45,000 - £50,000 a year
- Monday to Friday
- Hybrid work
- Engineering
- Bachelor's degree
- Continuous improvement
- Employee assistance programme
- Employee discount
Quick apply
Project Manager
CPC Technologies LLC —Canary Wharf
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Analysis skills
Model Validation Analyst - AI Trainer - Freelance - 8-20 hrs/week - Remote
10x Team —London
- £84 - £156 an hour
- Remote
Quick apply
Global Payroll & EOR Onboarding Implementation Manager
Papaya Global —London
- Full-time
- Analysis skills
- Bachelor's degree
- No degree
Quick apply
Manager, Validation Team - 18 month FTC
Lloyd's of London —Chatham
- Full-time
- Analysis skills
- Continuous improvement
- Team management
1d
Sustainability & ESG Manager
Tait —London
- Full-time
- Continuous improvement
- Mentoring
- Communication skills
Regulatory Affairs & Quality Manager – Medical Devices / IVD
Mitra Bio —London
- Full-time
8d
Consumer Insights Manager - Innovation and Campaign Development (mat cover FTC)
Anglo American / De Beers Group —London
- Full-time
- Leadership
- Annual leave
- Employee assistance programme
11d
Team Leader, Pilot Plant Support and Analytical Equipment Validation
GlaxoSmithKline —Ware
- Full-time
- Hybrid work
- In-person
- Leadership
12d
Higher Scientist - £37,456-£42,084 p.a. + benefits
Medicines and Healthcare Products Regulatory Agency —South Mimms
- £37,456 - £42,084 a year
- Full-time
- Laboratory experience
- Presentation skills
- No degree
- Annual leave
- Sick pay
11d
Researcher – Data Center Infrastructure & Technology Impact
Schneider Electric —South East London
- Full-time
- Hybrid work
- Engineering
- Master's degree
- Analysis skills
Business Analyst - Supplier Data Cleansing
Vantage Point —London
- Full-time
- Hybrid work
- Analysis skills
- Communication skills
IT Network Manager
Indra Group UK & Ireland —Redhill
- Continuous improvement
- Organisational skills
- Leadership
- Work from home
- Employee assistance programme
Quick apply
Reporting Manager - Controls & Reporting team
STACK Infrastructure EMEA Limited —London
- Full-time
- Hybrid work
- Data analysis skills
- Analysis skills
- Continuous improvement
Quick apply
Global Incentives Programme Manager
M3EU —London
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Organisational skills
- Annual leave
- Employee discount
Quick apply
Compliance Senior Analyst - Temporary
Boston Consulting Group —London
- Full-time
- Microsoft Powerpoint
- English
- Analysis skills
Business Analyst / Project Manager – CRM(+) 12 months / 18 months Fixed Term Contract
WildBrain CPLG —London
- Full-time
- Hybrid work
- CRM software
Quick apply

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QA Executive

Crescent Pharma -
Park Royal

Quick apply

Job details

Permanent | Full-time
£30,000 - £35,000 a year
2 days ago

Benefits

Free parking
Life insurance
On-site parking

Qualifications

Document control
Non-conformance investigation
Quality management change control procedures
Internal quality management system auditing
Quality control within general manufacturing industry
Microsoft Office Suite
Complaint handling
Microsoft Office
Quality assurance
Continuous improvement
Quality control
Environmental monitoring
Document control software
Supply chain quality assurance
Pharmaceutical industry setting experience
Communication skills
Internal quality assurance

Full job description

About Crescent Manufacturing

Crescent Manufacturing is part of the Crescent Pharmaceutical Group, an independent UK pharmaceutical business supplying generic medicines to the NHS and international markets. We hold an MHRA Manufacturer's Licence and operate to full EU GMP standards, manufacturing and packaging licensed medicines for Crescent Pharma and third-party Marketing Authorisation Holders.

We are a close-knit, hands-on team where quality is everybody's business. This is a role where you will see the whole picture – from raw material sampling on the production floor to the batch paperwork that lets a Qualified Person certify a product for release.

The role

You will support the Quality Manager and our Qualified Persons in maintaining and improving the site Quality Management System. The role is a genuine mix of desk-based QA and practical in-process work, so you will split your time between reviewing and compiling batch documentation and carrying out testing, sampling and monitoring within production.

What you will be doing

Batch documentation and release

Review batch manufacturing, packaging and testing records for compliance with approved procedures and the product licence, and compile release packs for submission to the MAH
Manage the archiving of QMS documentation, retained samples and batch release paperwork in line with company procedures and regulatory requirements

Quality systems

Write and review Deviation Reports, investigations and CAPAs, and report outcomes to the MAH
Investigate customer complaints and report findings back to the MAH
Ensure changes are raised through Change Control and fully implemented, with all supporting activities completed
Support regulatory variations by preparing data packages and reports
Help maintain the site Documentation System, and write and revise SOPs covering GxP activities
Prepare Product Quality Review (PQR) reports
Create, review and approve validation protocols and reports (process, analytical, equipment and systems)
Record and report Quality department KPIs

Audit and inspection

Take part in the internal audit programme
Support audits of Crescent Manufacturing suppliers and sub-contractors, in the UK and overseas
Support MHRA and customer inspections of the site

In-process quality (production floor)

Perform periodic in-process checks within the production department
Sample raw materials
Carry out environmental monitoring

General

Deliver GxP training as requested, in line with internal training policy
Contribute to project work and continuous improvement initiatives
Plan and prioritise your own workload to meet agreed timelines and departmental objectives

Who you will work with

Internally: QA, Production, Supply Chain and Planning, Customer Services and Warehouse teams
Externally: Marketing Authorisation Holders and QP consultants

What we are looking for

Essential

Degree (or equivalent) in a scientific discipline – Chemistry, Pharmacy, Biochemistry, Microbiology or Biology preferred
Good attention to detail and the discipline to follow defined procedures and regulatory guidelines
Self-motivated and well organised, able to work on your own initiative and as part of a team
Effective time management and a flexible approach to shifting priorities
Strong interpersonal and written communication skills
Confident with Microsoft Office (Excel, Word, PowerPoint, Outlook)

Desirable

5 years Experience in a GMP-regulated pharmaceutical environment (QA, QC or production)
Working knowledge of EU GMP, deviation and CAPA management, or validation
Familiarity with electronic QMS or document management systems

What we offer

£30,000 - £35,000
25 days Holiday Entitlement
Broad exposure across the full GMP quality lifecycle at an owner-led, growing pharmaceutical group

How to apply

Please send your CV and a short covering note to [email / application link]. We review applications as they arrive and may close the advert early if we find the right candidate.

How we handle your data

CVs submitted in response to this advert will be shared with relevant staff within the Crescent Group for shortlisting. Your CV may be retained on our system until the vacancy is filled. If you attend an interview, any interview notes or test results will be retained alongside your CV as part of your personnel record should you join us. If you are not offered a position, these records will be deleted six months after the campaign closes, in line with our retention policy.

You have the right to access, rectify and restrict processing of your personal data, and in some cases to request erasure or data portability. To exercise these rights, please contact us via the Contact Us page on our website, quoting "Personal data" in the subject line.

Job Types: Full-time, Permanent

Pay: £30,000.00-£35,000.00 per year

Benefits:

Free parking
Life insurance
On-site parking

Experience:

Quality Assurance: 4 years (preferred)

Work Location: In person

Quick apply

Refine Your Search

analytical validation manager jobs in canary wharf, gtl

QA Executive

Technology Innovation – Senior Consultant/Associate/Engagement Manager – London

Senior Technical Project Manager - SDLC - Fintech

Quality Lab Manager

Project Manager

Model Validation Analyst - AI Trainer - Freelance - 8-20 hrs/week - Remote

Global Payroll & EOR Onboarding Implementation Manager

Manager, Validation Team - 18 month FTC

Sustainability & ESG Manager

Regulatory Affairs & Quality Manager – Medical Devices / IVD

Consumer Insights Manager - Innovation and Campaign Development (mat cover FTC)

Team Leader, Pilot Plant Support and Analytical Equipment Validation

Higher Scientist - £37,456-£42,084 p.a. + benefits

Researcher – Data Center Infrastructure & Technology Impact

Business Analyst - Supplier Data Cleansing

IT Network Manager

Reporting Manager - Controls & Reporting team

Global Incentives Programme Manager

Compliance Senior Analyst - Temporary

Business Analyst / Project Manager – CRM(+) 12 months / 18 months Fixed Term Contract

I want to receive the latest job alerts for analytical validation manager in canary wharf, gtl

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