Distribution associate Work, Jobs in Wokingham, Brk (with Salaries)

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
Marketing Associate
IRISH DISTILLERS PERNOD RICARD —London
- Hospitality
- Sales
- Marketing
Quick apply
5d
Retail Associate
TK Maxx —Bracknell
- Part-time
- No experience needed
- Employee discount
2d
Warehouse Associate
Montu UK —Winnersh
- £30,000 - £32,000 a year
- Full-time
- Warehouse experience
- Communication skills
Quick apply
4d
Retail Associate
Homesense —Farnborough
- Part-time
- No experience needed
- Employee discount
Retail Associate
TK Maxx —Maidenhead
- Part-time
- No experience needed
- Employee discount
4d
Retail Associate
TK Maxx —Woking
- Part-time
- No experience needed
- Employee discount
2h
Retail Associate
TK Maxx —Weybridge
- Part-time
- No experience needed
- Employee discount
7d
Clinical Trial Supplies Associate ** Farnborough, UK **
Syneos - Clinical and Corporate - Prod —Farnborough
- Full-time
- English
- Microsoft Office
- Travel
Clinical Trial Supplies Associate ** Farnborough, UK **
サイネオス・ヘルス —Farnborough
- English
- Microsoft Office
- Travel
National Account Manager
SC Johnson Lifestyle Brands —Frimley
- Full-time
- Microsoft Powerpoint
- Sales
- In-person
- Flexible schedule
SALES ACCOUNT MANAGER – GROCERY (Maternity Cover)
SC Johnson Lifestyle Brands —Frimley
- Full-time
- Hybrid work
- Sales
- Analysis skills
- Presentation skills
- Flexible schedule
B2B Account Manager - Private Ecosystem
Eli Lilly —Basingstoke
- Full-time
- Hybrid work
- Sales
- Travel
- Leadership
8d
Compliance Administrator
Active Care Group —Thame
- £28 - £30 an hour
- Full-time
- Microsoft Outlook
- Administrative experience
- Organisational skills
Quick apply
10d
Reservoir Programme Lead
South East Water —Aldershot
- £38,498.00 - £50,971.50 a year
- Full-time
- Customer service
- Project management
- Continuous improvement
- Annual leave
9d
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International —Marlow
- £66,814 - £134,641 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
Quick apply
IT Asset Management Associate
HighPoint —Greenford
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Microsoft Office
13d
Global Logistics Associate
HighPoint —Greenford
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Microsoft Office
13d
Customer Activation Manager - Functional Bars, Clif
Mondelēz International —Uxbridge
- Full-time
- Marketing
10d

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Associate Director Global CMC QU – Clinical GMP/GDP

Kyowa Kirin International plc -
Marlow

Apply Now

Job details

Permanent | Full-time
£80,000 - £140,000 a year

Qualifications

Bachelor's degree
Leadership

Full job description

Overview

Associate Director Global CMC QU – Clinical GMP/GDP

at Kyowa Kirin International plc

Marlow, UK or Hoofddorp, Netherlands

WE PUSH THE BOUNDARIES OF MEDICINE.

LEAPING FORWARD TO MAKE PEOPLE SMILE

At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. We’re an inclusive pharmaceutical company that takes time to understand what really matters to our patients, their families, and their healthcare professionals, helping our people to take bold actions that deliver life-changing solutions sooner. Our culture is rooted in our values: Teamwork, Commitment to Life, Innovation, and Integrity. They help us to push boundaries to deliver extraordinary impact and make KKI a brilliant place to work.

Job Purpose

You will be responsible for providing end-to-end quality oversight of clinical investigational medicinal products (IMPs) in accordance with EU GMP (EudraLex Volume 4), including Annex 13, and EU GDP Guidelines (2013/C 343/01)

The role provides independent QA oversight and regulatory support to EU Qualified Persons (QPs), ensuring that certification and release of investigational medicinal products is performed in compliance with EU legal and regulatory requirements. The position maintains quality oversight of CDMOs, packaging sites, laboratories, and Third-Party Logistics providers (3PLs) involved in the manufacture, storage, and distribution of clinical trial material (CTM)

Responsibilities

Key Responsibilities:

Provide QA oversight of clinical IMP manufacturing, packaging, testing, release, and distribution activities
Support EU Qualified Person (QP) certification and batch release processes
Ensure compliance with EU GMP Annex 13 requirements, including labeling, traceability, accountability, and retention samples
Review and approve GMP documentation, including batch records, CoAs, deviations, investigations, and quality events
Lead QA support for clinical technology transfers, process start-ups, and product lifecycle activities
Provide quality oversight of clinical supply chain operations, including transportation, temperature-controlled logistics, and distribution
Ensure clinical trial materials remain fully traceable throughout the supply chain.
Manage Quality Technical Agreements (QTAs) with CDMOs, laboratories, distribution partners, and 3PL providers
Plan, conduct, and support risk-based GMP and GDP audits of external partners.
Support regulatory submissions, inspections, and health authority interactions
Author, review, and maintain Clinical GMP/GDP procedures and quality system documentation
Ensure compliance with data integrity requirements, including EU GMP Annex 11 and ALCOA+ principles

Qualifications

Position Requirements:

Bachelor’s degree in a relevant scientific/technical discipline or equivalent experience in the pharmaceutical industry
Solid leadership experience within Pharmaceutical Quality in the pharmaceutical Industry, with significant exposure to EU Clinical GMP and GDP
Prior experience working with a Qualified Person (QP) responsible for investigational medicinal products, as well as experience in batch disposition (release), is preferred for success in this position
Strong knowledge of EU GMP (EudraLex Volume 4, Annex 13) and EU GDP Guidelines
Experience with biologics and/or small molecule clinical products.
Demonstrated ability to assess quality and regulatory risk and provide sound compliance judgments
Experience in QA, QC, auditing, or regulatory affairs within a clinical development environment

UK salary - £80,000-121,000

Netherlands salary - €93,000-140,000

Apply Now

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distribution associate jobs in wokingham, brk

Associate Director Global CMC QU – Clinical GMP/GDP

Marketing Associate

Retail Associate

Warehouse Associate

Retail Associate

Retail Associate

Retail Associate

Retail Associate

Clinical Trial Supplies Associate Farnborough, UK

Clinical Trial Supplies Associate Farnborough, UK

National Account Manager

SALES ACCOUNT MANAGER – GROCERY (Maternity Cover)

B2B Account Manager - Private Ecosystem

Compliance Administrator

Reservoir Programme Lead

Associate Director Global CMC QU – Clinical GMP/GDP

IT Asset Management Associate

Global Logistics Associate

Customer Activation Manager - Functional Bars, Clif

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