Director of program management Work, Jobs in Liverpool, Eng (with Salaries)

Associate Director, CMC Lead – Biologics (12 Month Fixed Term Contract)
Pharmaron —Liverpool
- Doctoral degree
- Master's degree
- Leadership
8d
Director of Homes & Compliance
The Riverside Group —Liverpool
- Full-time
- Continuous improvement
6d
Assistant Director of Building Safety
The Riverside Group —Liverpool
- Full-time
- Leadership
- Communication skills
6d
Associate - Engagement & Consultation
WSP —Liverpool
- Part-time
- Hybrid work
- Management
- Business development
- Organisational skills
- Flexitime
- Work from home
13d
Technical Director, Capture Management Lead – Nuclear
AECOM —Warrington
- Full-time
- Hybrid work
- Sales
- Business development
- Travel
Associate Director of TPM
AstraZeneca —Liverpool
- Monday to Friday
- Maintenance
- Continuous improvement
- Leadership
7d
Senior Manager, Customer Success Engineering
Veeam Software —Liverpool
- Remote
- Leadership
- Annual leave
- Employee assistance programme
Associate Director, Procurement Enablement – ESG, Governance, Training & Development
CSL Behring —Liverpool
- Full-time
- Bachelor's degree
- Training & development
- Business
Business Development Manager (BDM) - Birkenhead - Circa 41k Package- 53k OTE Uncapped
Yell Ltd —Birkenhead
- £35,875 a year
- Full-time
- Business development
- Presentation skills
- Referral programme
Quick apply
Assoc Dir Global Category Manager Devices
Teva —Runcorn
- Communication skills
- Annual leave
Senior Project Manager - Water Sector
AECOM —Liverpool
- Full-time
- Hybrid work
- Engineering
- Business development
- Team management
Consultant
American Bureau of Shipping (ABS) —Warrington
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Data analysis skills
Business Development Manager (BDM) - Liverpool - Circa 41k Package- 53k OTE Uncapped
Yell Ltd —Liverpool
- £35,875 a year
- Full-time
- Business development
- In-person
- Referral programme
Quick apply
Solutions Architect – Marketing Technology
UK, West London, Chiswick —Liverpool
- Full-time
- Annual leave
- Employee assistance programme
7d
Crematorium & Cemetery Assistant
WesterleighGroup —Manchester
- From £26,842 a year
- Weekend availability
- Computer literacy
- Computer skills
- Free parking
- Employee discount
Associate Director – Transport Planning and Advisory
AECOM —Liverpool
- Full-time
- Hybrid work
- Engineering
- Business development
- Business
Digital Marketing Executive
Bellrock Property and Facilities Management —Liverpool
- Hybrid work
- Social media management
- AI
- Health & wellbeing programme
- Annual leave
Quick apply
Project Director - Controls Analytics
AECOM —Liverpool
- Full-time
- Hybrid work
- Engineering
- Business development
- Leadership
International Trade & Customs Manager EMEA
Univar Europe Ltd. —Cadishead
- Hybrid work
- Management
- English
- Communication skills
Trust HR Assistant
The Heath Family Trust —Borough of Halton
- £27,269 - £30,060 a year
- Full-time
- Hybrid work
- Customer service
- Writing skills
- Administrative experience
Quick apply
22h

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director of program management jobs near liverpool, eng

Associate Director, CMC Lead – Biologics (12 Month Fixed Term Contract)

Pharmaron -
Liverpool

Apply Now

Job details

Fixed term contract
8 days ago

Qualifications

Doctoral degree
Stakeholder collaboration
Quality management
Master's degree
Risk management
Multidisciplinary collaboration
Leadership

Full job description

Job Introduction

Position: Associate Director, CMC Lead – Biologics (12 Month Fixed Term Contract)

Location: Liverpool

Pharmaron is a global CRO helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

We’re proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules to biologics and gene therapies, and we work with more than 3,000 global customers. To learn more, visit www.pharmaron.com.

About the Role

We have a new opening for a Associate Director, CMC Lead on a 12 Month Fixed Term Contract to lead the CMC strategy for client programs, ensuring alignment with regulatory expectations and successful progression through development and licensure.

This successful candidate will act as a technical and strategic bridge between customers and functional teams (Process Sciences, Analytical Sciences, Manufacturing) and ensure effective strategy for delivery of client programs both internally and externally also be expected to deliver high-quality consultancy and submission support to both customers and internal teams.

At Pharmaron we offer:

Vibrant and dynamic employment – we are a highly specialised, growth company operating in a critical sector of the economy – our future is strong and exciting!
Opportunities to develop your skills and yourself – our rapid growth brings greater opportunities for you to learn and grow faster!
A great team where we all support each other – enjoy your work – after all you spend about a third of your time here!

Key roles and responsibilities:

Lead CMC strategy for assigned client programs across development stages (early development through to commercialisation).
Responsible for ensuring alignment of development, manufacturing and control strategies with current global regulatory expectations (MHRA, EMA, FDA).
Lead preparation and / or review of CMC regulatory submission dossiers for the customer and review, manage and interpret regulatory guidance and translate into practical development and control strategies
Act as CMC sponsor on client projects, lead and support the project team to ensure robust and phase-appropriate control strategies are in place and risks to regulatory submissions are flagged and managed.
Oversee validation activities for manufacturing processes, analytical methods, and cleaning procedures to align with customer needs, regulatory guidance and internal procedures.
Provide consultancy services to customers and support project delivery by overseeing the technical design and reporting of CMC technical studies including process and analytical tech transfer, product comparability, process characterisation, and process validation
Responsible for identifying regulatory trends and implementing changes within the organisation and internal procedures.
Creates strategy for external partnering and collaboration as appropriate for internal/client requirements and oversees delivery.

Requirements:

Essential

PhD or MSc in Life Sciences discipline or equivalent industrial experience
10+ Years experience including significant experience leading process and analytical transfer activities for development and GMP projects within the biotechnology industry as well as extensive CMC leadership across multiple / highly complex biologics programs
Experience supporting process validation, analytical validation, and GMP manufacturing and risk management approaches
Strong knowledge of global CMC regulations
Clear understanding of science and a passion for keeping abreast of regulatory and industry changes across multi-modalities.

Desirable

Experienced in the manufacturing and testing of multi-modality biologics.
Knowledge of GMP and Quality Management Systems.

Why Pharmaron?

Collaborative Culture: Thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators.

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Salary Competitive
Frequency Annual
Job Reference ukpharmaron/TP/78/729
Contract Type Fixed-Term Contract
Closing Date No expiry date
Job Category Scientific (Biologics Development, Manufacturing & Control Operations)
Division Biologics R&D Organisation
Location Liverpool, United Kingdom
Posted on 19 August, 2026

Apply Now

Refine Your Search

director of program management jobs in liverpool, eng

Associate Director, CMC Lead – Biologics (12 Month Fixed Term Contract)

Director of Homes & Compliance

Assistant Director of Building Safety

Associate - Engagement & Consultation

Technical Director, Capture Management Lead – Nuclear

Associate Director of TPM

Senior Manager, Customer Success Engineering

Associate Director, Procurement Enablement – ESG, Governance, Training & Development

Business Development Manager (BDM) - Birkenhead - Circa 41k Package- 53k OTE Uncapped

Assoc Dir Global Category Manager Devices

Senior Project Manager - Water Sector

Consultant

Business Development Manager (BDM) - Liverpool - Circa 41k Package- 53k OTE Uncapped

Solutions Architect – Marketing Technology

Crematorium & Cemetery Assistant

Associate Director – Transport Planning and Advisory

Digital Marketing Executive

Project Director - Controls Analytics

International Trade & Customs Manager EMEA

Trust HR Assistant

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