Site Director - Biologics CDMO in Ely

Site Director - Biologics CDMO in Ely

Ely Full-Time 90000 - 110000 £ / year (est.) No working from home possible
Integrated Talent Partnership

At a Glance

  • Tasks: Lead a multidisciplinary team in biologics manufacturing and ensure compliance with industry standards.
  • Company: A top-tier CDMO specialising in biologics, serving global biotech and pharmaceutical clients.
  • Benefits: Competitive salary, leadership opportunities, and a chance to drive site growth.
  • Other info: Join a dynamic environment with opportunities for professional development and career advancement.
  • Why this job: Make a significant impact in the biopharmaceutical industry while leading innovative projects.
  • Qualifications: Extensive senior leadership experience in biologics manufacturing and strong regulatory knowledge.

The predicted salary is between 90000 - 110000 £ per year.

My client is a leading Contract Development and Manufacturing Organisation (CDMO) specialising in biologics, supporting clients across mammalian cell culture, microbial fermentation, and downstream purification for clinical and commercial-scale production. Our UK site is a centre of excellence for biologics manufacturing, serving a global client base of biotech and pharmaceutical innovators. We are seeking an experienced Site Director to take full operational and strategic leadership of our facility, ensuring safe, compliant, and efficient delivery of manufacturing programmes while driving continued growth and site development.

The Role

As Site Director, you will hold overall accountability for the performance, compliance, and culture of the site. You will lead a multidisciplinary team spanning manufacturing, quality, engineering, supply chain, and technical operations, ensuring the facility consistently meets GMP standards, client commitments, and business objectives.

Key Responsibilities

  • Provide overall leadership and P&L accountability for the site, ensuring delivery against safety, quality, delivery, and cost targets
  • Act as the site's Responsible Person/Qualified Person liaison, maintaining full compliance with MHRA, EMA, and FDA GMP requirements
  • Lead, coach, and develop the senior site leadership team across Manufacturing, Quality, Engineering, and Supply Chain functions
  • Own the site's health & safety culture, ensuring robust EHS systems and continuous improvement
  • Drive operational excellence initiatives (Lean/Six Sigma) to improve right-first-time rates, capacity utilisation, and cost efficiency
  • Serve as a key point of contact for major clients, supporting business development, technology transfer, and new project onboarding
  • Oversee capital investment planning, site expansion projects, and long-term facility strategy
  • Ensure inspection readiness and lead engagement with regulatory bodies during audits and inspections
  • Represent the site within the wider corporate leadership structure, contributing to group-level strategy

About You

  • Significant senior leadership experience within biologics manufacturing, ideally within a CDMO, biopharmaceutical, or biotech manufacturing environment
  • Proven track record of managing large, multidisciplinary teams and full site P&L responsibility
  • Strong working knowledge of biologics manufacturing processes (upstream/downstream, fill-finish, or drug substance/drug product) and associated GMP regulatory frameworks
  • Demonstrated success leading regulatory inspections (MHRA, FDA, EMA) with strong outcomes
  • Commercially astute, with experience supporting client relationships and business growth
  • Excellent leadership, communication, and change management skills
  • Degree in a relevant scientific, engineering, or technical discipline; advanced degree or professional qualifications advantageous

Site Director - Biologics CDMO in Ely employer: Integrated Talent Partnership

As a leading Contract Development and Manufacturing Organisation (CDMO) in the biologics sector, our UK site offers an exceptional work environment that prioritises safety, compliance, and operational excellence. We foster a collaborative culture where employees are empowered to lead and innovate, with ample opportunities for professional growth and development. Joining our team means being part of a global network dedicated to advancing biopharmaceutical solutions, all while enjoying the benefits of working in a state-of-the-art facility at the forefront of the industry.

Integrated Talent Partnership

Contact Details:

Integrated Talent Partnership Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Site Director - Biologics CDMO in Ely

Get Involved in Local Research Communities

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Show Off Your Projects

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Stay Up-to-Date with Industry Trends

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We think you need these skills to ace Site Director - Biologics CDMO in Ely

Operational Leadership
P&L Accountability
GMP Compliance
Biologics Manufacturing Processes
Regulatory Inspections
Lean Six Sigma
Health & Safety Management

Some tips for your application 🫡

Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show Integrated Talent Partnership that you have the hands-on skills they need.

Tailor Your Technical Skills:Make sure to emphasise your technical skills, especially those relevant to the biotechnology sector. Include any software tools or programming languages you've used, like R or Python for data analysis, which could be key for this role at Integrated Talent Partnership.

Craft a Compelling Cover Letter:Since this is a full-time role, your cover letter should reflect not only your passion for biotechnology but also your long-term career ambitions. Share why you're excited about the work that Integrated Talent Partnership does and how you envision contributing to their goals. This shows that you’re not just looking for any job, but you're genuinely invested in this opportunity.

Include Your Papers and Projects:If you've published any papers or contributed to significant projects, mention them! These documents can boost your application and provide tangible evidence of your expertise in the biotechnology field. Don’t forget to link to any relevant publications or project summaries—this can set you apart from other candidates.

How to prepare for a job interview at Integrated Talent Partnership

Brush Up on Lab Techniques

Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at Integrated Talent Partnership. You might even be asked to demonstrate your understanding of these processes.

Know Your Bioinformatics Tools

Get comfortable with bioinformatics tools that are commonly used in the industry, like BLAST or Bioconductor. These are key in biotechnology, and having hands-on experience or at least familiarity can set you apart. Prepare to discuss any relevant projects you've worked on, especially if they involved data analysis or genomic research.

Show Your Teamwork Skills

Biotech often involves collaboration across multiple disciplines. Be ready to share stories that highlight your teamwork and communication skills, especially in research projects. Think about working with different teams at university or any internships – this is where you can show how well you fit into Integrated Talent Partnership's culture.

Research Recent Biotech Innovations

Stay updated on the latest trends and breakthroughs in biotechnology. Knowing what's happening in the field can help you engage in more meaningful discussions during your interview. Bring up recent articles or advancements that excite you, especially those related to the work being done at Integrated Talent Partnership. This shows your passion for the industry!