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- Tasks: Lead mechanical design for pharmaceutical projects, ensuring compliance and performance standards.
- Company: Global project management consultancy with a strong track record in life sciences.
- Benefits: Competitive salary of £95,000 - £100,000 plus additional benefits.
- Why this job: Join a dynamic team and make a significant impact in the pharmaceutical industry.
- Qualifications: Degree qualified, chartered, with 8+ years in large-scale construction projects.
- Other info: Opportunity for career growth in a thriving sector.
The predicted salary is between 78000 - 120000 £ per year.
We are currently partnering with a multi-national Project Management consultancy with a global track record of Life Sciences and Pharmaceutical project delivery. Due to continued expansion in the UK region, they are now seeking an experienced Mechanical Associate Director to lead their Mechanical Arm in North London.
Responsibilities
- Lead Mechanical Building Services Design Delivery: Own the full mechanical design lifecycle for the project, including HVAC, cleanroom air handling, process ventilation, chilled & heating water systems, ensuring all outputs meet pharma-grade performance and GMP standards.
- Develop Mechanical Design Concepts & Technical Solutions: Produce and oversee mechanical design concepts, technical calculations, equipment selections and system schematics that comply with regulatory, contamination-control and pharmaceutical environmental requirements.
- Review, Approve & Assure Mechanical Design Outputs: Carry out technical reviews of drawings, specs, models and mechanical design deliverables produced by external consultants, ensuring accuracy, completeness and alignment with the projects design strategy.
- Manage Mechanical Design Interfaces with Process & Validation: Coordinate closely with process engineering and validation teams to ensure mechanical systems (HVAC, utilities, pressure regimes, cleanroom zoning, etc.) integrate seamlessly with critical production environments.
- Drive Mechanical Risk Management, Compliance & Change Control: Lead mechanical-focused design risk assessments, ensure compliance with UK regulations and GMP expectations, and manage change control processes for all mechanical modifications, deviations and technical queries.
Requirements
- Successful candidate must be both Degree Qualified and Chartered.
- Must have 8+ years experience in a similar role on large-scale construction projects (Preferably Pharmaceutical).
- Must be based within a commutable distance of North London.
Benefits
£95,000 - £100,000 + Benefits
Associate Director Mechanical Engineering in Stevenage employer: LJB & Co
Contact Detail:
LJB & Co Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director Mechanical Engineering in Stevenage
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical and engineering sectors. Attend industry events or webinars, and don’t be shy about introducing yourself. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews! Research the company and their recent projects in the life sciences sector. We want you to be able to discuss how your experience aligns with their needs, especially in mechanical design and compliance with GMP standards.
✨Tip Number 3
Showcase your expertise! Bring along a portfolio of your previous work, especially any large-scale projects you've led. We want to see your mechanical design concepts and how you’ve tackled challenges in past roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always on the lookout for talented individuals like you to join our team in North London.
We think you need these skills to ace Associate Director Mechanical Engineering in Stevenage
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Mechanical Associate Director role. Highlight your experience in mechanical design, especially in pharmaceutical projects, and don’t forget to mention your degree and chartered status!
Showcase Your Achievements: When writing your application, focus on showcasing your achievements in previous roles. Use specific examples that demonstrate your ability to lead mechanical design delivery and manage compliance with GMP standards.
Be Clear and Concise: Keep your application clear and concise. Avoid jargon and ensure that your points are easy to understand. We want to see your skills and experience without having to sift through unnecessary fluff!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at LJB & Co
✨Know Your Mechanical Stuff
Make sure you brush up on your knowledge of HVAC systems, cleanroom air handling, and other mechanical design concepts relevant to the pharmaceutical industry. Be ready to discuss specific projects you've worked on and how you ensured compliance with GMP standards.
✨Showcase Your Leadership Skills
As an Associate Director, you'll be leading a team. Prepare examples of how you've successfully managed teams in the past, particularly in high-pressure environments like large-scale construction projects. Highlight your ability to coordinate with different engineering disciplines.
✨Prepare for Technical Reviews
Expect to discuss how you approach technical reviews of design outputs. Think about how you ensure accuracy and completeness in drawings and specifications. Be ready to explain your process for managing design interfaces with other teams.
✨Demonstrate Risk Management Expertise
Familiarise yourself with mechanical risk management and compliance processes. Be prepared to talk about how you've led risk assessments in previous roles and how you handle change control for mechanical modifications. This will show your understanding of the regulatory landscape.