Pharmaceutical engineering consultants
Consulting Services
We´re different in ways that will matter to you
We´re different in ways that will matter to you
What’s the difference between a highly trained expert and a practical, hands-on person who can implement cross-functional know-how to move your business forward? At KeyPlants, they're one and the same.
Not only do we match junior and senior consultants with your specific needs, we also match their personalities with your corporate culture and project team. Our consultants are supported by the expertise of the whole organisation. So, experienced consultants on both the project and consulting sides of our business are always ready to assist their colleagues. That can mean contributing specific expertise, or nuts-and-bolts, problem-solving insight into the challenges of the ongoing assignment. It's testimony to KeyPlants’ extensive project experience all over the world.
Commissioning, qualification and validation (CQV)
Quality assurance
Automation
Process design
Facility design
Project management
Work as a consultant
Our CQV consultants are experienced in leading and performing commissioning testing, qualification and validation of equipment, cleanroom and automation, as well as IT systems in the life sciences industry.
Their training and background in turnkey delivery of industry facilities, gives them a practical, solution-focused outlook and an ability to see projects through from beginning to end.
From construction quality assurance to automation systems, they’ll show you how to meet the most stringent quality, cost, and schedule requirements. Our Project Delivery services include:
- Development of commissioning and qualification plans
- Design review and qualification
- FAT/ SAT planning and execution support
- Commissioning protocol development, site execution, and reporting
- IQ/OQ protocol development, execution, and reporting
- Process validation and cleaning validation support
Our Quality Assurance consultants can help you with your daily QA work, in accordance with your existing quality system. Alternatively, they can help you develop or expand your quality system.
Our Quality Assurance consultants are backed by an organisation that has worldwide experience with regulations. They are able to see the full picture, as well as make those tough decisions. Their training and background in turnkey delivery of facilities for the industry also gives them a practical, solution-focused approach, and an ability to see projects through from beginning to end.
When you partner with us, you become part of a creative and welcoming company where everyone has the opportunity to develop their skills. We also hope that you will learn as much from us as we will learn from you. In addition to an attractive work environment, we offer a wide range of benefits. For many of our job openings, you will need a bachelor’s or master’s degree, or a similar qualification in engineering.
KeyPlants automation delivers a full range of automation services, from complete project delivery to on-site consultancy services. Based on our own quality systems and project development methodology, we offer complete application development, testing, quality assurance and documentation for your projects. This includes:
- System independent conceptual and basic automation designs
- Full Distributed Control Systems design and implementation
- Full PLC/SCADA solution design and implementation
- System upgrade/replacement
- Both batch and continuous system design
- Cabinet I/O Layout and design
- Site based consulting and troubleshooting support 15:54
- In-house development and test systems
The team at KeyPlants automation has extensive experience across multiple industries, with particular focus on GMP-regulated environments, such as pharmaceuticals and biotechnology. All of our consultants work according to established international standards and guidelines, including ISA S88, ISA S95 and GAMP. Our automation team also has extensive experience and skills with Emerson
Using modern design tools and the industry’s sharpest engineers, we will develop your process from intial plans to a GMP-compliant process design for procurement, installation and validation. Our process engineers can support your team and organisation with expertise in such areas as:
- OSD
- Aseptic formulation and filing
- Biopharmaceuticals
- Small molecule APIs
Our design managers draw on their practical experience to steer your project design around all possible challenges, avoiding unnecessary gold-plating, so you can meet your schedule and budgets. Product quality is always the top priority.
KeyPlants’ engineering experts are ready to assist you in ensuring your design and operation complies with all regulatory requirements. We are accustomed to working in an international environment, complying with local building codes and guidelines, and cooperating with local engineering firms all over the globe. We will perform efficient design reviews of your design in relation to GMP or other applicable regulations, based on extensive global experience.
KeyPlants knows what it takes to manage a project and make it profitable. After all, that's been our business from the very start. Over many years, we have executed a large number of projects around the world, and we have experience of working with both large and small clients, many of whom are leading A/E’s and construction companies.
Today, our experienced project managers are sharing that expertise, by ensuring successful project deliveries through effective planning, backed by an experienced team. We offer senior project teams for large projects, including technical project leaders, as well as project planning or project administration.
We have the experience and tools in place for monitoring progress and maintaining robust control throughout the lifecycle of a project. This ensures any challenges are effectively addressed, so as to meet your time, cost, and quality objectives. Through an execution model that's proven through many project deliveries over the years, we help reduce our clients’ risk and deliver projects in a predictable manner, for any project phase in which we are involved.
We’re recruiting for a new hybrid project/consulting business that will offer expertise to the lifescience industry. Are you curious, adventurous, and ready for an amazing journey? If so, we offer an international work environment in which you can collaborate on interesting technical solutions that improve people’s lives.
Our CQV consultants are experienced in leading and performing commissioning testing, qualification and validation of equipment, cleanroom and automation, as well as IT systems in the life sciences industry.
Their training and background in turnkey delivery of industry facilities, gives them a practical, solution-focused outlook and an ability to see projects through from beginning to end.
From construction quality assurance to automation systems, they’ll show you how to meet the most stringent quality, cost, and schedule requirements. Our Project Delivery services include:
- Development of commissioning and qualification plans
- Design review and qualification
- FAT/ SAT planning and execution support
- Commissioning protocol development, site execution, and reporting
- IQ/OQ protocol development, execution, and reporting
- Process validation and cleaning validation support
Our Quality Assurance consultants can help you with your daily QA work, in accordance with your existing quality system. Alternatively, they can help you develop or expand your quality system.
Our Quality Assurance consultants are backed by an organisation that has worldwide experience with regulations. They are able to see the full picture, as well as make those tough decisions. Their training and background in turnkey delivery of facilities for the industry also gives them a practical, solution-focused approach, and an ability to see projects through from beginning to end.
When you partner with us, you become part of a creative and welcoming company where everyone has the opportunity to develop their skills. We also hope that you will learn as much from us as we will learn from you. In addition to an attractive work environment, we offer a wide range of benefits. For many of our job openings, you will need a bachelor’s or master’s degree, or a similar qualification in engineering.
KeyPlants automation delivers a full range of automation services, from complete project delivery to on-site consultancy services. Based on our own quality systems and project development methodology, we offer complete application development, testing, quality assurance and documentation for your projects. This includes:
- System independent conceptual and basic automation designs
- Full Distributed Control Systems design and implementation
- Full PLC/SCADA solution design and implementation
- System upgrade/replacement
- Both batch and continuous system design
- Cabinet I/O Layout and design
- Site based consulting and troubleshooting support 15:54
- In-house development and test systems
The team at KeyPlants automation has extensive experience across multiple industries, with particular focus on GMP-regulated environments, such as pharmaceuticals and biotechnology. All of our consultants work according to established international standards and guidelines, including ISA S88, ISA S95 and GAMP. Our automation team also has extensive experience and skills with Emerson
Using modern design tools and the industry’s sharpest engineers, we will develop your process from intial plans to a GMP-compliant process design for procurement, installation and validation. Our process engineers can support your team and organisation with expertise in such areas as:
- OSD
- Aseptic formulation and filing
- Biopharmaceuticals
- Small molecule APIs
Our design managers draw on their practical experience to steer your project design around all possible challenges, avoiding unnecessary gold-plating, so you can meet your schedule and budgets. Product quality is always the top priority.
KeyPlants’ engineering experts are ready to assist you in ensuring your design and operation complies with all regulatory requirements. We are accustomed to working in an international environment, complying with local building codes and guidelines, and cooperating with local engineering firms all over the globe. We will perform efficient design reviews of your design in relation to GMP or other applicable regulations, based on extensive global experience.
KeyPlants knows what it takes to manage a project and make it profitable. After all, that's been our business from the very start. Over many years, we have executed a large number of projects around the world, and we have experience of working with both large and small clients, many of whom are leading A/E’s and construction companies.
Today, our experienced project managers are sharing that expertise, by ensuring successful project deliveries through effective planning, backed by an experienced team. We offer senior project teams for large projects, including technical project leaders, as well as project planning or project administration.
We have the experience and tools in place for monitoring progress and maintaining robust control throughout the lifecycle of a project. This ensures any challenges are effectively addressed, so as to meet your time, cost, and quality objectives. Through an execution model that's proven through many project deliveries over the years, we help reduce our clients’ risk and deliver projects in a predictable manner, for any project phase in which we are involved.
We’re recruiting for a new hybrid project/consulting business that will offer expertise to the lifescience industry. Are you curious, adventurous, and ready for an amazing journey? If so, we offer an international work environment in which you can collaborate on interesting technical solutions that improve people’s lives.
Global experience in pharmaceutical engineering
KeyPlants’ pharmaceutical engineering consultants bring extensive international experience, enabling us to support your capital projects from equipment and plant design through to commissioning, qualification and validation.
We specialize in designing and validating pharmaceutical facilities that meet strict quality, cost, and schedule requirements. Combining a multicultural mindset with hands-on problem-solving, we deliver solutions that bring value to your projects.
With KeyPlants, you gain a partner who understands pharmaceutical industry challenges and ensures compliance at every stage of your pharmaceutical project.
Turnkey project delivery by pharmaceutical engineering consultants
At KeyPlants, our pharmaceutical engineering consultants manage every phase of your turnkey project, from concept through to commissioning and qualification. With our expertise, we ensure that your project meets the highest industry standards and regulatory requirements.
Combining technical excellence with hands-on problem-solving, our pharmaceutical plant design consultants ensure that your facility is fully GMP compliant when ready for operation. Our focus on efficiency and quality ensures that your project is completed on time, on budget, and tailored to your business goals.
Why choose KeyPlants' pharmaceutical engineering consultants?
KeyPlants’ pharmaceutical engineering consultants provide tailored solutions to meet the complex needs of the pharmaceutical industry. From conceptual design to commissioning and validation, we bring a unique combination of technical expertise and hands-on problem-solving to ensure projects are delivered efficiently on time, and in full compliance with GEP and global GMP.
With extensive experience in designing and optimizing pharmaceutical production facilities, our team focuses on streamlining processes while maintaining the highest quality and safety standards. By choosing KeyPlants, you gain a reliable partner with a global mindset and a proven track record of delivering solutions that align with your business goals.
FAQ
FAQ
What services do KeyPlants' pharmaceutical engineering consultants provide?
KeyPlants' pharmaceutical engineering consultants offer comprehensive solutions, including process- and facility design, automation, commissioning, qualification, validation (CQV), quality assurance (QA), and project management for the pharmaceutical and life sciences industries.
What is a turnkey project in pharmaceutical engineering?
A turnkey project refers to a fully managed solution where KeyPlants’ consultants handle every phase of the project — from design and execution to commissioning and validation — ensuring the facility is ready for operation.
How do pharmaceutical engineering consultants ensure GMP compliance?
KeyPlants’ pharmaceutical engineering consultants follow strict Good Manufacturing Practice (GMP) guidelines during design, construction, and validation to meet regulatory requirements and ensure product quality and safety.
What industries do pharmaceutical engineering consultants work with?
KeyPlants' consultants primarily serve the pharmaceutical, biopharma, biotech, and medtech industries, delivering tailored engineering and validation solutions.
Why choose KeyPlants’ pharmaceutical engineering consultants?
KeyPlants’ consultants combine technical expertise with hands-on experience, ensuring projects are delivered on time, on budget, and fully compliant with global regulatory standards.
Can KeyPlants’ pharmaceutical engineering consultants lead large-scale projects?
Yes, KeyPlants’ consultants have extensive experience managing large-scale pharmaceutical projects, delivering end-to-end solutions that meet the highest quality and performance standards.
Experts on call
Every company is different, with its own complexities and parameters. We offer a range of expertise both for large assignments, or for when you need an extra resource within your company or project team. Some of our more experienced consultants can also act as team leaders within your business.
Our specialist consultants work across the life sciences industry, including:
- Pharma
- Biotech
- Medtech
Specific expertise includes project management, QA, validation leadership, validation engineers, process engineers, and project leadership.
The KeyPlants difference
Our consultants come from a project management background in the life sciences industry. This makes all the difference when it comes to tackling challenges in a practical, hands-on manner. For a start, our consultants are not just specialists in their own fields, they also have experience working in cross-functional teams on our own projects. This means that they’re not ‘silo’ thinkers but are used to seeing how all the parts of a project fit together. In other words, they work in a cross-functional way to get things done. You’ll find that they really know what they’re talking about and will instinctively see how their own work fits into the bigger picture, i.e., your business.
Our consultants take ownership and responsibility for their individual work. That means they have an ingrained understanding of what ‘follow-through’ really means, all the way to the completion of a given assignment.
On the project side of KeyPlants' business, quality, safety, precision, agility, and sustainability are our main areas of focus. Because our consultants are experienced in these values, they bring the very same standards to your projects.
As our consultants are trained on KeyPlants’ own projects, they often have experience of not just working in a team, but leading a team. This gives you the option of choosing a consultant to lead a team within your own company
Worldwide experience, cross-cultural mindset
Worldwide experience, cross-cultural mindset
At KeyPlants, we work with some of the largest and most prestigious corporations in the life sciences industry. We also work with small, entrepreneurial companies and start-ups. We work on large, multi-million-dollar projects and those that are much smaller. And we work or parts of larger projects too. We work in Sweden, and all around the world.
Our international experience means that as we've grown, we've evolved a distinctly multicultural mindset. Today, our consultants are comfortable working with teams of people from anywhere in the world, all over the world. We believe there is no substitute for leaving our comfort zones, challenging our own assumptions, and experiencing how people in other cultures think and act. Our international experience also means that we are accustomed to working with regulators, authorities, and standards agencies setting different rules.
All of this means we’ll never make you choose between a consultant who is a highly-trained expert and one who is a practical, hands-on person who can implement cross-functional know-how to move your business forward. Because all our consultants are both.
Our Projects
