Senior Process Specialist (2576)

Senior Process Specialist

Introduction
Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you. With us, you will not only have the opportunity to influence the production and development of our products - you will also have the opportunity to develop in our Process Support team.

One of our Senior Process Specialists, says the following about the job:

“As Senior Process Specialist in Process Support, you'll have the opportunity to influence the production and be the expert in problem solving. You'll have many roles and responsibilities working with many different stakeholders in a versatile working day. I look forward to welcoming you as part of the Process Support Team. “

About Ferrosan Medical Devices
Ferrosan Medical Devices is a leading player in the medical devices industry, dedicated to providing innovative and high-quality solutions that improve patient outcomes. With a commitment to excellence and a focus on cutting-edge technology, we are at the forefront of advancing healthcare. Our products, used globally every second, exemplify our dedication to making a meaningful impact on the lives of patients around the world.

Position overview
The Process Support team consists of 13 committed and skilled employees. It is, among other things, our responsibility that our production processes and equipment are always in a validated state and are thus ready to produce on. A large part of this is running CR-cases to ensure that necessary improvements and optimizations in production are implemented. In addition, it is our responsibility to handle production deviations, risk assessments, continuous updates of instructions and procedures so that they meet current authority requirements along with driving and implementing continuous improvements.

Your role
You will become a process- and equipment owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, periodic evaluations, revalidations, and risk assessments for the specific process. You will also be responsible for systematic problem solving, deviation management, optimization of equipment and processes as well as general support for production. You will have a central and cross-organizational role in connection with development projects and the implementation of new equipment and act as a link between production, the support team, project team, development, and maintenance.

Key responsibilities
• Improvement activities in production, including facilitation of problem solving on equipment and processes

• Identify potential improvements by analyzing production data

• Handle deviations; includes close sparring with operators, technical department, QA etc.

• Prepare and maintain documentation e.g., risk assessments and periodic evaluation

• The change applications with associated documentation

• Production specialist in connection with development and equipment projects

About you
Curious, independent and with experience within process support
We are looking for a technically grounded profile that can independently find the way forward and make decisions. You are motivated by working in a dynamic environment and you are good at planning and take pride in moving tasks forward and meeting deadlines. As a person, you look positively on the challenges that working life can offer. You thrive working independently and in groups across departments and organizations.

You can challenge those around you in an empathetic and respectful way - and do not fall into a headwind.

You must be able to work in a structured and analytical manner, and to be successful in the job it is important to be able to collaborate with colleagues in different functions.

In addition, your CV contains:

• A relevant academic background; engineer, chemist, pharmacist or similar, preferably with at least 5 years of experience from a production environment

• Experience with filling- and/or Multivac manufacturing equipment is an advantage

• Experience working with change requests, requirements specifications, validation, and testing

• Experience of working in a GMP-regulated environment

• Good written and verbal competencies in both Danish and English

We offer an exciting workplace, where you can have real influence
We offer an exciting and challenging job and a workplace with strong values. What this means quickly becomes clear to our new employees. We are driven to create better outcomes for patients, and we bring our values ​​to work every day – we care about each other, our environment and our customers and we win for patients with innovative, high-quality products. You will meet a Danish-rooted company that is growing in the number of international colleagues and a way of working where hybrid, digital, learning and innovation are keywords. And we take pride in having fun! :-)

Location
Søborg, Denmark