QC Instrument Engineer for QC Instrument Team

FLBD FUJIFILM Life Sciences Biotechnologies Denmark ApS; Hillerød; On-site; DKK 650,000 - 850,000; Full time

Benefits offered by this job

Competitive salaries

Bonuses

Health insurance

Wellness options

Fitness center

Social club events

Flexible working

Canteen and Friday breakfasts

Job summary

FLBD FUJIFILM Life Sciences Biotechnologies Denmark ApS in Hillerød is seeking a qualification professional to coordinate instrument and software qualification across labs and manufacturing units, ensuring cGMP compliance and data integrity.

You will drive improvements, support end-users, and collaborate with stakeholders in a fast-paced, international environment, contributing to the QC/Manufacturing team’s goals and embracing new technologies.

Qualifications

• Passion for implementing instruments and technology with a user-benefit focus, understanding the crucial role of teamwork.
• Ability to juggle tasks and adapt to changing priorities in a dynamic GMP environment.
• Excellent communication and collaboration skills for achieving stakeholder buy-in.
• Experience in instrument/equipment qualification, maintenance, data integrity, and support functions.
• IT skills are advantageous but not required.
• More than 3 years of experience in cGMP and pharmaceutical manufacturing.
• Fluent English proficiency as we operate internationally.

Responsibilities

• Coordinate and perform instrument and software qualification across diverse labs and manufacturing units.
• Identify and implement solutions that boost compliance, integration, automation, and empower end-users.
• Deliver exceptional support to stakeholders within a cohesive team that makes the most of each member's strengths.
• Drive and support projects, collaborating closely with stakeholders.
• Ensure instrument systems and documentation adhere to cGMP and Data Integrity standards.
• Use your expertise to innovate and champion continuous improvement within the team.

Skills

Instrument qualification

Data integrity

Collaboration

GMP experience

English fluency

Education

Bachelor's degree or equivalent

Job description

About the Job

Are you someone who thrives on energizing teams to find automated, agile solutions for end-users? Do you excel in coordination and have a big-picture mindset that flourishes in collaborative environments with multiple stakeholders? Join our lively and engaged team where collaboration is not just a practice but a joy! At QC Instrument, we ensure that laboratory instruments and software are qualified and maintained according to cGMP guidelines in both QC and manufacturing. Our mission is to support internal stakeholders in QC and production by enhancing processes, automating solutions, and embracing new technologies. We work together, leveraging each other's strengths to achieve our ambitious goals.

Key Responsibilities

• Coordinate and perform instrument and software qualification across diverse labs and manufacturing units.
• Identify and implement solutions that boost compliance, integration, automation, and empower end-users.
• Deliver exceptional support to stakeholders within a cohesive team that makes the most of each member's strengths.
• Drive and support projects, collaborating closely with stakeholders.
• Ensure instrument systems and documentation adhere to cGMP and Data Integrity standards.
• Use your expertise to innovate and champion continuous improvement within the team.

Qualifications and Education

• Passion for implementing instruments and technology with a user-benefit focus, understanding the crucial role of teamwork.
• Ability to juggle tasks and adapt to changing priorities in a dynamic GMP environment.
• Excellent communication and collaboration skills for achieving stakeholder buy-in.
• Experience in instrument/equipment qualification, maintenance, data integrity, and support functions.
• IT skills are advantageous but not required.
• More than 3 years of experience in cGMP and pharmaceutical manufacturing.
• Degree in Natural Sciences, Health and Medical Sciences, Pharmacy, Engineering, or equivalent.
• Fluent English proficiency as we operate internationally.

About Our Quality Control Department

Our QC department at site Hillerød has over 200 dedicated team members divided into support and testing teams, including QC Instrument Support. We embody a OneQC spirit, helping and supporting each other to achieve our goals, foster collaboration, and enable personal growth. Our success is driven by passionate colleagues committed to making a global difference. As a leading CDMO company, we continually pursue dynamic improvements in a flat organizational structure enabling rich co‑decision making. The culture at FUJIFILM Denmark (FDBD) is our cornerstone.

Benefits

• competitive salaries
• bonuses
• health insurance
• wellness options
• a fitness center
• social club events
• flexible working
• Enjoy our canteen services with Friday breakfasts and monthly afternoon cake
• celebrate achievements with our "bell ringing" tradition
• access to fitness and an attractive canteen

Development Opportunities

• Enhance project management and stakeholder interaction skills.
• Learn to create impactful business cases with stakeholders and SMEs.
• Expand your knowledge in instrument digitalization, interfacing enterprise systems, and automation with a focus on user experience.
• Master analytical instrument qualification and lifecycle management.
• Deepen personal and team insights in a group that values close collaboration.

Working at FUJIFILM Biotechnologies

We offer a competitive compensation package in a site/company growing rapidly, with many opportunities for individual growth. We also offer access to fitness and an attractive canteen. FUJIFILM Biotechnologies is an industry‑leading Biologics Contract Development and Manufacturing Organization (CDMO) with locations in Hillerød, Denmark, Teesside, UK, RTP, North Carolina and College Station, Texas, USA. We use our skills, dedication, and ambition to enable impact for the world’s most innovative biotech and biopharma companies reimagining healthcare’s potential. We work across the entire lifecycle of our customers’ products—enabling success throughout. Every cure, vaccine, biologic, and advancement we contribute to starts with our people and our passion. We fuel one another’s passion, help accelerate progress, expand capabilities, strengthen innovation, and improve processes to improve lives. Our Manufacturing site in Hillerød, Denmark, brings together a complete range of expertise, capabilities, and technologies to manufacture advanced biologics.

Diversity and Inclusion

Deeply committed to diversity and inclusion, we ensure that everyone - no matter their background or gender—has an opportunity to develop. We take pride in enriching our communities, caring for our environment, and cultivating a world of opportunity for future generations. We aim to foster a collaborative, innovative, and rewarding environment, where diverse perspectives and people come together united by a common purpose and shared values. We pursue our fullest potential as individual contributors and team members. We strive to be the employer of choice and offer a competitive compensation and benefit package.

Equal Opportunity Employer

FUJIFILM Biotechnologies Denmark is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identity, or any other protected class.