Danimarka İş ilanı: Process Engineer Automated Visual Inspection Drug Product, Hillerød, Denmark

FUJIFILM Diosynth Biotechnologies Denmark ApS

Company logo

Work place location Hillerød municipality

Description of the company

Biogen Idec creates new standards of care in therapeutic areas with high unmet medical needs. Founded in 1978, Biogen Idec is a global leader in the discovery, development, manufacturing and commercialization of innovative therapies. Patients in more than 90 countries benefit from Biogen Idec's significant products that address diseases such as multiple sclerosis (MS), lymphoma and rheumatoid arthritis. In 2007, Biogen Idec's total revenues grew 18 percent over 2006 to almost $3.2 billion.

Reference

JUE

Important dates

Created: 9 May 2022

Application deadline: 4 July 2022

Date of employment: As soon as possible

The company offers

Permanent position

Full-time

Contact person

- -

Employer

FUJIFILM Diosynth Biotechnologies Denmark ApS

Biotek Allé 1

3400 Hillerød

Danmark

Process Engineer / Sr. Process Engineer Automated Visual Inspection Drug Product, Hillerød, Denmark

We are looking for an experienced and motivated Process engineer / Sr. Process engineer to join Mfg. Sciences and Technology (MSAT) for Drug product in Hillerød. The successful candidate will be accountable for Engineering and Technology SME support for our new Fully automated Visual Inspection line under construction in Jutland and for being the go-to person and specialist in the Automated Visual Inspection Engineering and Technology matters during qualification and when the line is in commercial mfg. 

Follow Your Genki to FUJIFILM Diosynth Biotechnologies

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us. We’re growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. Here, you will work alongside and learn from some of the most dedicated scientists, engineers, and manufacturers in the industry. We’re proud to cultivate a culture that will fuel your passion, energy, and drive—what FDB calls Genki. Join us and discover a community that thrives on diversity and never scares away from a complex challenge. At FDB, you determine what’s possible.

Our Manufacturing site in Hillerød, Denmark, brings together a complete range of expertise, capabilities and technologies to manufacture advanced biologics. We are on a journey of expansion in Denmark and in the US and work in a dynamic and varied environment.

The team

The MSAT for DP department contains the Drug Product Process and Technology Scientists / SMEs as well as the Tech Transfer Leads and Program Managers. We are growing from the current 6 colleagues to more than 10 over the coming year as we get closer to clinical and commercial DP mfg. operations. We work in an informal way with emphasis on trust, delegation, proactivity, teamwork and learning and sharing with each other.

The role

The main purpose of the job is to act as Process Engineer / Responsible Engineer (Technology SME) within Drug Prodcut MSAT on the Automated Visual Inspection line work in cooperation with relevant scientists / SMEs in additional areas as relevant. These are the focus areas:

Support and drive MSAT engineering activities and deliverables in connection with Construction, FAT, SAT, Qualification and Process Validation of an Automated Visual inspection  Line for Fujlifilm Diosynth Biotechnologies in Hillerød and developing into technology SME

Acting as second line support to maintenance organization in complex and unforeseen equipment issues. Leading troubleshooting teams and activities and being point of contact to suppliers.

Drives and provides inputs to creation of processes and procedures towards having shortest mean time to repair ( getting it right first time) and longest Mean time between failure. Creating clear data driven structures to understand and prioritize on solving and eliminating equipment potential failure modes.

Provides support to activities around maintenance strategy and experimental development towards most reliable process parameters (ranges) ensuring high uptime and least possible product loss.

Provides support towards operational readiness for the Inspection processes, including support for training, procedures etc.

Drives continuous improvement of the Inspection process, being up to date with new technologies and equipment.

Participates in deciding future equipment technologies as fit to Fujifilm Strategy.

Qualifications

We are ideally looking for a person who brings with her/him the below mentioned:

• experience from the Pharmaceutical industry working in a GMP environment.
• experience from Automated Visual inspection technologies in Pharma or transferable from elsewhere.
• experience from working with strategies for equipment uptime and preventive, predictive and corrective maintenance for complex mfg. equipment
• interest and bandwidth for continually learning about new technologies, processes and products
• Strong communication skills in English (spoken and written).
• Profound analytic skill
• Self-drive, proactivity and skills in managing complex assignments.
• Please upload your CV and cover letter as soon as possible as we are screening candidates on a continuous basis:

https://fujifilmdiosynth.wd3.myworkdayjobs.com/en-US/External/details/Process-Engineer---Sr-Process-Engineer-Automated-Visual-Inspection-Drug-Product_JR1358

About FUJIFILM Diosynth Biotechnologies

FUJIFILM Diosynth 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 site in Hillerød, Denmark, brings together expertise, capabilities and technologies to manufacture advanced biologics. The large scale manufacturing facility has a capacity of 120,000 liters to reliably manufacture biologics for late phase and commercial use. We commenced 6 billion DKK projects to double our manufacturing capacity and to add fill finish to the site.

We offer the chance to be part of a global workplace where passion, drive and commitment are met with opportunities for professional and personal development. 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.

As we continue to enhance and expand our capabilities, we are looking for people who share our passion, drive, and energy – what we call Genki – to join our team.

www.fujifilmdiosynth.com

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