Are you our new Quality Specialist?

We are committed to excellence and continuous improvement, and we are looking for a dedicated new colleague to join our team

Responsibilities:

• drive the implementation of a new quality system ensuring that it meets the highest standards and ensuring its seamless integration into our existing processes
• Your focus will be on maintaining and enhancing our quality processes

You will have professional growth opportunities for career advancement and professional development.

Manufacturing Associate - Operator

We are currently looking for candidates within our Drug Substance Manufacturing (DSM) for the two departments; Upstream and Downstream.

These are covering different steps in the biopharmaceutical production such as Media/Buffer preparation, CIP, SIP of equipment, expansion of cell cultures, and purification via multiple column steps.

We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools.

Distinguished Engineer for Large Scale Business Unit

Do you have extensive experience with the management of large technical projects in a complex pharmaceutical environment?

In this role you will assist in Antibody Drug Conjugates, process engineering and automation activities. You will ensure alignment on shared goals through collaboration with Holly Springs location, engaging with other sites and stakeholders as needed.

Bachelor's degree required in Electrical, Biochemical, Chemical, or other Engineering disciplines.

Technical Supporter med interesse for optimering og vidensdeling!

Som Technical Supporter skal du være med til at drive, vedligeholde og forbedre fabrikkens forsyningsenheder ved at optimere vores arbejdsgange, samt sikre vidensdeling på tværs af hele afdelingen.

Arbejdet omfatter drift og vedligehold af mange forskellige systemer og foregår i et til tider hektisk miljø – du skal derfor være i stand til at have mange bolde i luften. Du vil desuden få en bred kontaktflade til leverandører og tværfagligt internt i organisationen på tværs af sitet.

Du tilbydes et dynamisk arbejdsmiljø, hvor du får mulighed for at påvirke din egen fremtid gennem kreativitet og innovation.

Sales Executive - Cruise & Offshore new building (Sweden/Europe)

Joining the Cruise Sales Team as a Sales Executive, you will be the face of Johnson Controls towards our customers, and you will focus on always delivering excellent value and service with integrity.

At Johnson Controls Cruise & Advanced Offshore division, we are a dynamic global team committed to delivering state-of-the-art HVAC & R solutions to a diverse clientele across the Cruise, Offshore, Luxury & Passenger vessel industries. We operate with a robust global presence, supported by dedicated service teams located in 10 strategic sites worldwide.

Operators for Drug Product Manufacturing

Would you like to be part of an international pharmaceutical company in rapid growth, which offers good development opportunities and set shifts?

This project is in the early phase of establishment and in the beginning, you will help design and establish processes for the upcoming production.

Main tasks:

• Participate in running and validation of equipment on site
• Assist during installation of equipment on site and carry out qualification tests afterwards

Operations Data Coordinator for Drug Substance Production

The primary task within the position is to collaborate with various departments (e.g., automation, tech transfer, and manufacturing departments) to collect and translate information required for building efficient production campaigns and daily task schedules.

You will be part of a team with a great sense of humor and a high willingness to support where needed.

Manufacturing Support Documentation Associate

Do you have a flair for compliance and can handle many stakeholders? Are you looking for a position where you can take on responsibility?

About the position:

• Create and maintain records and procedures by collecting information from stakeholders to supply manufacturing with compliant documents.
• Start-up events and support investigations by giving input as procedural SME.
• Support the change process by writing SME assessment to ensure procedural alignment. Perform timely closure of action items to ensure reliable execution of production.
• Continuously improve the department processes and support stakeholder improvement projects.