Job Description

Do you have a passion, and are motivated by setting the right compliance standards, ensuring continuously improvement of processes and ways of working?
Then you may be the new GMP Partner at Agilent, Site Glostrup, Denmark.

At Agilent, we develop and produce reagents, instruments, and software for in vitro diagnostic of cancer. So here is an opportunity for a career in the fight against cancer!

The position
You will be part of a two-person GMP Partner team where you and your colleague will report directly to the Country General Manager & Associate Vice President.
The GMP Partner team have a vital role in supporting Senior Management ensuring compliance, fostering the quality strategy, and promoting the quality culture within production.

This position involves a dynamic mix of leading, coordinating, and participating in management-related compliance and quality activities.

Responsibilities
Your key responsibilities will include:

• Coordinating preparation, participation-, and follow up on audits and inspections.
• Set direction via quality KPI´s, report trends and drive relevant actions in collaboration with production management.
• Take leadership and set direction for the compliance initiatives in production.
• Drive continuous improvement of quality performance and processes.
• Support compliance and represent production in cross-functional quality projects.
  

Qualifications

To succeed in this role, it is advantageous to have:

• Solid experience and understanding of GMP production.
• A bachelor's or master´s degree within pharmacy, engineering, or similar.
• 3+ years of experience from the medical device or pharmaceutical industry or similar; experience from manufacturing.
• A LEAN mindset with a track record of systematic problem-solving.
• Demonstrated ability to work with stakeholders at all levels of the organization.
• Fluent in Danish and English; both spoken and written.

On a personal level, you thrive and get motivated by working with and across all levels of the organization. You are known for your ability to set direction, work proactively and systematically and see solutions from a broader perspective. You solve challenges with a simplicity mindset, active involvement of stakeholders and as close to the operational process as possible.

We offer:

• An opportunity to be part of a dynamic production team with appropriate 280 colleagues. A team driven to provide the best solutions, to ensure accurate and early diagnosis, to improve treatment, and enhance survival rates and quality of life!
• Agilent offers core global benefits to all staff - but in addition to these, the DK business offers Agilent Result Bonus, Stock Purchase Plan, Life Insurance, Pension, Healthcare, Physiotherapy and much more.

Additional Details

This job has a full time weekly schedule.
Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations
Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

Travel Required

Occasional

Shift

Day

Duration

No End Date

Job Function

Manufacturing