*QA Scientist, Training Partner

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Training Partner

Would you like to be a part of shaping the future for our employees, and do you have what it takes to play a pivotal role in our Quality Assurance Department? Are you a quality-conscious Training Partner? Do you want to work with skilled colleagues and stakeholders throughout the organization connecting business strategy with training and human performance solutions to achieve significant results that align with business strategy? who enjoys implementing structure, providing superior training support and can facilitate newcomer onboarding? Then join a dynamic and international company where everyone is responsible for delivering Right On Time as one team!

As our new Training Partner your main responsibility is to support QA management in ensuring efficient and compliant training and competence development set-ups. You will work at our multiproduct facility in Copenhagen and play a central role in ensuring effective training strategy of the QA department.

What will you do?

You tackle specific business challenges by facilitating a training needs analysis and subsequently designing and developing high impact training solutions. As Training Partner, you support and drive implementation of best practice within training standards, technologies, and solutions. Furthermore, you facilitate training design workshops and the training in our training standards. Together with the training coordinators, managers and other key stakeholders, you will coordinate training events, documentation and onboarding logistics for the growing number of employees in our Quality Assurance teams. AGC Copenhagen continues to expand, not only in the number of employees in Copenhagen, but also with our new facility, due for completion in 2024. As the Training Partner you will ensure that our training systems, standards and approach to training can support this growth, the needs of the business and the needs of our Quality Assurance employees. You will be optimizing training documentation, develop innovative training material.

As the Training Partner you will;

  • Take lead in implementing a modern and user friendly training system.
  • Act as a strategic partner to QA Management supporting accelerated competence development and a culture of continuous improvement.
  • Collaborate closely with managers to identify and execute new training requirements.
  • Improve, align and structure the content of our training systems, training plans and documentation etc.
  • Ensure correct completion of training documentation in accordance with GMP legislation and requirements and create monthly compliance reports.
  • Ensure coordination of all onboarding activities in collaboration with our Training Coordinators and secure that our newcomers receive a very warm welcome.
  • In collaboration with SMEs; create efficient training material.
  • Support the training coordinators and improvement projects.

Not a pre-requisite, but definitely a bonus if you…

  • Experience with coaching is an advantage and/or behavioral design/nudging is an advantage.
  • Experience with digital learning technologies is an advantage. You are familiar with Training within Industries (TWI)

What do you need to succeed in this role?

  • We imagine that you hold a relevant master’s degree within adult learning, learning management, organizational development, psychology or similar. A minimum of 3-5 years of experience developing and implementing competence development programs, preferably within pharma
  • A proven track record of driving change management projects and engaging stakeholders, as well as experience as a trainer and facilitator
  • Comprehensive knowledge of training principles.
  • Knowledge or experience within LEAN and continuous improvement is an advantage.
  • You have an independent, yet team-oriented and service minded approach. You tackle tasks in a structured way with energy, curiosity and a positive attitude.
  • It is of utmost importance that you have a proactive personality, with a pragmatic attitude and approach to the daily work - without compromising quality. The environment is dynamic and challenging, which requires the ability to find solutions and deliver on time.
  • Professional and effective communication skills in English, verbal as well as written. Danish is not a pre-requisite, but is definitely a bonus.
  • You know Office 365 features by heart (Power Bi Pro is an advantage)

AGC offers

AGC offers a dynamic working place with good opportunities of working with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments throughout a contract manufacturing organization interact in order to achieve success. Exciting and challenging assignments will constantly come your way, and you will to a large extend be able to plan your daily work yourself. AGC offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. AGC’s employees have a flexible attitude and we help each other to reach deadlines together as one team.

What’s next?

Submit your application as soon as possible. We treat the applications as we receive them, and conduct interviews with qualified candidates. When the right candidates are found, the ad will close.

Want to keep posted about our growth and to learn more about our company?

We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !

AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.

Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.


Information og data

Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 5.3.2024, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Forsker
  • København
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