Team Leader, Quality Control at Orion Pharma

Työnkuvaus:

Uusimmat työtiedot yritykseltä Orion Pharma tehtävään Team Leader, Quality Control. If the Team Leader, Quality Control avooin työpaikka kohteessa Espoo vastaa pätevyyttäsi, lähetä uusin hakemuksesi tai CV:si suoraan päivitetyn Jobkos-työpaikkaportaalin kautta.

Huomioithan, että työpaikan haku ei ole aina helppoa, sillä ehdokkaiden on täytettävä yrityksen asettamat vaatimukset. Toivomme, että uramahdollisuus yrityksessä Orion Pharma tehtävään Team Leader, Quality Control vastaa tavoitteitasi.

Job Description
We are seeking Team Leader to work in chemical quality laboratory (Tablet Team) at Orion Pharma's Espoo site.

Job Description
Your responsibilities include supervising a team of laboratory technicians, guiding and reviewing analytical work, and handling deviation in accordance with GMP (Good Manufacturing Practice). Depending on your interests and expertise, you may also take on other chemical quality control tasks.

The work is 2-shift work from Monday to Friday (evening shift every sixth week). The Tehtävä is permanent.

What We Offer
We offer you diverse, interesting, and challenging tasks at the heart of Orion Pharma's supply chain, surrounded by a strong and professional team, as well as opportunities for continuous personal and professional development.

At Orion Pharma, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life.

Please visit our website to find further information about our values and Orion Pharma as an employer .

Our expectations

• A Master's degree in chemistry, chemical engineering, or equivalent education
• proficiency in Finnish and English. Our working language is Finnish.
• an open attitude and desire to learn
• ability to follow the guidelines and instructions
• basic IT skills (e.g. MS office)

Experience in supervisory roles, liquid chromatography, working in a GMP environment and quality control is considered an advantage.

We expect you to work in a systematic and goal-oriented manner. You are proactive, efficient, and take responsibility in your area. You plan, execute, and investigate actively and collaborate closely with laboratory staff. You have strong teamwork skills even in urgent and high-pressure situations. We continuously develop our operations according to Lean principles, so you are eager to improve work practices and adapt to changing conditions. Additionally, we expect you to have a strong safety mindset.

How To Apply And Additional Information
If you are interested, please apply for the Tehtävä by We review applications already during the application period and may start interviewing candidates before the application deadline. Therefore, we invite you to send your application (Cover Letter and CV in Finnish/English) as soon as possible.

For additional details, do not hesitate to contact QC Manager Mikko Laitinen (Tel on any of the following times (Finnish Time): between 14pm – 15pm and between 15pm – 16pm

Approved medical examination which also includes drug testing is required prior to the employment. We will also carry out a security clearance prior to the employment for the selected person.
Unit Description
Quality management (QM) is responsible for ensuring the quality of materials, products and operations, as well as maintaining and developing the quality system and monitoring the regulatory environment. Pharmacovigilance and Patient Safety unit is responsible for the global pharmacovigilance system of Orion Corporation and for the continuous safety surveillance, regulatory reporting and safety risk management activities of human and veterinary medicinal and non-medicinal products.

The QM function consists of about 350 experts who work in Quality Control, Quality Assurance, Quality System, Method Development and the Pharmacovigilance & Drug safety unit. We are located in Espoo, Turku, Salo and Kuopio plants, in addition to the Quality Assurance team in India reporting dotted-line to QM.

The Chemical Quality Control (CQC) is responsible for the quality control of products, raw materials, and packaging materials, stability studies of commercial products and production's cleaning validation analytics. There are around 160 professionals working in CQC, as a significant part of the supply chain. Our Tablet Team employs approximately 60 people.

Tietoa meistä
Orion Pharma is a globally operating Nordic pharmaceutical Yritys – a builder of well-being for over a hundred years.

We're Koti to more than 4,000 Orionees around the world, and we're proud to be known as a responsible employer and a great place to work. At Orion Pharma, people are truly valued and trusted, encouraged to grow, and supported by a culture where every voice is heard. We appreciate each other, strive for excellence, and build the future.

Together we develop, manufacture, and market human and veterinary pharmaceuticals and active pharmaceutical ingredients. Our extensive portfolio includes proprietary and generic medicines as well as consumer health products. The core therapy areas of our pharmaceutical R&D are oncology and pain. Proprietary products developed by Orion Pharma are used to treat cancer, neurological diseases, respiratory diseases, and more.

We offer careers with a clear purpose: empowering people to live their lives to the fullest.

Tiedot työpaikasta:

• Yritys: Orion Pharma
• Tehtävä: Team Leader, Quality Control
• Työskentelypaikka: Espoo
• Maa: FI

Näin lähetät työhakemuksen:

Kun olet lukenut ja ymmärtänyt kriteerit sekä vähimmäisvaatimukset, jotka on mainittu työpaikkailmoituksessa Team Leader, Quality Control at the office Espoo yllä, valmistele välittömästi hakuasiakirjat, kuten työhakemus, CV, kopio tutkintotodistuksesta ja muut liitteet. Lähetä hakemus 'Seuraava sivu' -linkin kautta alta.