QA Manager, QP

Orion Oyj; Turku; On-site; EUR 90,000 - 120,000; Full time

Job summary

Orion Oyj in Turku is seeking a QA Manager, QP for quality assurance in Gel and Ointment production. The role focuses on approving batches for sale, QA reviews, and document approvals at the Turku plant.

You will join a team responsible for quality systems and cooperation with production, QC, and lifecycle management. The position emphasizes GMP proficiency, collaboration, and bilingual capability in Finnish and English.

Qualifications

• Master's degree in pharmacy or equivalent with readiness to obtain QP qualification via experience.
• Experience in the pharmaceutical industry, preferably drug production or QA/QC tasks.
• Knowledge of GMP basics and strong communication skills in Finnish and English.

Responsibilities

• Approve batches for sale as QP and assess deviations and changes.
• Handle quality assurance activities such as product quality reviews and document approvals.
• Participate in quality meetings and operations development with production, QC, and PLM.
• Work primarily on-site at Turku plant with hybrid remote options.

Skills

QP (Qualified Person)

Quality Assurance

Teamwork

Negotiation

Regulatory

Education

Master's degree in pharmacy

Job description

We are looking for a QA Manager, QP (Qualified Person) for quality assurance in Gel and Ointment production at Orion’s Turku plant for permanent job.

Your role and responsibilities

As a QP, your tasks will include approving batches for sale and assessing deviations and changes. You will be responsible for quality assurance activities in your area, such as product quality reviews and document approvals, and you will participate in quality meetings and operation development. You will work closely with production, quality control, and product lifecycle management organizations. Your workplace is located at Orion’s Turku plant. The job mainly requires on-site work, but you can work part of the time remotely according to our hybrid model.

What you can expect from us

We offer you a position at the heart of Orion’s operations, as ensuring the quality, reliability, and safety of our products and operations is one of the cornerstones of our activities. Your role will be diverse and challenging, and you will have the opportunity to develop yourself as an expert in the quality aspects of industrial drug manufacturing.

At Orion, 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.

What are we looking for?

We require you to have a master's degree in pharmacy or another suitable higher education degree (e.g., a degree in pharmacy supplemented with specialization studies in industrial pharmacy) and good readiness to achieve QP qualification through work experience. Experience in the pharmaceutical industry, preferably in drug production or quality assurance or quality control tasks, is an advantage. Knowledge of different parts of the supply chain is also considered an advantage.

The position requires knowledge of GMP basics. You get along well with different people, are convincing, have negotiation skills, and are proactive. You are curious, willing to learn new things, and take responsibility as part of the whole. You can manage your work and have excellent teamwork skills. Quality, reliability, and safety are important values to you. Successful performance in the position requires good proficiency in Finnish and English.

Your new team

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 QMfunction 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 Quality Assurance Department for production employs approximately 60 people. The Gel and Ointment team within this department comprises QPs and QA Pharmacists whose responsibilities include quality assurance activities related to the manufacture and packaging of non‑sterile gel, ointment, and solution products at the Turku site.

About Us

Orion Pharma is a globally operating Nordic pharmaceutical company – a builder of well‑being for over a hundred years.

We’re home 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.

About Orion

Please visit our website to find further information about our values and Orion as an employer https://www.orion.fi/en/careers/orion-as-an-employer/.

For more information about the position, please contact Anne‑Mari Virtanen, Head of QA Team, QP, tel. [phone] (available on Tuesday August 18, between 15:30-16:30, Friday August 21, between 9-10 and Monday August 24, between 15-16).

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.

• Apply Before 08/25/2026, 09:59 PM
• Job Schedule Full time
• Locations Tengströminkatu 8, Turku, 20360, FI (Hybrid)