Validation Engineer Job at NextPharma in Tampere

NextPharma is recruiting a Validation Engineer for its Technical Department in Tampere, Pirkanmaa, Finland. The post suits an engineer with experience in pharmaceutical-industry validation and qualification who can work independently while applying knowledge of GMP and ISO 9000 quality systems. Fluent spoken and written Finnish and English are required, alongside a customer-oriented approach to technical work.

The Tampere-based position centres on the qualification of small equipment within a pharmaceutical manufacturing setting. It is appropriate for a technically grounded applicant able to support equipment qualification, packaging and filling-machine validation, risk assessment and change-control activities. The role also calls for an engineering degree or Master of Science in Engineering and practical experience that connects validation work with quality-system expectations.

Opportunity Details

Overview of the Vacancy

Location, Sector, and Role Context

Situated in NextPharma's Technical Department, the Validation Engineer contributes to the controlled status of production equipment and related validation activity at the Tampere site. Day-to-day work has a particular emphasis on qualifying small equipment, while also covering validation work for packaging and filling machines. The engineer maintains production-equipment qualifications, carries out risk assessments and addresses technical change control. Participation in projects takes place as the validation representative, bringing validation considerations into project work. The role therefore combines hands-on technical documentation and assessment with the quality-system knowledge expected in pharmaceutical manufacturing.

A suitable background combines an engineering degree or Master of Science in Engineering with experience from pharmaceutical industry work, validation and qualification. The vacancy requires fluent written and spoken Finnish and English, independent working and a customer-oriented approach. Knowledge of GMP and ISO 9000 quality systems is also required because the remit includes qualification, validation, risk assessment and technical change control. The work is based in Tampere, Pirkanmaa, Finland, in an environment focused on pharmaceutical manufacturing and small-equipment qualification. The published employment information describes the role as a full-time fixed-term parental-leave replacement of about one year.

About the Employer: NextPharma (NextPharma Oy)

Organization and Relevant Services

Verified Employer Overview

NextPharma describes itself as a European contract development and manufacturing organisation specialising in pharmaceutical and nutraceutical development, clinical-trial supply and commercial manufacturing. Its network supports work across the product lifecycle, from formulation and analytical development through clinical-trial supply to commercial manufacturing and packaging. The group states that it operates 10 specialised manufacturing sites across Europe and supplies finished products to customers serving 70 global end markets. This breadth gives context to a validation role within an organisation whose stated activities span development, supply and commercial production.

The organisation states that all of its sites operate under GMP conditions and that its quality systems align with ICH Q9 and ICH Q10. For the Validation Engineer, those stated operating conditions are relevant to responsibilities involving equipment qualification, packaging and filling-machine validation, risk assessment and technical change control. NextPharma's published description places pharmaceutical development, clinical-trial supply and commercial manufacturing within the same wider network. The vacancy itself is located in the group's Technical Department in Tampere, where the position focuses on a pharmaceutical manufacturing environment and the qualification of small equipment.

Professional Setting and Role Context

Work Environment, Operations, and Facilities

The Tampere site has been part of the NextPharma Group since 2019. NextPharma reports continuous ophthalmic production experience in Tampere since 1981 and an FDA approval track record since 1995. Within the group, Tampere is described as the dedicated centre of excellence for sterile ophthalmic and otic liquids. The site uses BFS, three-piece and preservative-free multidose platforms. These published site characteristics provide the local context for a Validation Engineer whose duties include maintaining production-equipment qualifications and undertaking validation for packaging and filling machines.

At the Tampere facility, NextPharma states that formulation development, analytical-method development and validation, clinical-trial supply, scale-up and registration-batch manufacturing are provided on site. The Validation Engineer vacancy sits in the Technical Department at this Tampere location and focuses on small-equipment qualification in a pharmaceutical manufacturing setting. The employer also describes an environment involving both new technologies and technologies approaching the end of their lifecycle. That context aligns with the post's stated work on technical change control, risk assessments, equipment qualifications and project participation as the validation representative.

---

Open Positions

1. Validation Engineer

Official title: Validointi-insinööri — Validation Engineer

Location: Tampere, Pirkanmaa, Finland | Employment information: Full-time temporary parental-leave cover

This Validation Engineer position is defined by the need to keep qualifications current while completing validation activity for packaging and filling machines. Small equipment is the main stated focus, although the remit also includes production equipment more broadly. The Technical Department role requires the engineer to assess risks, manage technical changes and represent validation in projects. It calls for independent work, but the vacancy also states that support is available from a skilled and encouraging validation team in Tampere. The position is therefore closely tied to practical qualification and validation responsibilities at the local pharmaceutical manufacturing site.

Responsibilities

• Qualify small equipment used within the pharmaceutical manufacturing environment at the Tampere site.
• Carry out validation activities for packaging machines in line with the stated remit of the Technical Department role.
• Complete validation work for filling machines as part of the post's assigned technical responsibilities.
• Keep production-equipment qualifications current through the maintenance activities assigned to the engineer.
• Undertake risk assessments connected with the validation and qualification work covered by this position.
• Manage technical change-control activity within the scope of the advertised validation responsibilities.
• Take part in projects as the validation representative, providing the role-specific validation perspective.
• Work in a pharmaceutical manufacturing setting with small-equipment qualification as the principal stated focus.

Qualifications

• Hold an engineering degree or a Master of Science in Engineering relevant to the technical demands of this validation post.
• Demonstrate fluent spoken and written Finnish and English for the communication required by the vacancy.
• Be able to work independently when carrying out qualification, validation, risk-assessment and change-control tasks.
• Bring experience from the pharmaceutical industry together with practical experience in validation and qualification.
• Apply knowledge of quality systems, including GMP and ISO 9000, to the responsibilities described for the role.
• Use a customer-oriented approach in the technical work associated with the Validation Engineer position.
• No professional licence is stated for this post.

Skills and Competencies

• Use equipment-qualification capability to support the small-equipment focus of the Tampere manufacturing role.
• Apply process and packaging-validation knowledge when completing the packaging-machine activities assigned to the post.
• Use filling-machine validation competence for the filling-equipment work explicitly included in the remit.
• Carry out risk assessments that support the qualification and validation responsibilities of the Technical Department.
• Handle technical change control as part of maintaining an appropriate qualification and validation status.
• Apply GMP knowledge in the pharmaceutical manufacturing environment described for this position.
• Use ISO 9000 quality-system knowledge in connection with the role's stated validation and qualification work.
• Contribute validation input to projects while working independently and maintaining a customer-oriented approach.

Benefits and Employment Information

• The employer lists flexible working hours among the stated benefits for the Tampere Validation Engineer role.
• A lunch benefit is included in the benefits published for this position.
• The vacancy lists a well-being benefit for the successful applicant.
• Leisure-time accident insurance is identified as a stated employee benefit.
• The role offers support from a skilled and encouraging validation team in Tampere and an opportunity to develop expertise in GMP manufacturing and validation.
• This Validation Engineer post is full-time, fixed-term parental-leave replacement of about one year, and the vacancy does not publish a salary.

Application Guidance

Prepare a Focused Application

CV, Evidence, Documents, and Interview Preparation

As general preparation guidance, applicants can organise clear examples of equipment qualification and validation work undertaken in pharmaceutical settings. A concise account may distinguish work on small equipment from experience with packaging or filling machinery, where relevant. It can also be useful to prepare examples showing how risk assessments and technical changes were approached within GMP and ISO 9000 quality systems. Candidates may set out their engineering education accurately and be ready to explain how independent working and a customer-oriented approach have informed technical decisions. Treat these points as optional preparation; NextPharma's listed criteria stay unchanged.

For interview preparation, applicants may select factual examples that demonstrate validation, qualification and quality-system knowledge without presenting them as duties beyond the advertised remit. Discussion can focus on how previous experience relates to equipment qualification, production-equipment qualification maintenance, packaging validation, filling-machine validation, risk assessment or technical change control. Candidates can also prepare to describe professional communication in Finnish and English, as both spoken and written fluency are required. General preparation may include a structured explanation of how validation input has been provided in project work and how independent technical tasks have been prioritised.

• Prepare a CV in English that accurately identifies the engineering degree or Master of Science in Engineering held.
• Outline pharmaceutical-industry experience with validation and qualification in clear, factual terms.
• Select examples of small-equipment qualification, packaging validation or filling-machine validation that are relevant to this post.
• Prepare a concise explanation of experience using GMP and ISO 9000 quality systems in validation work.
• Review examples of risk assessment, technical change control and participation in projects as a validation representative.
• Be ready to describe fluent spoken and written communication in Finnish and English, together with independent and customer-oriented working.

---

How to Apply

Submit Your Application Through the Verified Route

Apply Through the Official Employer Portal

Prepare a CV in English for the Validation Engineer role and submit the application through the official employer application portal opened by the button below these instructions. Review the material for an accurate account of the required engineering background, validation experience and Finnish and English fluency. A short 10-second countdown precedes the final portal link.