3.8.2026 | Avoimet työpaikat
https://duunitori.fi/tyopaikat/tyo/target-discovery-lead-cancer-genomics-scsom-19902349?utm_source=loimu&utm_medium=site
Job description
We are seeking an accomplished Target Discovery Lead to join our client’s Cancer Genomics Research Team. The Target Discovery Lead drives innovation in cancer genomics by identifying and validating novel therapeutic targets. This role combines strategic thinking, scientific leadership, and cross-functional collaboration to advance high-impact ideas through the discovery pipeline. The ideal candidate will have a strong track record in target identification and validation, preferably within the small molecule space.
Key Responsibilities
Scientific Strategy & Innovation
- Monitor emerging trends and breakthroughs in cancer genomics to inspire new target concepts.
- Lead ideation sessions and foster a culture of creativity and scientific rigor in target discovery.
Target Identification & Prioritisation
- Design and implement strategies for identifying high-potential therapeutic targets in collaboration with bioinformatics and translational research teams.
- Evaluate and prioritise target ideas based on biological relevance, feasibility, and clinical impact.
Validation & Advancement
- Oversee experimental validation of selected targets, ensuring robust scientific evidence. Develop and conduct complex assays. Analyse and interpret experimental data, synthesise insights, and communicate results effectively in internal reviews and external presentations.
- Define clear advancement criteria and decision-making frameworks to progress targets through the pipeline.
Leadership & Accountability
- Act as the primary owner for target ideation goals, ensuring timely delivery and alignment with organisational strategy.
- Collaborate cross-functionally internally and externally to integrate insights from genomics, bioinformatics, and clinical research.
- Initiate and manage strategic collaborations with CROs, academic institutions, and industry partners to accelerate target discovery and validation.
- You will work closely with a multidisciplinary team to discover and validate novel cancer targets and help develop first- or best-in-class targets from concept to clinical candidate. This is a unique opportunity to contribute to cutting-edge cancer therapies that can make a real difference for patients.
What We Offer
- A chance to work with experienced scientists in a dynamic R&D environment.
- A supportive workplace with opportunities for growth.
- The opportunity to contribute to innovative therapies that improve patients’ lives.
- A culture of friendliness, respect, mutual appreciation, and diversity, creating a safe environment to strive for excellence.
- Career paths and development opportunities that support innovation and impact on quality of life.
Key Qualifications
- Ph.D. in Molecular Biology, Cancer Genomics, Genetics, or related field.
- Postdoctoral industry experience in oncology research, target discovery, or drug development.
- Proven track record in target identification and validation within cancer biology.
- Strong understanding of genomics, bioinformatics, and translational research.
- Demonstrated ability to lead teams and drive projects to completion.
- Excellent communication and strategic thinking skills.
- Experience with CRISPR-based functional genomics and gene-editing technologies.
- Proficiency in multi-omics data analysis (genomics, transcriptomics, proteomics), with experience in flow cytometry, advanced microscopy techniques.
Preferred Skills
- Familiarity with computational biology tools and pipelines for target discovery.
- Knowledge of tumor biology and resistance mechanisms.
- Strong ability to interpret large-scale datasets and integrate insights into experimental design.
- Prior experience in pharma or biotech environments with drug discovery exposure.
TSP Talent Solutions and our customers are affirmative action/equal opportunity employers (Minorities/Females/Veterans/Disabled)
3.8.2026 | Avoimet työpaikat
https://duunitori.fi/tyopaikat/tyo/qa-manager-development-scsom-20455198?utm_source=loimu&utm_medium=site
Apply latest by 30.8.2026
Job description
Are you looking for an exciting professional challenge?
We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.
NextPharma Tampere has several decades of extensive experience in pharmaceutical development, commercial manufacturing and packaging of ophthalmic products BFS (Blow Fill Seal), MD (Multi dose) and PFMD (preservative free multi dose ophthalmic products). The products we manufacture are globally exported.
Interested in shaping Quality Excellence in Pharmaceutical Development?
We are seeking an experienced and highly motivated QA Manager – Development to join our Quality organization in Tampere. In this critical leadership role, you will provide QA oversight for late-stage pharmaceutical development activities, process validation, technology transfer and commercial readiness. You will ensure that development programs progress in compliance with GMP requirements while supporting the successful transition from development to commercial manufacturing. You and your team (3-4 Specialists) work closely together especially with the site Product Development Team and Production.
This is an exciting opportunity for a quality professional who combines People skills, strong GMP expertise, scientific understanding and a collaborative mindset to support innovative pharmaceutical products through pivotal development stages.
Key Responsibilities:
Leadership
- Coach and develop QA professionals within the Development Quality function.
- Serve as a trusted business partner to cross-functional development teams.
- Influence quality decisions while maintaining independent quality oversight.
Quality Oversight of Development Activities
- Provide QA support for late-stage development programs, including Phase III and registration-enabling activities.
- Ensure compliance with applicable GMP, ICH, FDA, EMA, and other regulatory requirements.
- Review and approve development documentation, protocols, reports, and other quality-related documents.
Process Validation & Commercial Readiness
- Lead QA oversight of process validation activities, including:
- Process validation
- Cleaning Validation
- Hold Time Studies
- Analytical Method Validation and Transfer
- Review and approve validation master plans, protocols, and final reports.
- Ensure validation strategies are scientifically sound and compliant with regulatory expectations.
- Support process characterization and risk management activities.
Technology Transfer
- Act as QA representative for technology transfer projects.
- Partner with Manufacturing, Product Development, Engineering, Validation, and Supply Chain teams.
- Ensure readiness for commercial manufacturing and regulatory inspections.
Quality Systems & Compliance
- Manage investigations, deviations, CAPAs, change controls, and risk assessments related to development and validation activities.
- Monitor quality metrics and identify opportunities for continuous improvement.
- Support internal audits, supplier audits, and regulatory inspections.
- Promote a culture of quality excellence and compliance throughout the organization.
What we hope you bring:
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, Life Sciences, Engineering or a related scientific discipline.
- Minimum of 3 years of experience in the pharmaceutical or other highly regulated industry.
- Strong expertise in GMP regulations and pharmaceutical quality systems.
- Leadership Experience / Potential, Excellent communication and stakeholder management skills.
- Hands-on experience with process validation and late-stage product development.
- Experience supporting technology transfer and commercialization activities.
- Fluency in Finnish and English.
We Appreciate:
- Experience interacting with health authorities and supporting regulatory inspections.
What We Offer:
- Opportunity to contribute to innovative therapies that improve patients’ lives.
- A pivotal role within a growing and dynamic organization.
- Collaborative international environment with strong cross-functional exposure.
- Competitive compensation and benefits like flexible working hours, lunch and well-being benefit, leisure insurance and company events.
- Professional development and career growth opportunities.
It is a permanent senior white-collar position and you would report to Head of Quality Tampere. We hope you could start working in September-October 2026.
Say yes to what’s next: Would you like to know more about the position? Please contact: Head of Quality Stefan Weber Stefan.weber@nextpharma.com / +358 44 430 4739. The best time to reach him is 4th or 11th Aug between 2 p.m. and 5 p.m. We look forward to receiving your application preferably on our website nextpharma.com/careers before 31st of Aug 2026. Please also include your earliest possible start date. NextPharma Oy Niittyhaankatu 20, Tampere.
14.8.2025 | Avoimet työpaikat
https://career2.successfactors.eu/sfcareer/jobreqcareer?company=ABE&jobId=476
The role
In your role as a laboratory analyst/technician, your work is to skilfully and precisely perform laboratory experiments related to gene technology, microbiology, enzyme analytics, and automation. The daily tasks would include e.g. production of enzymes in fungal platform, analysis of laboratory scale cultivations and documentation of the results. We expect you to adhere to our agreed high standards and HSE practices.
The position is a permanent and located in Rajamäki, Finland.
About you
You hold a Bachelor´s degree from University of Applied Sciences or a technician´s degree and have hands-on skills in molecular biology methods (PCR, DNA extraction etc.) and microbiology methods, especially using bacteria or fungi. Laboratory experience in enzyme or other biotechnology industry is a clear asset. We are expecting a pragmatic and independent working style with the ability to prioritize and organize individual tasks for efficient throughput. We are looking for a reliable team player and value a high level of responsibility and accountability, as well as a willingness to further develop your skills. Good written and verbal communication skills in English are essential. Finnish language skills are considered as an advantage.
Please send your CV and cover letter with a salary expectation by latest September 14th, 2025. Please note that applications are processed already within the application period.
