Are you a student looking for internship or thesis project? Apply here!

PolyPeptide is on a transformative growth journey – expanding globally, investing in new technologies, and increasing our production capacity through major site expansions and strategic projects. As part of this journey, we are launching a global SAP S/4HANA implementation and building a new ERP function from the ground up. We’re looking for an experienced IS/IT Compliance & Validation Specialist to help ensure that our new enterprise systems – especially the ERP platform – are implemented and maintained in line with industry standards, regulatory requirements, and best practices. This is a unique opportunity to join in the ERP journey and take a central role in securing validation of a modern, global ERP system in close collaboration with Global QA. About us PolyPeptide Group AG and its consolidated subsidiaries (“PolyPeptide”) is a specialized Contract Development & Manufacturing Organization (CDMO) for peptide- and oligonucleotide-based active pharmaceutical ingredients. By supporting its customers mainly in pharma and biotech, it contributes to the health of millions of patients across the world. PolyPeptide serves a fast-growing market, offering products and services from pre-clinical through to commercial stages. Its broad portfolio reflects the opportunities in drug therapies across areas and with a large exposure to metabolic diseases, including GLP-1. Dating back to 1952, PolyPeptide today runs a global network of six GMP-certified facilities in Europe, the U.S. and India. PolyPeptide’s shares (SIX: PPGN) are listed on SIX Swiss Exchange. United by Purpose At PolyPeptide, we take pride in contributing to medicines that make a real difference to people's lives and health. Here, you will become part of work that truly matters, every single day. We are driven by our core values: trust, innovation and excellence. This is reflected in how we collaborate, solve problems, and uphold our responsibility for quality and safety for the patients ultimately affected by our work. We are a company undergoing rapid development. Our growth brings a fast-paced environment, change and new opportunities for both employees and the business. Here, you will grow together with us. If you are looking for a workplace where purpose, community and development go hand in hand, then PolyPeptide is the right place for you. About the Role In this role, you will be part of our global IS/IT organization and act as a key resource in securing regulatory compliance across enterprise systems – with a primary focus on the new ERP program. You’ll be responsible for system validation (CSV), audit readiness, change control, and risk management, with a strong emphasis on maintaining compliance with GxP, 21 CFR Part 11, EU Annex 11, and GAMP 5. You will work closely with Global QA, IT, regulatory affairs, and external vendors to ensure that the new ERP platform and other digital systems are inspection-ready, properly documented, and aligned with pharmaceutical regulations and expectations. Key Responsibilities * Develop and execute validation strategies for GxP-relevant systems in accordance with GAMP 5 and biotech/pharma industry standards. * Author and review validation documentation such as validation plans, IQ/OQ/PQ protocols, traceability matrices, and summary reports. * Ensure systems comply with electronic records and signature regulations (21 CFR Part 11, Annex 11). * Perform risk assessments for new systems, upgrades, and system changes, and integrate validation into the change management process. * Maintain audit-ready documentation and support both internal and external audits, including regulatory inspections. * Address audit findings and contribute to corrective and preventive actions (CAPAs). * Collaborate with QA, regulatory, manufacturing, and IT stakeholders as well as external vendors to align on compliance and validation requirements. * Provide training and guidance on validation procedures, regulatory expectations, and documentation standards. Your Profile We are looking for a structured and proactive specialist who thrives in a regulated environment and enjoys collaborating across functions. You bring: * A Bachelor’s or Master’s degree in Life Sciences, Engineering, Computer Science, or similar. * 5+ years of experience in IT compliance, system validation, or QA in biotech, pharma, or another regulated industry. * Solid knowledge of GxP, GAMP 5, 21 CFR Part 11, and EU Annex 11. * Experience with computerized system validation (CSV) and quality documentation. * Familiarity with enterprise platforms like ERP, MES, LIMS, or QMS. * Excellent analytical, documentation, and communication skills. * Full professional proficiency in English. As a person, you are detail-oriented and accountable – and you take pride in building systems and documentation that stand up to inspection and support safe, efficient operations. FIND THIS INTERESTING? APPLY NOW! Are you ready to take the next step in your career? The position will be open until August 31 but we are applying ongoing selection so do not hesitate to send us your application. Due to summer vacation we will start going through the applications later in August. For more information, please contact Krister Svärd at krister.svard@polypeptide.com. Swedish applicants are welcome to contact the local union chairman for Akademikerföreningen or Unionen at +46 040-36 62 00 for support.

Who We Are Allgon is a leading manufacturer of wireless machinery control systems, delivering customized solutions to companies across the industrial sector. Our customers engage with us through our subsidiaries, Tele Radio, Åkerströms and Sistematica. We are passionate about developing industrial remote control solutions that enhance safety and efficiency worldwide. Our R&D department values fast decision-making, open communication, and a flat organizational structure while offering strong resources and excellent development opportunities. We have a team of around 50 professionals working across multiple locations, including Gothenburg, Björbo, Malaga. ---------------------------------------------------------------------------------------------------------------------------------- About the Role We are growing our R&D team and are looking for dedicated Mechanical Engineers to join us. As a Mechanical Engineer, you will play a key role in the development and maintenance of the mechanical design across our product portfolio. You will work hands‑on with product innovation, design improvements, and problem‑solving, ensuring our solutions meet the highest standards in performance, durability, and compliance. You will be part of the R&D Hardware team, working cross-functionally and collaborating with colleagues in R&D, production, and product management. The position is based in Gothenburg and reports to the Manager R&D Hardware. Key Responsibilities: * Develop and maintain mechanical designs for our products. * Drive mechanical design work within assigned development projects. * Lead investigation and root-cause analysis for mechanical product deviations and maintenance issues. * Evaluate existing technology and product functionality, proposing improvements where needed. * Assess and explore new technologies within the mechanical field. * Support NPI activities, including first builds and debugging. * Execute design testing of mechanical components. * Plan, set up, and carry out mechanical compliance testing. ---------------------------------------------------------------------------------------------------------------------------------- What We’re Looking For We are looking for both junior and senior engineers with a strong interest in mechanical engineering and a solid technical understanding. Whether you are early in your career or bring several years of experience, you are a proactive team player who takes initiative, enjoys hands‑on work, and collaborates effectively both independently and across cross-functional teams. You approach complex challenges with a structured, analytical, and solution‑oriented mindset. Your communication skills enable you to contribute clearly in a dynamic environment and support sound technical decision‑making. Key qualifications include: * MSc or BSc in Mechanical Engineering, Electrical Engineering, or equivalent. * Experience in mechanical design for embedded systems. * Experience with one or more of the following areas is an advantage: * Injection molding * Chemical regulations * LVD * Functional safety * Sustainability * Electronics * Mechanical testing, IP ratings, drop testing, etc. * Knowledge of SolidWorks and Jira is meritorious. * Fluent in English, Swedish skills are a plus ---------------------------------------------------------------------------------------------------------------------------------- What We Offer * Work with cutting-edge, high-quality products in a dynamic environment. * Opportunities for continuous professional growth and career development. * A challenging and rewarding role within a growing organization. * Collective agreement, including 9 extra days off per calendar year through reduced working hours. * 3,000 SEK annually for wellness benefits. ---------------------------------------------------------------------------------------------------------------------------------- About Allgon Allgon is a Swedish company specializing in industrial radio control, with a strong track record in wireless technology innovation. Through our brands Tele Radio, Åkerströms and Sistematica, we have built a global presence, employing over 470 professionals and presence in 26 countries. We offer an exciting work environment in a profitable and growing organization with a strong technical focus. Despite our global reach, we maintain the close-knit atmosphere of a smaller company, where every employee has a voice and can influence the projects they work on. At Allgon, sustainability is a key priority—ecologically, socially, and financially. We are committed to attracting passionate individuals who share our vision of a safer, more efficient world through advanced wireless technology. We look forward to your application! ⭐