Environmental Liability Project Manager - Europe

Incluso AB

We are looking for a Supplier Quality Engineer for a global company in Gothenburg. Start is ASAP, 8 months limited contract to begin with, possibility of extension after that. This role is 100% onsite in Gothenburg. Description The Supplier Quality Engineer (SQE) is part of the Supply Network Quality (SNQ) Organisation within our client´s Purchasing and reports to the Director for SNQ.   Purpose The SQE performs quality assurance activities to ensure that sourced components and suppliers’ production processes meet the necessary quality standards and specifications, ultimately contributing to the overall quality of the final product as well as high quality performance of suppliers.  Responsibilities Assess and evaluate potential suppliers based on their quality systems, capabilities and performance history. Conduct audits and site visits to ensure suppliers comply with quality standards. Perform assessments, evaluations and approval of materials and components sourced from suppliers. Perform quality assurance activities in Projects (including performing APQP activities where necessary) according to DVP to meet necessary deadlines. Participate in cross-functional teams to address quality issues and improve product quality. Monitor supplier performance through regular reviews and audits. Collaborate with suppliers to improve their processes and quality systems. Educate and provide support to suppliers in order to develop their quality standards, performance, and best practices. Make sure that quality objectives and expectations are known to suppliers. Maintain comprehensive records of supplier evaluations, audits, and performance metrics. Work closely with Technology, Operations, and Purchasing teams to ensure alignment of quality expectations. Ensure that we utilize and enhance synergies. Contribute to Risk Assessments of suppliers within assigned commodities. Participate in and contribute to the fulfilment of company strategy, operational and personal development activities. Contribute to cost reduction and sustainability goals, including lowering CO₂ emissions and supporting environmentally responsible initiatives.  Authority In accordance with the valid our client´s governance and processes, the SQE has the authorities to act to fulfill the above tasks and responsibilities. Represent SNQ in projects and sourcing cases for their commodities. Approve or reject PPAP submitted by external suppliers. Propose suppliers to be entered into LPS, put on business hold or phased out per the LPS escalation process. Perform and approve/reject audit performance results.  Competencies Bachelor’s degree in engineering, Quality Management, or a related field or experience in supplier quality engineering or quality assurance in a manufacturing environment, preferably in the automotive or marine industry. Strong knowledge of quality management systems (e.g., ISO 9001) and quality improvement methodologies (e.g., Six Sigma, Lean). Proficient in statistical analysis and quality tools (e.g., SPC, FMEA, root cause analysis). Excellent communication and interpersonal skills, with the ability to work effectively with suppliers and cross-functional teams. Strong problem-solving skills and a proactive approach to quality management. Proficient in using digital tools including Microsoft Office 365 applications. Understanding of sustainability concepts and strategies, including the 9Rs, carbon footprint (CO₂) analysis, and related environmental frameworks.  This role requires fluency in English. Application: Please submit your CV and application in English. This is a full-time consultant position in Gothenburg through Incluso. Start is ASAP, 8 months limited contract to begin with, with possibility of extension after that. This role is 100% onsite in Gothenburg. Please submit your CV as soon as possible since we will review the applications on an on-going basis. For more information about this role, please contact Marianne Nilsson recruiter at Incluso.

CCRM Nordic AB (svb)

About CCRM Nordic CCRM Nordic breaks down the bottlenecks that slow life-changing therapies from lab to patient. Based at GoCo Health and Innovation City in Mölndal, we provide ATMP teams across Sweden, the Nordics and Europe with the infrastructure, know-how and partner network they need, whether that means a single consultation or a long-term manufacturing collaboration. We have invested in a brand-new GMP manufacturing facility with five processing rooms on floor 16 of GoCo House. We are now building the founding team that will shape how this facility runs, and are looking for a Manufacturing Team Lead ready to be part of something genuinely exciting. The opportunity This is a founding role. As one of the first hires into the manufacturing team, you will help build the structure, not just step into it. From authoring SOPs and batch records to training operators and leading quality investigations, this role sits at the operational heart of CCRM Nordic's manufacturing capability. You will lead a team of up to six GMP operators across multiple processing rooms, manage day-to-day scheduling and training, and act as the department's SME for quality systems. You will work alongside PD and MSAT colleagues on new product introductions and technology transfers, and collaborate with our Validation team on equipment qualification and process establishment. Key responsibilities Manufacturing Operations Lead day-to-day GMP manufacturing operations across multiple processing rooms, ensuring clinical materials are delivered on time and to the highest quality standard. Perform and oversee hands-on processing including cell culture, bioreactor operation, Tangential Flow Filtration (TFF) and chromatography. Schedule and manage housekeeping, environmental monitoring and cleaning activities, internally and with external contractors. Maintain full inventory control, ensuring consumables and raw materials are stocked and within expiry. People & Team Leadership Line manage a team of up to six pharmaceutical operators, including performance management, workload planning and day-to-day support. Design and deliver training plans to ensure every team member is qualified for all processing and ancillary activities. Act as a role model for a collaborative, high-performance culture: mentoring and developing the people around you. Quality & Compliance Serve as the manufacturing SME for all GMP quality matters, leading incident investigations, root cause analyses, change controls and CAPAs. Ensure all operations are executed in strict accordance with approved SOPs, Batch Manufacturing Records and current GMP guidelines. Author and review SOPs, batch records, logbooks, COSHH assessments and User Requirement Specifications for new equipment. Support regulatory inspections and ensure the facility is always inspection-ready. Collaborate with the Validation Department on equipment calibration, qualification and shutdown planning. New Product Introduction & Tech Transfer Partner with PD and MSAT teams to introduce new products and processes into the GMP suite. Support technology transfers into and out of the facility, including handovers to clients or CMOs. What we are looking for Essential Minimum 5 years' GMP manufacturing experience, with a strong focus on bioproduction or ATMPs. Proven track record as a line manager of a GMP manufacturing team. Hands-on experience with ATMPs, ideally including Viral Vectors or similar advanced modalities. Degree in bioprocessing, microbiology or a related life science discipline, or equivalent experience. Deep working knowledge of GMP QMS systems: quality incidents, change controls and CAPA management. Experience authoring SOPs, batch records and validation documentation. Strong communication skills and ability to collaborate across functions. Highly Desirable Experience in Tech Transfer and process validation. Hands-on operation of TFF systems, including Repligen platforms. Experience supporting or participating in regulatory inspections. The person We are looking for someone who is: A strong team player who invests in the people around them and understands that great manufacturing is a collective achievement. Adaptable and calm under pressure, able to pivot when processes change, timelines shift or unexpected challenges arise. Energised, not overwhelmed, by the complexity of a new facility and evolving product portfolio. Service-oriented and delivery-focused, with high personal standards for accuracy and thoroughness. An excellent organiser who can hold multiple priorities without letting quality slip. Why join CCRM Nordic? CCRM Nordic is an innovation-led organisation at the frontier of ATMP development. Joining now means helping to shape the team, culture and operational standards of a facility that will directly contribute to getting advanced therapies to patients faster. A rare opportunity to join a founding manufacturing team and leave your mark on how things are built. Work alongside world-class scientists and process development experts on cutting-edge ATMP programmes. A collaborative, supportive environment where your expertise is genuinely valued. Clear pathways for growth as the team expands from Phase 1 through to full multi-project manufacturing capacity. Competitive salary in line with the Swedish pharmaceutical market. Ready to build something important? We'd love to hear from you.

Digitalenta AB

You’ll join a forward-thinking R&D environment focused on building next-generation infotainment and software-driven driving experiences, where data is at the core of innovation. Based in Gothenburg, this on-site assignment runs from April 27, 2026, to April 30, 2027. About the Role As a Data Engineer within the infotainment software factory, you will contribute to building and evolving a data product that provides visibility into CI/CD pipelines, engineering environments, and software products. Working in a team of skilled data engineers, you’ll transform complex engineering data into actionable insights, supporting efficient and high-quality software development. You will collaborate closely with platform, CI/CD, and product teams. Responsibilities Design and develop scalable data pipelines for ingesting, transforming, and storing engineering and CI/CD data Define and implement canonical data models and metrics in collaboration with architects and senior engineers Build and maintain the ConX engineering data product to support software development workflows Develop event-driven and batch data processing solutions Ensure high data quality, reliability, and observability across pipelines Apply data governance, security standards, and access controls Deliver self-service datasets and analytical layers for engineering teams and stakeholders Monitor, troubleshoot, and continuously improve pipeline performance and efficiency About You You are a hands-on Data Engineer with a strong interest in data-intensive systems and modern software development practices. With a few years of experience under your belt, you are comfortable working in cross-functional environments and enjoy solving complex data challenges. Your ability to bridge technical implementation with business needs makes you a valuable contributor to high-impact engineering teams. Experience and Skills Bachelor’s or Master’s degree in Computer Science, Engineering, Data Science, or similar 3–7 years of experience in data engineering or software engineering Strong experience with Python, SQL, or similar for building data pipelines Solid understanding of data modeling, transformation layers, and modern data platforms Experience working with CI/CD systems and engineering data sources (e.g., Jenkins, GitLab CI, Grafana, ELK, Git) Knowledge of distributed systems, data storage formats, and streaming/event-driven architectures Familiarity with cloud platforms (AWS, Azure, or GCP) and containerized environments is a plus Understanding of data governance, security, and compliance practices is meritorious About the assignment For this assignment you will be hired as a full-time consultant by Digitalenta. We offer our consultants a generous package including healthcare allowance, insurance policy, paid vacation days and pension savings. In addition, you'll also have a dedicated consultant manager available throughout your employment with us, in addition to optional networking activities with our network of consultants.