Lab Technician

DAVA Foods Sweden AB

Tjänstebeskrivning Som Laborant hos DAVA Foods Sverige arbetar du med att stödja kvalitetskontroll och produktutveckling genom provtagning, analys och dokumentation av livsmedelsprodukter. Rollen är viktig för att säkerställa att produkterna uppfyller gällande lagstiftning, kvalitetskrav och säkerhetsstandarder samt bidra till innovation och förbättringsarbete. Primära Ansvarsområden · Analysera inkommande prover enligt provplan (provberedning, registrering, analysering, skicka prover till externt Lab, rapportering) · Ta fram analysföreskrifter och SOP:er · Genomföra och rapportera hygienkontroller enligt provplan · Delta i ringtester · Frisläppa produkter efter godkänt analysresultat · Rapportera analysresultat (interna & externa) till Laboratoriekoordinator / Kvalitetschef · Utfärda och skicka analyscertifikat till kunder · Planera, genomföra och rapportera hållbarhetstester enligt plan tillsammans med teamet · Kalibrera och underhålla laboratorieutrustning · Medverka vid felsökning och utredningar vid kvalitetsavvikelser · Följa gällande rutiner för livsmedelssäkerhet, god laboratoriesed och arbetsmiljöregler · Bidra till förbättringsarbete och innovation i produktutveckling Kvalifikationer · Laborantutbildning eller relevant högskoleutbildning inom bioteknik, livsmedelsvetenskap, kemi eller mikrobiologi · Erfarenhet av laboratoriearbete, gärna inom livsmedel · Erfarenhet av att genomföra tester, protein- och aktivitetsanalyser samt mikrobiologiska analyser · Grundläggande kunskaper i mikrobiologi och kemiska analysmetoder · God kommunikativ förmåga, både skriftligt och muntligt, inklusive kontakt med kunder och externa laboratorier · Svenska och engelska i tal och skrift Meriterande · God datorvana och erfarenhet av arbete i kvalitetssystem (ISO, HACCP) · Förståelse för livsmedelssäkerhet och hållbarhetskrav Personliga Egenskaper · Noggrann och strukturerad: Du arbetar metodiskt och har öga för detaljer · Ansvarstagande: Du tar ansvar för dina arbetsuppgifter och förstår vikten av att följa rutiner · Analytisk förmåga: Du har lätt att förstå och tolka analysresultat samt identifiera avvikelser · Samarbetsvillig: Du trivs med att arbeta i team och bidrar till ett positivt arbetsklimat · Flexibel och lösningsorienterad: Du kan anpassa dig till förändrade förutsättningar och bidra med idéer för förbättringar · Kommunikativ: Du är tydlig i din dokumentation och kan kommunicera resultat och observationer professionellt · Proaktiv och innovativ: Du har intresse för utveckling och innovation Vad Vi Erbjuder · En trygg och stabil arbetsgivare inom en växande och samhällsviktig bransch. · Ett nära samarbete i ett engagerat team där vi värdesätter kunskapsdelning, öppenhet och laganda. · Moderna laboratoriemiljöer och tillgång till avancerad utrustning. · Friskvärdsbidrag och hälsofrämjande aktiviteter – din hälsa är viktig för oss. · Kollektivavtal med marknadsmässiga löner, försäkringar och pensionsavsättningar. · En arbetsmiljö med fokus på hållbarhet, kvalitet och ständig förbättring.

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.

Graphcore

Job Summary Our team is at the forefront of the artificial intelligence revolution, enabling innovators from all industries and sectors to expand human potential with technology. The availability of specialised artificial intelligence compute will be a decisive factor in AI’s rate of progress. Graphcore allows innovators to go further, faster. What we do, really makes a difference. As an Electronics Laboratory Technician you will be part of the team responsible for the Bristol laboratories within Graphcore ensuring the lab facilities are always operational and available to support cross-functional operations. You will also help develop and implement standard operating procedures to ensure compliance with ESD, safety, quality and regulatory standards, and other relevant policies. The Team The Laboratory team supports the installation, maintenance, repair and modification of electronic systems, cables, and equipment within the laboratory. Providing support to cross-functional teams to troubleshoot issues to ensure reliable and safe operation of all lab equipment. The team also maintains accurate technical documentation, manages tools, assets, and test equipment, and contributes to efficient, high-quality technical operations. Responsibilities and Duties • Support the installation, setup, and calibration of electronic test equipment (oscilloscopes, logic analysers, power supplies, etc). • Execute preventative maintenance programs. • Maintain a clean and safe lab environment, ensuring compliance with health and safety requirements. • Check and maintain ESD countermeasures. • Responsible for asset management and goods in/out process for the laboratories. • Support engineering teams in setting up test benches, configuring equipment, and ensuring technical readiness for hardware bring up, validation, and characterisation. • Generate standard operating procedures providing technical guidance, training, and procedures to support the requirements of multidisciplined lab teams. • Support engineering teams with board, cable, and wire modifications. Candidate Profile Essential: • Experience in working in an electronics lab environment. • Strong technical understanding of electronic test equipment, including setup, calibration, and troubleshooting. Job Description Template 2024• Good understanding of ESD prevention and controls. • Working knowledge of health & safety requirements in an electronics laboratory, ensure safe working practices are implemented and controlled. • Ability to collaborate with cross-functional engineering teams in the laboratory environment, ensuring setups meet technical requirements while adhering to defined working practices and project timescales. • Experience in Repair and Modification of PCB assemblies to IPC-7711/21 and J-STD-001 standards. • Experience in cable and wire harness assemblies to drawings and IPC-620 standards. • Experience in IPC-A-610 Inspection. • A pragmatic approach, the ability to improvise and get the job done. • Ability to mentor junior members of the team. • Effective communication skills. Desirable • Experience using asset management systems including tracking of test equipment, security- controlled devices, and calibration status. • Experience in collaborating with external subcontractors for technical services including periodic maintenance and calibration of lab equipment, facilities upgrade, or specialist equipment maintenance.