Sökresultat för "GMP"

På Läkemedelsverket gör vi skillnad tillsammans. I livet och för livet. Vi jobbar för människors och djurs hälsa, för ett bättre Sverige idag och i framtiden. Vill du använda din kompetens inom kvalitetssäkring av läkemedelstillverkning eller partihandel med läkemedel, har ett öppet, objektivt förhållningsätt och ett genuint intresse för inspektioner? Har du goda kunskaper om GMP eller GDP? Sök jobb hos oss! Vår verksamhet Enheten för inspektion av industri och sjukvård ansvarar för tillsyn av kliniska prövningar, tillverkning, distribution och system för säkerhetsövervakning av läkemedel. Tillsynen omfattar aktörer inom industri och sjukvård och bedrivs huvudsakligen via fältinspektioner både nationellt och internationellt. Vi deltar även aktivt i utformning av regelverk och riktlinjer inom respektive område. För närvarande arbetar drygt 40 personer på enheten indelade i fem grupper: inspektion GMP/GDP 1 och 2, inspektion GVP/GCP, inspektion sjukvårdsnära tillverkning samt inspektion kansli. Vi söker nu nya kollegor till grupperna inspektion GMP/GDP 1 och 2. Dina arbetsuppgifter Arbetet som inspektör består till stor del av fältinspektioner av läkemedels- och substanstillverkning, import respektive partihandel.  Som ny inspektör får du en gedigen introduktion till inspektionsarbetet anpassad efter tidigare erfarenhet och efter certifiering kommer du att delta i och leda inspektioner. Med mer erfarenhet från inspektioner kommer nationella inspektioner att varvas med internationella inspektionsuppdrag för bland annat EMA (European Medicines Agency). Som inspektör kommer du att ingå i olika arbetsgrupper och samarbeta med andra verksamheter inom Läkemedelsverket och förväntas bidra i hantering av olika ärenden samt till samsyn och harmonisering vad gäller regelverk och inspektionsverksamhet. I arbetsuppgifterna ingår även att informera om regelverk i olika sammanhang samt hantera inkommande frågeställningar ifrån företag, andra myndigheter eller allmänheten. Baserat på tidigare erfarenheter finns olika vägar att utvecklas framåt i en expertroll hos oss. Det finns goda möjligheter att vidareutvecklas i rollen med till exempel deltagande i nationella och internationella arbetsgrupper. Din bakgrund Vi söker dig som har en naturvetenskaplig universitets- eller högskoleexamen och mångårig, gedigen yrkeserfarenhet från kvalitetssäkring av läkemedelstillverkning eller partihandel med läkemedel. Du har goda aktuella kunskaper om GMP och GDP och vi ser gärna att du har god insikt i regelverk gällande kvalitet och godkännande av läkemedel. Du bör till stor del uppfylla de formella kraven för sakkunnig person (QP) enligt HSLF-FS 2021:102. Det är meriterande om du har erfarenhet från kommersiell läkemedelstillverkning, inspektioner/auditering eller om du har arbetat som sakkunnig person (QP eller RP). Det är även meriterande om du har djupare kunskaper inom tillverkning av aktiva substanser, sterila eller biologiska läkemedel. Det dagliga arbetet ställer krav på mycket god förmåga att kommunicera i tal och skrift på såväl svenska som engelska. Körkort är ett krav i och med att arbetet medför regelbundna resor. Dina personliga egenskaper Du har hög integritet och god analytisk förmåga. Arbetet som inspektör kräver god kommunikations- och samarbetsförmåga samt ett strukturerat arbetssätt från planering till genomförande och rapportering av inspektioner. Du behöver kunna granska och utvärdera uppgifter från olika system, prioritera och självständigt fatta beslut även under tidspress vid fältinspektioner. Du har ett nyfiket förhållningssätt och är öppen för att ta in ny information. Du är tydlig i din kommunikation med andra såväl internt som externt samt värnar om ett gott bemötande. Vi lägger stor vikt vid personlig lämplighet. Bra att veta Sista ansökningsdag: 2026-09-04   Anställningsform: Tillsvidare   Tillträde: Enligt överenskommelse   Enhet: Inspektion av industri och sjukvård   Diarienummer: 2.4.1-2026-051207   Vi tillämpar 6 månaders provanställning.   Vi värdesätter mångfald och välkomnar sökande med olika bakgrund.   På Läkemedelsverket får du goda förutsättningar för balans i livet. Vi erbjuder dig bland annat flextid, förmånliga semestervillkor, friskvårdsbidrag samt friskvård på arbetstid. I den mån arbetsuppgifterna tillåter finns det möjlighet att delvis arbeta på distans efter överenskommelse med chef. Läs mer om de förmåner du får hos oss här: https://www.lakemedelsverket.se/sv/om-lakemedelsverket/jobba-pa-lakemedelsverket/formaner-hos-oss  Läkemedelsverket är beredskapsmyndighet, vilket innebär att vi genomför vissa bakgrundskontroller i samband med rekryteringar. Du kommer vid en eventuell intervju att behöva styrka din identitet samt uppvisa examensbevis och relevanta intyg. All tillsvidareanställd personal vid Läkemedelsverket är krigsplacerad inom myndigheten. Kontakt Du är välkommen att kontakta gruppcheferna Marianne Weisner eller Jenny Bjurström. Du kan även kontakta de fackliga företrädarna Jonas Walldén, Saco och Pia Wictor, ST. Vi finns alla på telefon 018-17 46 00 eller nås genom e-post fornamn.efternamn@lakemedelsverket.se. Mer om Läkemedelsverket Du tänker kanske inte så ofta på Läkemedelsverket, men vi kan lova att du möter oss i din vardag. Resultatet av det vi gör märks på apotek, sjukhus, hos veterinären och i ditt badrumsskåp. Vi ser nämligen till att du och alla andra i Sverige får tillgång till säkra och effektiva läkemedel och medicintekniska produkter, allt från plåster och graviditetstester till rollatorer och appar. Det gör vi genom att godkänna och ge tillstånd, övervaka och kontrollera och genom att informera och ge råd. Vi som arbetar på Läkemedelsverket är stolta över vårt viktiga samhällsuppdrag: att bidra till den svenska folk- och djurhälsan. Läs mer om vårt uppdrag och vad det innebär att arbeta på Läkemedelsverket här: https://www.lakemedelsverket.se/sv/om-lakemedelsverket/jobba-pa-lakemedelsverket Välkommen med din ansökan! Denna rekrytering sker helt genom Läkemedelsverkets försorg. Vi undanber oss därför telefonsamtal från rekryteringsföretag och annonsförsäljare.

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry. Assignment Description We are looking for an experienced Automation Engineer What You Will Work On Develop and configure automation solutions for pharmaceutical manufacturing systems Design and implement control logic, sequences, phases, and interlocks Configure and optimize DeltaV or equivalent DCS automation platforms Develop HMI screens and operator interface solutions Configure alarm management and control strategies Integrate process equipment with control systems and higher-level applications Support batch control and recipe implementation Participate in FAT, SAT, commissioning, and system verification activities Troubleshoot automation systems during testing and startup Prepare and maintain automation documentation and technical specifications Support qualification and Computerized System Validation (CSV) activities Collaborate with process, validation, commissioning, and engineering teams Ensure compliance with GMP, GxP, and pharmaceutical quality standards Support system improvements and automation optimization throughout the project lifecycle What You Bring Experience as an Automation Engineer within the pharmaceutical industry or another GMP/GxP-regulated environment Strong hands-on experience with DeltaV or similar DCS/process automation platforms Experience configuring control logic, sequences, phases, interlocks, and alarm functions Experience developing HMI applications and operator interfaces Experience integrating process equipment with automation and supervisory systems Good understanding of GMP, GxP, and Computerized System Validation (CSV) Experience performing FAT, SAT, commissioning, startup, and automation verification Experience troubleshooting, testing, and documenting automation solutions in regulated environments Ability to work effectively with process, validation, and commissioning teams Strong analytical, troubleshooting, and communication skills

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry. Assignment Description We are looking for an experienced Technical Sub Project Manager – Equipment & Systems What You Will Work On Lead technical equipment packages or engineering sub-projects Coordinate technical systems and multidisciplinary engineering activities Define technical requirements and develop equipment specifications Manage suppliers, technical vendors, and engineering partners Coordinate technical design reviews and engineering approvals Ensure technical deliveries meet project quality, cost, and schedule objectives Monitor project progress and manage technical risks Drive technical issue resolution and decision-making Collaborate with Process, Automation, Validation, Commissioning, QA, and Engineering teams Support procurement activities and supplier evaluations Review technical documentation, drawings, and specifications Participate in FAT, SAT, commissioning, and project handovers when required Ensure compliance with GMP, engineering standards, and project requirements Coordinate cross-functional stakeholders throughout the project Support continuous improvement of engineering execution and project delivery What You Bring Experience leading technical sub-projects or engineering work packages Background in industrial investment or capital projects Experience managing technical equipment and engineering systems Strong technical coordination and stakeholder management skills Experience preparing technical specifications and requirements Experience managing suppliers and contractor deliveries Experience conducting technical reviews and engineering evaluations Knowledge of project planning, scheduling, and risk management Ability to coordinate multiple engineering disciplines Strong communication and leadership skills Experience working in multidisciplinary engineering teams

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry. Assignment Description We are looking for an experienced Process Engineer What You Will Work On Translate process requirements into practical manufacturing solutions Develop process descriptions, process parameters, operating limits, and process documentation Support process development for GMP manufacturing operations Develop and optimize batch processes and recipe management Work with DeltaV or equivalent automation platforms Define process parameters, setpoints, and operating boundaries Support commissioning, process verification, testing, and startup activities Troubleshoot process and production issues Collaborate closely with automation, validation, and commissioning teams Support process safety through alarm philosophy and interlock design Ensure compliance with GMP/GxP standards and regulatory requirements Participate in process optimization and continuous improvement initiatives Prepare and maintain technical documentation throughout the project lifecycle What You Bring Experience as a Process Engineer within the pharmaceutical, biotech, or other GMP/GxP-regulated industries Strong understanding of batch manufacturing processes and recipe development Experience with DeltaV or similar Distributed Control Systems (DCS) Experience defining process parameters, setpoints, and operating limits Understanding of alarm philosophy, interlocks, and process safety principles Experience with process verification, testing, commissioning, and troubleshooting Experience collaborating with automation and validation teams Strong technical documentation skills Experience working in highly regulated manufacturing environments Good communication and collaboration skills

Vill du arbeta i framkant av framtidens cell- och genterapier? Är du disputerad inom biomedicin, bioteknik eller annat relevant område och vill kombinera kvalitetsarbete, teknisk utveckling och forskning i en högspecialiserad verksamhet? Då kan du vara den vi söker som tekniskt ansvarig till aferes- och stamcellslaboratoriet inom Klinisk immunologi och transfusionsmedicin (KITM) i Huddinge. Du erbjuds en central roll med ansvar för kvalitetssäkring av metoder och medicintekniska instrument inom våra aferesmottagningar möjlighet att arbeta med utvecklingsprojekt inom stamcellstransplantation samt avancerade cell- och genterapier (ATMP) ett stimulerande och utvecklande arbete i en högspecialiserad verksamhet med forskning, innovation och avancerad laboratorieverksamhet ett nära samarbete med engagerade kollegor inom flera professioner i en dynamisk och föränderlig sjukhusmiljö. Självklart får du också ta del av våra generella förmåner som Karolinska Universitetssjukhuset erbjuder dig. Om tjänsten På sektionen för Hemoterapi bedrivs högspecialiserad verksamhet inom aferes, stamcellsterapi och avancerade cell- och genterapier. Sektionen består av en aferesmottagning där patienter behandlas och stamceller tillvaratas samt ett GMP-laboratorium med dedikerat renrum för avancerad cellhantering. Verksamheten regleras av Socialstyrelsens och Läkemedelsverkets föreskrifter och är ackrediterad enligt flera nationella och internationella kvalitetsstandarder, däribland SWEDAC och JACIE. Här kombineras klinisk verksamhet med forskning och utvecklingsprojekt inom framtidens behandlingar. Tjänsten är huvudsakligen placerad vid Stamcellslaboratoriet och Aferesmottagningen i Huddinge, men arbete förekommer även vid vår aferesmottagning i Solna. Under introduktionsperioden kommer du främst att vara verksam på mottagningen i Huddinge. Som tekniskt ansvarig har du en central roll i verksamheten och arbetar nära medicinskt ansvarig läkare, sjuksköterskor, biomedicinska analytiker, kvalitetsansvariga och övriga tekniskt ansvariga inom kliniken. Dina arbetsuppgifter omfattar bland annat att: ansvara för validering, verifiering och förvaltning av medicintekniska instrument och metoder dokumentera och utveckla verksamheten inom kvalitetsledningssystemet delta i upphandlingar och driva utvecklingsprojekt initiera och leda digitaliseringsprojekt samt arbeta med vetenskaplig uppföljning av patientbehandlingar bidra till utveckling, kvalitetssäkring och produktion av nya avancerade terapiläkemedel (ATMP). Du kommer även att ingå i ledningsgruppen för Hemoterapi och rapportera till sektionschefen för Utveckling och IT. Vi söker dig som tar ansvar för ditt arbete och driver processer framåt på ett strukturerat och självständigt sätt planerar, organiserar och prioriterar arbetet effektivt samt håller uppsatta tidsramar har en god samarbetsförmåga och trivs med att arbeta tillsammans med olika professioner kommunicerar tydligt och bygger goda relationer genom ett lyhört och prestigelöst förhållningssätt. Stor vikt läggs vid personlig lämplighet. Kvalifikationer Krav: doktorsexamen inom biomedicin, bioteknik eller annat relevant ämnesområde mycket goda kunskaper i svenska och engelska, både i tal och skrift erfarenhet av utvecklings- eller kvalitetsarbete inom ATMP eller annan relevant cell- eller genterapi erfarenhet av kvalitetssäkring eller förvaltning av medicintekniska instrument och metoder Meriterande: erfarenhet av läkemedelstillverkning enligt GMP erfarenhet av aferes- eller stamcellsverksamhet erfarenhet av digitalisering och dataanalys kunskaper inom flödescytometri utbildning och erfarenhet inom projektledning Om rekryteringsprocessen I samband med din ansökan behöver du bifoga CV. Istället för ett personligt brev ber vi dig besvara urvalsfrågor samt kort motivera varför du passar för rollen. Att besvara frågorna är en förutsättning för att din ansökan ska anses komplett. Varmt välkommen med din ansökan - Tillsammans är vi Karolinska! Inför tillsättning av befattning som innefattar vård av barn och ungdom, kontrolleras den som erbjuds tjänsten mot misstanke- och belastningsregistret. Här kan du läsa mer om rekryteringsprocessen och om vilka kontroller som utförs på Karolinska. Som anställd på Karolinska Universitetssjukhuset kan du komma att krigsplaceras. Läs mer om vad det innebär här. Om du är eller tidigare har varit anställd i Region Stockholm kommer vi att ta interna referenser från din nuvarande eller tidigare chef om du blir aktuell för anställning. För tillsvidaretjänster kan provanställning komma att tillämpas. Att söka jobb i Region Stockholm Vi eftersträvar jämställdhet och jämlikhet på vår arbetsplats och ser gärna sökande med olika bakgrund och förutsättningar. Vi tar endast emot ansökningar via detta system. Ansök genom att klicka på knappen ”Ansök”. Ansökningar per brev eller e-post beaktas inte. Vi undanber oss direktkontakt med bemannings- och rekryteringsföretag samt säljare av ytterligare jobbannonser. Vårt rekryteringssystem kan inte hantera anonyma ansökningar eller sökande med skyddade personuppgifter. Om du har skyddade personuppgifter ber vi dig att kontakta den kontaktpersonen som finns angiven i annonsen. Din ansökan kommer då att hanteras utanför rekryteringssystemet. Du bör även vara försiktig med vilken information du lämnar i din ansökan och endast ta med information som är relevant för den aktuella befattningen. Region Stockholm ansvarar för hälso- och sjukvård, kollektivtrafik, regional utveckling och bidrar till kulturlivet. Varje dag, dygnet runt. I landets snabbaste växande region. Tillsammans skapar vi Europas attraktivaste storstadsregion. Läs mer om hur det är att jobba hos oss i Region Stockholm

YOUR MISSION To manage incoming materials and support Good Manufacturing Practice (GMP) compliant activities for the QC release of product and incoming materials.  Support QC Materials Team in other activities where requested. JOB DESCRIPTION MAJOR ACTIVITIES * Perform inspection of incoming materials, following SOPs and GMP practices to ensure seamless supply of material to support aseptic manufacture of ATMP product. * Monitor the material inspection programme ensuring materials are suitable for the manufacture of gene therapy products to the required standards. * Physical inspection of raw materials. Ensure the warehouse storage environment is acceptable for the materials being inspected (Can be multiple warehouse locations). * Coordinate incoming material testing where required. * Maintain all incoming material documentation meets GMP requirements. * Ensure adequate control of the material status for release or Reject. * Comply with MeiraGTx procedures including Health and safety and GMP. * To ensure all equipment used is calibrated/maintained and in line with SOP’s. * Identify and report procedural problems and deviations. * Perform and support environmental monitoring activities for the sampling room, in line with GMP requirements, ensuring results are recorded and reported. * Perform sampling of incoming raw materials, following SOPs and GMP practices to ensure seamless supply of material to support aseptic manufacture of ATMP product. * Participate in the planning of duties to ensure the facility is acceptable and customers receive products on time and in full. * Any other duties/projects within the skills and ability of the post holder. * Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures. * Responsible for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken. * Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions is closed timely and in a RFT state. KEY PERFORMANCE INDICATORS * HR process compliance. * Material release KPIs. * GMP compliance. * Data integrity.   KEY JOB COMPETENCIES * Experience of working within a GMP manufacturing environment. * Quality Management - looks for ways to improve and promote quality; demonstrates accuracy and thoroughness. * A high Level of attention to detail. * Problem Solving - Identifies and resolves problems in a timely manner; able to gather information; develops alternative solutions; works well in group problem solving situations. * Motivation - sets and achieves challenging goals; demonstrates persistence and overcomes obstacles; measures self against standard of excellence. * Planning/Organizing - prioritizes and plans work activities; uses time efficiently. * Professionalism - approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments. * Innovation - meets challenges with resourcefulness; generates suggestions for improving work; develops innovative approaches and ideas. * Oral Communication - speaks clearly; listens and gets clarification; responds well to questions; demonstrates good presentation skills; participates effectively in meetings. * Written Communication - writes clearly and informatively; edits work for spelling and grammar; varies writing style to meet needs; presents numerical data effectively; able to read and interpret written information. * Physical & mental requirements - occasional lifting; the noise level in the work environment is usually moderate.   JOB RESPONSIBILITIES * Compliance with GMP.   JOB BACKGROUND * Minimum 1 years experience working in a GxP environment. * Experience of quality documentation. * Proficiency in Microsoft Office software (Word, Excel and PowerPoint) preferred.

Role: Team Leader Career Step Level: Step level 3 Location: Blyth, Worksop   📣A bit about the role Do you have the passion and desire to constantly strive for better? Have genuine care for dogs, their humans and our team (squad members), want to create a best in class customer experience and all whilst making it a great place to work. Then this is the job for you! As a Production Team Leader, you will lead a team to deliver our production plan to feed our happy and healthy dogs. Doing this whilst driving high team performance, embracing all aspects of the culture and functional requirements, making continuous improvements and elevating us to the next level. Reporting into the Shift Operations Manager, you’ll support the daily operations and ensure our dogs are provided with the very best human-quality meals. A bit more detail Operational Requirements  * Accountable for our health and safety standards on shift, the upkeep and delivery through conducting daily Health and Safety audits with your Squad members, raising corrective actions to any nasties you may find and owning the resolution. * Be competent in completing thorough Accident Investigations through root cause analysis and completing near-miss reports. Ensuring that corrective actions are raised and closed out in a timely manner.  * Review training and development of staff through all areas of the kitchen by ensuring that Squad members are trained against relevant SOPs and other required training and documentation. * Ensure that labour is managed effectively to ensure production can be maintained through the management of holidays and absences. Proactively managing and identifying issues. * Quality & hygiene standards are increasingly important to us, so we ensure that GMP standards are maintained at all times. As well as verification of IMS checks from the cooking of our products to the cleaning of all our equipment.  * Provide supervision, support and leadership to the Production team in pursuit of key operational metrics of quality, output and waste. Ensuring that you are reactive in times of deviations from the agreed targets. * Have had some experience in leading continuous improvements and problem-solving initiatives, which contribute to savings within the department/company. Communication & Partnership * Be able to communicate clearly and effectively with the SLT team when needed, particularly in times when the Shift Operations Manager may be away from the business.  * Ensure daily handovers between departments are completed - ensuring the relevant detail is captured so each shift oncoming is a success.  * Work closely with the procurement and planning team to ensure meal output meets sales demand. * Work well with multiple functional teams, including People, Engineering, Technical, Warehouse and Order fulfilment to drive well thought-out and cohesive plans Our Culture & Values  * Understanding that squad member engagement drives operational excellence and People Leaders play a crucial role in making Butternut Box the best place they’ve ever worked. * Be present in the Kitchen, ensuring you are available to proactively support the team, help find solutions and take action to change.  * Messages and key communications are delivered to the teams and key stakeholders in a timely and accurate manner. You’ll have an excellent awareness of how your communication style impacts others, and you’ll tailor this to your audience.  * Confidently undertake meaningful and regular 1:1’s with Squad members, ensuring they feel heard and that their feedback is important to you. You’ll consider their career aspirations, skills and background and tailor your style to their needs. 🔎 A bit about you * Strong production background in an FMCG manufacturing environment * Experience in a high-speed volume manufacturing environment * Leadership experience with a broad working knowledge of relevant safety legislation * Pragmatic, adaptable, resilient and humble * Well-practised planning, organisation and scheduling skills * Someone who loves the pace and excitement of FMCG manufacturing * Hungry for a challenge and keen to build something from the ground up * Easily approachable with good interpersonal skills, with creative thinking and analytical skills * Drives for results, action-oriented, problem-solving, and priority setting * Loves dogs (naturally)   🐶  A bit about Butternut Delivering on our promise of "Fresh food, Happy dogs" requires operational excellence at every step. Our Doncaster site, made up of Rudie’s Kitchen (manufacturing) and Ace’s Pantry (Order Fulfilment and Warehouse) are where our meals are gently cooked, and then packed with care for our customers, through the people who manage our flow, quality, and distribution. We are moving beyond the scale-up phase of the operation to a place where excellence happens every day. To do this, we need forward-thinking individuals who see the big picture and want to play a hands-on role in a complex, fast-moving operation. If you believe dogs deserve better and you have the drive to help us deliver it, we want to hear from you.   🥳What's In It For You?🥳 * Enjoy 257.5 hours of holiday per year, plus an extra 8 hours for each year of service (up to 40 hours).* * 39 hours of pre-booked paws days to support good wellbeing and self-care.* * Enrollment into our EAP Telus offering free financial planning, counselling, mental health support and more * Unlock a £500 annual budget for personal learning and development. * Get discounted Private Medical Insurance and dental cover. * Discounted Gym membership with “MyGymDiscounts” helping you stay fit and healthy * Satisfy your taste buds with subsidised food from a variety of street food vans, and of course, pay day pizza! * Butternut branded uniform provided (fleece, footwear, hi-vis) * Enrolment into the company pension scheme and sick pay * Enhanced parental leave * Get discounted Private Medical Insurance with Aka Healthcare. * Private showers, changing facilities and dedicated locker space * Treat your furry friend with an employee discount on Butternut Box. * Comfy, bright and airy kitchen space with lunch making facilities and large screen TVs * Free tea, coffee, and fruit (and pay day pizzas) * Opportunity to grow, develop and learn with internal training programmes * Be part of an energetic and high performing team * Team socials & events * Refer a friend bonus of up to £500 * Say goodbye to parking woes with free parking and electric car charging. ‼️  A few things to note * There is no closing date for this role. However, we normally experience a high volume of applications so if you are interested we suggest applying as soon as possible. * We aim to respond to all applicants personally. Our recruitment team is small so do bear with us. * Butternut Box is an equal opportunity employer and we value diversity and inclusion. We welcome people of different nationalities, backgrounds, experiences, abilities and perspectives. * We're not afraid of putting extra weight on candidates from underrepresented groups. We want strong, diverse teams built from different backgrounds, experiences, and identities. We're ready for the ongoing work that goes into building an inclusive, supportive place for you to do the best work of your career. * You might know this role as a Shift Manager, Production Manager, Team Manager or Assistant Operations Manager, in Butternut Box we call this role a Team Leader * We are not looking for external agency support with this role.

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.

Location: THG Labs, Meridian Business Park, Trowbridge, BA14 0BP About THG Labs THG acquired Acheson & Acheson in 2018 to bring full service, product development & manufacturing in-house to supply innovative branded and THG Beauty Brand products to the industry. In 2022 Acheson & Acheson became THG Labs. Capabilities include: * In-house market knowledge & trends * End-to-end service from idea generation through to manufacturing and launch * Technical, commercial and production expertise * Outstanding customer service About The R&D Team Based within the Technical division of the business, The R&D team are responsible for formulating products and seeing them through, from concept to the factory, whilst also ensuring all testing elements required for the PIF are carried out. Why be a Laboratory Technician at THG Labs?  The position of Laboratory Technician is intended to facilitate the smooth and efficient running of the laboratory teams. The position provides a foundation in essential aspects of the laboratory environment, from basic formulation development, through to laboratory and factory hygiene. The position requires compliance with company policy, including Good Manufacturing Practices (GMP) and Control of Substances Hazardous to Health (CoSHH). As a Laboratory Technician you will: * Assist Chemists in the day to day running of the laboratory. * Follow company Standard Operating Procedures (SOP’s). * Follow company Work Instructions (WIN’s). * Make formulations under the instruction of Chemists, prepare samples for customer evaluation, product stability and compatibility testing. * Prepare bulks for user trial, clinical efficiency testing, safety testing and any other appropriate purposes. * Assist Chemists with stability and compatibility testing, including evaluating samples, recording, and reporting of results. * Maintain hygiene standards within the laboratory, ensuring it remains a clean, safe, and efficient workplace. * Maintain accurate records relating to the development and production of safe and legal cosmetics and personal care formulations. * Monitor and manage laboratory raw material stock levels, maintaining clean storage conditions, and ensuring safe handling of chemicals in accordance with company policy. * Assist Chemists with pilot batches when required. * Demonstrate effectiveness as a member of the Technical team through consistent professional conduct and role model behaviour. * Communicate effectively and positively with all teams, colleagues, and managers. * Take reasonable care for the health and safety for yourself and other persons who may be affected by your work. * Cooperate with regards to all company health & safety measures, following H&S training when using equipment. * Report to a person in authority any work situation which may represent a serious or imminent danger to health & safety or any shortcomings in the protection arrangements to health & safety. In respect of any hazards remember ‘see it, report it’. * Help to promote a positive working atmosphere within the company. * Any other duties that may be required from time to time. What skills and experience do I need for this role? * Must be competent in maths. * Must have in interest in science. * High level of attention to detail. * Must be a team player. * Good organisational skills. * Must be willing to learn. What’s in it for me? Career Development * Access bespoke development programmes that have been designed and developed by our in-house L&D team. * Continued development through our upskilling programme that is delivered in partnership with an industry-leading training provider. Enhanced Leave * 25 days annual leave plus bank holidays. * Don’t want to work on your birthday? We don’t either! Enjoy your day off on us! * Enhanced maternity and paternity pay, depending on length of service. * Up to 10 days compassionate leave. * Buy back up to 3 days each year. * Unlock 2 days volunteer leave after 12-months. Wellbeing Support * Access face-to-face and virtual appointments with our in-house GP (Manchester Head Office). * Access our 247 Employee Assistance Programme (EAP) which is provided by Bupa. Other Perks * Save up to 12% on the cost of personal tech through our salary sacrifice scheme. * Up to 50% staff discount on THG brands. * Know someone who would be perfect for THG? Refer them and get up to £1000 when they pass their probation. * Anniversary gifts when you hit 5 and 10 years of service.