Lediga jobb Agardh Consulting AB i Lund

Optimizing blood for life - solutions for improved quality of life and better health economy!

Glycorex’s unique molecular level technology that specifically selects and removes antibodies in the blood has opened revolutionary treatments and solutions in healthcare.

Glycorex Transplantation AB provides products that enables transplantations across the blood group barrier and thereby help saving lives. The first transplantation using Glycosorb® ABO was performed in September 2001 at the Karolinska Hospital in Stockholm, Sweden. Since then, more than 5,000 transplants have been performed in 28 countries at more than 200 transplant centers. More than 60 scientific papers in reputable medical journals show excellent short- and long-term results fully comparable to blood group compatible transplants. Glycorex technology not only saves lives and improves patients’ quality of life, it also has very positive health economic effects. Each kidney transplant saves about 150 dialysis treatments per year, which means that the more than 5,000 kidney transplants performed after Glycosorb® ABO treatments, can be estimated to save over 700,000 dialysis treatments per year.

Glycorex is entering an expansive phase with the development of new products based on the company’s unique technology platform. The company has recently launched a new product version designed to produce universal blood plasma that can be given regardless of the recipient’s blood group, which means major improvements in the logistics, safety, and availability for blood donor centres. Read more about Glycorex! (http://www.glycorex.com/)

We are seeking an energetic Organic Chemist with strong communication, leadership, technical and operational skills to join our dynamic and fast paced team in Lund. In this role you will be a part of the R&D team and report to our Head of Development.

Responsibilities

You will follow SOPs and work in compliance with safety, regulatory and quality guidelines. You develop products, lead process and upscaling from pilot to manufacturing level.

Responsibilities will include process testing of products and manufacturing protocols.

Furthermore, you will:

- Address and report problems in daily manufacturing and propose effective countermeasures
- Communicate the results effectively by written and oral reports, including electronic laboratory notebooks
- Interact effectively in a cross functional setting
- Critically review processes and provide input
- Proactively identify areas for opportunity and drive efficiency results
- Be proficient in manufacturing processes
- Can organize and prioritize work to ensure on-time delivery
- Meet minimum productivity standards
- Use highly specialized equipment and instrumentation in daily manufacturing


Experience and education

You have:

- A relevant post-secondary education, for example a Bachelor or Master’s in Science, Engineering or equivalent (preferably a degree in Biochemistry/Molecular Biology with an emphasis on proteins/enzymes)
- >3 years’ laboratory experience
- Experience from fermentation techniques and instruments
- Experience from aseptic technique for protein and biomolecular analysis
- A good knowledge of GLP
- Excellent communication skills, both written and verbal in English
- A good knowledge in Excel and the Office suite


The ideal candidate has a working knowledge of manufacturing environments and

direct experience with protein/enzyme biochemistry. An additional experience from production, purification and analysis of proteins, enzymes and biomolecules is a plus.

About you

You are easygoing and can work in a team and share responsibilities and tasks. You are well organised, structured with a good planning ability. You are good at writing and reporting in a well-structured and logical way. You possess an analytical mindset.

Also, we think that you are driven and engaged and able to work independently. Finally, you keep to schedules and follow procedures and policies with a positive mindset.

You will be based at our laboratory in Lund.

Glycorex Transplantation AB was founded in 1996 and is listed on NGM Equity Stockholm since 2001. Head office, production, development, and laboratory units are based at Ideon Gateway in Lund.

Recruitment process

In this recruitment we work together with recruitment consultant Pernilla Agardh. For questions regarding the position or process please call +46 72-249 94 80, or email [email protected]. We look forward to receiving your CV and cover letter and will review applications and make selection on an ongoing basis. Visa mindre

Are you looking for a new challenge as an IT Manager? Maybe this job as IT Manager is for you!

We are looking for an IT manager - with a focus on strategy and project management - to be responsible for establishing initiatives that affect the organization's IT strategy. This person will have the overall responsibility and accountability for the smooth running of our computer systems according to the requirements, specifications, costs and timelines. The person will develop, implement, manage, maintain and support IT applications and infrastructure with the aim to constantly improve and adapt to the needs of the company and if needed initiate and supervise the implementation of new systems. The successful candidate will have a proven professional experience and a detailed knowledge of industry’s best practice processes.

Responsibilities

Key Responsibilities of the role:

- Have the overall responsibility for the IT department, e.g. software solutions, including processes, requirements and configurations.
- Together with the line organization assess the current IT system structure and suggest developments and prioritization of these in order identify the optimal combination of applications that meet the requirements of the company.
- Coordinate and manage continuous improvement of IT systems and processes across the company.
- Ensure compliance of the company’s IT systems, structure and strategy with regulatory requirements (GxP), particularly within Europe and the USA (e.g. secure and non-manipulable storage of data, ongoing validation of systems used for GxP related data).
- Ensure that that quality requirements made of systems outside of GxP operations are met.
- Lead IT projects and implement solutions and applications within the company.
- Enhance general IT­ skill sets within the company by training and "missionizing" (develop training material and conduct user training)
- Overall managerial responsibility for staff (currently one person) within the unit
- Knowledge of and understanding of business goals within the company and familiarity with developments in other departments.


Qualifications

Practical experience

You need to have several years of experience from a similar role in the pharmaceutical industry and in an international environment and extensive experience of GxP regulatory requirements. You also need to have experience of ensuring, leading and implementing continuous improvement/ optimization of IT systems and processes and experience of following good standards in the pharmaceutical industry. Since BioInvent is an international company it is necessary that you have excellent verbal and written communication skills in English.

You should also have experience of the following:

- Extensive experience of IT security/routines
- Previous experience of project leadership and staff management
- Previous experience with relevant industry tools, e.g. protein databases is a bonus


Education

Master of science in engineering, B.Sc. or equivalent higher education in a relevant specialization (preferably within systemization).

Personal profile

- Efficient, analytical, solution-oriented mindset, good organization skills, multi-tasking, respond to urgent needs of the team.
- Curious and flexible, able to be at ease with frequent changes, delays, or unexpected events.
- Self-motivated and independent
- Ability to get things done and implemented as needed
- Capable of handling strategic issues, yet ready to be hands-on if needed
- Knowledge and understanding of the importance of creating efficient working environment and contributing to ensure continuous improvements
- Genuine interest in natural science and the medical world
- Solid ability to communicate and educate
- Nurture a culture of teamwork, positive team spirit, promoting the development of each member in the team.


About the company

BioInvent International AB (Nasdaq Stockholm: BINV) is a clinical-stage biotech company that discovers and develops novel and first-in-class immuno-modulatory antibodies for cancer therapy, with currently three drug candidates in four ongoing clinical programs in Phase 1/2 trials for the treatment of hematological cancer and solid tumors, respectively. The Company’s validated, proprietary F.I.R.S.T™ technology platform simultaneously identifies both targets and the antibodies that bind to them, generating many promising new drug candidates to fuel the Company’s own clinical development pipeline or for additional licensing and partnering.

The Company generates revenues from research collaborations and license agreements with multiple top-tier pharmaceutical companies, as well as from producing antibodies for third parties in the Company’s fully integrated manufacturing unit. More information is available at www.bioinvent.com (http://www.bioinvent.com/). Follow us on Twitter: @BioInvent. Visa mindre

Glycorex Transplantation AB produces products that enables transplantations across the blood group barrier and thereby help saving lives. The first transplantation using Glycosorb® ABO was performed in September 2001 at the Karolinska Hospital in Stockholm, Sweden. Since then, more than 5,000 transplants have been performed in 28 countries at more than 200 transplant centers. More than 60 scientific papers in reputable medical journals show excellent short- and long-term results fully comparable to blood group compatible transplants. Glycorex technology not only saves lives and improves patients’ quality of life, it also has very positive health economic effects. Each kidney transplant saves about 150 dialysis treatments per year, which means that the more than 5,000 kidney transplants performed after Glycosorb® ABO treatments, can be estimated to save over 700,000 dialysis treatments per year.

Glycorex is entering an expansive phase with the development of new products based on the company’s unique technology platform. Glycorex has recently launched a new product version designed to produce universal blood plasma that can be given regardless of the recipient’s blood group, which means major improvements in the logistics, safety, and availability for blood donor centres. Read more about Glycorex! (http://www.glycorex.com/)

We are looking for a CFO with a proven track record that will report directly to the CEO and be part of the senior management team. As CFO you will play a critical role in driving the future of the company and be a strategic leader building robust systems that can meet the company’s vision.

Responsibilities

In this role you will be:

- Responsible for financial activities such as accounting, management control, reporting, audit, budget process and annual report
- Contact person for financial stakeholders
- A strategic leader working closely together with the CEO and management team
- Contributing with IR and preparing presentations and participate in investor meetings
- Leading the process for an eventual change of listing
- Oversee long-term budgetary planning and cost management in alignment with the company’s strategic plans


Furthermore, you will:

- Ensure knowledge of economic and accounting principles and practices
- Together with CEO report and follow up to capital market, shareholders, management team, board, and other stakeholders
- Develop tools and systems to provide critical financial and operational information to the CEO
- Ensure financial and regulatory compliance with listing requirements
- Work closely together with administration, finance department and CEO


Experience and education

You have:

- Bachelor's or master’s degree in Business Administration, Accounting, Finance, Economics or related field AND post-graduate finance/finance leadership experience
- A strong IFRS experience
- Track record from working as a CFO, > 5 years, preferably from a manufacturing med tech company
- Experience from working at a stock listed company and/or having prepared for an IPO
- Investor Relations experience
- An operational and strategic mindset and a “can-do” attitude to driving business growth
- Knowledge of economic and accounting principles and practices, the financial markets, banking and reporting of financial data
- Experience from consolidated financial statement is meriting


You are fluent in Swedish as well as English, both written and spoken. Preferably you have experience from working with distributors in an international company. In this role you will have responsibility for direct reports.

About you

To succeed in this role, you have an open and positive mindset and like to work in a smaller company. You can work both on strategic and operational level. You are a person with high integrity who are used to work both independently and in a team. As a person you are flexible and engaged, you like to be challenged and contribute to developing the company. You have social and communications skills and are used to give presentations in both Swedish and English. You can be both analytical and meticulous as well as hands on and proactive.

Glycorex Transplantation AB was founded in 1996 and is listed on NGM Equity Stockholm since 2001. Head office, production, development, and laboratory units are based at Ideon Gateway in Lund.

Recruitment process

In this recruitment we work together with recruitment consultant Pernilla Agardh. For questions regarding the position or process please call +46 72-249 94 80, or email [email protected]. We look forward to receiving your CV and cover letter and will review applications and make selection on an ongoing basis. Visa mindre

Om jobbet

Vill du driva förbättringsarbete, aktivt delta i projekt samt arbeta tvärfunktionellt i ett spännande företag med många olika läkemedelsprodukter? Trivs du i en miljö med komplexa frågeställningar där din förmåga att strukturera och aktivt göra skillnad får full potential?

Då är detta rätt jobb för dig!

APL, Apotek Produktion & Laboratorier AB, är en av Europas största tillverkare av extemporeläkemedel. APL är också en etablerad kontraktstillverkare inom Life science i Skandinavien med resurser för utveckling, tillverkning och analys av läkemedel. APLs ca 500 medarbetare är verksamma vid fem tillverkningsenheter runt om i Sverige samt vid beredningsenheter i anslutning till sjukhus. APL har till uppgift att tillverka extemporeläkemedel som skräddarsys för den enskilde patienten. Många beredningar görs till barn och till patienter med olika typer av överkänslighet. APL bidrar till läkemedel som förbättrar och räddar liv. Läs gärna mer på (http://www.apl.se/)

Vi söker nu en Processingenjör som kommer att ingå i Process & Teknik teamet. Du kommer tillsammans med ca 10 kollegor, vara delaktig i att driva och medverka i förbättringsarbetet, utreda avvikelser och ta fram CAPA, samt arbeta mycket nära produktionen.

Om tjänsten

Som Processingenjör kommer du främst att arbeta med förbättringsarbete både i och utanför projektform. Du kommer vara aktiv i att leda och medverka i införandet av nya uppdrag, processförändringar och effektiviseringar inom tillverkningen.

Arbetsuppgifter

Du kommer att:

- Utveckla och utarbeta metoder för tillverkningsmoment.

- Ta fram och ansvara för kvalificerings- och valideringsdokument (IQ, OQ, PQ) samt rengöringsvalideringar

- Leda och strukturera tvärfunktionella förbättringsarbeten.

- Driva standardisering och effektivisering av processflöden.

- Bidra till genomförande av Tech Transfer, såväl in som ut från storskalig produktion.

- Ta fram underlag till kravspecifikationer och delta i investeringsprojekt.

- Utföra/delta i riskbedömningar avseende säkerhet-hälsa-miljö och kvalitet.

- Genomföra kvalificerade orsaksutredningar och korrigerande åtgärder.

- Skriva och sammanställa rapporter

- Utforma underlag till satsdokumentation för nya eller reviderade uppdrag.

- Utarbeta instruktioner.

Dina kontaktytor kommer vara medarbetare inom våra avdelningar Tillverkning, QC, QA och Farmaceutisk utveckling både i Malmö och vid våra övriga anläggningar. I förkommande fall har du även kontakt med externa kunder.

Din bakgrund och profil

Du har en högskole-/civilingenjörsutbildning i kemiteknik, farmaceutisk examen eller likvärdig utbildning. Du har minst 5 års arbetslivserfarenhet från en reglerad verksamhet som läkemedels- eller livsmedelstillverkning. Erfarenhet och utbildning inom GMP är meriterande.

Viktiga personliga egenskaper är att du kan arbeta självständigt, är drivande och strukturerad samt har lätt för att samarbeta. Du är bra på problemlösning och har en god analytisk förmåga. En viktig del i din roll är att kunna hantera komplexa frågeställningar och skapa resultat.

En god kommunikationsförmåga både muntligt och skriftligt på svenska och engelska är ett krav.

För att lyckas i rollen är det viktigt att du är flexibel och tycker den höga pulsen i produktion är stimulerande. Vi fäster stor vikt vid personlig lämplighet.

Vi erbjuder

APL är ett företag som befinner sig i en spännande utvecklingsfas inom såväl tillverkningsprocesser, digitalisering och hållbart förbättringsarbete. APL kännetecknas av en öppen och dynamisk atmosfär med korta beslutsvägar. Våra värderingar, som APLs chefer och medarbetare arbetar efter, är affärsmässig, lyhörd, lösningsorienterad och ansvarstagande. För att du ska trivas hos oss bör dessa värderingar även passa in på dig.

Tjänsten är på heltid, 40 timmar/vecka med placering i Malmö. Vi erbjuder förmåner som flextid, Rikskortet och ledighet på klämdagar.

Ansökan: Sista ansökningsdag är den 5 december 2021.

I denna rekrytering samarbetar vi med rekryteringskonsult Pernilla Agardh. För mer frågor angående tjänsten eller ansökningsförfarande är du välkommen att ringa 072-249 94 80.

Övrigt: Innan ev. anställning kommer du att få göra en alkohol-/drogtest samt kommer vi att göra en bakgrundskontroll på dig via Bakgrundskollen.se.

Välkommen att dela en spännande framtid med oss på APL! Visa mindre

Bioextrax is an innovation-driven company using industrial biotechnology to contribute to a more sustainable future. The company is originally a spin-off from the Department of Biotechnology at Lund University and is today a rapidly growing publicly traded company.

The vision is to be a world-leader in bio-based technologies accelerating the transition to a sustainable, green global economy. The company is consistently working to develop innovative and green solutions based on microbiology and biotechnology.

The core of our business is a highly scalable bio-based platform technology for the hydrolysis of protein-rich materials. This technology has many applications contributing to a sustainable and circular economy. Based on this platform, we are developing chemical-free methods to produce the bio-based and biodegradable biopolymers PHAs (polyhydroxyalkanoates) and turn various protein-rich materials such as poultry feathers into valuable ingredients for feed, textile, and cosmetic applications. Read more about our company and work at www.bioextrax.com (http://www.bioextrax.com).

About the position

We are looking for a Downstream Bioprocessing Scientist to join our team at the head office in Lund, Sweden. You will be working closely with our Chief Technology Officer in a creative role where your tasks will range from designing and executing lab/pilot experiments to exploring new downstream processing methods. You will be responsible for downstream process conceptualisation, definition of new processes and the development and testing of strategies to improve purity and yield in a cost-efficient way.

Your responsibilities will be:

- Management, design, and lab operation of pilot-scale (3-60 and 1000 L) experiments.

- Presentation and interpretation of results and project outcomes.

- Actively contribute to the improvement of processes and methods, as well as evaluation of the patentability of the results.

- Management of R&D and customer related projects.

- Preparation and review of protocols and Standard Operating Procedures for technology transfers.

- Writing patents and project reports.

- Leading DSP team and facilitate integration between DSP and USP teams.

Specific responsibilities include developing and enhancing downstream processing of microbial cells and products, extracting and purifying extracellular and intracellular microbial products, and analysing their purity. The position involves managing the laboratories' day-to-day running, data collection, analysis, reporting, and leading and collaborating with other team/s members.

Qualifications

You are an ambitious Scientist with a Ph.D. degree in biochemical engineering, environmental engineering, biotechnology, or related discipline with an emphasis on downstream processing. Industry or industry related experience of 4+ years is necessary. Applicants with MSc and 8+ years of related industry or R&D experience will be also considered.

You have experience of management and design lab operation and leading/participating in projects.

You are fluent in English, both written and spoken.

Required lab experience:

- Lab and pilot scale practical engineering experience in optimizing and scaling harvesting of microbial cells (centrifugation, membrane filtration, coagulation, sedimentation, etc.), cell disruption, extraction, and purification technologies of microbial and natural products.

- Strong knowledge and practical experience in separating microbial intracellular and extracellular metabolites products and cellular components, such as lipids, proteins, organic and amino acids, etc. Large-scale separation experience is a significant advantage.

- Experience in softwares like Aspen, SuperPro, SchedulePro, DOE).

Desired experience:

- Bioprocess modelling experience for upscaling and downscaling of industrial processes.

- Large scale or industrial scale experience in downstream bioprocessing and bioproduction.

- Experience in process cost estimation and in statistical experimental design.

- Downstream processing of scl and mcl PHAs (polyhydroxyalkanoates) and/or natural fibers.

- Extraction and purification of the bioplastic, PHA and/or protein hydrolysates.

- Knowledge and practical experience in microbial fermentation technologies.

About you:

You have an entrepreneurial mindset and the ability to take advantage of new opportunities and let go of things that do not work. You also possess a willingness to learn new things, collaborate, and critically assess new ideas.

We think that the right person can work on a stand-alone basis. It is also important that you are flexible, solution-oriented, innovative and at the same time being reliable. You are a down to earth person and possess good social skills.

Bioextrax is growing fast, and you consider it an exciting opportunity to be part of our journey.

The position may require occasional shift work (eg. evenings, night or weekends). It is a full-time position based in Lund.

Welcome with your application no later than the 15st of August. We will evaluate the applications on an ongoing basis.

For further questions please contact Recruitment consultant Pernilla Agardh at +46 72 249 94 80 being responsible for this recruitment.

Start date: September 1st 2021. Visa mindre