Consultants spécialisé
dans le secteur pharmaceutique

This is a great opportunity for someone who comes from a technical background and wants to take his/her career a step further. You will be able to expand on your experience and continue your professional career even more within a fast-paced environment with lots of accountability in the role.

This company is middle sized so you will have a chance to bring on your existing experience and take on more responsibilities as your role will be quite varied which normally happens in smaller companies so definitely a great opportunity to have a fast development.

You will be working closely with the R&D teams coordinating the technical requirements of the projects, implementing necessary operations for optimal project management (liaising closely with R&D, Supply Chain, Finance, Engineering, Quality and Production). You will also be a contact person with the clients and develop strong long term relationships. You will also be able to do some coaching with more junior members of the team as well as be the right hand of the PMO manager.

Please get in touch if you meet the below requirements:

• Good command of French and English
• Degree in Chemistry, Biochemistry, Engineering, Pharmaceutical sciences or similar
• Minimum 3 years of relevant experience in a sterile production environment
• Strong PM experience (PMP, PINCE 2 or other relevant certification)
• The role is located in Waterloo, Belgium

Interested? Please apply and we can discuss further.

Please forward your CV in the Word format to Oksana Kolesnichenko or recommend this role to someone who would be suitable: [email protected]

Hiring now, apply to avoid missing out on this great opportunity! Please make sure you live in the area or are able to relocate quickly, no visa sponsorship is provided.

The job market changes very quickly so do not forget to connect with me on Linked in, check other roles that I am hiring for at the moment and follow for any future relevant roles.

Nonstop is dedicated to raising the standard of ethical recruitment and comprises a number of brands, each having their own niche sector focus.

Strategic Purchaser Components/Investment (m/w/d) - Urgently needed, start soon!

My client is currently searching for a strategic purchaser with focus on the procurement of mechanical components and investments. The company is one of the most successful, international market leaders in the biopharmaceutical industry and research. In 2019 they managed to achieve a revenue of more than 1.83 billion euros. With more than 9.000 employees in 60 countries around the globe you will be met with a truly international culture. This dynamic paves the way for strong development opportunities. Apply today!

Your responsibilities:

• Strategic Purchaser of mechanical components and investments
• Price and contract negotiation
• Supplier management and selection
• Key Account function but no operative assignments

Your profile:

• Economic or scientific degree
• Experience in strategic procurement
• Ideally experience in procurement of mechanical components and investments, most ideally with a background in the biopharmaceutical industry
• German and English fluency

Interviews are being conducted in the very near future, start ASAP. Apply today to take the next big step in your career in procurement. Call me today at NonStop Recruitment and dial my extension 7139 or ask for Sebastian Bell when speaking to one of my fellow consultants.

On behalf of one of the top 3 Pharma companies who are looking for a Senior Scientist, on a contract basis for at least 12 months to be based in Basel. This is a chance to be a part of one of the largest pharmaceutical companies in the world, where extensions are expected allowing you to gain exposure with a reputable name and ultimately build further value for your profile. This is a contract with guaranteed working hours of 40 hours per week, working on their development of solid dose formulations.

Job purpose to support drug product manufacturing process related development and supply activities for oral small molecule drug products in Post POC phase. This includes the scientific evaluation and presentation of data, authoring of technical and GMP documentation, integrity checks against raw data and on-site manufacturing support to technical and clinical manufacturing campaigns. You work in a cross-functional team with manufacturing operations, analytics and QA and contribute to the overall Technical Research and Development strategies and goals. You work under minimal guidance of more experienced formulation project leaders.

This position is ideal for somebody with a pharmaceutical background wishing to gain or expand first experience in the field of pharmaceutical development

Major accountabilities:

• support drug product formulation development and manufacturing activities at internal or external manufacturing sites for assigned projects in line with the project plan, guidelines and procedures *collaborate with operational colleagues working on your process at the respective manufacturing sites *take accountability for formulation and manufacturing process deliverables incl. GMP related aspects and change control *author manufacturing instructions for clinical manufacturing campaigns, compile data and interpret results, evaluate data, draw relevant conclusions and contribute to development reports and Quality risk assessment documents in close collaboration with the project teams *perform document reviews and data integrity checks against raw data *support deviation investigations and drive change control * exchange regularly within your project team as well as seek guidance with internal experts on diverse aspects

Education:

Master degree or higher in life sciences, ideally in the Pharmaceutical field

Experience:

Ideally up to 3 years industrial experience in the development and / or clinical manufacturing of pharmaceutical formulations for small molecules Interdisciplinary thinking and interest in collaboration with other functions Good knowledge of GMP and GLP Good knowledge of oral solid dosage form technologies and laboratory and/or technical tools Good scientific / technical writing skills Good collaboration skills and team spirit enabling you to work in a matrix environment, good communication and negotiation skills

Languages:

Fluent in English (oral and written), German is an advantage.

Call me Daniel Watson at NonStop Recruitment now for a confidential conversation. Contact me on [email protected] or +41 435 080 817, please send your CV in word format OR if this does not sound like the opportunity for you, but you are a Contract professional within the pharmaceutical, medical device or biotech industry, please feel free to get in touch, to see other opportunities we may have within this field.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

One of our clients, one of the biggest and most dynamic healthcare communication agencies in UK, is looking for a Creative Director, to help one of their clients - a TOP 5 Pharmaceutical Company.

Are you an art director or an senior copywriter looking for a short-term superb collaboration? This is the perfect opportunity for you! You will not only have leading responsibilities but you have to be ready to get involved in the creative process!

Responsibilities

Develop creative concepts and sign off on creative projects

Lead projects from conception to completion

Provide strategic input and oversight of the creative department

Interpret and understand utilisation figures, working within budgets and timeline management

Stakeholders management

Leading and team management responsibilities

Qualifications

Fluent in English

Artwork and Copy-writing experience

Digital Savvy

At least 4 year's experience as Art Director/ Sr Copywriter

Healthcare Agency

A global Medical Devices company, leader on the cardiology market, is looking for a Quality System Specialist to ensure the quality of all the clinical QMS processes. One of the job duty is also to take part in the project of digitising all clinical activities, in order to ensure the compliance with regulations and guidelines. Therefore, you will assess the impact of software changes on those good practices. This is an opportunity to work for a leader in innovative medical devices, with a lot of autonomy and flexibility, as well as a broad-range of tasks.

Job duties -

• Maintain and improve the QMS procedures on clinical trials and clinical evaluation.
• Participate to projects to digitise the clinical activities.
• Set up a yearly audit program.
• Define and follow up KPI's to monitor the clinical processes.
• Collaborate closely with Clinical Operation team

• Monitor regularly all QMS processes in the clinical department and optimise where needed.
• Coach the clinical associates in QMS requirements.
• Responsible for non-conformity handling related to clinical processes.

• Participate in the internal audits.
• Support regulatory, corporate and customer audits for the QMS processes on clinical trials and clinical investigation.

Your profile -

• You have a university or technical degree in engineering, scientific, medical or pharmaceutical oriented education, or equivalent by experience.
• You're specialising in clinical trials and clinical evidence for medical devices or pharmaceuticals.
• You have a profound knowledge of EN ISO 13485, 21 CFR Part 820, MDD, ISO 14155, ICH GCP E6
• You have a minimum of 5 years of professional experience in a medical and/or pharmaceutical environment.
• You have a proficient knowledge of English (written and spoken).
• You are a team player featured with strong communication skills.

I have a great opportunity for someone with a true passion for law and science to work in a pharmaceutical field whilst honing on your legal experience.

A very interesting and niche opportunity that doesn't come on the market too often and will actually suit both: someone with a legal degree who would like to work within a pharma world as well as someone from a scientific background who wants to pursue a legal career.

Your role will involve negotiations of contracts as well a keeping up to date with regulations concerning clinical trials.

I would love to hear back from the candidates with the following experience:

* Degree in Law or Science
* Minimum 1 year of relevant work experience would be preferred (clinical, pharmaceutical)
* Fluency in Hebrew and English is compulsory!

Share your CV to discuss this opportunity further!

Please bear in mind that the role is located in Israel, RAmla area so please only apply if you are eligible to live and work here and can relocate locally.

Please forward your CV in the Word format or recommend this role to someone who would be suitable: [email protected]

If you do not hear from me you might not have the exact skills required for the position, however, I will make sure to keep your profile for any other possible opportunities.

The job market changes very quickly so do not forget to connect with me on Linked in, check other roles that I am hiring for at the moment and follow for any future relevant roles.

NonStop is dedicated to raising the standard of ethical recruitment and comprises a number of brands, each having their own niche sector focus