We are looking for a Quality Manager for a rapidly-growing company that does analyses for the Pharmaceutical Industry under GMP-guidelines.You implement and own the QMS, and lead a small team of Quality Officers.Apply today if this is a good step for you! Job Description This position is completely new within this fast-growing company as they previously outsourced their Quality work.You pioneer the Quality team by implementing, maintaining and updating the Quality Management System.You initially supervise the external quality officers until they are completely phased-out and you supervise internal quality officers.This company does niche analyses for the pharmaceutical industry and delivers Certificates of Analyses (Co As) to the client, which you and your team check for quality, completeness, and compliance.You will be in contact with quality departments from clients to set quality agreements and discuss quality-related matters regarding analytical studies and Co As.We are looking for someone with about 5-10 years of QA-experience in a GMP environment.The ideal candidate has a background in a small and rapidly-growing company, or in a dynamic environment like a CRO or CDMO, to uphold quality standards while simultaneously being flexible where quality guidelines allow you to do so.The team you will manage is relatively small (1-3 employees), so a strong background in management is not a hard requirement.Responsibilities Implement, maintain, and improve the QMS Supervise a few Quality Officers Review Certificates of Analysis (Co As) for GMP-compliance Client contact for quality agreements and quality matters Profile University-level education At least 5 years of QA-experience in a GMP-environment Experience in a rapidly-growing or dynamic environment is a plus Professional English is a hard requirement, Dutch is a plus Experience as a supervisor, team lead, or manager is a big plus Benefits and practical information Long-term position.Contract directly with our client Fulltime position in office hours (32-40 hours) On-site presence is required Salary range: €4500-€5500,- gross monthly, depending on experience Location: Amsterdam Vacaturenummer: 25323
Our client is dedicated to helping patients with advanced cancer by making their therapy more affordable and accessible.They have developed kits for use in hospitals based on cell culture and immunology.We are looking for candidates with an immunological background.As a laboratory technician, you will be involved in assembling these kits, including preparing buffers and reagents, as well as correctly connecting tubes and other components.This role combines technical work with hands-on laboratory tasks.Additionally, there are various quality-related aspects such as documentation, logistics, and inventory management.Responsibilities Prepare and distribute therapeutic kits for cell-based cancer therapies.Support production activities including training, process validation, and laboratory testing.Contribute to the improvement and automation of the entire material supply chain, including the implementation of an ERP system.Support QC incoming goods, warehouse management, and material logistics as needed.Draft documentation such as SOPs and protocols.Profile MLO-4 or Bachelor diploma in biotechnology/Molecular Biology.Attention to detail and experience in a GMP environment.Practical experience with pharmaceutical material management, warehousing, logistics, packaging, and distribution of GMP materials.High sense of responsibility.Must be fluent in English and have a valid Dutch work permit, if you have no permit you will not be considered! Benefits Contract: Initially 6 months through Oxford, with realistic long-term prospects.Salary: €3000 - €4000 gross per month based on a full-time position.Working hours: Full-time Region: Leiden Vacaturenummer: 25324
Our client is an innovative organisation within the pharmaceutical and biotechnology sector, focusing on advanced CAR-T immunotherapies for the treatment of cancer.These therapies are manufactured on site in hospitals, simplifying logistics and ensuring faster patient treatment and better outcomes.As part of their growth, they are seeking a motivated Quality Assurance Specialist for the Quality Control (QC) department.You will work in a dynamic and fast-growing environment where quality assurance and compliance are key.Job Description: In the Quality Assurance role for the QC department, you will be responsible for supporting the quality control processes within a laboratory environment.You will work closely with the QC team to ensure that all materials and products meet required quality standards and regulations.You will manage and update work instructions and SOP's, monitor materials intake and participate in the product release process.This position is critical to maintaining high quality standards and ensuring compliance in the production of CAR-T cells.Responsibilities : Support quality assurance activities within the laboratory and QC department, with emphasis on compliance with applicable pharmaceutical and biotechnology guidelines.Manage and update laboratory work instructions and SOP's to ensure consistency, precision and regulatory compliance.Check and verify incoming materials and products, ensure proper documentation according to quality standards.Assist in quality control and laboratory testing to ensure all materials and products meet established specifications.Participate in the release process by ensuring complete and accurate documentation of QC checks and test results.Actively collaborate with the QC team to identify and resolve quality issues within the laboratory in a timely manner.Contribute to the improvement of quality processes within the laboratory environment, based on data analysis and best practices.Support the implementation and compliance of quality management systems (QMS) within the QC department, focusing on compliance with EU and US regulations.Profile : Graduate degree in biotechnology, pharmacy, or a related field, with experience in quality assurance or quality control within a laboratory.In-depth knowledge of quality standards, pharmaceutical regulations, and GMP (Good Manufacturing Practice) within the biotechnology industry.Experience working in laboratory environments, with a focus on product quality and process control.Strong communication skills in English, both oral and written.Attention to detail and the ability to work accurately in a dynamic environment.Ability to work independently, but also function well within a team of professionals.Working conditions: Minimum 60% FTE, with flexible working hours and opportunities to work from home.Salary between €5000 and €7000 per month on a secondment basis, depending on experience.A contract of at least 6 months, with the possibility of extension depending on project needs.The possibility to work one or two days a week at the Leiden office in a stimulating, international working environment.Extensive opportunities for professional development and growth within the biotechnology and pharmaceutical sector.Vacaturenummer: 25290 if you do not have a valid working permit in the Netherlands you will not be considered for this position
We are looking for a Pharmaceutical Development Scientist / Technical Writer.Your responsibility will be to optimize and validate manufacturing processes for pharmaceutical compounds intended for clinical trials.This position involves both hands-on pharmaceutical experiments, development, and validation tasks, as well as drafting scientific documentation.you will conduct lab experiments in collaboration with experienced production technicians, focusing on method setup and/or optimization during the development phase.You will also contribute to process validation experiments alongside the production and QC teams.Once validation is complete, you will play a key role in training new technicians and resolving process-related issues.In addition to the above responsibilities, you are primarily responsibility will be to optimize and validate automated manufacturing processes for pharmaceutical compounds intended for clinical trials.A significant aspect of your work will involve contributing to the establishment of a validation strategy and drafting scientific documentation required for clinical manufacturing in compliance with GMP and ICH guidelines.This includes preparing procedures, validation plans, scientific reports, and chemical and pharmaceutical data for the Investigational Medicinal Product Dossier (IMPD).Key Tasks and Responsibilities: Assist in establishing clinical production processes for pharmaceutical investigational medicinal products (IMPs), progressing from test synthesis to a validated GMP-compliant manufacturing process.Contribute to the development of a validation strategy in alignment with ICH standards.Prepare and review documentation, including feasibility study reports, procedures, validation plans, and validation reports.Support the Head of Development in managing project documentation and timelines.Perform pharmaceutical syntheses activities using automated synthesis modules in a cleanroom environment during the development phase.Present results in a structured and professional manner, both verbally and in writing.Ensure compliance with all applicable regulations regarding radiation safety and Good Manufacturing Practices (GMP).Requirements: A completed BSc or MSc degree in a relevant field (e.g., organic or analytical chemistry, chemistry, or biochemistry).Very strong English communication skills and a proven ability to draft scientific and technical documentation.Demonstrated experience in drafting scientific and technical documentation.You excel at summarizing scientific content and validation strategies.You can easily translate laboratory procedures into precise and structured documentation.You possess excellent organizational skills Are able work with individuals from diverse backgrounds, including internal team members and international external partners.You are able to manage multiple projects simultaneously and keep track of deliverables and timelines.Familiarity with working in a GMP-compliant environment and cleanrooms At least two years of relevant laboratory experience in industry or academia, preferably in the pharmaceutical field Benefits: Contract: start via Oxford Global Resources - Prospect of a permanent contract Salary: €3300 to €4400 per month Hours: 36 hours per week.Location: Nijmegen.Vacaturenummer: 25236
Our client is a leading biotechnology company focused on developing advanced CAR-T immune therapies for cancer treatment.Using innovative technologies such as the point-of-care cell therapy production model, the company offers efficient and effective treatment options.They are looking for an experienced Senior Technician to join the Manufacturing Sciences and Technology team and optimise their production processes.Job Description As a Senior Technician in the production process, you will be directly involved in executing automated production activities within a controlled laboratory environment.You will be responsible for managing production in GMP-certified clean room spaces and supporting process design, optimisation, and scale-up of cell therapy production.You will contribute to the implementation of process improvements and collaborate with various internal teams, such as Process Development and Quality Control, to ensure production efficiency and quality.Responsibilities Execute and monitor production activities within a controlled production environment (Grade D clean room), including Cocoon runs and positive fraction generation.Lead process optimisation, scale-up experiments, and late-stage development activities in a GMP-compliant environment.Oversee technology transfer and support the implementation of new production strategies in collaboration with other departments.Actively contribute to process improvement and efficiency projects within cell therapy production.Ensure compliance with GMP guidelines and maintain high-quality standards throughout the production process.Profile A completed BSc in HLO, life sciences, biotechnology, engineering, or a related field.At least 5 years of experience in biotechnological production, with expertise in cell therapy processes, automated bio reactors, and GMP-controlled production environments.Experience in process optimisation, scale-up, and technology transfer within the pharmaceutical or biotechnology sector.Strong knowledge of GMP guidelines and experience working in a regulated production environment.Strong communication skills in English, both written and verbal.Full-time availability required, with part-time possible for a perfect profile.Employment Conditions Full-time position with the possibility of part-time based on the ideal candidate's profile.Salary range of €3800 to €4600 gross per month, depending on experience and qualifications.Initial 6-month contract with the possibility of extension and potential for permanent hire.Work in an innovative and rapidly growing biotechnology environment with excellent career development opportunities.Attractive employment conditions, including a modern work environment and access to cutting-edge technologies in cell therapy production.Vacaturenummer: 25091
Are you an experienced Product Developer with a keen eye on quality? We are looking for an engineer working in a high-tech environment on the quality and reliability of our products.In this role you will become a specialist on complex, high-tech laboratory systems, focusing on the development of low-volume parts.About the Role As a Product and Quality Assurance Engineer, you will focus on the quality in module projects and integration within the system.As a strategic engineer you will implement and perform test plans, risk- and mitigation analysis, to test reliability and verification of the system.You will perform root-cause-analyses with statistical engineering, to hypothesize and implement the product improvement.Furthermore, by defining the entry- and handover criteria necessary, you can assure quality of the system.By collaborating with the design teams and supporting the development, you will assure the design reliability for new innovations.Requirements BSc or WO degree in mechanical, mechatronic-, or electronical engineering 5+ year's experience in product development, preferably in low-volume and/or complex high-tech systems Experience with developing and testing complex systems, including hardware, software, and mechanics Design for Six Sigma Green Belt certification Excellent communication and interpersonal skills in English, with Dutch a plus What We Offer Contract: long term with prospect of permanent employment Salary: €5000, to €6000,- depending on experience A challenging and dynamic work environment with development and grow possibilities A talented team, working together as specialists on cutting-edge projects Region: Eindhoven Vacaturenummer: 25222
Introduction Our client is an innovative company focused on developing CAR-T immunotherapies for the treatment of cancer.This cutting-edge approach utilizes point-of-care cell therapy, resulting in efficient treatments and better patient outcomes.The organization offers a modern and dynamic working environment in a new building.Job Description As an Audit Coordinator, you will be responsible for supporting the audit and inspection department in coordinating logistical processes and managing documentation.You will ensure that all operational activities comply with Good Practice (Gx P) guidelines.Additionally, you will collaborate with various stakeholders to schedule audits, track timelines, and generate and manage corrective and preventive actions (CAPA).You will maintain accurate records of all audit and inspection activities and produce reports summarizing findings and operational insights.Responsibilities Support the audit and inspection department with logistical and operational tasks.Ensure compliance with Gx P guidelines in all operational processes.Collaborate with internal and external parties to schedule and track audits.Generate CAPA plans and follow up on actions until closure.Maintain accurate audit and inspection documentation and prepare reports.Profile Bachelor's degree in Life Sciences or a related field.Minimum of 3-4 years of experience in a biotech, pharmaceutical, or CRO environment with a focus on Gx P compliance.Knowledge of Gx P areas such as GMP, GDP, GCP, and GLP, as well as regulations in the EU, US, and other regions.Strong organizational skills and attention to detail.Employment Conditions Salary depends on the experience and background of the candidate.Contract type: Contract through Oxford A challenging role for professionals with audit experience who enjoy coordinating projects.A dynamic work environment with opportunities for professional growth.Vacaturenummer: 25149
Our client is dedicated to helping patients with advanced cancer by making their therapy more affordable and accessible.They have developed kits for use in hospitals based on cell culture and immunology.We are looking for candidates with an immunological background.As a laboratory technician, you will be involved in assembling these kits, including preparing buffers and reagents, as well as correctly connecting tubes and other components.This role combines technical work with hands-on laboratory tasks.Additionally, there are various quality-related aspects such as documentation, logistics, and inventory management.Responsibilities Prepare and distribute therapeutic kits for cell-based cancer therapies.Support production activities including training, process validation, and laboratory testing.Contribute to the improvement and automation of the entire material supply chain, including the implementation of an ERP system.Support QC incoming goods, warehouse management, and material logistics as needed.Draft documentation such as SOPs and protocols.Profile MLO-4 diploma in biotechnology.experience with working in a cleanroom is a must.Attention to detail and experience in a GMP environment.Practical experience with pharmaceutical material management, warehousing, logistics, packaging, and distribution of GMP materials.High sense of responsibility.Must be fluent in English and have a valid Dutch work permit.Benefits Contract: Initially 6 months through Oxford, with realistic long-term prospects.Salary: €3000 - €4000 gross per month based on a full-time position.Working hours: Full-time Region: Leiden Vacaturenummer: 25097
Who We Are…
Since 1984, Oxford Global Resources has focused on building trust with each interaction.
We're proud to create long-lasting relationships with the brightest minds in industry, while continuing to identify and drive initiatives that advance our clients' business.
Oxford is known for our unmatched ability to deliver The Right Talent. Right Now.®
As a leading Staffing and Consulting company with offices across North America and Europe, we focus on proactively building a network of highly skilled professionals across 4 key disciplines - Life Sciences, IT, Lab Services & Engineering – to assist our most valued asset, Our Clients, in achieving their goals
As a Sales Account Manager working in our specialist Lab Services Business, you will be in constant communication with new and current clients across Europe, and the world, to understand their critical skill gaps, consulting needs, budgets, and more.
With a focus on representing the full scope of our services, you'll identify new opportunities by building relationships with your current and prospect clients to support the growth of your accounts.
You'll embark in an immersive training program that will give you the tools and knowledge you need to hit the ground running, and you'll discover what it is like to have uncapped earning potential.
If you are an energetic, self-motivated, networker, you'll develop an extremely rewarding sales career
Responsibilities:
· Establish high value relationships with new and existing clients
· Build rapport and strengthen relationships with clients to unearth consulting opportunities
· Negotiate bill rates with clients.
· Responsible for pre-sale planning and post-sale execution.
· Collaborate with Recruiters to identify optimal candidate matches.
· Manage consultants while on assignment for Oxford.
· Input client information and all communication notes into the database.
· Business Development: Create Outbound lead generation campaigns by profiling and researching new clients to build your client database.
· Perform outbound calls & prospecting campaigns to generate and nurture leads to develop your client base.
Qualifications:
Excellent verbal and written communication skills in Dutch & English – additional major European languages would be beneficial.
Self-motivated, high-energy personality, agile.
Competitive, goal-oriented mindset to stay on track to meet and exceed production goals.
Any Science / Lab Experience or a Science focused educational background would be a distinct advantage.
Ability to multitask in a fast paced environment.
What We Offer:
· Competitive, combined package of base salary, uncapped commissions, and various other bonus opportunities.
· A Dynamic Career Opportunity with travel opportunities to client sites across Europe, and to our own offices in Cork, Barcelona, Dusseldorf, Antwerp and Zug.
· Opportunity to sell unique, highly-specialized staffing solutions and to become a trusted partner to some of the largest and best companies in the world.
· A collaborative work environment where you can thrive as an individual, and know that you are supported every step of the way.
· Team-building activities and social events in and outside of the office.
· Ongoing training and career advancement.
· Opportunity for high-performers to qualify for President's Club.
