Chemical laboratory technician HPLC (m/f/d)Permanent position, full-time I am currently looking for a chemical laboratory technician with expertise in GC/HPLC for a leading and innovative pharmaceutical company. This position involves the execution of various laboratory and technical-based processes, including GC/HPLC analyses, stability tests as well as the documentation and qualification of the corresponding processes and substances within quality control. The ideal candidate has initial experience in a GMP-regulated environment and is familiar with GC/HPLC techniques. Your tasks Analytical release testing of finished medicinal products and pharmaceutical starting materials using GC/HPLC in accordance with the requirements of the Pharmacopoeia (Ph. Eur.).Conducting stability studies to monitor quality over time.Creation and regular updating of documentation such as standard operating procedures (SOPs), test methods and test protocols.Ensuring the functionality of the GC and HPLC equipment and carrying out minor maintenance and repair work.Qualification of reference substances for analysis. Your profile Successfully completed training as a chemical laboratory technician, chemical-technical assistant or a comparable qualification.Basic knowledge and initial practical experience in instrumental analysis, especially with GC and HPLC.Willingness to work in a regulated environment according to GMP guidelines.Confident handling of chemical calculations.Experience in using chromatography software, ideally OpenLab.Very good knowledge of German and English, both written and spoken.Experienced in using MS Office, especially Excel and Outlook.Strong sense of responsibility and quality.Independent and methodical way of working.Ability to work effectively under pressure and a high level of adaptability. Information about the customer: The company is a leading supplier in the chemical industry, known for its innovative and high-quality products. It offers tailor-made solutions for various industries and attaches great importance to the highest quality standards and strict compliance with regulations. With a dynamic team and modern working conditions, it creates an inspiring and supportive working environment that offers space for creative ideas and professional development.

In this position you will be part of the IT team and be the interface between IT and pharmaceutical management. You have the opportunity to manage exciting IT projects and to drive digital transformation. These tasks are waiting for your:IT Demand ManagementLeading IT projects, including creating project plans and specifications, and organizing workshopsManaging external service providersSupporting departments in the SAP environment and connected systemsAnalyzing, optimizing, and integrating business processes into IT systemsConducting system validation, including documentation This completes your profile:Degree in a technical or scientific field (preferably in the field of Information Technologies, Science or similar)Initial experience in computer system validation in the pharmaceutical sector, EU GMP guidelines, and knowledge of GAMP5Knowledge and experience in dealing with QMS softwareFluent German and English language skillsProficient in MS Office This is what the position offers you: Further training opportunitiesAdditional social benefitsModern corporate health management programCollaborate and inspiring atmosphere About our client:Our client is a German pharmaceutical company specializing in the production and distribution of medicinal products. Known for its long tradition, the company focuses on natural medicines, particularly for treating respiratory and cold-related illnesses. It emphasizes quality and research, blending traditional healing methods with modern scientific knowledge.

QA & CSV Manager (m/f/x) | Munich Area | PharmaAs a competent contact for Quality Assurance and Computer System Validation topics, you can be an asset to a pioneer in the pharmaceutical industry. These tasks are waiting for you: Execution of Computer System ValidationReview, approval, and tracking of deviations, changes, and CAPAs, including the corresponding risk assessmentCreation and review of SOPs, validation/qualification plans, and reportsContinuous monitoring and annual review of product qualityImplementation and optimization of validation processesApproval and qualification of new suppliers This is what the position offers you:Opportunity to be part of a team designing one of the most innovative production facilities for the manufacture of novel medicationsDedicated and competent teamAn appreciative company culture and a collegial work environment with flat hierarchiesThe opportunity to develop further within a growing company This completes your profile:Degree in Pharmacy, Chemistry, Engineering, Pharmaceutical Engineering or related with strong knowledge in the field of Quality Assurance and Software ValidationAt least 3 years of professional experience in the pharmaceutical industry within a GMP-regulated environmentVery good self-management and organizational talentExcellent team and communication skillsHigh degree of flexibility and commitmentFluency in German (C1) Information about our client: Our client is a German pharmaceutical company specializing in the development and production of innovative drugs, particularly for the treatment of chronic pain. The company focuses on advanced manufacturing processes and the creation of novel medications. They value a collaborative work environment, with opportunities for professional growth and development within a supportive and innovative team.

SciPro is partnering with a leading UK Healthcare company, holding close ties with the NHS, to find their next Quality Director. Role Overview: As part of the Senior Leadership team, the Quality Director will ensure the quality and compliance of products, services, and processes across the organisation. The role involves establishing quality control measures, driving continuous improvement initiatives, and maintaining the company's reputation. Key Responsibilities:Develop and implement quality strategies aligned with company objectives.Design and maintain quality management systems compliant with industry regulations and standards.Ensure regulatory compliance and manage relationships with regulatory bodies.Lead continuous improvement initiatives using methodologies like Lean Six Sigma.Oversee quality assurance processes to meet customer expectations.Manage supplier and vendor quality programs.Analyse quality data, prepare reports, and recommend corrective actions.Provide quality-related training and development across the organisation.Identify and mitigate risks to product quality and safety.Lead and develop a high-performing quality team.Experience & Qualifications:Bachelor's degree in a relevant field; advanced degrees/certifications preferred (e.g., Six Sigma Black Belt).Strong knowledge of quality management systems (ISO standards, GMP guidelines, MHRA regulations).Qualified Person (QP) certification is essential.Proven success in quality improvement initiatives and team leadership.Experience in the medical/pharma industry; NHS experience is desirable.Hands-on approach with a willingness to engage in various quality department activities.

SciPro is currently partnered with a clinical-stage biotechnology company targeting novel drug delivery platforms. The company is looking for a formulation subject matter expert to join the Technical Operations team and contribute to formulation development, scale-up, and tech transfer activities.   Responsibilities: Formulate novel inhalation drug delivery platforms Manage raw material development and preformulation through late-stage process development Process design and development for drug product manufacturing Coordinate with other cross functional CMC teams   Qualifications: PhD in Biochemistry, Chemical Engineering, or related field with ideally 3+ years of industry experience (combined experience in biotech and pharmaceutical environment is ideal) Hands on experience working with inhalable drug delivery formats   All interested applicants are encouraged to apply below.