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 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.

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 lead all drug product development strategy.   Responsibilities: Lead a small team of formulation scientists working inhalation drug delivery platforms Oversee raw material development and preformulation through late-stage process development Coordinate with other cross functional CMC teams   Qualifications: PhD in Biochemistry, Chemical Engineering, or related field with ideally 12+ years of industry experience (combined experience in biotech and pharmaceutical environment is ideal) Hands on experience working with inhalable drug delivery formats People leadership experience strongly preferred   All interested applicants are encouraged to apply below.

Engineering / Capital Project Manager Raleigh NC   PROFILE:   This individual will develop, implement, and oversee capital projects and equipment purchases to support biopharmaceutical Operations. This role is focused on managing projects ranging in size of up to $5 million. Duties include interfacing with cross-functionally with both internal teams and groups, and external suppliers to ensure projects are delivered on time and within budget. This position will utilize breadth of knowledge across facilities and engineering to ensure regulatory compliance and effective project execution   REQUIRED COMPETENCIES   Strong pharmaceutical project management skills and proven experience in having managed capital projects with emphasis on Biologics, clinical and/or manufacturing and development laboratories in a cGMP environment. Project Management skills including the development and management of work breakdown structures, RACI diagrams, schedules, budgets, action trackers and meeting minutes. Understanding of GMP, regulatory, environmental, and OSHA regulations as it relates to Engineering, Facilities Operations and Construction Understanding of financial management as it relates to capital and expense spending and project cash flow forecasting. (i.e. Purchase Orders, Invoicing) Experience in total project delivery in a cGMP environment (from concept to validation and startup process). Leads the development of the capital project scope and objectives in support of the business strategy dealing with clients and stakeholders. Exhibits project leadership and effective decision making throughout each project. Leads and promotes effective teamwork by engaging both Facilities as well as including key clients and stakeholders.   QUALIFICATIONS & EXPERIENCE:   BSc in Engineering or equialvent discipline Previous cGMP Project Management experience Right to work in the USA without Sponsorship