Projektingenieur Prozesstechnik für pharmazeutische/ biotechnologische Anlagen (m/w/d)

Description du poste

Join CRB as a Process Engineer for pharmaceutical/biotech projects! Enjoy a dynamic workplace with great benefits. Tasks Manage planning and execution of process engineering projects. Collaborate with clients and teams to meet project goals. Create and document process designs and specifications. Skills Bachelor's in Chemistry/Biotechnology or equivalent; 5+ years experience. Strong knowledge of FDA/EMA standards and cGMP compliance. Proficiency in 3D software like AutoCAD and Revit. Project Engineer Process Technology for Pharmaceutical/Biotechnological Plants (m/f/d) Full-time Company Description CRB consists of over 1,100 visionary employees who develop innovative, sustainable engineering solutions for the life sciences industry. We support our clients throughout the entire lifecycle of their plants – from strategic planning of new plants, expansion or conversion of existing plants to commissioning. We have successfully expanded our presence in Europe over the last 10 years with locations in the DACH region in Basel (Switzerland), Böblingen and Penzberg (Germany) and are now looking for a Project Engineer Process Technology (m/f/d) for our office in Basel. Job Description In this position, you are responsible for planning and implementing exciting projects in the pharmaceutical industry. Your scope of work includes planning a defined project scope, for example for a specific area or a series of equipment and systems. Through regular communication with our clients, you ensure that all requirements are met and that budget and schedule are adhered to. The process units, areas and systems to be managed range from small to medium-sized projects with corresponding complexity. What to expect: You coordinate collaboration with internal and external engineers, clients, site managers, partners and suppliers You independently structure, prioritise and delegate complex tasks within the team You communicate effectively and regularly with clients or suppliers You are responsible for creating, documenting and evaluating mass and energy balances You identify deviations from the agreed project scope as well as changes in design direction and, if necessary, forward these to the discipline or project manager You have extensive experience in preparing common project documentation and can support other colleagues in this You create block flow diagrams (BFDs), process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs) You prepare technical documentation and functional specifications for process equipment and qualification requirements You conduct technical bid evaluations Due to your experience and technical skills, you also take on additional tasks such as: FAT (Factory Acceptance Tests) Risk analyses HAZOP/HCCP or similar safety analyses Management of supplier packages Review of 3D models and coordination Resolution of 3D model collisions You act as a mentor for younger team members Our office is less than ten minutes from Basel SBB main station and offers flexible options regarding commuting and catering. Modern and well-equipped workstations in an open-space concept complete our location. What we offer: A family-like and team-oriented working environment where our employees are the focus Individual career and development opportunities Flexible working hours and mobile working Onboarding with mentor and buddy programme At least 25 days of holiday 20 days of workation per year in Europe Subsidy for public transport subscription Attractive occupational pension benefits Exciting projects in the DACH region Great passion for complex industrial challenges and enjoyment in jointly developing innovative, sustainable solutions Qualifications University degree in chemistry or biotechnology, process engineering or equivalent qualification Project experience (at least 5 years) within the pharmaceutical industry as a process engineer and/or project manager and excellent technical understanding Social skills, leadership talent and ability to work in a team Sound knowledge of FDA / EMA standards as well as cGMP and their interpretation in projects Ideally, you already have experience with 3D viewer software such as Navisworks, Revit, AutoCAD Willingness to travel to project sites in the DACH region Very good language skills in German (B2+ including technical and industry-specific vocabulary) and English (C1+) Additional Information All your information will be kept confidential according to EEO guidelines. CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails. If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. If you click on the above link or any third-party link in this post, you will leave this website and be redirected to a third-party website where the terms of use and privacy policies of that website apply.