Technical Assistant, Quality Control - Entry into the Pharmaceutical Industry - Halle, Germany Are you looking to kick-start your career in the pharmaceutical industry? If yes, then this is the position for you! Planet Pharma is currently working with a clinical development manufacturing organisation (CDMO) offering a range of services in the development for manufacturing injectables. As the Technical Assistant for Quality Control, you will be responsible for the quality control of production processes. You will also be responsible for: Observation, documentation and evaluation of the aseptic behaviour of employees in the production areas Instruction of immediate corrections in the event of observed process deviations and escalation of these deviations Instruction of correct and timely documentation in the batch documentation Checking the proper cleanroom status of the aseptic areas Carrying out cleanroom studies Collaboration in the continuous improvement of aseptic processes and cross-departmental projects Collaboration in the continuous improvement of aseptic processes and cross-departmental projects For this position, our client is looking for someone who has a keen interest in joining the pharmaceutical industry with a particular passion of working in quality control. You must also have: A bachelor's degree in life science Native German language skills Strong communication skills For this position, you will be expected to work shifts and some weekends so you must be comfortable taking this on. For more information on this position or any similar opportunities, please contact Chanel Hicken on or email your CV in German (and English if possible) to and we can arrange a time for a confidential discussion on how you can get involved in this exciting opportunity and kick-start your career in the pharmaceutical industry!
Position Overview: We are currently looking for a dedicated Associate Quality Assurance to join our client, a large CDMO. In this role, you will ensure that aseptic production processes are carried out accurately and continuously improved. You will monitor these processes closely, deriving and tracking corrective actions based on your observations. Key Responsibilities: Observe, document, and evaluate aseptic behavior of employees in the production areas Instruct and implement immediate corrections in the event of observed process deviations Escalate deviations as necessary Ensure correct and timely documentation in batch records Check the cleanroom status of aseptic areas and carry out cleanroom studies Actively contribute to the continuous improvement of aseptic processes Collaborate in cross-departmental projects related to aseptic processes Your Profile: Completed MINT studies (Bachelor) or vocational training in the technical/pharmaceutical field (e.g. pharmaceutical technician, chemical technician, PTA/BTA/CTA) Good knowledge of English is advantageous Strong analytical skills, communication abilities, and structured work style Willingness to work shifts and weekends If you're passionate about making a difference in the pharmaceutical industry and meet the above qualifications, we would love to hear from you! About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
