Equipment Engineer Parenteral Pilot Plant

pAt Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. /p pAs guided by Our Credo, Johnson Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson Johnson, we respect the diversity and dignity of our employees and recognize their merit. /p h3Job Function: /h3 pRD Product Development /p h3Job Sub Function: /h3 pRD Mechanical Engineering /p h3Job Category: /h3 pScientific/Technology /p h3All Job Posting Locations: /h3 pBeerse, Antwerp, Belgium /p h3Job Description: /h3 h3About Innovative Medicine /h3 pOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. /p pJoin us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. /p pLearn more at /p h3We are searching for the best talent for Equipment Engineer Parenteral Pilot Plant to be in Beerse. /h3 h3The role is fixed for three years. /h3 br/ h3About the Department /h3 pThe Drug Product Research Development (DPRD) is part of the Pharmaceutical Development organization and plays a crucial role in delivering medicines to our patients during the development phase of a new product. Within this organisation the Pharmaceutical Supply Engineering Sciences team (PSES) is responsible for the upscaling and fine tuning of formulation and processes which result in the successful clinical manufacturing of new Drug Product (DP). Our activities include all in‑house and outsourced planning, manufacturing and distribution of clinical supplies through a global network. We supply more than 60.000 patients in more than 300 clinical trials every year. /p pPSES DP Pilot Plant includes two operational area’s: /p pSolids area: Oral Solid Dosage forms using Batch manufacturing technology like Granulation, Tabletting, Coating and Spray Drying, but also Continuous Manufacturing technology, which will fundamentally change the development and manufacturing of oral solid dosage forms in the near future. /p pLiquid Parenterals area: Early development in the liquids/parenterals area for both Small Molecules and Large Molecules (monoclonal Antibodies). /p pFor our DP Pilot plant in Beerse, Antwerp, Belgium we are looking for an Equipment Engineer Solids. This role will report to the Senior Manager Engineering. /p h3Purpose: /h3 pAs part of our equipment and qualification engineering team (both internal and external team members), you will contribute to improving existing installations and delivering new equipment. /p br/ h3You will be responsible for: /h3 h3Equipment engineer /h3 ul liDevelop a thorough understanding of assigned equipment's and its interaction with manufacturing processes. /li liAct as the “go to” person for questions and problems regarding your area of expertise /li liTranslate process and user needs into practical technical solutions. /li liIdentify improvement opportunities and help implement them. /li liParticipate in technical, quality and safety risk assessments. /li liLearn how equipment is designed, installed, commissioned and qualified in a regulated pharmaceutical environment. /li liBuild effective relationships with operators, engineers, quality partners, safety specialists and suppliers. /li liContinue developing your expertise through training, contact with equipment suppliers, peer learning and hands‑on experience. /li liShare lessons learned and contribute to the technical knowledge of the team. /li liBuild technical expertise in Parenteral manufacturing equipment such as processors, fill‑finish equipment, autoclaves, dry heat ovens, Sterilize‑In‑Place systems, lyophilizes, nano milling equipment and manufacturing processes such as surface decontamination, steam sterilization, dry heat sterilization, and depyrogenation /li liUnderstand how equipment design affects process performance, product quality, safety and operability. /li liAnalyze technical and process requirements and help define suitable solutions. /li liSupport troubleshooting and continuous improvement of existing equipment. /li liParticipate in Change Control (CHG) and risk assessments such as Hazard and Operability Studies (HAZOP), Structured What‑If reviews (SWIFT) and Failure Modes and Effects Analysis (FMEA) /li liWork with internal specialists and suppliers to evaluate new techn