Job Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to making a positive impact on the lives of the patients and families we serve. Genzyme's portfolio of transformative therapies, which are marketed in countries around the world, represent groundbreaking and life-saving advances in medicine.
As a Sanofi company, Genzyme benefits from the reach and resources of one of the world's largest pharmaceutical companies, with a shared commitment to improving the lives of patients. Learn more at www.genzyme.com.The Manufacturing Engineering Group at the Allston Landing manufacturing site is responsible to ensure that the manufacturing equipment/systems and Automation systems used in the manufacture, storage, testing, and distribution of Genzyme products are fit for purpose in accordance with Genzyme Corporate standards and industry regulatory requirements. This encompasses work processes that originate with the identification of a new or revised asset, the design, installation, verification and validation of the asset, the maintenance of the asset in its commissioned/qualified/validated state and the retirement of the asset at the end of its life.This position is responsible for the configuration, administration and maintenance of the Emerson DeltaV process control system.Automation Engineer I This individual will have the ability to translate manufacturing process information into the design of control systems that will be utilized by equipment systems employed in the manufacture of biological products. Additionally, the individual must troubleshoot control system problems and then document and recommend the solution to that problem.This position supports manufacturing by working with other groups to identify process control gaps and rectify them through an approved change control process.
The goal for this position is to constantly identify continuous improvement opportunities and manage them from conception through implementation.The ability to operate self-sufficiently and to motivate oneself is crucial for the success of this position. In addition, the ability for this person to develop and maintain good communication between departments is essential Qualifications Basic QualificationsBachelor's degree in Engineering, Computer, Science or related technological fieldExperience with Emerson DeltaV or similar process control systemTypically 3+ years of relevant work experience with 1+ year experience in operations/manufacturing environment.Preferred QualificationsExperience in operations/manufacturing environmentExposure to or direct experience with regulated environments (i.e. cGMP, OSHA, EPA)Allen Bradley PLC, RS3, cGMP experience, computer software validation, computer programming and process experience in a Biopharmaceutical environment.Experience with GAMPValidation experience related to control and computer systems.Ability to effectively and appropriately escalate operational issuesExperienced in establishment of safe practices in a cGMP environmentBasic equipment knowledge (valve, pump, replacement part, skid control system).Basic understanding of GMPs as applied to individual equipment or process steps. Special working conditionsAbility to gown and gain entry to manufacturing areas
CareersInPharmaceutical.com - 10 months ago
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