27 Aug
Sr. manufacturing Technician
Massachusetts, Framingham , 01701 Framingham USA

Vacancy expired!

Department Description:8 NYA is an integrated, continuous, biomanufacturing facility (ICBF). The facility is operated by upstream, downstream and support services groups which support a 24/7 large-scale therapeutic protein manufacturing facility housing multiple products.Position Overview with Key Responsibilities:This is a 12 hour, rotating position in a flexible, single-use technology, large scale cGMP biologics facility. Initial job responsibilities will include leading a team responsible for a diverse range of manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and commercial operations.The Sr. manufacturing Technician will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs.Core Responsibilities: Maintains a safe working environment and reporting of incidents/accidentsto Manufacturing management. Effectively demonstrates understanding of GMPs and how they apply tospecific responsibilities. Follows verbal and written procedures in operating production andequipment and performing processing steps; accurately completesappropriate production documentation. Maintains cleanliness and orderliness in process area. Ensures production area is stocked with supplies. Performs EWI (Electronic Work Instruction) revisions and work ordergeneration. Interacts with other support functions such as Quality Assurance, QualityControl, Manufacturing Engineering, MSIT, Validation, etc. Utilizes manufacturing knowledge to improve process operations and affectpositive change. Demonstrates ability to troubleshoot basic mechanical operations. Effectively utilizes Microsoft Office applications. Mentors less experienced operators. Performs in process analytical testing. Demonstrates general knowledge of automation systems (INFOR, MES,ERP, DeltaV). Demonstrates general knowledge and practice of aseptic techniques.Continuous Improvement: Contributes to continual improvement of all manufacturing documentation(SOP’s, EWI’s, MBR’s, OJT’s) to ensure they are current, accurate, andclear. Supports plant floor continuous improvement initiatives.Key Responsibilities may differ among employees with the same job title andmay change over time, in accordance with business needs.Leadership Qualification: N/ABasic Qualifications: High School diploma/GED with 1-3 years of experience in a cGXP environment, or a Bachelor’s degree with 1-3 years of experience.Preferred Qualifications Bachelor’s degree with 1-3 years of experience in bulk biologics GMP manufacturing. Effectively uses process automation systems to operate production processes (i.e. Delta V).Special Working Conditions:Ability to lift up to 50 lbs. 0 Ability to stand on average 10 hours per shift. Ability to gown and gain entry to manufacturing areas. Ability to work a twelve hour rotating shift and every other weekend, including holidays as scheduled.At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Vacancy expired!


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