Manufacturing Technician I/II/III - MA (1st Shift)

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.  WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY Manufacturing performs all required process steps and in process controls, in close collaboration with MSAT, QC, QA, Engineering and Validation. With general supervision the individual will perform routine and non-routine manufacturing operations, including but not limited to work functions in Cell Culture, Purification, Solution & Equipment Prep areas. Operates production equipment according to SOPs for the production of clinical and/or commercial products.  This position is located in Lexington, MA and reports to the MFG Supervisor. ESSENTIAL JOB FUNCTIONS This individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Production Records and Solution prep records. Primary responsibilities include the following: Attend daily meetings including shift hand off and ensure relevant information is shared between shifts Perform weekly/monthly walkthroughs and ensure areas are maintained in a safe and compliant state  Maintaining orderliness of process area and stocking production area with supplies from collaboration with Supply Chain Demonstrating general knowledge of aseptic techniques  Perform troubleshooting activities according to SOPs  Execute routine and non-routine production operations according to MFG schedule, including off shift production activities when needed Document operations according to GDP principles in Batch Production Record (BPR), Solution records (SLR), Logbooks and Forms    Perform page reviews in BPRs, SLRs, Logbooks, and Forms   Carry out work in a safe manner, notifying management of safety issues and risks  Maintain up-to-date training folder for applicable processes  Required to work holidays and overtime as needed to support the manufacturing process This individual will manage equipment and support facility related projects by: Perform scheduled cleaning of equipment  Perform standardization of equipment  Support product change over activities  Support equipment and process qualifications if needed  Escalate work requests to Senior or Lead Technicians for submission in work request management system  Staff Technical Training and Development: Propose continuous improvement, process, and human performance document revisions Escalate and contributes to process improvement and manufacturing Continuous Improvement items Develop and maintain personal development plan Provide annual performance self-assessment SPECIAL JOB REQUIREMENTS Normally requires a high school diploma and 2-4 years related cGMP industry experience or an Associate’s Degree in Life Sciences/Engineering field with 1 year of cGMP Manufacturing experience or Bachelor’s degree in life Sciences/Engineering field Preferably working experience in a comparable position (similar type of work, similar group dynamics), preferentially in an industrial organization   Ability to adhere to company internal and regulatory (EMA, FDA) policies, processes and procedures   Hands-on experience in writing and reviewing documentation   Experience in (bio)-manufacturing unit operations (USP and/or DSP) Good writing and oral communication skills   Applies experience and skills to complete assigned work within own area of expertise Works within standard operating procedures and/or scientific methods Comfortably able to lift up to 40lbs   Adaptability required as work schedule may change based on business needs Criminal background check required Other duties as assigned KNOWLEDGE, SKILLS AND EXPERIENCE EDUCATION / CERTIFICATIONS / LICENSES Essential/Desired High School Diploma Essential Associate’s Degree in Life Sciences/Engineering Desired Bachelor’s Degree in Life Sciences/Engineering Desired ON-THE-JOB EXPERIENCE 2-4 years related industry experience Desired SKILLS / ABILITIES Has process-oriented way of thinking and working  Essential Is detail oriented  Essential Is self-organized  Essential Is able to communicate in professional way on diverse levels and channels  Essential Is capable of taking initiative when necessary  Essential Has a flexible attitude in a challenging environment  Essential Is intrinsically motivated  Essential COMPENSATION RANGE: The hourly compensation range for this position is $28-$40/hour.  PHYSICAL DEMANDS  While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment Regularly sit for long periods of time Movement Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl Lifting Frequently lift and/or move up to 20 pounds Rarely lift and/or move up to 40 pounds Vision Frequently utilize close vision and the ability to adjust focus Communication Frequently required to communicate by talking, hearing, using telephone and e-mail GENEZEN'S CURES VALUE-BASED COMPETENCIES C ommitted to Science We are committed to scientific exce