Manufacturing Technician Salary at Enovis BETA

Aseptic Manufacturing Technician Philadelphia, PA (Onsite) 6-Month Contract-to-Hire **Day & Night Shifts Avaliable - 12 hour shifts Sunday to Wednesday OR Wednesday to Saturday** Compensation: AMT II: $31.75/hr Sr. AMT: $35/hr Lead AMT: $40/hr MUST HAVE EXPERIENCE: 1+ year - Aseptic Technique, GMP, Gowning, Cell Culture/Cell Processing About: At the forefront of cutting-edge biotechnology, our organization is dedicated to advancing innovative solutions in the autologous cell therapy space. We’re looking for passionate, detail-oriented professionals to join our team and play a pivotal role in our mission to transform lives through groundbreaking treatments. Why This Role? As an Aseptic Manufacturing Technician, you will be at the heart of our manufacturing process, contributing to the development and production of life-changing cell therapies. You will apply your expertise in aseptic techniques, cell culture, and GMP practices in a fast-paced, dynamic environment. This is an exceptional

Job Description Job Description As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations is strongly desired. Essential Functions and Responsibilities Develop a Subject Matter Expert (SME)-level understanding of and be able to skillfully execute as well as troubleshoot GMP cell therapy manufacturing process(es). Complete training sessions and ensure training documentation is maintained. Understand and comply with quality standards and requirements as documented. Provide operational support functions including materials stocking and transfer, kit preparation, reagent preparation, room readiness, cleaning activities, and equipment maintenance. Perform document review, including executed Batch Records and Logbooks. Aseptic Manufacturing Technicians are required to work their assigned schedule. The first few months of onboarding training for this position w

Manufacturing Technician needed! Overview: As an Aseptic Processing Technician, you will focus on the documentation for our processes. The ideal candidate will have a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed. This position working a 4 day week - Tuesday - Friday, 7am - 5pm OR 2:30pm-1am Essential Functions and Responsibilities: Complete training sessions and ensure training documentation is maintained. Proficiently carry out procedures to achieve a consistent, error-free execution of daily job assignments Work as part of a team to produce each lot accurately and fully complete batch records, forms, and documentation. At all times, understand and comply with quality standards and safety guidelines. Perform materials stocking, kit preparation,

Manufacturing Technician needed! Overview: The Manufacturing Technician role is crucial for the autologous cell therapy manufacturing program. This position requires a broad understanding of theories, techniques, and principles to support manufacturing processes. The Manufacturing Specialist will be responsible for various tasks, such as cleaning, sanitization, preparation, and fulfilling products for commercial and clinical use. To excel in this role, it is strongly desired that the candidate has a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations. This position works across different shifts. Depending on your assigned shift, you may be required to work on weekends and holidays. Shifts: A or B Shift A-Rotation Week 1: Sunday to Tuesday: 6:00PM – 6:30AM Week 2: Sunday to Wednesday: 6:00PM – 5:30AM OR Shift B-Rotation Week 1: Wednesday to Saturday: 6:00PM – 5:30AM Week 2: Thursday to Saturday: 6:00PM – 6:30AM Essential Functions and Resp

Job Description Job Description Seasonal Contract Position Starts in mid-February/early March, and contact ends around late Sept/early October. 1st, 2nd, and 3rd Shifts Available 1st Shift- 0600-1430 (Mon-Fri) 5x8 hour shifts 2nd Shift- 2nd: 1400-2230 (Mon-Fri) 5x8 hour shifts 10% differential included in rate 3rd Shift- 3rd:2200-0630 (Sun-Thu) 5x8 hour shifts 15% differential included in rate Job Summary: Performs a variety of tasks related to the processing of ingredients and/or pharmaceutical products. Operates general manufacturing equipment, such as autoclaves, and automated aseptic filling lines. Handles raw materials and intermediate or finished products. Handles cleaning and sanitization of the facility. 25% of 8hr day is cleaning the stage area/rooms. Role and Responsibilities • Assists in direct manufacturing support functions such as Thaw, Blend, Fill, Stage, Prep, Environmental Monitoring (EM), and equipment preparation. • Assists in indirect manufacturing support functions

Overview: This role is primarily responsible for suite preparation for cell processing, material transfer, environmental monitoring, BSC runner duties, final product inspection, and final product cryopreservation in controlled rate freezers, for commercial and clinical use. Duties: Materials stocking and transfer. Equipment cleaning activities. Feeder cell retrieval from liquid nitrogen (LN2) tanks. Able to perform final product visual inspection. Final product cryopreservation in controlled rate freezers. Perform biosafety cabinet (BSC) runner duties as assigned. Perform in-suite environmental monitoring during the day of process Perform logbook review. Qualifications: Bachelor’s degree or equivalent experience. Minimum 0-1 year of experience in biopharmaceutical-based GMP manufacturing operations, including, aseptic technique, aseptic liquid transfers, use of welders and sealers, BSC aseptic operations and associated downstream processing is a plus. Why Choose R&D Partners? As an emp

Primary Responsibilities: Proficiently execute cell therapy manufacturing process(es). Performs cell counts utilizing cell counting machines. Harvesting/seeding single use high density bioreactors Perform aseptic tube welding, sealing and connections Perform in-suite environmental monitoring during the day of process Perform real-time document review, including executed Batch Records and Logbooks. Qualifications: Bachelor's degree or equivalent experience. Minimum 1+ years of experience in biopharmaceutical-based GMP manufacturing operations, including experience in cell culture and associated downstream processing, including but not limited to cell culture, single use high density bioreactors, Bio Safety Cabinets (BSCs), cell count machines, liquid transfers, cell wash and concentration machines, tube welders and sealers, controlled rate freezers, grade B (ISO7) gowning and liquid nitrogen amongst others. Why Choose R&D Partners? As an employee, you have access to a comprehensive bene

Openings for multiple levels: II, Senior, and Lead Shift: Wednesday - Saturday, 4 days a week, 10 hour days Pay between $31.75-$40 based on experience 6 month contract to hire Specific Responsibilities Develop a comprehensive understanding of and be able to proficiently execute current cell therapy manufacturing process. Complete training sessions and ensure training documentation is maintained. Understands and complies with quality standards and requirements as documented. Provides operational support functions including materials stocking, kit preparation, reagent preparation, cleaning activities, and equipment maintenance. Supports technical transfer and additional research level testing activities. Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP). Completes recording of data to comply with regulatory requirements. Support documentation needs, which may including drafting and approval of SOPs, Batch