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Job Requirements of Biomanufacturing Technician:
-
Employment Type:
Contractor
-
Location:
Memphis, TN (Onsite)
Do you meet the requirements for this job?
Biomanufacturing Technician
Careers Integrated Resources Inc
Memphis, TN (Onsite)
Contractor
Job Title: Biomanufacturing Technician
Location: Memphis, TN
Duration: 6 months+
Shift: 6 :00 am - 6:30 pm/ once trained potentially moved to 10:30am-11pm -training is 6-8 weeks
Additional Requisition Requirements :
2nd Shift: 10:30am-11:00pm (2 shifts on, 2 shifts off, 3 shifts on, 2 shifts off, 2 shifts on, 3 shifts off with the 3-days falling Friday – Sunday)
Built in OT based off the 2-2-3 set up (i.e., 48 hr. week + 36 hr. week = 84 hours for two week period) -Training class on
The Biomanufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of Client cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description.
Essential Duties And Responsibilities:
Qualifications:
#sczr2
Location: Memphis, TN
Duration: 6 months+
Shift: 6 :00 am - 6:30 pm/ once trained potentially moved to 10:30am-11pm -training is 6-8 weeks
Additional Requisition Requirements :
2nd Shift: 10:30am-11:00pm (2 shifts on, 2 shifts off, 3 shifts on, 2 shifts off, 2 shifts on, 3 shifts off with the 3-days falling Friday – Sunday)
Built in OT based off the 2-2-3 set up (i.e., 48 hr. week + 36 hr. week = 84 hours for two week period) -Training class on
The Biomanufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of Client cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description.
Essential Duties And Responsibilities:
- Obtain and maintain qualifications necessary for the performance of aseptic activities.
- Responsible for the production, formulation, and banking of cellular products (including GMP, GDP, and aseptic processing).
- Write, under supervision, GMP required documents including standard operating procedures, product specifications, equipment specifications and batch production records.
- Provide support in validation efforts related to the manufacturing process.
- Participate in all aspects of manufacturing activities including raw material support, cell culture, and continuous improvement.
- Consistently practice appropriate clean room behaviors and upkeep of clean room
- areas.
- Perform all other related duties as assigned.
Qualifications:
- Associate degree in a scientific field is strongly preferred.
- High school diploma or equivalent required.
- Zero to 1 year of applicable experience in biotech or cell therapy.
- May consider less education and professional experience upon successful completion of Client internship program.
- Must be able to work in a clean room environment that potentially includes hazardous materials and medical equipment (including blood, tissues, and needles)
- Must have ability to perform algebraic math.
- Must be detail oriented and have excellent organizational skills.
- Must possess effective written and oral communication skills.
- Must display a high degree of professionalism and confidentiality.
#sczr2
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