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Job Requirements of Clinical Manufacturing Associate:
-
Employment Type:
Contractor
-
Location:
Warren, NJ (Onsite)
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Clinical Manufacturing Associate
Careers Integrated Resources Inc
Warren, NJ (Onsite)
Contractor
Job Description: Clinical Manufacturing Associate
This role is Onsite in Warren
Work Schedule: Friday- Tuesday, 8:30 AM-5 PM
•*Note there are FOUR openings on this req**
Detailed Position Responsibilities
Production of blood component lots through cell culture, harvest, and cryopreservation.
Aseptic technique
Become fully trained and qualified in all aspects of assigned processes
Develop a high level of technical knowledge of project(s)
Weigh and measure in-process materials to ensure proper quantities are added/removed.
Adhere to the production schedule ensuring on-time, internal production logistics.
Record production data and information in a clear, concise, format according to proper GDPs.
Work in a team based, cross-functional environment to complete production tasks required by shift schedule.
Assist tech transfers in and out of the clinical facility.
Motivated, team consciousness individuals are needed to fulfill job requirements.
No direct reports will be assigned to this job role.
Perform other tasks as assigned.
Desired Experience Required:
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique
- Experience within cGMP/FDA regulated industry
- Basic mathematical skills
- Technical writing capability
- Proficient in MS Office applications
- Background to include an understanding and application within industry of biology, chemistry, medical or clinical practices
Ideal Candidates Would Also Have:
- Advanced understanding of cell culture
Other Qualifications:
- Bachelor s degree in an applicable science or engineering field and a minimum of 2 years relevant experience
Additional Job Requirements:
None
This role is Onsite in Warren
Work Schedule: Friday- Tuesday, 8:30 AM-5 PM
•*Note there are FOUR openings on this req**
Detailed Position Responsibilities
Production of blood component lots through cell culture, harvest, and cryopreservation.
Aseptic technique
Become fully trained and qualified in all aspects of assigned processes
Develop a high level of technical knowledge of project(s)
Weigh and measure in-process materials to ensure proper quantities are added/removed.
Adhere to the production schedule ensuring on-time, internal production logistics.
Record production data and information in a clear, concise, format according to proper GDPs.
Work in a team based, cross-functional environment to complete production tasks required by shift schedule.
Assist tech transfers in and out of the clinical facility.
Motivated, team consciousness individuals are needed to fulfill job requirements.
No direct reports will be assigned to this job role.
Perform other tasks as assigned.
Desired Experience Required:
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique
- Experience within cGMP/FDA regulated industry
- Basic mathematical skills
- Technical writing capability
- Proficient in MS Office applications
- Background to include an understanding and application within industry of biology, chemistry, medical or clinical practices
Ideal Candidates Would Also Have:
- Advanced understanding of cell culture
Other Qualifications:
- Bachelor s degree in an applicable science or engineering field and a minimum of 2 years relevant experience
Additional Job Requirements:
None
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