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PROCESSING APPLICATION
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Job Requirements of Process Engineering, Scientist:
-
Employment Type:
Contractor
-
Location:
New Brunswick, NJ (Onsite)
Do you meet the requirements for this job?
Process Engineering, Scientist
Careers Integrated Resources Inc
New Brunswick, NJ (Onsite)
Contractor
Pay Range: $51.81 - $65.81/hr.
Job Description: 50 % onsite is required
Work Schedule: Mon-Fri(normal business hours)
Responsible for supporting pharmaceutical Active Pharmaceutical Ingredient (API) and Drug Product (DP) development-to-launch teams.
Responsibilities:
-Responsible for supporting MS&T Active Pharmaceutical Ingredient (API) and Drug Product (DP) development-to-launch teams.
- Design and run experiments
- Perform risk assessments, including but not limited to Material and Process Risk assessment, Nitrosamines Risk Assessment, Elemental Impurities Risk assessment etc.
- Complete, analyze and present data analysis
- Support tech transfer activities in the form of generating test plans, change controls, executing and compiling results into reports
- Supports validation efforts in the development of validation strategies and testing plans
- Provide input into process related investigations and complete MST investigations as required.
- Advise on root-cause analysis of undesired trends or deviations related to process equipment.
-Support monitoring of studies at manufacturing areas, Contract Manufacturers, as needed
- Support the Change Control process
- Position does handle hazardous material
Education and Experience Required:
- Bachelor's Degree in a Science Related field required
- Experience working in or supporting pharmaceutical operations required--minimum of 4 years
- Comfortable wearing proper PPE and working in a Laboratory -- time in Laboratory will fluctuate
- Strong communication skills, working with a team, and accountable for their work
Qualifications:
6+ years of DP technical experience, support during experimental phase and process validation and the Pharma space for oral solids. Experience writing OSD strategies, study plans, study reports, validation protocols and reports.
4+ years of expertise in data evaluation, 4+ years of expertise managing Risk Assessments
5+ years of expertise working process related Investigations and change controls.
Job Description: 50 % onsite is required
Work Schedule: Mon-Fri(normal business hours)
Responsible for supporting pharmaceutical Active Pharmaceutical Ingredient (API) and Drug Product (DP) development-to-launch teams.
Responsibilities:
-Responsible for supporting MS&T Active Pharmaceutical Ingredient (API) and Drug Product (DP) development-to-launch teams.
- Design and run experiments
- Perform risk assessments, including but not limited to Material and Process Risk assessment, Nitrosamines Risk Assessment, Elemental Impurities Risk assessment etc.
- Complete, analyze and present data analysis
- Support tech transfer activities in the form of generating test plans, change controls, executing and compiling results into reports
- Supports validation efforts in the development of validation strategies and testing plans
- Provide input into process related investigations and complete MST investigations as required.
- Advise on root-cause analysis of undesired trends or deviations related to process equipment.
-Support monitoring of studies at manufacturing areas, Contract Manufacturers, as needed
- Support the Change Control process
- Position does handle hazardous material
Education and Experience Required:
- Bachelor's Degree in a Science Related field required
- Experience working in or supporting pharmaceutical operations required--minimum of 4 years
- Comfortable wearing proper PPE and working in a Laboratory -- time in Laboratory will fluctuate
- Strong communication skills, working with a team, and accountable for their work
Qualifications:
6+ years of DP technical experience, support during experimental phase and process validation and the Pharma space for oral solids. Experience writing OSD strategies, study plans, study reports, validation protocols and reports.
4+ years of expertise in data evaluation, 4+ years of expertise managing Risk Assessments
5+ years of expertise working process related Investigations and change controls.
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