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Upstream Manufacturing Associate

  • Upstream Manufacturing Associate job type Posted on: Nov 04, 2026
  • Upstream Manufacturing Associate experience level Planet Pharma
  • Upstream Manufacturing Associate employment type Pennington, New Jersey
  • Upstream Manufacturing Associate employment type Onsite
  • Upstream Manufacturing Associate salary Full-time

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Job Title :

Upstream Manufacturing Associate

Job Type :

Full-Time

Job Location :

Pennington New Jersey United States

Remote :

No

Jobcon Logo Job Description :

Upstream Manufacturing Associate I, II or II (depending on experience)Location: 100% onsite in Pennington, NJDuration: 6 month contract, potential for extension or conversionSchedule: 1st, 2nd, 3rd shiftThese positions require a lot of flexibility – may require OT, evening work, overnight work, weekends, & holidays.Position OverviewThe Upstream Manufacturing Associate I is responsible for executing day-to-day upstream manufacturing operations in a cGMP cleanroom environment. This position supports cell culture manufacturing activities including media and buffer preparation, seed train expansion, bioreactor operations, harvest processing, equipment cleaning, and aseptic processing while ensuring compliance with GMP requirements.Key ResponsibilitiesUpstream Manufacturing Operations• Prepare media and buffers according to approved procedures and batch records.• Perform vial thaw, shake flask culture, seed train expansion, and bioreactor support activities.• Support fed-batch and perfusion bioreactor operations.• Execute harvest and filtration activities.• Perform equipment setup, cleaning, sanitization, and routine maintenance activities.Aseptic Processing• Perform manufacturing activities within classified cleanroom environments.• Adhere to aseptic techniques and contamination control procedures.• Follow gowning and cleanroom behavior requirements.Documentation & Compliance• Complete batch records, logbooks, and associated GMP documentation accurately and contemporaneously.• Follow SOPs, batch records, and work instructions.• Report deviations, equipment issues, and atypical events to supervision.• Support internal audits and inspection readiness activities.Continuous Improvement• Participate in training programs and qualification activities.• Support process improvement initiatives and operational excellence projects.QualificationsEducation & Experience• Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, Life Sciences, or a related discipline with 0-2 years of relevant experience.• High School Diploma/GED with 4+ years of relevant biopharmaceutical manufacturing experience may be considered.Required Skills• Basic understanding of biological manufacturing and cell culture processes.• Ability to follow detailed instructions and procedures.• Strong attention to detail and documentation practices.• Effective communication and teamwork skills.• Knowledge of cGMP requirements is preferred.Preferred Skills• Experience with:o Cell culture operationso Shake flask cultivationo Bioreactor systemso Buffer and media preparationo Single-use technologieso Aseptic processingPhysical Requirements• Ability to stand for extended periods.• Ability to bend, reach, and lift up to 50 pounds.• Ability to work in cleanroom environments while wearing required PPE.

Jobcon Logo Position Details

Posted:

Nov 04, 2026

Reference Number:

10440_4478801525

Employment:

Full-time

City:

Pennington

Job Origin:

APPCAST_CPC

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Upstream Manufacturing Associate I, II or II (depending on experience)Location: 100% onsite in Pennington, NJDuration: 6 month contract, potential for extension or conversionSchedule: 1st, 2nd, 3rd shiftThese positions require a lot of flexibility – may require OT, evening work, overnight work, weekends, & holidays.Position OverviewThe Upstream Manufacturing Associate I is responsible for executing day-to-day upstream manufacturing operations in a cGMP cleanroom environment. This position supports cell culture manufacturing activities including media and buffer preparation, seed train expansion, bioreactor operations, harvest processing, equipment cleaning, and aseptic processing while ensuring compliance with GMP requirements.Key ResponsibilitiesUpstream Manufacturing Operations• Prepare media and buffers according to approved procedures and batch records.• Perform vial thaw, shake flask culture, seed train expansion, and bioreactor support activities.• Support fed-batch and perfusion bioreactor operations.• Execute harvest and filtration activities.• Perform equipment setup, cleaning, sanitization, and routine maintenance activities.Aseptic Processing• Perform manufacturing activities within classified cleanroom environments.• Adhere to aseptic techniques and contamination control procedures.• Follow gowning and cleanroom behavior requirements.Documentation & Compliance• Complete batch records, logbooks, and associated GMP documentation accurately and contemporaneously.• Follow SOPs, batch records, and work instructions.• Report deviations, equipment issues, and atypical events to supervision.• Support internal audits and inspection readiness activities.Continuous Improvement• Participate in training programs and qualification activities.• Support process improvement initiatives and operational excellence projects.QualificationsEducation & Experience• Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, Life Sciences, or a related discipline with 0-2 years of relevant experience.• High School Diploma/GED with 4+ years of relevant biopharmaceutical manufacturing experience may be considered.Required Skills• Basic understanding of biological manufacturing and cell culture processes.• Ability to follow detailed instructions and procedures.• Strong attention to detail and documentation practices.• Effective communication and teamwork skills.• Knowledge of cGMP requirements is preferred.Preferred Skills• Experience with:o Cell culture operationso Shake flask cultivationo Bioreactor systemso Buffer and media preparationo Single-use technologieso Aseptic processingPhysical Requirements• Ability to stand for extended periods.• Ability to bend, reach, and lift up to 50 pounds.• Ability to work in cleanroom environments while wearing required PPE.

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