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Location
In office (Pennington)
Seniority
Middle · 4+ years exp
Employment
Contractor

Confirmed on the employer's own hiring board on Nov 8, 2026. First seen by Alion on Nov 5, 2026. Planet Pharma scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Planet Pharma is a life sciences recruitment and staffing firm headquartered in Deerfield, Illinois, that places contract and permanent professionals with pharmaceutical, biotechnology, medical device and contract research organizations. Founded in 2012, it offers contract and direct hire staffing, strategic resourcing, executive search, functional service provider models and global workforce solutions, with offices in Deerfield, Chicago and Raleigh and placements in the United States, Europe and Asia. Planet Pharma recruits for clients research scientists and associates, clinical trial managers, quality engineers, compliance specialists, medical writers and production supervisors.

Pay range: 20-28/hr

*depending on experience

Position Overview

The 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 Responsibilities

Upstream 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.

Qualifications

Education & 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 operations

o Shake flask cultivation

o Bioreactor systems

o Buffer and media preparation

o Single-use technologies

o Aseptic processing

Physical 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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