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Process Development Associate - Onsite

Confidential ClientConsulting
Entry LevelContractOn-Site$69,521
West Greenwich, Rhode Island
17 Hours Ago

The Process Development Associate supports cell culture and downstream purification processes at a global biotechnology company, working onsite with flexible shifts including weekends. This entry-level role involves executing aseptic techniques, operating bioreactors, performing routine lab tasks, and documenting scientific data to ensure process integrity and quality. The position offers hands-on experience in biopharmaceutical manufacturing and process development within a contract setting.

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Description

About Careertakes

👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, Scientific & QA.

Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.


What You’ll Do

This is an onsite, entry-level Process Development Associate role supporting cell culture and downstream process activities for a confidential client in the life sciences. You will work under supervision to execute experiments, collect process data, and support scale-up and routine manufacturing operations.

  • Support cell culture workflows: aseptic vial thaw, flask passaging, benchtop wave bioreactors, and 200L/500L single-use bioreactors
  • Assist large-scale harvests and downstream purification steps (chromatography, filtration, UF/DF)
  • Perform in-process sampling and operate laboratory analyzers
  • Record experimental and process data using electronic laboratory notebooks (ELNs)
  • Prepare media and buffers; perform CIP (Clean-In-Place) and SIP (Steam-In-Place) procedures
  • Assemble/disassemble equipment, conduct routine maintenance of benchtop analyzers, and maintain lab organization and cleanliness
  • Apply scientific principles to execute experiments and support basic data analysis
  • Follow good documentation practices for all process and data records

Requirements

  • Bachelor’s degree in Engineering or Science OR
  • Associate’s degree plus 1 year of lab/manufacturing experience OR
  • 2+ years of lab or manufacturing experience
  • Ability to work onsite and be available for scheduled weekend shifts (typically 1–3 times per month)
  • Willingness to work the flexible shift (approx. 7:30 AM – 4:00 PM)

Desired skills

  • Hands-on experience with pilot- or large-scale cell culture or downstream purification (preferred)
  • Familiarity with automated, computer-controlled biopharmaceutical equipment
  • Basic experience compiling and analyzing process data
  • Strong attention to detail and problem-solving aptitude
  • Good written and verbal communication skills

Compensation & Schedule

  • Pay: up to $29.58 per hour (hourly, contract opportunity)
  • Location: West Greenwich, RI (onsite)
  • Duration: 6+ month contract (contingent on client needs)
  • Schedule: Day shift with occasional weekend work (1–3 times monthly)

Benefits

When employed through the engagement model used by our client, typical benefits may include:

  • Medical
  • Dental
  • Vision
  • Sick pay (where applicable by state or municipality)

Employment notes

This role is administered via Careertakes supporting the hiring process for a confidential client. Candidates must be able to work as employees of the client (or the client’s authorized staffing partner) to be considered.


Equal Opportunity & Hiring Transparency

Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.

If you have questions about how your data is used, please contact us directly.

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