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In office (Tucson)
Seniority
Senior · 6+ years exp
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H-1B filings in 12 months: 2
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Contractor

Confirmed on the employer's own hiring board on Nov 11, 2026. First seen by Alion on Nov 11, 2026. Planet Pharma scores B on the Alion truth index.

Overview
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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.

Target Pay Rate: 32-38/hr **salary will be commensurate with experience

SUMMARY

As a member of the Assay Transfer team, you will facilitate the seamless transition of new and existing reagent products from Development to Manufacturing. This role involves initiating, directing, and executing process characterization, scientific research, and manufacturing process strategies to support product manufacturability and improve process capability.

KEY RESPONSIBILITIES & ESSENTIAL DUTIES

  • Laboratory Execution & Protocol Design:
    • Lead the design, execution, and troubleshooting of complex laboratory protocols, bench experiments, process characterization, and scale-up activities with minimal supervision.
    • Execute bench experiments, record meticulous observations, and conduct quantitative data analysis.
  • Process Transfer & Quality Standards:
    • Prepare manufacturing documentation and complete transfer activities for new products.
    • Champion “Quality First Time” standards while identifying and implementing process capability improvements in the laboratory environment.
  • Problem Solving & Subject Matter Expertise:
    • Serve as a technical resource to troubleshoot complex technical problems, institute corrective actions, and resolve intangible variables.
    • Optimize workflows and identify potential patent or publication opportunities.
  • Documentation & Technical Reporting:
    • Generate comprehensive technical reports, summaries, and experimental procedures.
    • Present findings and scientific data clearly to project teams, group meetings, and organizational stakeholders.
  • Collaboration & Leadership:
    • Partner actively across organizational boundaries and lead or participate in cross-functional technical teams (e.g., core teams, failure investigations).
    • Contribute to project planning, provide creative solutions, and mentor or train team members in areas of expertise.

CANDIDATE REQUIREMENTS & QUALIFICATIONS

  • Education & Experience:
    • Bachelor’s degree in Science with 6+ years of post-college relevant experience, OR
    • Master’s degree with 1+ year of relevant experience.
  • Technical Expertise:
    • Hands-on experience with wet lab and biological techniques, specifically IHC (Immunohistochemistry) and ISH (In Situ Hybridization).
    • Direct experience in a regulated environment, product development, and/or manufacturing operations.
    • Proficiency in standard laboratory techniques, scientific literature retrieval, and software tools (word processing, spreadsheets, graphical/presentation applications).
  • Methodologies: Ability to apply Design for Six Sigma and Design for Quality and Manufacturability (DQM) principles to optimize processes and solve potential inventions or production issues.
  • Candidate Guidelines: Candidates must meet the minimum post-college experience requirements (6+ years for Bachelor’s). Please do not submit Ph.D. candidates (considered overqualified).
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