Process Development Engineer

{
  "content_hash": "7b3f2173993f065aa7b879c13479d5bebe745ae95cf98ef88a816e16880ec0c9",
  "source_hash": "ac095cfc567f82207e470df200222be9427beee52e5d859f5521c07fce1d4c73",
  "last_changed_at": "2026-06-03T12:27:01.776Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "Emeryville, CA",
    "city": "Emeryville",
    "region": "CA",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
  },
  "salary_max": 125000,
  "salary_min": 85000,
  "inferred_at": "2026-06-06T20:02:59.567Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Emeryville, CA",
      "city": "Emeryville",
      "region": "CA",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.9
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": "year",
  "workplace_type": "on_site",
  "salary_currency": "USD"
}

{}

{
  "lists": [
    {
      "text": "Qualifications",
      "content": "\n<li>MS, or BS in Chemical Engineering, Mechanical Engineering, Manufacturing Engineering, Chemistry, Biochemistry, Chemical Biology, or a similar field. For candidates with a BS, we’d like to see significant experience in process development and GMP environments (2-5 years).</li>\n<li>Experience in CMC (Chemistry, Manufacturing, and Controls), pharmaceutical/biopharmaceutical manufacturing, or related process development and automation is strongly preferred.</li>\n<li>Hands-on experience with operation of process equipment, solid mechanical aptitude, record keeping in a QMS, aseptic processing/clean rooms, and automation.</li>\n"
    },
    {
      "text": "Skills and Qualities",
      "content": "\n<li>Process operation and development – Demonstrated ability to execute process development activities, evaluate process performance, and provide recommendations through data-driven analysis and practical problem solving.</li>\n<li>Prior experience with GMP manufacturing process and managing relations with equipment providers is a huge bonus, as we expect this role to involve several collaborations with equipment providers.</li>\n<li>Meticulous attention to detail and record keeping. You take pride in generating clear, accurate, and traceable documentation.</li>\n<li>Familiarity with operating in a GMP QMS environment (batch records, deviations, CAPA, change control) is strongly preferred.</li>\n<li>Strong mechanical aptitude and experience in the use of tools for operation, assembly, and maintenance of development laboratory equipment and infrastructure.</li>\n<li>Familiarity with CAD and mechanical design would be a plus, especially when it comes to sourcing parts or working with equipment design.</li>\n<li>This role may require some domestic and international travel to CMO sites for on-the-ground tech transfer support and troubleshooting.</li>\n"
    }
  ],
  "country": "US",
  "createdAt": 1780420803486,
  "updatedAt": null,
  "categories": {
    "team": "4:59 - Prolynx",
    "location": "Emeryville, CA",
    "commitment": "Full-time",
    "department": "4:59 Initiative",
    "allLocations": [
      "Emeryville, CA"
    ]
  },
  "salaryRange": {
    "max": 125000,
    "min": 85000,
    "currency": "USD",
    "interval": "per-year-salary"
  },
  "workplaceType": "onsite"
}