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Process Engineer​/Scientist II - 1st shift

Job in Pittsfield, Berkshire County, Massachusetts, 01201, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-02-28
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Pharmaceutical Manufacturing, Operations Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Role Summary

Process Engineer/Scientist II, 1st shift. Provide hands‑on support to pharmaceutical manufacturing operations, ensuring adherence to procedures and regulatory guidelines. You will execute production activities, assist in technology transfer and startup efforts, and maintain compliant technical documentation to support process approvals. This role requires strong organizational skills and the ability to work in a structured environment on defined procedures.

Responsibilities
  • Execute production activities using knowledge of process equipment, systems, and manufacturing operations.
  • Participate in operational qualification training and assist the Team Lead as needed.
  • Ensure all activities comply with company policies, standard operating procedures, Pfizer values, and global regulatory and environmental guidelines.
  • Work in a structured environment using established procedures.
  • Ensure work is regularly reviewed for technical judgment, completeness, and accuracy.
  • Assist in troubleshooting, technology transfer, and startup activities.
  • Oversee technical documentation for production and process approvals, ensuring compliance with Current Good Manufacturing Practices, and manage process activities by adhering to Standard Operating Procedures.
Qualifications
  • Required:

    BA/BS degree with any years of experience, or Associate's degree with 4+ years of experience, or high school diploma (or equivalent) with 6+ years of relevant experience.
  • Knowledge of process equipment and manufacturing operations.
  • Ability to follow standard operating procedures and regulatory guidelines.
  • Basic understanding of Current Good Manufacturing Practices.
  • Strong organizational skills to manage project tasks and meet deadlines.
  • Technical documentation skills for production and process approvals.
Preferred Qualifications
  • Experience with in the pharmaceutical industry.
  • Familiarity with Six Sigma or other operational excellence programs.
  • Proficiency in troubleshooting and technology transfer activities.
  • Strong analytical skills for process monitoring and data analysis.
  • Excellent communication skills for presenting data in project team meetings.
  • Strong problem‑solving skills.
Additional Requirements
  • Non-standard Work Schedule, Travel Or Environment:
    First Shift, Monday – Friday, 7:30 AM – 4 PM. On‑site work location.
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