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Engineering Scientist

Job in Fort Lauderdale, Broward County, Florida, 33336, USA
Listing for: LanceSoft, Inc.
Seasonal/Temporary position
Listed on 2025-12-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 35 - 45 USD Hourly USD 35.00 45.00 HOUR
Job Description & How to Apply Below

This range is provided by Lance Soft, Inc.. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$35.00/hr - $45.00/hr

Direct message the job poster from Lance Soft, Inc.

Director Delivery Services at Lance Soft, Inc.

Job Title: Manufacturing Science and Technology Engineer/Scientist

Location: Davie, FL 33314

Duration: 12 Months

  • Temp to Perm role: Possibility based on workers performance and openings

Core essential skill sets candidates must have to be considered for the role:

  • College fresh PhD with chemistry
  • Basic certifications in areas of Power Platform, AI, Project Management, preferred

Position Summary:

  • This position is responsible for performing activities related to critical aspects of products and processes with focus on process engineering.
  • Maintains expertise related to process engineering and chemistry is necessary
  • Digital literacy including basic knowledge of AI (working knowledge of Power

    BI, Power Platform, Python and various presentation tools), JMP, R, etc. is necessary.

Essential Areas of Responsibility:

All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.

  • Coordinate manufacturing of batches if required and prepare technical reports.
  • Perform continuous process and cleaning verification, statistical assessments and trend analysis for the development and commercial products.
  • Perform investigations to identify the root causes and actively seek remediation approaches and implement Corrective and Preventive Actions (CAPAs).
  • Provide Technical assessments/ product impact assessment summaries on time to avoid back-order situation.
  • Execute the experimental and process confirmation studies in coordination with planning, manufacturing, quality, LTS and PM groups.
  • Review and analysis of the analytical and statistical data to support the pre-validation work. Analysis of data to ascertain the data meets protocol and product acceptance criteria: writes deviation reports and technical assessments as required.
  • Supports pre-validation commercial scale report that includes detailed summary of the equipment and qualified equipment parameters (QEPs) assessment, CPPs and CQAs identified during pre-validation work.
  • Participation in internal (Corporate and QA audits) and external (FDA, MHRA) audits.
  • Remediation of the audit related observations (if any) and timely completion of the action items (if any)
  • Maintenance of appropriate documentation of protocols, reports, and laboratory notebooks as required by Standard Operating Procedures (SOPs) and internal policies.
  • Actively participate in commercial pre-validation and provide technical support to the manufacturing and quality teams as required.
  • Leading multiple new product introduction, site transfer projects and cleaning validation activities.
  • Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) and Batch Record instructions.
  • Responsible for performing additional related duties as assigned.

Position Requirements:

  • Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.

Education/Certification/

Experience:

  • Requires a college fresh Ph.D. With chemistry
  • Basic certifications in areas of Power Platform, AI, Project Management, preferred

Skills/Knowledge/Abilities:

  • Ability to prepare various types of complex high quality technical documentation (Batch Records (BR), Change Controls (CC), protocols, summary reports, technical assessments, validation reports and deviation/investigation reports etc.
  • Ability to handle multiple projects, duties, and assignments.
  • Solving practical problems and considering a variety of concrete variables in situations where only limited standardization exists.

Seniority level: Associate

Employment type: Contract

Job function: Science, Research, and Engineering

Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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