Process Engineer II

LanceSoft Inc

Elkton (VA)

On-site

USD 60,000 - 85,000

Full time

14 days+

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Job summary

A leading biopharmaceutical company is seeking candidates for a technical role focused on supporting manufacturing processes. Responsibilities include creating and maintaining detailed spreadsheets, providing technical support, and conducting investigations. The ideal candidate demonstrates strong problem-solving abilities, excellent communication skills, and a passion for continuous learning. Experience in a cGMP environment is preferred, along with an excellent academic record. Join our team for a rewarding career in the biopharmaceutical industry.

Qualifications

  • Experience working in a cGMP environment preferred.
  • Initiative and enthusiasm needed for continuous learning.
  • Leadership, judgment, and project management abilities required.

Responsibilities

  • Create & maintain highly detailed spreadsheets.
  • Provide technical support for manufacturing processes.
  • Conduct technical investigations and analyses.

Skills

Strong verbal and written communication skills
Problem solving skills
Technical/analytical data comprehension
Attention to detail

Education

Excellent academic record

Job description

Responsibilities

Responsibilities may include:

  • Create & maintain highly detailed spreadsheets
  • Providing technical support for vaccine, biologic, and sterile manufacturing processes in the form of data analysis, troubleshooting, problem-solving, report writing
  • Supporting change control implementation
  • Learning new processes and procedures
  • Recommending, creating, writing process control and automation instructions
  • Performing shift work as needed
  • Conducting technical investigations and analyses
  • Recommending and implementing corrective and preventative actions, and helping lead reduction of atypical events
  • Writing, reviewing, and improving procedures for operation of equipment and processes
  • Contributing to process and equipment safety reviews
Qualifications

Preferred Experiences:

  • Experience working in a cGMP environment
  • Work, co-op, or internship experience in industry

Qualifications:

The successful candidate must have:

  • Excellent academic record
  • Strong verbal and written communication skills, team skills, personal character, and ethics
  • Strong problem solving skills and a hands‑on approach to problem solving, with a bias towards going to see problems for oneself in the field.
  • Ability to examine an issue from diverse perspectives (safety, compliance, maintenance, automation, equipment, process, and people) in order to best understand and resolve it.
  • Enthusiasm, confidence, and initiative‑taking ability needed for continuous learning and its applications.
  • Strong desire to succeed and to help others to do the same.
  • Technical/analytical data comprehension
  • Leadership, judgment, organization and project management abilities - Create & maintain highly detailed spreadsheets
  • Independent decision making and coordination of activities
  • Attention to detail and follow‑up skills
Additional Information

All your information will be kept confidential according to EEO guidelines.

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