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Senior Process Engineer / Lead Process Engineer

Verista Inc.Dallas, TX
On-site Full-time $85K/yr - $154.4K/yr

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Experience Level

Senior

Qualifications

Job Requirements:Bachelor’s or Master’s degree in Chemical Engineering.5 to 10+ years of experience in the pharmaceutical industry focusing on manufacturing or process engineering. Strong problem-solving skills and ability to lead cross-functional teams. Proficiency in process optimization and quality assurance methodologies. Excellent communication and interpersonal skills. Experience with regulatory compliance in pharmaceutical manufacturing.

About the job

Description

Verista is a dynamic organization comprising 500 dedicated professionals who collaborate with leading names in the life sciences sector to address their business challenges. Our mission is to foster growth and innovation within the scientific community, assisting researchers, organizations, and companies in tackling some of the most urgent healthcare issues worldwide. We deliver innovative solutions and services that facilitate informed decision-making, stemming from our substantial investment in our workforce and capabilities.

Our growth is fueled by exceptional individuals who excel in a collaborative atmosphere and share our commitment to empowering life sciences clients in enhancing lives. Our skilled and passionate team members are devoted to making a significant impact every day.

Company Culture Guidelines & Values:

  • We empower and support our colleagues.
  • We are committed to client success at every opportunity.
  • We possess the courage to do what is right.
  • We promote an inclusive environment where colleagues feel respected, engaged, and challenged.
  • We continuously acquire new skills and learn from our experiences to enhance our collective expertise.

Lead Process Engineer Responsibilities:

  • Lead and implement Design of Experiments (DOE) studies to assess and enhance pharmaceutical manufacturing and packaging processes.
  • Provide technical leadership for process optimization initiatives, concentrating on efficiency, reliability, and product quality.
  • Support and refine liquid/gel filling and bottle/tube packaging operations within pharmaceutical manufacturing settings.
  • Conduct root cause analyses for process deviations or performance challenges and develop sustainable corrective actions.
  • Work collaboratively with cross-functional teams, including manufacturing, quality, and engineering, to support process development and enhancement initiatives.
  • Act as a client-facing technical expert, engaging directly with customers and stakeholders to resolve process issues.
  • Document process studies, experimental outcomes, and improvement initiatives in alignment with industry and company standards.

About Verista Inc.

Verista Inc. is committed to empowering innovation in the life sciences industry, providing comprehensive solutions and services that help organizations overcome complex healthcare challenges. Our team's expertise and dedication drive our mission to improve lives through scientific advancement.

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