21 час назад
Process Engineering Consultant (Pharmaceutical Manufacturing)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Process Engineering Consultant (Pharmaceutical Manufacturing): Developing and optimizing pharmaceutical and biotechnology manufacturing processes through concept development, detailed design, and implementation with an accent on process calculations, PFDs, P&IDs, equipment specifications, and GMP compliance. Focus on analyzing complex technical challenges, designing compliant process solutions, and coordinating engineering deliverables across multidisciplinary project teams.
Location: Clayton, North Carolina, United States; must be based in Clayton
Salary: Competitive salary with annual adjustment increases
Company
delivers engineering and consulting solutions for pharmaceutical, biotechnology, and life sciences manufacturing projects.
What you will do
- Develop process engineering deliverables, including process flow diagrams, process descriptions, equipment specifications, calculations, and technical reports.
- Execute engineering tasks across conceptual, basic, and detailed design phases while meeting quality, budget, and schedule expectations.
- Collaborate with multidisciplinary teams, clients, vendors, and subject matter experts on practical and compliant process solutions.
- Analyze technical challenges, evaluate alternatives, and recommend solutions supporting client and project objectives.
- Contribute to knowledge sharing, process improvements, and engineering best practices.
Requirements
- Must be based in Clayton, North Carolina, United States.
- Must have unrestricted authorization to work in the United States and must not require current or future employer sponsorship.
- Bachelor's or master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Pharmaceutical Engineering, or a related discipline.
- At least 3 years of relevant engineering experience in pharmaceutical, biotechnology, life sciences, or another regulated industry.
- Experience with process calculations, PFDs, P&IDs, equipment sizing, and technical documentation.
- Familiarity with GMP-regulated environments and pharmaceutical manufacturing processes, plus strong communication and collaboration skills.
Nice to have
- Experience with commissioning, qualification, validation, or process optimization.
Culture & Benefits
- Agile, fast-paced, project-oriented environment with multidisciplinary collaboration.
- 160 hours of paid time off, prorated from the hire date, plus 14 paid holidays.
- Health, dental, and vision insurance from the first day.
- 8% guaranteed 401(k) company contribution.
- 14 weeks of paid parental leave, company-paid life and disability insurance, and employee referral bonuses.
Hiring process
- Applications are accepted through the online system only.
- Interviews are scheduled on a rolling basis.
- Application deadline: September 25, 2026.
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