5 дней назад
Product Engineer I (Life Sciences Manufacturing)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Product Engineer I (Life Sciences Manufacturing): Supporting customer and manufacturing issue resolution and new product introduction activities with an accent on data collection, root cause analysis, process validation, and quality documentation. Focus on analyzing process performance, executing test protocols, maintaining controlled manufacturing documentation, and supporting regulated life sciences production.
Location: On-site in Pensacola, Florida, United States
Company
is a Danaher operating company developing solutions for biological research, vaccines, medicines, and cell and gene therapies.
What you will do
- Support structured problem-solving activities, including 5 Whys and basic root cause analysis.
- Collect and analyze process and quality data to identify and monitor critical-to-quality characteristics.
- Participate in new product introduction activities, including data collection, protocol execution, and documentation for process validation and qualification.
- Support raw material changes by collecting supplier data, executing test protocols, and documenting engineering assessment results.
- Maintain process documentation, including SOPs, work instructions, and control plans, in line with change control requirements.
Requirements
- Bachelor of Science in Engineering or a related technical discipline, or an equivalent combination of education and internship or co-op experience.
- 0–3 years of experience in engineering, manufacturing, or quality; internships and co-ops are valued.
- Basic understanding of manufacturing processes, statistics, data analysis, SPC, and DOE concepts.
- Foundational knowledge of problem-solving methodologies and basic root cause analysis.
- Ability to work on-site in Pensacola, Florida, United States.
Nice to have
- Exposure to polymeric materials or life sciences manufacturing.
- Familiarity with Danaher Business System concepts.
- Experience in a regulated manufacturing environment using cGMP or ISO standards.
Culture & Benefits
- Continuous improvement culture focused on measurable impact in life sciences.
- Collaborative environment centered on customers, patients, and innovation.
- Healthcare programs and paid time off.
- Equal opportunity employment and reasonable accommodation for candidates and employees with disabilities.
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