2 часа назад
Sr. Maintenance Compliance Engineer
82 700 - 137 900$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Sr. Maintenance Compliance Engineer (Pharmaceutical Manufacturing): Supporting the redesign, maintenance, repair, and compliance of utility systems, buildings, and production equipment with an accent on reliability engineering, cGMP, and maintenance optimization. Focus on root cause failure analysis, preventive maintenance improvements, CAPA investigations, and coordinating engineering activities with Production and Quality teams.
Location: On-site in Rochester, Michigan, United States. Standard Monday–Friday daytime schedule with overtime, shutdown-period work, and occasional national or international travel.
Salary: $82,700–$137,900 annual base salary, plus eligibility for a 10% bonus target.
Company
develops and manufactures medicines and pharmaceutical products.
What you will do
- Manage maintenance and reliability engineering activities for utility systems, buildings, and production and non-production equipment.
- Develop scopes of work, project execution plans, engineering studies, and equipment installation or modification plans.
- Review preventive and corrective maintenance work orders, equipment history, and maintenance optimization opportunities.
- Ensure maintenance and engineering activities comply with current Good Manufacturing Practices, GxP requirements, and aseptic practices.
- Lead or participate in root cause failure analyses, investigations, change controls, and CAPA implementation.
- Coordinate troubleshooting and investigation closure with Production, Quality Operations, and engineering teams.
Requirements
- Bachelor’s degree with at least 2 years of experience, master’s degree with more than 0 years of experience, associate’s degree with 6 years of experience, or high school diploma with 8 years of relevant experience.
- Experience in manufacturing, reliability, plant, or project engineering.
- Experience with root cause failure analysis, equipment criticality ranking, preventive or predictive maintenance optimization, and/or FMEA.
- Strong knowledge of current Good Manufacturing Practices and working knowledge of Microsoft Office applications.
- Strong written and verbal communication, planning, problem-solving, and teamwork skills.
- Permanent U.S. work authorization is required; visa sponsorship is not available. Candidates must not be allergic to penicillin and must be able to work in clean-room conditions.
Nice to have
- Certified Maintenance and Reliability Professional certification or equivalent.
- Experience with pharmaceutical manufacturing equipment and utility systems.
Culture & Benefits
- On-site work at a penicillin manufacturing facility with a standard daytime schedule.
- Overtime, late work during unexpected equipment downtime, and extended hours during scheduled manufacturing shutdowns may be required.
- Benefits include a 401(k) plan with matching and retirement contributions, paid vacation and holidays, caregiver, parental and medical leave, and medical, prescription, dental, and vision coverage.
- Relocation assistance may be available depending on business needs and eligibility.
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