Process Engineer (Pharmaceutical Manufacturing)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Location: San Fernando, California, United States. The role splits time between office-based work and manufacturing or operational environments, including production-area walking, stair or platform climbing, PPE use, and occasional light lifting. Up to 20% travel is required to support other locations and special or new projects.
Salary: $80,000–$133,000 national target base pay annually. For candidates in California and New York metro areas, the target base pay range is $88,000–$146,000 annually. Compensation may also include an annual performance bonus and benefits.
Company
develops and manufactures vitamins, supplements, and other healthy-living products, including Nature Made.
What you will do
- Develop process understanding and capability for assigned dosage forms, establish controls and guardrails, and continuously optimize products and processes.
- Use data analysis and problem-solving to identify root causes and implement short- and long-term corrective actions.
- Collect and review product and process data, then make and implement improvement recommendations.
- Prepare, review, and approve technical documents, including change controls, non-conformance reports, SOPs, batch records, validation protocols, and technical reports.
- Support equipment testing and qualification, including FAT, SAT, PQ, IQ, and OQ activities.
- Lead cross-functional improvement initiatives that increase manufacturing and packaging efficiency while maintaining safety, SOP, and GMP compliance.
Requirements
- Bachelor's degree or equivalent work experience in Industrial, Mechanical, or Chemical Engineering, Food Science, or a related scientific field; equivalent directly related experience may be considered.
- 4–6 years of related experience, including at least 2 years in pharmaceutical, nutritional, food, or other consumer-packaged-goods industry experience.
- 1–3 years of experience in manufacturing technical support, process or product development, quality engineering, and/or testing.
- Comprehensive knowledge of product and process development, manufacturing and packaging equipment, processing and testing laboratory techniques, and regulatory requirements.
- Strong oral and written communication skills, with the ability to present recommendations.
- Ability to use hand-held data collection devices and instrumentation.
- Results-oriented planning, prioritization, organization, and execution skills.
- Immigration sponsorship or support is not available, including completion of the Form I-983 training plan required for STEM OPT.
- U.S. work authorization must be accurately represented during the application process.
Nice to have
- ASQ Certified Quality Engineer.
- Certified Packaging Professional, Lean Manufacturing, Six Sigma, or other related problem-solving certification.
- Understanding of Lean concepts and application of DOE and QbD.
Culture & Benefits
- Growth-oriented environment focused on learning, experimentation, curiosity, and continuous development.
- Medical, dental, and vision benefits, 401(k) match, wellness benefits, and an annual performance bonus may be included.
- Overtime is compensated for non-exempt hourly employees in accordance with applicable state and federal law; overtime may be required based on business needs.
- Work includes manufacturing noise, moving equipment, temperature variation, and other operational conditions requiring safety precautions.
Hiring process
- Applications must accurately disclose U.S. work authorization and any need for immigration sponsorship or support; misrepresentations may result in rejection or termination.
- 's hiring process does not include text-based conversations or interviews and never requires payment or fees from applicants.
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