Process Engineer

HELP US BRING THE GIFT OF HEALTH TO LIFE. Working at Pharmavite is an experience like no other. With a focus on complete nutrition for all, each endeavor is urgent and every day counts. You’ll have the opportunity to work on the #1 selling national vitamin and supplement brand, Nature Made, as well as an exciting portfolio of other products that are shaping the future of the healthy living industry. Consumer‑driven innovation, high quality products and a promising portfolio, all driven by a team with a shared sense of purpose – that’s Pharmavite. Join us to bring the gift of health to life. This role is not available for any form of immigration sponsorship or support, including completion of the Form I-983 training plan required for STEM OPT. Position Summary Optimizes products and processes by establishing process capabilities and controls, and ensures adherence to standards through continuous verification. Leads site functional technical support for assigned dosage form as it relates to finding and implementing creative solutions that maximize value to our customers. Establishes specifications and appropriate process guardrails to ensure we deliver a reliable and repeatable process to Operations. Leverages data and an analytical mindset to draw insights on our products and champions change across our supply chain. Responsibilities Demonstrates a high level of subject matter expertise for the assigned dosage form and is capable of influencing internal and external groups to make improvements Uses problem‑solving skills to identify root cause and implement short and long‑term corrective actions related to improving the reliability of our products or processes Develops a high level of process understanding and capability for the assigned dosage form, establishes an appropriate level of controls for repeatability, and works to optimize the product or process to maximize customer value Supports periodic review of our products and processes by collecting data, analyzing it, and making and implementing recommendations related to improvements Develops and executes cleaning validations Supports Quality and Operations through troubleshooting, change controls, and Non‑Conformance Report (NCR) reduction Serves as a technical approver for equipment change requests and Installation Operations Qualification (IOQs) documentation Prepares, reviews, and/or approves technical documents to include but not limited to: Quality Change Requests (QCRs), Non‑Conformance Report (NCRs), Technical Reports, SOPs, Master Batch Records (MBRs), Change Controls, Cost Quotes, Product and Process Verification/Validation Protocols (IQ, OQ, PQ), P&PV Summary Reports and Stability Protocols. Serves on cross‑functional team leads who address specific problems, facilitates discussion and research, enabling manufacturing and packaging operations to become more efficient and to build and enhance interdepartmental relationships. Maintains documentation on all projects and submits written reports in a timely fashion. Performs equipment testing and qualification as required. Will support the following: factory acceptance test (FAT), site acceptance tests (SAT), and performance qualification (PQ), will also require participation in Installation qualification (IQ) and operational qualification (OQ) activities Trains Technical Operations, Product Development, and Manufacturing staff on new processes and/or equipment technologies. Ensures efficient operations in assigned project areas in accordance with Pharmavite Safety Requirements, SOPs, and GMPs. Ensures functional operation and preventative maintenance of equipment to reduce/eliminate accidental injury Reviews current and new processes; applies state‑of‑the‑art technology to our processes. Occasional after‑hours operations and or project support may be required. Performs other related duties as assigned. Education Requires a four‑year college or university degree in Industrial Engineering, Mechanical Engineering, Chemical Engineering, Food Science, or other related science fields. Certification None. Certified Packaging Professional, Lean Manufacturing, Six Sigma, or other related problem‑solving tools are a plus. Experience Requires two years of industry (preferably in pharmaceutical, nutritional, food, or other consumer‑packaged goods) experience in manufacturing technical support and/or process/product development, Quality Engineering, and/or testing. Knowledge/Skills/Abilities Comprehensive knowledge of product and process development, manufacturing/packaging equipment, processing/testing laboratory techniques, and regulatory requirements. A firm foundation in chemistry, mathematics, pharmaceutics, and/or food science. Well‑developed oral and written communication skills. Results‑oriented and able to effectively organize and develop plans; prioritize and execute actions. The ability to make presentations and recommendations in the assigned area. Understanding of Lean concepts and application of DOE and QbD are a plus. Use of hand‑held data collection devices and instrumentation. Physical Requirements Manufacturing, Pilot Lab, and general office environment, which may occasionally require lifting up to 35 lb. Environment Exposure to disagreeable elements is negligible. Frequent work in pilot plants and production facilities. Travel Overnight travel for training or to support other Pharmavite regional facilities is anticipated. Up to 10% of routine travel to support other locations and up to 25% travel to support special/new projects. Safety The incumbent must be able to perform this job safely in accordance with standard operating procedures and good manufacturing practices, without endangering their own or others’ health or safety. Supervisory Responsibility Guides and assigns the work of Technicians, and may include coordinating and supervising outside engineers/vendors and technical support personnel. Compensation and Benefits National Target Base Pay Range: $80,000.00 - $133,000.00. The salary range for this position is based on national standards. For candidates in California and the New York metro, the Target Base Pay Range is $88,000.00 - $146,000.00, to reflect the cost of living and market conditions in those areas. Actual compensation will take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location, education, experience, qualifications, and job‑related skills. It is not typical for an individual to be hired above the midpoint of the range for their role, and compensation decisions depend on the facts and circumstances of each case. This information is provided to applicants in accordance with state and local laws. Base pay is only one component of our total rewards offerings, and we will take the full offering into consideration when presenting an offer of employment. Our total rewards package for this position may also include an annual performance bonus, Medical, dental and vision benefits, 401K match, and other wellness benefits. Equal Opportunity Employer Pharmavite is an equal opportunity employer. We prohibit employment discrimination and harassment based on race, color, religion, age, sex, sexual orientation, gender, national origin and any other basis protected by state and federal law. Pharmavite recruits, hires, employs, trains, promotes, and compensates individuals solely based on job‑related qualifications and abilities. Pharmavite also provides reasonable accommodation to qualified individuals with disabilities or based on a sincerely held religious belief, in accordance with applicable laws. If you need to inquire about an accommodation to complete the application process, please email View email address on click.appcast.io. #J-18808-Ljbffr