Aseptic Process Engineer
Decatur, Illinois

Job ID: 11259
Start Date: ASAP
Type: Direct Hire
Job Industry: Engineering

Onsite: On location at the Client’s site 100% of the time. No telecommuting or remote work.

Additional Information: Full benefits, relocation assistance, and interview travel reimbursement are available.

Description: Our Client, a pharmaceutical company, is looking to hire an Aseptic Process Engineer II in Decatur, IL.

Responsibilities:

• Support and troubleshoot day-to-day operations, capital projects, and pipeline products in aseptic manufacturing processes;
• Be responsible for engineering and process optimization for aseptic manufacturing processes and related operations;
• Perform financial analysis activities to determine project cost savings and return on investment;
• Manage the procurement of process equipment;
• Assess current processes to reduce processing times and reduced utility consumption by measuring key performance indicators;
• Perform process design improvements to reduce the quantity of lost batches and improved quality of product;
• Manage third party vendors to optimize detail designs of engineering projects;
• Deliver strategic and technical expertise to drive continuous process improvement that generate cost savings and optimize efficiencies;
• Assist with design of new facilities and systems from conceptual design, specifications, budgeting, scheduling, and construction management;
• Develop documents for FAT and SAT activities for process equipment;
• Participate in FAT, SAT, the startup and commissioning of process equipment after design phase;
• Manage the life-cycle documentation of the equipment including generation and approval of user requirement;
• Provide direction to contractors to meet project schedule and financial goals while ensuring technical success;
• Participate in procurement efforts for process and facility related equipment and facilitate change orders during the project;
• Drive remediation work for design improvement or correction for process equipment and processes.

Requirements:

• Experience in process engineering in a pharmaceutical or similar manufacturing environment (5+ years);
• Experience with aseptic manufacturing processes (3+ years);
• Experience in process development, experimental design / statistical analysis, process optimization, and scale-up;
• Experience with new product introduction, technology transfer, and process / equipment validation;
• Working knowledge of various manufacturing processes and unit operations including, vial filling, sterilization formulation, and secondary packaging;
• Basic knowledge of process automation / control systems;
• Continuous improvement background with knowledge of Lean Manufacturing / Six Sigma / OE tools and techniques (preferred);
• Understanding and application of GMP Documentation as it relates to the job function;
• Bachelor degree required, preferably in Chemical Engineering, Engineering, or Pharmacy.

If this job is not for you, earn a $2,100.00 referral bonus in cash by referring a Candidate or a Client to us. Vitaver Referral Program is one of the most generous on the market!

Please feel free to apply directly and contact me with your questions at mary.andreas@vitaver.com

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* In compliance with the Federal Law, all persons hired to work in the United States will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire.

Vitaver & Associates, Inc. is an equal opportunity employer. It is the Company's policy to make all employment decisions including hiring, promotion, compensation, benefits, termination and others, without regard to age, race, color, religion, national origin, sex, disability, veteran status, or any other protected status in accordance with applicant federal, state, and local laws.
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