Validation Engineer I
Akorn 2

Decatur, Illinois

This job has expired.

  • Maintains and coordinates the Validation Master Plan.
  • Assists in the development, review, execution and closure of validation protocols (IQ, OQ, PQ, VQ) by collection of raw data used as supporting documentation.
  • Assists the Manager in the scheduling and coordination of staff to meet aggressive project timelines.
  • Provide management oversight for the Validation efforts at Akorn, Decatur.
  • Work towards improving validation practices and procedures; ensure site compliance with current FDA regulatory requirements.

This individual must have the expertise to interface with all levels of management, staff and internal departments, including outside contractors and vendors as applicable. They must be able to multitask within a high-stress environment to maintain critical timelines.

  • Track and report on progress to project deliverables, schedules.
  • Review, analyze and interpret system performance data for completed qualification and prepare final package to summarize data.
  • Demonstrate solid communication and documentation skills.
  • Develop Installation, Operational Qualification, and performance protocols for commissioning and validation.
  • Ensure that all work carried out is in compliance with the required standards conforming to company, cGxP, SOPs, regulatory regulations and guidelines, safety and environmental guidelines and assure that acceptance criterion related to the protocols are met.
  • Develop technical scope of work documents and estimate time and resources needed for projects.
  • Coordinate resources required to complete validation studies and tests in a timely manner.
  • Analyze test data and report issues/discrepancies. Lead and document investigations of failed validation test resultsthrough Root Cause Analysis.
  • Write summary reports to summarize test results and investigations.
    Lead the effort to gain approval of validation protocols and summary reports.
  • Conducting System Compliance Risk Assessment.
  • Assist cross-departmental teams in authoring validation related documentation, standard operating procedures, reports, system quality reviews, identifying deficiencies, preparing CAPA’s, test scripts and change controls.
  • Coordinate cleaning validation activities.Prepare and execute protocols and reports for cleaning development andvalidation.
  • Write technical cleaning evaluations as requested, including calculationsand deviations with root cause and impact assessment.
  • Coordinate training of new employees of the Validation Department.
  • Additional responsibilities as required.
  • The job may require travel to vendor sites and/or R&D facilities to complete required work. Expected travel of less than 10%.

  • Bachelor’s degree in Chemical Engineering, Computer, Industrial Engineering, Electrical Engineering or related engineering field, (or equivalent experience).
  • Minimum 2 years of previous validation experience, preferably at a parenteral or ophthalmic Pharmaceutical facility
  • Understanding manufacturing processes and process instrumentation.
  • Previous experience with liquid aseptic pharmaceuticals is highly preferred
  • Available to work non-standard shift, weekend and holidays if requested.
  • Strong writing ability required.
  • Knowledge of cGMP Cleaning Validation requirements and techniques, GMP Process and Product Validation requirements and techniques.
  • Experience with computer systems validation / QA within FDA (GxP) regulated environments.
  • Ability to read, analyze and interpret common scientific and technical journals. Ability to communicate to a group of individuals through oral and/ or written materials.
  • Knowledge of cGMP guidelines as well as international regulations pertaining to the production of APIs and drug products.

Company Overview
Who we are?

Aside from being a pharmaceutical industry leader with deep roots in the eye care community, Akorn has proven through the years, to be a company of clear vision. A vision of what it takes to continually develop and evolve in order sustain our mission, which is to improve patients’ lives through the quality, availability and affordability of our products. Along with developing and manufacturing branded and generic ophthalmics, Akorn manufactures injectable, oral liquid, optic, topical, inhalant, and animal health products. To learn more please visit our website at .

Why choose us?

Akorn employees are modern day superheroes! That might sound like an exaggeration; however, when you think of it, superheroes help those in need. That is exactly what we do here at Akorn. If you choose to work with us, you are not choosing to work an ordinary job. You are choosing to make an impact in this world. You are choosing to have a career with purpose. If you are seeking a rewarding opportunity where you can make a difference for others, then put on your cape and join the team!!

What do we offer?
  • Competitive pay
  • Growth and development opportunities
  • Tuition Reimbursement
  • 3 weeks PTO + Personal Days
  • 9 company holidays
  • 401K match
  • Medical, Dental and Vision Benefit Options
  • 100% Paid Maternity Leave
  • Fast paced, family-oriented work environment
  • Wellness Program
  • Inclusive and diverse culture
  • Adoption Assistance
  • Flexible Spending Accounts

EEO Statement
Akorn, Inc. is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

This job has expired.
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