Validation Engineer
- Location: Shreveport, LA
- Working Situation: Onsite
Position Overview: Assist in fostering collaboration with Quality, Manufacturing, Packaging, Technical Services, and Engineering teams to ensure effective quality oversight of new equipment, systems, and process validation. Additionally, this role will evaluate modifications to current equipment and processes within the pharmaceutical manufacturing DRL Shreveport Plant.
Responsibilities:
- Assures that systems and processes, in the following areas, are defined and executed in compliance with cGMP and applicable company policy.
- Develop and execute protocols for equipment validation, cleaning, equipment and process validation.
- Participate in cross-functional teams to provide technical support for new product development and launch.
- Knowledge of cGMP environments to review of GMP documents including but not limited to Change Control documents, Master Batch Records, SOPs, APRs, specifications, or Laboratory Data.
Qualifications:
- Bachelor's degree in a Science, Engineering or related field with 3-5 years of pharmaceutical industry experience.
- Experience necessary with pharmaceutical process validation, cleaning validation, equipment, utilities, and computer system qualification processes.
- Strong technical writing skills.
- Ability to work independently and as part of a team.
- Excellent communication skills.
