What are the responsibilities and job description for the Senior Validation Engineer position at Sovereign Technologies?
Job Details
Note: Must be local to IL and onsite interview in mount prospect
This position is on W2 basis
Job Description:
Pharmaceutical experience, ideally with cleaning validation expertise.
Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Oversees and reviews validation area processes.
- Design and develop cleaning procedures for new products and manufacturing equipment.
- Provide technical support to cleaning activities associated with the manufacturing process.
- Use of cleaning agents and the establishment of sound cleaning practices within new or refurbished manufacturing rooms and sampling suites areas.
- Designs and supports the implementation, i.e. provides training, of cleaning strategies for product transfer projects and product development projects.
- Investigates and conducts troubleshooting/root cause analysis of cleaning related incidents, deviations and cleaning out of specification results for non-validated or under development cleaning procedures.
- Leads the enhancement of cleaning practices, clean in place (CIP) equipment and introduction.
Reviews and approves Manufacturing Cleaning Working Instructions and Forms. - Supports the periodic review of cleaning validation studies.
- Performs successful and on time resolution of incidents and deviations related to cleaning validation exercises.
- Issues Change Controls required for the implementation of cleaning procedure changes, as needed.
- Trains manufacturing and QC/QA personnel on cleaning validation documentation.
Qualifications
- Bachelor's or Master's Degree in Science, Pharmacy or Engineering.
- Minimum of 5 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries.
- Proficient knowledge of cleaning validation, continuous process improvement and troubleshooting processes.
- Strong project management skills.
- Experience mixing solutions (formulations)
- Proficient time management skills, planning and organization capabilities.
- Proven leadership & teamwork skills, self-starter, results oriented and build and maintain strong relationships with multiple groups.
- Proficient in Risk Assessment/Management
- Proven assessment, analytical and problem-solving skills.
- Proficient presentation skills and Technical Writing/Oral communication skills (English)
- Proficient in cGMP's, OSHA and FDA Regulations as it applies to pharmaceutical industry.
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