Cleaning Validation Specialist Raleigh, NC

3 weeks ago


Durham, United States PharmEng Technology Full time

At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. **We are seeking a Cleaning Validation Specialist for an opportunity in Raleigh-Durham, NC.**

**Objectives of this Role:** * 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 existing manufacturing rooms and sampling suites areas.

* Design and support the implementation of cleaning strategies for product transfer projects and product development projects.

* Investigate and conduct troubleshooting/root cause analysis of cleaning related incidents, deviations and cleaning out of specification results for non-validated or under development cleaning procedures.

* Lead the enhancement of cleaning practices, clean in place equipment and introduction.

* Review and approve Manufacturing Cleaning Working Instructions and Forms.

* Support the periodic review of cleaning validation studies.

* Perform successful and on time resolution of incidents and deviations related to cleaning validation exercises.

* Issue Change Controls required for the implementation of cleaning procedure changes, as needed.

* Train manufacturing and QC/QA personnel on cleaning validation documentation.

* Bachelor's or masters degree in Science, Pharmacy or Engineering.

* Minimum of 3 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries.

* Proficient knowledge of cleaning validation, continuous process improvement and troubleshooting processes.

* Proficient time management skills, planning and organization capabilities.

* Proven team player, self-starter, results oriented and able to build 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.

* Proficient in cGMP's and FDA Regulations as it applies to pharmaceutical industry.



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