Cleaning Validation Engineer

Location England
Discipline: Cosmetics
Job type: Permanent
Salary: £Negotiable
Contact name: Mohammed Bellarbi

Contact email: mohammed.bellarbi@sciencesr.com
Job ref: BBBH4126_1655719219
Published: 14 days ago
Startdate: ASAP

Role: Cleaning Validation Engineer

Salary: DOE

Location: South East

A world leader in manufacturing of cosmetic and personal care products located in the south east are looking for Cleaning Validation Engineer to join their team. As a Cleaning Validation Engineer you will be technically sound in the comprehension of cleaning processes/procedures, specialised in cleaning validation, continuous process improvement and troubleshooting, experienced in designing and implementing new cleaning processes as well as have excellent organisation skills.

Main Duties

  • Create and develop cleaning procedures for new products and manufacturing equipment.
  • Offer technical support to cleaning actions associated with the manufacturing process.
  • To lead the cleaning validation plan and events.
  • Support qualification activities of cleaning agents and the establishment of good cleaning practices within new or refurbished manufacturing rooms and testing points
  • Designs and help the implementation, i.e. provides training, of cleaning strategies for product transfer projects and product development projects.
  • Examines 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.
  • Directs the enhancement of cleaning practices, "clean in place" 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.

Personal Profile:

  • Competent knowledge of cleaning validation, continuous process improvement and troubleshooting processes.
  • Robust project management skills.
  • Competent 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 in cGMP's, OSHA and FDA Regulations as it applies to pharmaceutical industry.
  • Ability to write SOPs, deviations, change controls and OOS reports
  • Proficiency in Microsoft Office Suite and SAP systems preferred
  • Proficient presentation skills and Technical Writing/Oral communication skills (English)