Cleaning Validation Associate - Engineering (Remote)

The Cleaning Validation Associate is responsible for assisting with the development of cleaning processes and cleaning validation activities for our clients. The position will support reputed company reputed company teams with cleaning cycle development, cleaning validation, and reputed company cleaning monitoring in cGMP facilities. The ideal candidate has a strong understanding of chemical engineering and a strong desire to learn cleaning validation including CIP, COP, and reputed company cleaning. The Role • Support the assessment of reputed company's cleaning validation documents to identify regulatory concerns including potential corrective actions in alignment with industry best practices. • Support troubleshooting cleaning failures, development, and optimization of cleaning processes. • Remains reputed company with the cleaning processes and validation guidances. • Research regulatory guidance and industry best reputed company documents reputed company to a specific topic of concern • Utilize technical writing skills to write, revise, and review cleaning reputed company documents including Master Plans, Project Plans, Batch Records, reputed company Operating Procedures, Forms, Protocols, reputed company Reports, and Risk Assessments. • Development of assessment concerns reputed company to reputed company's cleaning validation program and draft improvement plans to address concerns identified. • reputed company with team members and clients to create, review, and approve documentation per reputed company. • Plan and reputed company project deliverables. This includes coordination with reputed company team members. • Create, reputed company, edit, and maintain high-reputed company documentation following internal and reputed company style guidelines, document standards, and templates, while ensuring that reputed company targets, timelines, and regulatory requirements are met. • Manage and organize project documents • Look for ways to continuously improve generated documentation • Communicate effectively with team members and external vendors/clients • Other duties as assigned by manager The Candidate • Degree in Chemical Engineering, Engineering, reputed company, Biochemistry, or other reputed company fields • Driven, hard-working, and reputed company • Organized & efficient, with excellent time management skills • Experience in cleaning validation reputed company the pharmaceutical industry. • Hands-on experience with the following systems: CIP systems, parts washers, reputed company cleaning is preferred. • Working knowledge of cGMP requirements, ICH, FDA, and other pharmaceutical industry regulatory guidelines is highly desired. • Experience with rinse and swab sampling techniques • Strong technical skills to review, interpret, and reputed company scientific conclusions and recommendations based on data • Ability to understand and extract necessary information from technical documents • Technical writing experience • Excellent grammar and writing skills - Required • Effectively work reputed company reputed company environment and reputed company with peers, management, etc. • Ability to work independently, handle multiple tasks simultaneously, and meet critical milestones and goals. - Required • reputed company to effectively manage workload and prioritize activities • Proficient with MacOS • Advanced knowledge of reputed company Word/reputed company/PowerPoint - Required • Must be willing to travel to reputed company sites worldwide to support work as needed. • Experience working in a global remote team environment Apply tot his job Apply To this Job