b
bridgetidehen

Bridget Idehen

@bridgetidehen

Scientific Technical Document Expert: SOPs, GMP, GCP, QC, QA

Duitsland
Engels
Sommige informatie wordt in het Engels weergegeven.
Over mij
I am a Quality & Compliance Specialist with a Chemistry degree, certified in GMP, GCP, and as a TÜV certified Quality Representative. I specialize in proofreading SOPs, Specifications, Work Instructions, and technical Documents in regulated Environments. I ensure Clarity, Consistency, and professional English while preserving the original technical Meaning. My services are ideal for non-native English speakers in regulated Industries who need precise and reliable Documentation. I am committed to Confidentiality, Accuracy, and high-quality Delivery in every Project.... Lees meer

Skills

b
bridgetidehen
Bridget Idehen
offline • 

Bekijk mijn diensten

Proeflezen
I will sops and scientific document, gmp, gcp, quality

Werkervaring

Quality & Compliance Specialist

Confidential/Regulated Environment • Fulltime

Sep 2023 - Present2 yrs 8 mos

I am a Quality and Compliance Specialist with a Degree in Chemistry and over 5 years of experience working in regulated environments, including Pharma, Biotech, MedTech, and Laboratory settings. I am a certified GMP and GCP Specialist and a TÜV Certified Quality Representative, with extensive experience in Quality Systems, SOPs, Specifications, Work Instructions, and Technical Documentation. My expertise includes proofreading and improving Technical and Scientific Documents, ensuring clarity, accuracy, and professional English while preserving the original technical meaning. I am skilled in reviewing controlled documents such as SOPs, Work Instructions, Specifications, and Quality Reports, maintaining compliance with industry standards. I have worked on Quality Management Systems, Regulatory Compliance Documentation, and Standard Operating Procedures, providing professional and reliable support to internal and external teams. I am experienced in Technical Writing, Editing, and Document Control, helping professionals and organizations present accurate, clear, and well-structured documentation. I am committed to confidentiality, precision, and timely delivery of all projects. My background allows me to support non-native English speakers and international teams in producing high-quality Technical Documents suitable for regulated industries. I specialize in: Technical Proofreading, SOP and Specification Review, Quality Documentation, GMP and GCP Compliance, and Scientific Document Editing. My goal is to provide clients with professional, clear, and compliant documents that meet industry standards while saving time and reducing errors. I am highly detail-oriented, organized, and professional, with a deep understanding of Regulated Documentation Processes, Scientific Terminology, and Quality Standards. I offer my services to professionals and organizations looking for precise, accurate, and reliable English Technical Documents.