Aerospace ISO 9001 AS9120B Consultant

@govindasamyjgces

Hi, Greetings I am an Engineer, and I have 12 years of experience in QSHE ( Quality Safety Health, and Environment) I am a consultant for the ISO 9001, ISO 14001, ISO 45001, ISO 27001, and IATF 16949, and I have strong exposure to Quality Management Systems ( QMS) and Information Security Management Systems ( ISMS) I am also an expert in Quality Management Systems (QMS ) and PPAP document preparation. As I worked as a quality manager, I have rich experience in quality functions including the handling of Quality Tools, problem-solving tools, PPAP documents, SIx sigma, Lean, 5S, Kaizen, 7QC Tools, SPC, and other functions. I have rich experience in the preparation of Quality/ Environment/ Health and Safety Policies, Quality / Environment/ Health and Safety Manual, and Procedures. Internal audit, countermeasure implementation, Continuous improvement, and certification. I have supported the implementation of ISO 9001, ISO 14001, ISO 45001, and IATF 16949 systems in various organizations in the USA, UK, Europe, and India. I have read and understood your requirements, and I will do gap analysis, rewrite missing procedures, design controlled templates for forms and records, and create master list for traceability I will also provide guidance on linking supplier files, calibration certificates, FAI reports, and other aerospace-specific evidence directly to the QMS I want to work on this project. If you are OK, please revert so that we can discuss and proceed further

@uvucon

You are running ISO 9001:2015 and AS9120B in parallel, and the real blocker is that the procedures you already have are fragmented, inconsistent and not mapped to current clause numbering, so nothing is audit-traceable yet. I build clause-mapped QMS documentation sets on the manufacturing quality side: master document register, tier-2 procedures and controlled forms rebuilt so every record traces back to a numbered clause, a revision and a named owner. My ground is ISO 9001 quality systems and document control; the AS9120B layer I handle by explicit clause-by-clause mapping rather than by claiming an aerospace audit history I do not have. One scoping question: is your AS9120B scope distributor/stockist only, so counterfeit-parts control, certificates of conformance traceability and lot segregation lead the evidence set, or do you also do value-added processing that pulls further AS9100-family clauses into scope? How I would run it: 1) Gap analysis workbook, one row per ISO 9001:2015 and AS9120B clause: current document reference, verdict (conform / partial / missing), action and owner, plus a short written summary. 2) Rewrite the QMS manual and tier-2 procedures against that gap list, keeping your existing wording wherever it already conforms so your team still recognises the documents. 3) Controlled forms pack in Word/Excel with a standard header block: document number, revision, effective date, owner, approval. 4) Document control matrix as the master list, with linkage rows for supplier files, calibration certificates and FAI reports so evidence hangs off the QMS instead of loose folders. 5) Training notes plus an internal audit dry-run checklist your team can run before audit day. I work directly in your shared drive or eQMS folder structure, in writing. Sub-milestones: 30% on the approved gap analysis, 40% on manual, procedures and forms released, 30% on the control matrix, training notes and dry-run checklist. Happy to start with a small first batch, one clause block and two procedures, to confirm fit before the rest.