Cqa Dave Clymer

FAQ About Cqa Dave Clymer

• What is Cqa Dave Clymer's address?

  Cqa Dave Clymer is located at
  Port St Lucie, Florida, United States

• What is Cqa Dave Clymer's job title?

  Cqa Dave Clymer is a
  KEY WORDS: Quality, Compliance, Aseptic / Sterile Manufacturing, Sterility Assurance, cGMP Auditing, Coaching & Mentoring, Quality Management Systems (QMS), Data Integrity, Project Management, Technical Transfer, Deviation Management, CAPA Program, Change Control, Supplier Quality Management (SQM), Validation, Technical Services & Support CAREER SUMMARY: Technical Professional with over 25 years’ experience in the Pharmaceutical and Biotechnology Industries. A proven track record in Project Management, Managing, Directing and Supporting: Quality Assurance, Compliance, Sterility Assurance, Aseptic Manufacturing, cGMP Auditing, Quality Management Systems (QMS), Deviation Management, CAPA Programs, Change Control, HPLC/GC Data Integrity Review, Technical Transfer, Auditing, Supplier Quality Management (SQM), Process & Equipment Validation, Manufacturing & Operations, Coaching, Mentoring and Oversight, and Technical Service & Support projects. Well versed in FDA 21 CFR 210/211, 820, and Part 11, ICH Q7, Q9 & Q10, EMA EudraLex v.4. Project & Auditing experience in North America (US / Canada), Europe (England / Ireland / Italy / Hungary), and India. Significant Experience with parenteral / sterile products, vaccines & biologics manufacturing, API, excipients, and liquid & solid dose. Strong Mechanical Aptitude and hands-on approach. Please email / contact for current CV & Profile Elixir Biopharma Solutions

• What industry does Cqa Dave Clymer currently work in?

  Cqa Dave Clymer currently works in the
  Elixir Biopharma Solutions

• What is Cqa Dave Clymer's area of expertise?

  Cqa Dave Clymer specializes in
  KEY WORDS: Quality, Compliance, Aseptic / Sterile Manufacturing, Sterility Assurance, cGMP Auditing, Coaching & Mentoring, Quality Management Systems (QMS), Data Integrity, Project Management, Technical Transfer, Deviation Management, CAPA Program, Change Control, Supplier Quality Management (SQM), Validation, Technical Services & Support CAREER SUMMARY: Technical Professional with over 25 years’ experience in the Pharmaceutical and Biotechnology Industries. A proven track record in Project Management, Managing, Directing and Supporting: Quality Assurance, Compliance, Sterility Assurance, Aseptic Manufacturing, cGMP Auditing, Quality Management Systems (QMS), Deviation Management, CAPA Programs, Change Control, HPLC/GC Data Integrity Review, Technical Transfer, Auditing, Supplier Quality Management (SQM), Process & Equipment Validation, Manufacturing & Operations, Coaching, Mentoring and Oversight, and Technical Service & Support projects. Well versed in FDA 21 CFR 210/211, 820, and Part 11, ICH Q7, Q9 & Q10, EMA EudraLex v.4. Project & Auditing experience in North America (US / Canada), Europe (England / Ireland / Italy / Hungary), and India. Significant Experience with parenteral / sterile products, vaccines & biologics manufacturing, API, excipients, and liquid & solid dose. Strong Mechanical Aptitude and hands-on approach. Please email / contact for current CV & Profile

• Which languages does Cqa Dave Clymer speak? 

  Cqa Dave Clymer speaks the following languages:
  No languages available.

• Which industries has Cqa Dave Clymer previously worked in?   

  Cqa Dave Clymer has prior experience in the following industries:
  No prior industries available.

• What is Cqa Dave Clymer’s work experience?  

  Cqa Dave Clymer has the following professional experience:
  Elixir Biopharma Solutions .

• How can I find Cqa Dave Clymer on LinkedIn?  

  You can view Cqa Dave Clymer’s
  LinkedIn profile at LinkedIn URL.

• What are Cqa Dave Clymer’s work email addresses?  

  Cqa Dave Clymer’s work email addresses are
  [email protected] .

• What company does Cqa Dave Clymer work for?  

  Cqa Dave Clymer works at
  Elixir Biopharma Solutions