Pharmaceutical Quality/ Document Control Writer
2 weeks ago
Our client – a growing company with multiple plants in the US, urgently needs a Tech. Writer – Pharma / Med Device at their plant expanding to manufacture pharmaceutical products . Excellent salary + Relocation Assistance + Full Benefit Package.
Job Title : Tech. Writer – Pharma/Med Device
Relocation: YES - Client offers relo assistance with a lump Sum sign on Bonus
Benefits: Full package for medical, dental insurance, 401K, etc.
Our client is a privately held company with manufacturing sites in CA + KS with around 300 people
Group Info: Be part of the medical device and pharmaceutical contract manufacturing site with around 120+ employees and expected to grow to 150 people soon due to major expansion in Pharma manufacturing .
The new operation expansion is for Pharma Fill Finish Seal – FFS of Sterile Aseptic liquids.
This Quality group has around 25 people from Quality Control, Quality Assurance, Compliance. This person will be supporting quality people and write documents for them
Create, manage and oversee the generation of technical documents and Document control in support of the quality group for medical device and Pharma manufacturing FDA regulated plant
2 years of Hands-on Tech Writer and Document Control & Management experience for FDA regulated industry of Pharma, Med Device, Cosmetics, Food etc
Good computer skills – MS Office
Ability to produce and present clear, concise, and professionally written communications / Documents
Knowledge of Sterile Aseptic Filling Operations
Contract Manufacturing experience working closely with customers and clients
BioPharma, Pharma, Medical Device, Document control, Document Management, Validation, Quality, QC, QA, FDA, 483, Warning Letter, CMO, Sterile Aseptic, filling, CDMO, Manufacturing, Plant,
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