JO-2643-Tech. Writer

Job DescriptionJob DescriptionOur 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 Posting # 2643Job Title: Tech. Writer – Pharma/Med Device Location: Lawrence, KS Compensation: Salary of $60K - $75K per yearRelocation: YES - Client offers relo assistance with a lump Sum sign on BonusBenefits: Full package for medical, dental insurance, 401K, etc.Our client is a privately held company with manufacturing sites in CA + KS with around 300 peopleGroup 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 themNote 1: The right person with relevant experience will be considered even without any degree or certification.Job Summary: 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 plantCandidate Must Have:

• Min. 2 years of Hands-on Tech Writer and Document Control & Management experience for FDA regulated industry of Pharma, Med Device, Cosmetics, Food etc
• Good people, communication skills to work in a team environment
• Good computer skills – MS Office
• Ability to produce and present clear, concise, and professionally written communications / Documents

Candidate Nice to Have:

• AAS degree or some certification
• Knowledge of Sterile Aseptic Filling Operations
• Startup or Small company experience working in a dynamic and hands-on role.

• Contract Manufacturing experience working closely with customers and clients

Keywords: 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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