Tech. Writer – Pharma/Med Device from Management Recruiters of Edison

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 Posting # 2643

Job Title: Tech. Writer – Pharma/Med Device                        Location:  Lawrence, KS       
                     

Compensation: Salary of $60K - $75K per year

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

Note 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 plant

Candidate 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,