Technical Writer

Job Description:

Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and Quality Systems, with the ability to assess compliance risks.

Demonstrates analytical problem solving skills.

Demonstrates ability to explain complex concepts with clarity and simplicity.

Demonstrates ability to perform detail-oriented work with a high degree of accuracy.

Demonstrates strong verbal, written, and interpersonal communication skills.

Demonstrates proficiency in Microsoft Office applications and Adobe Acrobat Professional.

Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.

Experience with leading info mapping or Kaizen process mapping. Comfortable with working individually and in a team setting with minimal supervision.

Experience and Details:

Mid-Level role with at least 3 years of experience in Pharma/Bio Tech.

Quality Control experience is good to have, but not required.

Candidate will be working on a project with the main duty to complete Info Mapping (aka Process Mapping).

They will refine and create new documents of existing processes; quality and tech points are captured in Info Mapping.

Will be working on multiple procedures and projects at the same time. Need to have an understanding of GMP Technical experience in MS Office and Adobe Acrobat is required Candidate traits: Strong team player, but will be working as an individual contributor (team consists of 3 people: Chemists and Microbiologists).

Think Analytically. Good writing skills

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.

Thank you.

Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - (732)-844-8715

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