Documentation Coordinator, Process Technical Services

DOCUMENTATION COORDINATOR - PROCESS TECHNICAL SERVICES
Barr Pharmaceuticals, Inc. a holding company, is a global specialty pharmaceutical company engaged in the development, manufacture and marketing of generic and proprietary pharmaceuticals, biopharmaceuticals and active pharmaceutical ingredients. Operating through its principal subsidiaries including Barr Laboratories, Inc., Duramed Pharmaceuticals, Inc. and Pliva d.d. and its subsidiaries, the Barr Group of companies markets more than 120 generic and 25 proprietary products within the U.S. and more than 550 products internationally.

With more than 8,000 employees worldwide who share a commitment to bringing these affordable generic and unique proprietary products to our customers, Barr has annual revenues in excess of $2 billion through our commitment to and significant investment in new product research and development.

We have an outstanding career opportunity for a successful Documentation Coordinator - Process Technical Services located in our Pomona, NY offices.

Position Summary:

This position offers the ability to be a member of our dynamic Process Technical Services group and work closely with scientists and management in the generation, tracking and reporting of critical documentation related to the optimization of experiments. This is an excellent opportunity for a success driven professional with a strong background in writing and reporting to join a fast paced, rapidly growing organization.

Responsibilities include: Assist in generating technical and GMP documentation such as protocols, batch records and memos Assist scientists in routing and approval of documentation in a timely manner Maintain tracking mechanisms for documentation routing and approval Provide assistance to scientists where required for project related documentation activity such as report writing, reviewing data accuracy and consistency Write, track and manage the timely generation of experimental batch records, technical protocols and associated reports under the guidance of a scientist Prepare and coordinate review and approval of GMP documentation Assist scientists in compiling, tracking and timely completion of technical reports and compiling data for experimentsPosition Requirements include: Bachelor?s degree required 2+ years experience in technical writing ? reports, status updates Experience in GMP documentation strongly preferred Pharmaceutical experience will be a plus Demonstrated ability to work with other departments throughout the company to communicate, receive and provide information. Experience in technical writing ? reports, status updates Excellent communications skills - both verbal and written Strong computer skills - Microsoft Office applications Commitment to Excellence - Many companies talk about it. Barr delivers - every day, to our customers AND to our employees. Barr's commitment to employees is reflected in our total compensation and benefits package that includes competitive salaries and incentive compensation programs, career opportunities offering both personal and professional growth; a 401(k) plan that matches up to an additional 10% of your pay each year; a stock purchase plan that allows you to buy company stock at 15% below market; comprehensive medical and dental plans that provide coverage for you and your family with nominal employee cost; life and disability protection programs and so much more! Together, we raise the BARR!

We are an Equal Opportunity Employer m/f/d/v.