Technical Writer Formulation

Avet Pharmaceutical•East Brunswick Township, NJ

2d•$0 - $35•Onsite

About The Position

The RND- Technical Writer is responsible for creating new protocols, revising process validation protocols, manufacturing batch records and technical reports in accordance with site SOP’s. A technical writer will be responsible for preparing the development /validation/ investigation report with appropriate conclusions and recommendations under supervision. A Scientist I will work on the development/scale-up trials /technical transfer projects. They will also work cross functional with subject matter experts, operation, and quality as and when required.

Requirements

B.S. in Pharmacy, Chemistry or Chemical Engineering or other scientific discipline.
No previous experience required.
Math skills plus basic knowledge of statistical methodology and chemistry.
Computer skills including Word Processing, databases and spreadsheets.
Knowledge of cGMP and basic regulatory requirements.
Use of statistical methodologies.
Employees will be required to meet minimum English proficiency requirements.
All applicants must be legally authorized to work in the U.S. for any employer.
We are unable to sponsor any applicants for a work visa or take over sponsorship of a work visa for any applicants, at this time.

Nice To Haves

Hands-on technical writing, formulation research and development as well as formulation scale-up experience is desired, knowledge of US FDA registration guidelines.
Good team player and self-starter, innovative and comfortable in a multi-disciplinary team under defined timelines.

Responsibilities

Generate and execute all process characterization/validation protocols of all site transfer project to HPL in an FDA regulated environment
Technical writing and review of product development/validation reports, justification reports and FDA Deficiency Response for filed ANDAs.
Preparing Master manufacturing batch records, process characterization/validation protocols, cleaning verification/validation protocols.
Prepare process validation and cleaning validation reports at the conclusion of validation studies.
Analyze validation results and compile data into summary reports.
Writes and manages department SOP’s, training etc. to ensure regulatory compliance and operations enhancement.
Responsible for site transfer and technology transfer of new products.
Transfer of technology for new products from R&D or other sites to the manufacturing site.
Coordinate development activities for each drug product with the respective departments.
Work proactively with QA, Manufacturing, and other groups and coordinate/manage manufacture of registration/bio, validation, and initial commercial batches.