Gmp Document Reviewer Jobs

Excellent customer service and oral/written communication skills

Strong organization skills, attention to detail, and ability to multi-task

Prepare initial and final closing disclosures within required timeframe

Prepare and send closing documents timely for closing to buyers and title companies

Initiate funding wires for closings

Review signed packages for completeness prior to shipping

Remote/work from home opportunity, reviewers must reside in one of the following states: New York, New Jersey, or Connecticut

Proficient in the use of modern technology, especially computers and related remote, work from home office equipment

Experience reviewing and coding documents for responsiveness, relevancy, confidentiality, and privilege is preferred but not required

Critical thinking skills and ability to retain complex work direction

Excellent verbal and written communication skills

Duration depends on the project; opportunities vary from 1 week to 6 months; possibly longer

Proficient in the use of modern technology, especially computers and related remote, work from home office equipment

Remote/work-from-home opportunity, reviewers must reside in one of the following states: Minnesota, Missouri, or Texas

Experience reviewing and coding documents for responsiveness, relevancy, confidentiality, and privilege is preferred but not required

Critical thinking skills and ability to retain complex work direction

Excellent verbal and written communication skills

Pay rate: $28 per hour

Decision making, communication, planning and critical thinking skills are a must.

2 years of related experience and/or training preferred.

5 years of applicable experience required for Document Reviewer Lvl II position.

Working knowledge of Microsoft Office Suite is required.

Capable of ensuring QC documentation of all investigations and analysis were performed per cGMP and FDA rules.

Responsible for looking into method transfers or validation testing as required.

Provide support for the negotiation, drafting and management of Material Transfer Agreements, Sponsored Research Agreements, and Licensing Agreements.

The ideal candidate will have at least 4 years of experience working in or for life sciences companies.

Strong oral and written communication skills.

In-depth computer proficiency skills in MS Office suite.

Review general inquiries from internal stakeholders about agreements and provide analysis and guidance.

Strong analytical thinking and attention to detail.

Quality Tracking & Presentation skill.

Clear Communication skill (Verbal and written).

Knowledge of pharmaceutical unit process for solid dosage form and GMP documentation process.

Working knowledge of Quality Systems such as line clearance, logbook entries and other QA related activity preferred.

Main Tasks And Responsibilities Will Include

Address client comments and support comment resolution when needed.