Technical Writer

Key

Responsibilities :

Draft and maintain technical documents including summary

reports, test criteria, and conclusion reports.

Support validation activities by compiling data and

writing documentation (ability to read protocols

required).

Follow up on issues through change

control and deviation systems.

Collaborate

with validation, engineering, and QA teams to ensure compliance

with AbbVie standards.

Maintain version

control and documentation in electronic

systems.

Requirements :

Bachelor's degree in Life Sciences, Engineering, or

related field.

Minimum 2 years' experience in

technical writing, validation, or documentation in

pharma / biotech / medical devices.

Familiarity

with GMP, validation, and change control processes

preferred.

Strong attention to detail with

good written communication skills.

Ability to

manage multiple tasks under tight

timelines.