R & D Documentation Assistant
$ 2,200 - $ 2,200 / Per Mon
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Key Responsibilities:
Develop and maintain standard operating procedures (SOPs) for the RND department.
Create and update manuals, work instructions, and training materials.
Ensure that all documentation complies with regulatory requirements and pharmaceutical standards.
Collaborate with various teams to gather information and update documentation as needed.
Organize and maintain electronic and physical documentation systems for easy access and retrieval.
Review and edit documentation for accuracy, consistency, and clarity.
Assist in training staff on proper documentation procedures and requirements.
Identify opportunities for continuous improvement in the documentation process.
Qualifications:
Major in a related field such as pharmaceutical science, life science, or a related discipline to prepare for a successful career in the pharmaceutical industry.
Basic pharmaceutical manufacturing process and GMP knowledge are required
Proven experience in a documentation role, preferably in a manufacturing environment.
Strong writing and editing skills with excellent attention to detail.
Knowledge of document management systems and tools.
Ability to work collaboratively with cross-functional teams.
Familiarity with regulatory requirements and standards applicable to the pharmaceutical industry.
Strong organizational and time-management skills
other Informations:
5 days week
Develop and maintain standard operating procedures (SOPs) for the RND department.
Create and update manuals, work instructions, and training materials.
Ensure that all documentation complies with regulatory requirements and pharmaceutical standards.
Collaborate with various teams to gather information and update documentation as needed.
Organize and maintain electronic and physical documentation systems for easy access and retrieval.
Review and edit documentation for accuracy, consistency, and clarity.
Assist in training staff on proper documentation procedures and requirements.
Identify opportunities for continuous improvement in the documentation process.
Qualifications:
Major in a related field such as pharmaceutical science, life science, or a related discipline to prepare for a successful career in the pharmaceutical industry.
Basic pharmaceutical manufacturing process and GMP knowledge are required
Proven experience in a documentation role, preferably in a manufacturing environment.
Strong writing and editing skills with excellent attention to detail.
Knowledge of document management systems and tools.
Ability to work collaboratively with cross-functional teams.
Familiarity with regulatory requirements and standards applicable to the pharmaceutical industry.
Strong organizational and time-management skills
other Informations:
5 days week
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