What are the responsibilities and job description for the GMP Documentation Specialist (Pharma) position at Navitas Partners, LLC?
Title: GMP Documentation Specialist-I
Location: West Point, PA
Duration: 12 Months with possibilities of extension
Job Description:
The Release and Critical Documentation Specialist will be responsible for the generation and review of documentation for the submission, testing, and release of raw materials, culture media/buffers, and excipients. Primary responsibilities include release protocol development, preparing/maintaining appropriate critical GMP documentation.
Responsibilities also include:
Coordinate and maintain SOP review and approval process
Administering various functions within the Learning Management System (LMS)
Working with Subject Matter Experts, develop training requirements for Standard Operating Procedures, Analytical Procedures and other training material
Utilize templates for SOPs and supporting SOP documents
Qualifications:
Bachelor of Science or equivalent degree in a related field.
4 yr. Experience
Strong Technical Writing Skills
Good manufacturing practices experience
Ability to manage projects/work to schedule/deadlines
Coherent Communication skills (no proof reading).
Good project management skills
Working knowledge of cGMP requirements
Demonstrated ability to manage multiple tasks and priorities
Effective verbal and written communication skills
Understanding of applicable regulations and guidelines governing clinical supply manufacture and release (CFR, ICH)
Must have strong communication, interpersonal, and organizational skills, including time management.
Candidate must have the ability to work independently on several projects maintaining critical timelines.
