We are seeking a Document Control Specialist to support the management and organization of critical engineering and GMP documentation within our CICR (Engineering Library) system. This role ensures compliance with cGMP standards and internal document control processes while facilitating accurate record-keeping and storage of essential documents.
Qualifications
Experience: 1–2+ years in document control or related field.
Familiarity with GMP/cGMP documentation and compliance requirements.
Prior experience in a library or document management setting.
Strong attention to detail and organizational skills.
Ability to work collaboratively across departments.
Preferred Skills
Knowledge of engineering documentation and control systems.
Experience with EAMS or similar document management platforms.
Ability to manage large-scale document projects efficiently.
Seniority level
Associate
Employment type
Full-time
Job function
Other
Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Insight Global by 2x