Quality Systems Documentation Consultant job in Framingham, USA

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)

Location: United States

This vacancy has now expired. Please see similar roles below...

Proclinical is seeking a Quality Systems Documentation Consultant for a cutting-edge biotech company located in Framingham, MA.

This position provides cross-functional support of GXP activities as they relate to Quality Systems. This position will participate in the improvement of Quality Systems to ensure quality and adherence with current Good Manufacturing Practice (cGMP) and inspection readiness.

Must be eligible to work in the US.

Job Responsibilities:

Provide support of day-to-day operations of the Quality System department for multiple sites and support internal and external customers.
Participate in continuous improvement initiatives.
Review records and documents, for completeness and compliance with global regulations.
Generate standard operating procedures and/or guidelines to define and improve quality system functions.
Support and manage document lifecycle the Electronic Document Management System (EDMS).
Track and trend compliance paperwork (deviations, change controls, etc. both internal and external).
Oversee training documentation and compliance metrics through use of learning management system (LMS).
Assist with employee "on-boarding" training on general quality specific procedural requirements.
Ensure organizational charts are updated on a regular basis.
Participate in the internal audit program.
Create and modify user groups, training items, curricula, group trainings and assignments.
Conduct periodic review and audits of Quality Systems.
Assist with preparation of QMS metrics.

Skills and Requirements:

Highly motivated individual with excellent time management skills.
Strong organizational skills with the ability to effectively prioritize and manage multiple projects and tasks with attention to detail.
Ability to proactively resolve issues in a diplomatic, flexible, and constructive manner.
Proficient in Microsoft suite (Word, Excel, PowerPoint, Access and Outlook).
Excellent written and oral communication skills.
Bachelor's degree with practical experience in a regulated manufacturing environment or equivalent experience
A minimum of 4 years of relevant experience required.

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at +(1) 267-846-2026 or j.cerchio@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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