The Fountain Group
Contract Documentation Specialist III
The Fountain Group, Branchburg Township, New Jersey, United States
Overview
Bill: $74.80
Pay: $53-49
Spread: 324.4-520.1
Duration: 6 months
Job Summary Review documents, review document change requests and route document change requests to process document creation, maintenance, and implementation in eDMS. Control/distribution of controlled documentation. Preparation of records for issuance to production. Organize and maintain the Document Control System to meet current regulatory requirements.
Supervisory Responsibility N/A
Responsibilities
Implement, control and coordinate changes in documentation. Facilitates the updating and routing of controlled documents, including, but not limited to, Governance and Procedure documents, Master Forms and Master Batch Records within the eDMS.
Manage the change process for manufacturing documentation consisting of SOPs, policies, manufacturing documentation, specifications and other controlled documents.
Review, edit and process changes to controlled documentation such as procedures, manufacturing records, forms etc. in an electronic document management system.
Ensure proper approvals have been obtained prior to final release of document and coordinate effective dates with departments.
Preparation of records for issuance to production.
Coordination and maintenance of the periodic review system.
With minimal supervision, complete special projects and routine work on schedule.
Education and Experience
Bachelor's Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/ scientific area preferred.
3 years' experience in quality assurance, quality oversight or relevant experience. Experience in regulated pharmaceutical/medical device industry and document management areas preferred.
Proficient in Microsoft Word and Excel. eDMS experience (Veeva Vault) preferred.
Excellent proofreading skills. Excellent verbal and written communication skills. Good analytical, decision-making and problem-solving skills.
Experience working in both team setting and independently. Works well with manager guidance to complete tactical objectives while able to manage own time effectively.
Excellent interpersonal skills.
Ability to identify, communicate and follow through to completion action plans to resolve problems.
Essential Skills Refer to the role detail (or similar role details), located on My Allergan Career, to determine the appropriate Leadership and Professional skills. Leadership Skills: These skills evolve as colleagues move through different career stages. It is recommended that you select the up to 3 that are most important for success in the role. For skill definitions please hover over each listed skill.
Bussiness Unit:
Operations-Quality Assurance (OPQA)
Cost Allocation:
5120|CC|Quality-Change Mgmt (632947)
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Job Summary Review documents, review document change requests and route document change requests to process document creation, maintenance, and implementation in eDMS. Control/distribution of controlled documentation. Preparation of records for issuance to production. Organize and maintain the Document Control System to meet current regulatory requirements.
Supervisory Responsibility N/A
Responsibilities
Implement, control and coordinate changes in documentation. Facilitates the updating and routing of controlled documents, including, but not limited to, Governance and Procedure documents, Master Forms and Master Batch Records within the eDMS.
Manage the change process for manufacturing documentation consisting of SOPs, policies, manufacturing documentation, specifications and other controlled documents.
Review, edit and process changes to controlled documentation such as procedures, manufacturing records, forms etc. in an electronic document management system.
Ensure proper approvals have been obtained prior to final release of document and coordinate effective dates with departments.
Preparation of records for issuance to production.
Coordination and maintenance of the periodic review system.
With minimal supervision, complete special projects and routine work on schedule.
Education and Experience
Bachelor's Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/ scientific area preferred.
3 years' experience in quality assurance, quality oversight or relevant experience. Experience in regulated pharmaceutical/medical device industry and document management areas preferred.
Proficient in Microsoft Word and Excel. eDMS experience (Veeva Vault) preferred.
Excellent proofreading skills. Excellent verbal and written communication skills. Good analytical, decision-making and problem-solving skills.
Experience working in both team setting and independently. Works well with manager guidance to complete tactical objectives while able to manage own time effectively.
Excellent interpersonal skills.
Ability to identify, communicate and follow through to completion action plans to resolve problems.
Essential Skills Refer to the role detail (or similar role details), located on My Allergan Career, to determine the appropriate Leadership and Professional skills. Leadership Skills: These skills evolve as colleagues move through different career stages. It is recommended that you select the up to 3 that are most important for success in the role. For skill definitions please hover over each listed skill.
Bussiness Unit:
Operations-Quality Assurance (OPQA)
Cost Allocation:
5120|CC|Quality-Change Mgmt (632947)
#J-18808-Ljbffr