QA Documentation Specialist

6-month contract

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: (If Applicable)

Describe scope of authority to hire, promote, and manage performance of employees (include both numbers and responsibilities for direct and indirect reporting relationships) N/A

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 Client 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.

Job Type: Contract

Pay: $ $49.00 per hour

Expected hours: 40 per week

Benefits:

• Health insurance

Education:

• Bachelor's (Preferred)

Experience:

• QA Documentation: 4 years (Preferred)
• review document change requests: 4 years (Preferred)
• eDMS (electronic document management systems): 4 years (Preferred)
• Veeva Vault: 4 years (Preferred)
• change request or change control : 4 years (Preferred)
• quality assurance background: 4 years (Preferred)
• Pharma or medical device or biotech industry: 4 years (Preferred)

Ability to Commute:

• Branchburg, NJ Preferred)

Work Location: In person

Salary : $49