Orbis Clinical is seeking a Document Control Specialist, Quality located in Bedford, MA for up until the end of the year.

Job Title: Document Control Specialist, Quality

Location: Bedford, MA

Contract: Up until the end of the year

Summary:

This role will work closely with members of the Document Control team and support routine daily operations for Document Management. The position will have some additional responsibility for documenting processes and supporting continuous improvement. This position will primarily be responsible for the processing and maintaining of GxP documents throughout their lifecycle with a focus on issuance and reconciliation. 

This position is considered a CORE role and will require consistent on-site presence. It will support the Gene Therapy Manufacturing Therapy (GTMF) location in Bedford, MA. 

Responsibilities:

• Adhere to Standard Operating Procedures, Work Instructions, and other administrative practices.
• Manage activities associated with the Document Storage Room at both the GTMF and GTQC facilities.
• Organize and manage a high volume of documentation for archival in both electronic and paper-based processes.
• Assist with organizing and filing documents and records.
• Support issuance of controlled documents
• Assist with reconciliation, retention, and archival of documents and records.
• Retrieve documentation from document storage and/or offsite archival upon internal customer request
• Provide Document Control support in preparation of, during and after internal or external Audits/Inspections
• Provide guidance and support based on knowledge of GDP and cGMP principles during daily activities.
• Communicate effectively to assess daily interdepartmental needs and priorities; escalate where appropriate.

Requirements:

• Minimum of a Bachelor’s Degree in a science, engineering, or related discipline.
• 1-4 years’ experience in Quality with experience in the pharmaceutical, biotech or other related life-sciences industry a plus. 
• Experience in document control and electronic document management systems.
• Strong attention to detail and organizational skills, is required.
• Able to work independently, prioritize, and manage multiple tasks simultaneously.
• Demonstrates initiative and a strong sense of urgency.
• Proficient in MS Excel, Word, and PowerPoint.
• Effective teamwork and collaboration with internal and external SMEs.
• Knowledgeable in cGMP's and pharmaceutical industry regulations a plus.
• High ethical standards, good judgment, and professionalism.

Compensation Details:

• Orbis Clinical is an equal opportunity employer that provides a reasonable range of compensation for our positions. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.
• The Pay Range for this position is $36.00 per hour, can vary depending on employment status.
• Orbis Clinical offers eligible employees health benefits (medical, dental, and vision), employer-paid basic life and AD&D insurance, and a partial employer match on a 401(k). 

EEO and Reasonable Accommodation Statement:

Epic Staffing Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, genetic information, veteran status, or any other characteristic protected by law. We also consider qualified applicants with criminal histories, consistent with applicable law. If you need assistance or an accommodation during the application process, please contact us.

 By applying for this position, you agree that any calls from Orbis Clinical and its subsidiaries may be monitored or recorded for training and quality assurance purposes.