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- Some document control and records management responsibilities in past role
- Technical knowledge of Microsoft Word
- Willing and eager to learn
- Picks up on things quickly
- Ability to work in a fast paced environment
- Maintain document control systems (electronic/paper) compliant with regulatory requirements and company procedures/systems.
- Maintain external documents compliant with regulatory requirements and company procedures/systems.
- Maintain record control systems (electronic/paper) compliant with regulatory requirements and company procedures.
- Maintain sample control systems compliant with regulatory requirements and company procedures/systems.
- Maintain training matrices (electronic/paper) compliant with regulatory requirements and company procedures.
- Creates, reviews, and approves documents – procedures, protocols, reports, etc.
- Quality assurance review and disposition of products.
- Represents Quality on intra-/inter-departmental project teams.
- Conduct company-wide training (e.g., documents, records, and specimens/samples).
- Conducts internal and supplier audits.
- Ensures in a positive way compliance with regulatory/standards requirements and company procedures.
- Participates in professional organizations to ensure that state-of-the-art industry regulatory/standards requirements are communicated within the company and implemented in an efficient, timely, and accurate manner.
- Manages projects as assigned.
- Maintain and present quality indicator metrics.
- Has some independence for unreviewed action or decision.
- Effectively manage time and multiple task assignments.
- Other duties as assigned by management.
- Bachelor (or equivalent) degree in English/Technical writing with ≥5 years' experience with document and records control in regulated industry.
- Experience in document and records control.
- Working knowledge and experience with GMP or QSR / ISO 13485 or ISO 9001 required; GLP, GCP, and related ISO and ICH preferred.
- Working knowledge and experience with paper-/electronic-based document management systems.
- Excellent communication skills (oral, written, and presentation) and understands how to present information dependent upon the level of the audience.
- Must be detail oriented with excellent organizational skills.
- Must be able to work independently as well as in a team environment.
- Expert: MS Word, MS Excel, MS Power Point, Adobe and/or Adobe Creative Suite.
- Design/create product labels, product labeling (e.g., IFU, product inserts), audio-visual trainings
- Ability to work independently and collaboratively in a fast-paced environment
Document Control Specialist - Atlanta, United States - Randstad Life Sciences US
Description
Document Specialist
Duration: Direct hire
Location: Fully onsite in Atlanta
Are you ready to apply Make sure you understand all the responsibilities and tasks associated with this role before proceeding.
Must haves:
Summary:
Our client is currently seeking a highly skilled and detail-oriented Document Specialist to join their dynamic team. As a Document Specialist, you will develop and maintain document and record control systems in the FDA regulated biologics, pharmaceutical, and medical device industries.
Responsibilities:
Qualifications:
Education:
Experience: