What are the responsibilities and job description for the Technical Writer (Documentation/Change) (Pharma/Medical Device) position at Systems Ally?
- This onsite position is responsible for initiating and managing change control packages, primarily for device master records, to support product end-of-life documentation.
- The change control process may involve various document types, including Manufacturing Procedures, Quality Control Procedures, Certificates of Analysis, Material Specifications, and Labels/Package Inserts.
Key responsibilities include:
- Creating thorough and well-drafted change impact assessment documents.
- Ensuring quality documents are properly redlined and in-process revisions are controlled before approval.
- Conducting detailed reviews of document changes before submission to supervisors or approvers.
- Ensuring all necessary documents for routing change requests are in place before approval.
- Ensuring documentation is appropriate, justified, and approved by responsible functional areas according to timelines and established procedures.
Job Type: Contract
Pay: $26.56 - $31.98 per hour
Expected hours: 40 per week
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Flexible schedule
- Health insurance
- Internet reimbursement
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Education:
- High school or equivalent (Preferred)
Experience:
- Documentation: 2 years (Preferred)
- change control: 2 years (Preferred)
- Technical writing: 2 years (Preferred)
- healthcare or pharma or medical device industry: 2 years (Preferred)
Ability to Commute:
- Des Plaines, IL 60016 (Required)
Work Location: In person
Salary : $27 - $32
