OrciMed Life Sciences is hiring a Document Specialist with a strong science background to support its growing documentation and compliance needs. This role is ideal for candidates with 1–3 years of experience who are skilled in SOP formatting, MS Word guidelines, and document version control.
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If you are passionate about life sciences documentation, detail-oriented, and eager to contribute to high-quality standards, this could be the perfect career move for you.
📌 Job Responsibilities
As a Document Specialist at OrciMed Life Sciences, you will:
- Format and edit Standard Operating Procedures (SOPs), forms, and technical reports.
- Ensure compliance with MS Word documentation guidelines (headers, footers, version control, page setup, styles).
- Maintain document structure with headings, tables of contents, and version history.
- Support teams by developing, formatting, and managing company-wide controlled documents.
- Collaborate with quality and compliance teams to ensure regulatory-ready documentation.
🎓 Qualifications
- Bachelor’s or Master’s degree in Science, Pharmacy, or Life Sciences.
- 1–3 years of relevant experience in documentation or technical writing.
- Strong expertise in MS Word formatting and document control.
- Attention to detail and ability to manage multiple document workflows.
- Knowledge of SOP compliance and regulated environments is an advantage.
💼 Benefits of Joining OrciMed Life Sciences
- Opportunity to work in a fast-growing life sciences organization.
- Gain experience in regulatory documentation and SOP management.
- Exposure to industry best practices in document control and compliance.
- Collaborative and supportive work culture.
📩 How to Apply
Interested candidates can send their updated resume to:
careers@orcimedlifesciences.com
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