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Senior Talent Acquisition Specialist at Independent Solution | Hiring for Pharma & Biotech | Expert in Global Sourcing
Senior Technical Writer – Validation Protocols (Remote)- Part Time
Contract | Remote | Attractive Hourly Rate | Global Applicants Welcome
We are seeking an experienced Senior Technical Writer with a strong background in GMP environments to support the preparation, authoring, and review of validation protocols (IQ/OQ/PQ) for laboratory instruments. This is a remote, contract-based opportunity ideal for professionals with deep domain knowledge in equipment qualification, technical documentation, and regulatory compliance.
Key Responsibilities:
* Write and review qualification protocols (IQ/OQ/PQ) for a range of lab equipment (e.g., HPLC, LCMS, titrators, viscometers, balances).
* Collaborate remotely with validation, QA, and engineering teams.
* Ensure documentation aligns with GMP, FDA, EU Annex 15, and data integrity standards.
Requirements:
* 5+ years of experience in technical writing within GxP/laboratory validation or life sciences environments.
* Expertise in drafting protocols, reports, and validation documentation.
* Strong understanding of laboratory equipment and qualification processes.
* Excellent written communication and attention to detail.
* Ability to work independently across time zones.
Why Join Us?
* Fully remote role with flexible hours.
* Work with a reputable international pharma client.
* Attractive pay rates.
* Global professionals encouraged to apply.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Job function
Writing/Editing, Engineering, and Manufacturing
* Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Nanotechnology Research
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