A Technical Writer writes product instructions, user manuals or other material that helps to explain complex information or procedures. Writes help information available to customers online, or clear explanations of company policies. Supports internal communication among different technical, engineering and scientific specialists working on a project or product. Creates product documentation, and provides input for improving product design.
Validation Technical Writer | Pharmaceutical Manufacturing Bethlehem, PA Onsite $40-$50/hr. DOE Long-Term Contract (6-12 Months) US citizens or Green Card holders No C2C Love technical writing? Know cGMP inside and out? A well-established pharmaceutical manufacturing company is looking for an experienced Validation Technical Writer to support major validation initiatives, capital projects, and quality documentation. You'll partner with Engineering, QA, QC, and Operations to create audit-ready documentation supporting equipment, utilities, manufacturing processes, and validation activities. We're looking for experience with:
IQ / OQ / PQ
Protocols Validation Reports SOP Authoring cGMP Documentation FDA-Regulated Manufacturing API or Chemical Manufacturing (highly preferred) Document Control Cross-functional collaboration with Engineering & Quality Requirements Bachelor's degree in a scientific, engineering, quality, or related technical field Minimum 3 years of technical writing experience in pharmaceutical, API, or regulated chemical manufacturing Proven experience with qualification and validation documentation in a cGMP environment Strong understanding of cGMP principles and data integrity requirements Experience authoring
IQ OQ PQ
protocols and validation reports Excellent written communication skills with strong attention to detail and accuracy Ability to manage multiple priorities in a fast paced manufacturing environment Proficiency in Microsoft Word, Excel, Outlook, and document management systems This is an outstanding opportunity to join a respected pharmaceutical manufacturer on a long-term project with the potential for additional extensions! #MPGAll Masis Professional Group is committed to providing a workplace free of discrimination, harassment, and retaliation. We are an equal opportunity employer. Applicants, employees, and former employees are protected from employment discrimination based on race, color, religion, sex (including pregnancy, sexual orientation or transgender status), national origin, age (40 or older), veteran status, disability and genetic information (including family medical history).
