Sterling Engineering, Inc.
https://cdn.haleymarketing.com/templates/63335/logos/square_logo.png
https://www.sterling-engineering.com
https://www.sterling-engineering.com
USD
40.00
HOUR
true
Justin DiBlasi
Technical Writer
2024-03-19
2024-05-16
Employment Type:
Contract
Job Category: Technical Writer
Job Number: MC78575933
Compensation: $40.00 / hour
Job Description
Position: Technical Writer (Pharmaceutical or cGMP)
Location: North Chicago, IL 60064 onsite 5 days a week
Duration: 12-24 months
As a Technical Writer, you will play a crucial role in supporting Documentation in New Cosmetics Product line and Process development. The ideal candidate will have a meticulous eye for detail and proficiency in both paper and electronic documentation formats. Will have experience developing Batch Operating Procedures, protocols, Job Safety task management and a variety of documents related to pharmaceutical processes, quality control, and regulatory compliance. must have strong coordination skills to collaborate with SMEs.
- Conduct comprehensive review of existing documentation. Develop / Edit Standard Operating Procedures (SOPs) and Work Instructions: Create clear, concise, and accurate SOPs and work instructions related to processes used in a pharmaceutical Good Manufacturing Practices (GMP) environment. These documents must adhere to industry standards, templates, and best practices.
- Collaborate with Subject Matter Experts (SMEs): Work closely with SMEs, scientists, engineers, and other stakeholders to gather information and ensure accuracy in your documentation.
- Create and Revise Documents: Prepare a wide range of documents, including:
- Drive standardization of the documentation practices – identify non -conformance.
- Clinical Study Reports: Detailed reports summarizing clinical trial results.
- Regulatory Submissions: Documentation required for regulatory approvals.
- Precautions for Medications: Safety information and precautions.
- Reference Guides: Comprehensive guides for healthcare professionals.
- Ensure Compliance: Your work will contribute to maintaining compliance with cGMP regulations and industry standards.
Qualifications:
- Bachelor’s degree in a relevant field (e.g., life sciences, pharmacy, technical communication).
- Prior experience as a technical writer in the cosmetics or within a highly regulated environment
- Comprehensive knowledge of Batch Operating Procedures (BOPs), protocols, Job Safety Task Management (JSTms), and related documentation.
- Familiarity with regulatory requirements (e.g., FDA, cGMP) and quality standards in cosmetics manufacturing.
- Strong attention to detail and excellent written and verbal communication skills
- Strong understanding of cGMP regulations and pharmaceutical manufacturing processes.
Something you should know…about Sterling Engineering… As a Sterling Engineering W2 employee on contract, you are eligible to receive a Full Employee Benefits Package that includes Paid Time Off, paid holidays, 3 Medical plans to choose from, Dental & Vision plans, 401(k) with a match, and an Employee Stock Ownership (ESOP) plan.
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.
Meet Your Recruiter
Justin DiBlasi
Technical Recruiter
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