Technical Writer at Cosmetic Solutions
Boca Raton, FL 33487, USA -
Full Time


Start Date

Immediate

Expiry Date

12 Nov, 25

Salary

0.0

Posted On

12 Aug, 25

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Microsoft Word, Technical Writing, Chemical Engineering, Communication Skills, Chemistry, Netsuite, Excel, Compounding

Industry

Pharmaceuticals

Description

WHO WE ARE:

Cosmetic Solutions is a leader in the development and manufacturing of scientifically proven, innovative personal care products. With a focus on, face, body, hair, OTC, and professional use formulations, we create some of the most cost effective, high quality and powerful products on the market.
Providing world class services to up and coming businesses, large established brands, physicians, estheticians and other skin care professionals; we specialize in research & development, custom formulization, graphic design, manufacturing, packaging and delivery.
Job Title: Technical Writer – Manufacturing Instructions
Department: Technical Services
Location: Cosmetic Solutions, Boca Raton, Florida, 33487
Reports To: VP of Technical Services

POSITION SUMMARY:

The Technical Writer will be responsible for translating R&D product development data into clear, accurate, and actionable manufacturing instructions. This role is essential in bridging the gap between R&D and Compounding, ensuring a seamless transition from product development to scalable, production-ready procedures. The individual will work closely with R&D, Compounding, Engineering, and Quality teams to create first-draft batch manufacturing instructions (BMIs), define process parameters, and document critical formulation and processing steps.

QUALIFICATIONS:

  • Bachelor’s degree in Chemistry, Chemical Engineering, Cosmetic Science, related technical field preferred or 10-years if cosmetic/OTC manufacturing experience.
  • 2–4 years of experience in technical writing, manufacturing support, or process documentation within a cosmetics, pharmaceutical, or personal care environment.
  • Understanding of compounding processes, batch scale-up, and GMPs in a manufacturing environment.
  • Excellent written communication skills and attention to detail.
  • Ability to work cross-functionally with R&D, Manufacturing, and Quality Assurance teams.
  • Proficiency in Microsoft Word, Excel, and document control systems (e.g., MasterControl, NetSuite, etc.)
  • Ability to manage multiple projects with changing priorities.
Responsibilities
  • Author initial Manufacturing Instructions (MIs) and Batch Manufacturing Instructions (BMIs) for pilot and scale-up batches.
  • Translate R&D formulations into compounding-friendly instructions, considering equipment constraints and scale differences.
  • Collaborate with R&D to understand formulation intent, order of addition, heating and cooling requirements, and mixing speeds.
  • Work closely with the Pilot Specialist and Compounding team to collect in-process feedback and revise documents accordingly after pilots or first productions.
  • Ensure all instructions are written in compliance with internal SOPs and cosmetic/OTC GMP guidelines.
  • Maintain a document revision log and change history for all BMI documents.
  • Coordinate with Technical Services and Quality to ensure manufacturing instructions align with validated processes and specifications.
  • Assist with documenting learnings and adjustments from pilot, qualification, and first production batches.
  • Support the creation of master manufacturing documents and help transition instructions into ERP/document management systems.
  • Participate in cross-functional meetings for New Product Introductions (NPIs) and support timeline planning for document readiness.
  • Assists in writing validation and IOQ protocols.
Loading...