Technical Writer
TLDR
Manage controlled document life cycles from issuance through Quality Assurance archival, maintain GMP procedures, and train junior associates.
Job Title: Technical Writer
Location: Plainville, MA 02762
Duration: 12 Months
Responsibilities:
- Collaborates with area SMEs or technical specialist to build or revise existing procedures or documents for use in the manufacturing processes
- Acquires and verifies accuracy of technical details, manages documentation workflows and schedules and proofreads drafts for adherence to established document design and quality standards
- Performs administrative duties related to managing controlled document life cycles from issuance to Manufacturing through archival with Quality Assurance
- Responsibilities may include maintaining the GMP manual of Standard Operating Procedures and management of logbooks for the manufacturing operations
- Provides training to Junior associates on established writing standards for documentation design and quality
- Training provided may also Include company policies, programs and procedures commensurate with their experience as a qualified trainer
- Participates in initiatives to support. Innovation and continuous Improvement activities and improved compliance with quality procedures, policies and regulations
Keys to Success:
Minimum Requirements/Qualifications:
- Minimum High School Diploma required with 5+ years related experience
- 3-4 years industry related experience with an Associate's Degree
- 1-2 years Industry related experience with a Bachelor's Degree
Required Experience
- Strong interpersonal and communications skills; written and oral
- Must be skilled in the use of a personal computer and related software applications
- Must have strong Interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in diverse areas
Knowledge, Skills, Abilities:
- Must be skilled in meetings and interviews to eliciting technical details from subject matter specialists
- Must be able to provide effective written or verbal communication to peers, senior associates and area management within their operational group
- Must be able to develop logical structure for technical documents, content and illustrations
- Must be detail oriented while proofreading documents
- Must be able to recognize, understand and respond to situations requiring further evaluation and report these events (process, safety personnel, etc ) to senior specialists or area management
- Must be able to understand operational documents for GMP compliance, accuracy and completeness
Physical Requirements / Work Environment
- Gown aseptically and/or sterile gown as needed
- Fully onsite
Position Shift (Days/Hours):
Monday - Friday/ First shift (7:30 - 4pm)
All your information will be kept confidential according to EEO guidelines.
Techtrueup is a specialized job board designed specifically for the healthcare and engineering sectors, catering to companies in industries like Pharma, Medical Devices, and Aeronautical. What sets us apart is our AI-powered platform that enables rapid sourcing and screening of top talent, ensuring swift and high-quality matches for employers looking for skilled professionals in a highly competitive market.