Job Title: Technical WriterLocation: Plainville, MA 02762Duration: 12 MonthsResponsibilities:Collaborates with area SMEs or technical specialist to build or revise existing procedures or documents for use in the manufacturing processesAcquires and verifies accuracy of technical details, manages documentation workflows and schedules and proos drafts for adherence to established document design and quality standardsPerforms administrative duties related to managing controlled document life cycles from issuance to Manufacturing through archival with Quality AssuranceResponsibilities may include maintaining the GMP manual of Standard Operating Procedures and management of logbooks for the manufacturing operationsProvides training to Junior associates on established writing standards for documentation design and qualityTraining provided may also Include company policies, programs and procedures commensurate with their experience as a qualified trainerParticipates 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 experience3-4 years industry related experience with an Associate's Degree1-2 years Industry related experience with a Bachelor's DegreeRequired ExperienceStrong interpersonal and communications skills; written and oralMust be skilled in the use of a personal computer and related software applicationsMust have strong Interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in diverse areasKnowledge, Skills, Abilities:Must be skilled in meetings and interviews to eliciting technical details from subject matter specialistsMust be able to provide effective written or verbal communication to peers, senior associates and area management within their operational groupMust be able to develop logical structure for technical documents, content and illustrationsMust be detail oriented while prooing documentsMust 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 managementMust be able to understand operational documents for GMP compliance, accuracy and completenessPhysical Requirements / Work EnvironmentGown aseptically and/or sterile gown as neededFully onsitePosition Shift (Days/Hours):Monday - Friday/ First shift (7:30 - 4pm)
