Hello

Please check the below position and reply back withthe below details and 
updated resume if you are comfortable 

  

Title: Technical writer

Location: Devens,MA

Duration: LongTerm 

9+ Yearsof Experience needed

 

Key Responsibilities and Major Duties: 

• Write and revise standard operating procedures (SOPs) forGMP Biologics, 
Manufacturing and Downstream Commercial Manufacturing. 

• Ability to interview cross functional subject matterexperts and translate 
their description into actionable instructions- WorkInstructions, Job Aids 
using the templates prescribed by corporate policy

. • Schedule cross functional team meetings, collectfeedback, create draft 
documents, post on SharePoint, schedule reviews, collectand resolve feedback.

 • Work independentlybut recognize need to consult stake holders and keep them 
informed of progress.

 • Identify and leadimprovement efforts within current procedures. 

• Maintain a good understanding of GMP and GDP guidelines.Requirements: 

• Minimum 5 years' experience in writing and reviewingstandard operating 
procedures preferred, but not required. Any experiencewriting controlled 
documents will be considered 

• Science, Engineering or Math background preferred 

• Demonstrated ability to successfully manage completingdeadlines and balance 
priorities.

 • Excellent technicalwriting skills, close attention to detail and excellent 
follow up

. • Expertise in Microsoft Word and Share Point.

 • Proficient inMicrosoft outlook, MS team meetings, Share point. Able to 
conduct video conferencecalls via MS teams 4-6 hours a day

Thanks & Regards


Arun | Sr. Technical Recruiter
KLNtek324 E Foothill Blvd, Ste 206, 91006 Arcadia, California
a...@klntek.com
+1 (626)-346-9382










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