Technical Writer Job at TSR Consulting Services, Inc
Our client, an established pharmaceutical company is in search of a Technical Writer to join their team on contract.
Key Responsibilities and Major Duties:
- Write and revise standard operating procedures (SOPs) for GMP Biologics, Manufacturing and Downstream Commercial Manufacturing.
- Ability to interview cross functional subject matter experts and translate their description into actionable instructions- Work Instructions, Job Aids using the templates prescribed by corporate policy.
- Schedule cross functional team meetings, collect feedback, create draft documents, post on SharePoint, schedule reviews, collect and resolve feedback.
- Work independently but recognize need to consult stake holders and keep them informed of progress.
- Identify and lead improvement efforts within current procedures.
- Maintain a good understanding of GMP and GDP guidelines.
Requirements:
- 1 - 3 years experience in writing and reviewing standard operating procedures preferred, but not required. Any experience writing controlled documents will be considered
- Science, Engineering or Math background preferred
- Demonstrated ability to successfully manage completing deadlines and balance priorities.
- Excellent technical writing skills, close attention to detail and excellent follow up.
- Expertise in Microsoft Word and Share Point.
- Proficient in Microsoft outlook, MS team meetings, Share point. Able to conduct video conference calls via MS teams 4-6 hours a day.
Job Type: Contract
Schedule:
- 8 hour shift
- Monday to Friday
Application Question(s):
- Are you fully vaccinated against COVID-19?
- Are you local to the Devens, MA area?
- Will you now, or in the future, require sponsorship for employment visa status (e.g. H-1B visa status)?
Work Location: Hybrid remote in Devens, MA 01434
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