Author Jobs in Pennsylvania
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Search Results - Author Jobs in Pennsylvania
American Board of Internal Medicine-Philadelphia
Author technical reports and background/discussion papers related to assigned projects.
• Author and publish manuscripts in peer-reviewed journals.
• Presents scholarly research at professional meetings. Communicate research results to internal leadership...
appcast.io -
Shake Shack-Cranberry Township
of Union Square Hospitality Group and best-selling author of Setting the Table. Shack Fans lined up daily, making the cart a resounding success, and donating all proceeds back to the park beautification efforts. A permanent stand was eventually built...
jobget.com -
Insight Global-Malvern (PA)
Collaborate cross-functionally to represent Cell Banking department.
-Author, review, and approve technical documents, SOPs, and batch records.
Required Skills & Experienc
e-Bachelor's degree in scientific field, preferably Biotec
h-Minimum 1 year...
appcast.io -
Shake Shack-Cranberry Township
Hospitality Group and best-selling author of Setting the Table. Shack Fans lined up daily, making the cart a resounding success, and donating all proceeds back to the park beautification efforts. A permanent stand was eventually built…and the rest is Shack...
jobget.com -
1 similar job: Peabody
Alsinova-Collegeville (PA)
GPM stands for Global Pack Management]
• Liaise with other groups within Clinical Manufacturing & Supply Chain.
• Work in key IT systems – SMARTLS Compliance Author, Adobe InDesign, Prisym 360.
Experience Required
• Able to follow written...
appcast.io -
Shake Shack-Cranberry Township
Hospitality Group and best-selling author of Setting the Table. Shack Fans lined up daily, making the cart a resounding success, and donating all proceeds back to the park beautification efforts. A permanent stand was eventually built…and the rest is Shack...
jobget.com -
Siemens Energy-Mount Pleasant (PA)
Conduct risk assessments and author clear, executable work instructions for contracted scopes.
• Build and manage customer‑focused project schedules that drive commitment alignment and enable real‑time adjustments.
• Own tooling strategy, including...
Insight Global-Malvern (PA)
Banking department.
-Author, review, and approve technical documents, SOPs, and batch records.
Compensation:
$25-32/hr
Exact compensation may vary based on several factors, including skills, experience, and education.
Benefit packages for this role...
appcast.io -
PMRS-Horsham
environmental monitoring and product testing according to PMRS and international regulatory requirements (USP/NF, EP). Author necessary validations for processes and manage their execution.
Primary Duties:
Scheduling and performing all microbiological testing...
Johnson Controls-New Freedom
teams across factory sites on-site and remotely to resolve drawing conflicts, tolerance concerns, and producibility issues in existing product documentation.
• Participate in Change Control Board (CCB) reviews; author and process Engineering Change...
appcast.io -
Inizio Engage-Yardley
Author and review US MI responses by identifying and summarizing complex scientific literature in a scientifically accurate, fair balanced, concise and compliant manner to help inform clinical decision-making by HCPs.
• Plan and maintain a robust product...
Philadelphia
focused marketing campaigns, promotions, and events.
• Support experiential marketing efforts including author visits, bookstore activations, giveaways, and student programs.
• Research marketing trends and help identify new ways to connect with students...
icims.com -
Takeda Pharmaceutical-Cambridge
topics, as applicable.
• Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.
• Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan...
tdrct.com -
Michael Page-Philadelphia
management lead and SME, ensuring full lifecycle execution of risk processes in alignment with ISO 14971
• Coordinate design control activities while ensuring risk is properly integrated at every phase of product development
• Lead risk assessments, author...
michaelpage.com -
Takeda Pharmaceutical-Cambridge
on product specific value evidence topics, as applicable.
• Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.
• Monitor and anticipate trends that impact both the regulatory and access environments...
tdrct.com -
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