ZipRecruiter

Log In

1

Manager Ibm Technical Writing Jobs in Delaware (NOW HIRING)

Hologic Inc.

Manufacturing Quality Engineer

Newark, DE · On-site

$72K - $93K/yr

Responsible for planning, implementing and managing compliance of manufacturing and production ... Excellent technical writing skills with ability to write quality assurance reports and details ...

Hologic

Manufacturing Quality Engineer

Newark, DE · On-site

$72K - $93K/yr

Responsible for planning, implementing and managing compliance of manufacturing and production ... Excellent technical writing skills with ability to write quality assurance reports and details ...

Avani Technology Solutions, Inc.

Data Modeling

Newark, DE · On-site

$53.50 - $69.50/hr

... technical project teams. * Enterprise level delivery of reusable artifacts and interface ... Excellence in writing and maintaining clear enduser documentation including service API ...

Owens Community College

$33K - $41K/yr

Written/verbal communication, customer service skill, use of power tools i.e. drills/saws ... Ability to manage several projects at once. Essential Functions: * Coordinate events and facility ...

VIS IT Solutions Inc

Mainframe Developer

Wilmington, DE · On-site

$47.50 - $61.25/hr

Analyze business requirements and translate them into technical specifications. * Participate in ... Management) o IBM MQ (Message Queueing) * Familiarity with tools such as TSO/ISPF, File-AID, Abend ...

MDAEdge

LabWare LIMS-LES Developer

Port Penn, DE · On-site

... Management System (LIMS) and Lab Execution System (LES). The role involves configuring, customizing, and maintaining LabWare solutions while providing technical support to ensure smooth laboratory ...

Pennoni

Project Bridge Engineer

Newark, DE · On-site

Interacting with clients to showcase subject matter expertise and to perform project management if ... Produces high quality technical writing for use in bridge inspection reports, specifications ...

Pennoni

Project Bridge Engineer

Newark, DE

Interacting with clients to showcase subject matter expertise and to perform project management if ... Produces high quality technical writing for use in bridge inspection reports, specifications ...

THERMO KING

Service Writer, TK

Delmar, DE · On-site

$18 - $25/hr

Communicate effectively with customers and manage customer interactions to ensure customer ... or equivalent (Technical degree or certification a plus). * Experience in Service writing ...

previous pagenext page

Showing results 21-40

All JobsIbm Technical Writing JobsManager Ibm Technical Writing JobsManager Ibm Technical Writing Jobs in Delaware

Manager Ibm Technical Writing information

What is the difference between Manager Ibm Technical Writing vs Technical Writer?

AspectManager Ibm Technical WritingTechnical Writer
CredentialsBachelor's degree, experience in technical writing, leadership skillsBachelor's degree in English, Communications, or related field; technical writing experience
Work EnvironmentTeam leadership, project management, coordination with multiple departmentsIndividual content creation, editing, and documentation tasks
Employer & Industry UsageIBM and similar tech companies, corporate documentation teamsTech companies, software firms, engineering teams

The main difference is that a Manager Ibm Technical Writing oversees teams and manages projects within IBM, focusing on leadership and strategic planning. In contrast, a Technical Writer primarily creates and edits technical documentation. Managers handle team coordination, while Technical Writers focus on content development.

What are some common challenges faced by a manager IBM technical writing, and how can they be addressed?

Managers in IBM Technical Writing often face challenges such as coordinating documentation across global teams, ensuring consistency and quality in technical content, and keeping up with rapidly evolving technologies. Effective communication, implementing clear documentation standards, and leveraging collaborative tools can help address these challenges. Additionally, fostering a culture of continuous learning and feedback within the team is essential for adapting to new tools and maintaining high-quality outputs.

What are the key skills and qualifications needed to thrive as a manager IBM technical writing?

To thrive as a Manager IBM Technical Writing, strong leadership abilities, expertise in technical writing, and a background in computer science or a related field are generally required. Familiarity with documentation tools such as DITA, XML, IBM-specific platforms, and content management systems, as well as certifications in technical communication, are commonly expected. Exceptional communication, project management, and team collaboration skills set top performers apart in this role. These skills and qualifications ensure the delivery of clear, accurate, and user-focused documentation that supports IBM's complex technical products and enhances customer experience.

What is a manager IBM technical writing?

Manager IBM Technical Writing jobs involve overseeing teams of technical writers who create, edit, and maintain documentation for IBM products and services. These managers coordinate the documentation process, ensure quality and consistency, and work closely with engineers, product managers, and other stakeholders. Their responsibilities include developing documentation strategies, mentoring writers, setting timelines, and ensuring that all materials meet IBM's standards. Strong leadership, technical knowledge, and communication skills are essential for success in this role.

What does a manager IBM technical writing do?

A manager of IBM technical writing oversees teams responsible for creating and maintaining technical documentation, such as user manuals, product guides, and online help resources. They coordinate content development, ensure accuracy and clarity, and often use tools like XML or Markdown, while managing schedules and quality standards.
What cities in Delaware are hiring for Manager Ibm Technical Writing jobs? Cities in Delaware with the most Manager Ibm Technical Writing job openings:
Manager Ibm Technical Writing jobs near you

Technical Service Lead - Sterile Drug Products

WuXi AppTec

Middletown, DE • On-site

$99K - $150K/yr

Other

Posted 11 days ago

Job description

Overview
We are seeking a highly experienced and detail-oriented Technical Service Lead to join our Sterile Drug Product Engineering team. The Technical Service Lead will lead and oversee technical operations for a sterile injectable manufacturing facility. This role is responsible for supporting facility start-up activities, CQV execution, technical transfer, process implementation, and commercial product launch readiness. The position will serve as a key technical interface across Engineering, Manufacturing, Quality, Validation, and external vendors, clients, with future responsibility for building and leading a technical services team.
The ideal candidate will have strong hands-on experience with sterile injectable manufacturing processes, including aseptic filling, isolator technology, lyophilization, visual inspection, labeling, and packaging systems for vial, syringe, and cartridge presentations.
Responsibilities
Technical Oversight
  • Provide technical leadership for sterile injectable manufacturing processes including vial, syringe, and cartridge filling operations.
  • Oversee equipment and process support for formulation, aseptic filling lines, isolators/RABS, lyophilizers, automatic visual inspection, labeling and packaging equipment.
  • Support process design, technology transfer, scale-up activities, and process optimization for new product introductions.
  • Collaborate between engineering, quality department, vendors and manufacturing teams during equipment commissioning, qualification, and start-up activities.
  • Lead technical investigations, troubleshooting efforts, and implementation of corrective/preventive actions related to manufacturing and process performance.
  • As member of global engineering team, strongly connecting and involving in DP global engineering projects planning and implementation.
Regulatory Compliance
  • Ensure manufacturing processes and technical operations comply with cGMP requirements, FDA, EU GMP Annex 1, and internal quality standards.
  • Review and approve technical documentation including protocols, reports, SOPs, batch records, change controls, and deviation investigations.
  • Support regulatory inspections, customer audits, and internal audits by serving as a technical subject matter expert.
  • Partner with Quality Assurance to maintain validated state and continuous compliance of sterile manufacturing systems.
  • Drive contamination control strategy implementation and support aseptic process simulation/media fill activities.
Project Management
  • Lead cross-functional technical transfer and product launch activities from development through commercial manufacturing.
  • Manage technical deliverables, planning, risk management, and vendor coordination for new equipment and manufacturing initiatives.
  • Support continuous improvement, and operational readiness initiatives within the sterile manufacturing facility.
  • Work closely with external equipment suppliers, consultants, and contract partners to ensure successful project execution.
Team Leadership
  • Build, mentor, and lead a high-performing technical services team as the organization grows.
  • Provide technical guidance and coaching to engineers, production technicians, and manufacturing support staff.
  • Foster strong cross-functional collaboration with Manufacturing, Quality, Engineering, Supply Chain, and Program Management teams.
  • Establish a culture of accountability, continuous improvement, technical excellence, and proactive problem solving.
  • Support resource planning, workload prioritization, and talent development to meet business and project objectives.

Qualifications
Required Qualifications:
  • Excellent written and verbal communication skills, with attention to detail and clarity.
  • Bachelor's or Master's degree in engineering, Life Sciences, or related technical discipline.
  • Minimum of 8-10 years of experience in the pharmaceutical or biotechnology industry.
  • Preferably at least 3 years in a supervisory or managerial role.
  • Deep understanding of cGMP requirements, risk-based approach, and global regulatory expectations.
  • Proven experience in startup or expansion of manufacturing facilities is highly preferred.

Preferred Qualifications:
  • Strong knowledge of current Good Manufacturing Practices (cGMP), regulatory guidelines (FDA, EMA, ICH), and industry standards.
  • Experience with sterile filling, lyophilization, automatic visual inspection is a plus.
  • Prior experience supporting regulatory inspections and audits.

The anticipated base salary for this opening is $99,000 to $150,000
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

Apply