Technical Writer

Posted 2 Days Ago
Be an Early Applicant
2 Locations
In-Office or Remote
70K-80K Annually
Mid level
Healthtech • Pharmaceutical
The Role
Write and revise deviations, action plans, investigation reports, ECRs, SOPs, and trend reports for a GMP manufacturing distribution center. Lead deviation investigations, assign CAPAs, support audits/inspections, work with production SMEs, and use electronic systems to maintain compliance with FDA and cGMP requirements.
Summary Generated by Built In
Job SummaryThe Technical Writer is responsible for the writing of deviations, action plans, trend reports, and engineer change requests (ECR’s) for the Marketing Unit Distribution Center. Additionally, the role will assist with the writing and revision of standard operating procedures, assist with audit response development, and take direction from the Manager of Compliance regarding any related activities as needed.
Salary Range: $70,000 - $80,000 based on experience
• Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
• Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.
Hybrid role: Onsite 3 days per week
Applicants must be authorized to work for ANY employer in the United States. Fresenius Kabi is unable to sponsor or take over sponsorship of an employment visa either now or in the future.

Responsibilities

The Technical Writer is responsible for describing problems, identifying possible causes, collecting, understanding, and organizing existing data, comparing causes to facts, identifying probable root causes, and helping to determine the best solutions

Responsible for managing multiple deviation investigations simultaneously

Ensures investigations will withstand regulatory scrutiny and are compliant with cGMP regulations

Works with process experts and production personnel to fully understand and solve problems, provides technical expertise and recommends improvements

Writes and revises SOP’s based upon input from operations or other subject matter experts

Writes Impact Assessments and Investigation Reports, works within Kabi Track

Assigns corrective/preventive actions (CAPAs) as necessary in order to resolve problems

Informs Management on the progress of on-going investigations, provides information to and takes direction from the MRB Material Review Board

Takes the lead on the processing of Engineer Change Requests (ECR’s) based upon site needs

Creates trend reports necessary to meet compliance obligations and KPI’s

On-site presence before and during inspections to support the operations team

Utilizes Word, Excel, eDMS and other electronic systems to complete tasks

Maintains compliance with company policies, training requirements, cGMPs and safety standards

Requirements:

·            Bachelor of Science degree recommended

·            Requires advanced critical thinking skills and expert writing skills

·            At least three years’ experience in a GMP environment writing standard operating procedures and/or deviations/action plans 

·            Must be familiar with regulatory (FDA) requirements

·            Good organizational, communication, and interpersonal skills are required

Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.

Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is at‑will, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

Skills Required

  • Bachelor of Science degree
  • Advanced critical thinking skills and expert writing skills
  • At least three years' experience in a GMP environment writing SOPs and/or deviations/action plans
  • Familiarity with regulatory (FDA) requirements
  • Good organizational, communication, and interpersonal skills
  • Authorized to work in the United States; employer will not sponsor visas
  • Hybrid onsite schedule (onsite 3 days per week)
  • Proficiency with Word, Excel, eDMS and electronic document management systems (Kabi Track)
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Bad Homburg v. d. Höhe
21,388 Employees

What We Do

Fresenius Kabi is a global healthcare company that specializes in lifesaving medicines and technologies for infusion, transfusion, and clinical nutrition. The company’s products and services are used for the therapy and care of critically and chronically ill patients. Its product portfolio comprises a range of highly complex biopharmaceuticals, clinical nutrition, medical technologies, and I.V. generic drugs. Within biopharmaceuticals, Fresenius Kabi offers, among others, biosimilar drugs with a focus on autoimmune diseases and oncology. The company’s clinical nutrition offering includes a wide selection of enteral and parenteral nutrition products. In the segment of medical technologies, its offering includes vital disposables, infusions pumps, apheresis machines, cell therapy devices, and more. Fresenius Kabi puts essential medicines and technologies in the hands of people who help patients and finds the best answers to the challenges they face. Following its strategy “Vision 2026”, which is a key part of the #FutureFresenius program of the Fresenius healthcare group, the company is furthermore committed to increase efficiencies in the therapy and care of patients and improve access to high-quality healthcare around the globe. Fresenius Kabi aspires to be leading globally in its product segments – all for the benefit of patients, its customers, and its stakeholders. Fresenius Kabi Community Guidelines and User Information: https://www.fresenius-kabi.com/social-media-terms-conditions Imprint: https://www.fresenius-kabi.com/imprint

Similar Jobs

Aquia Inc. Logo Aquia Inc.

Technical Writer

Artificial Intelligence • Professional Services • Cybersecurity • Generative AI • Infrastructure as a Service (IaaS) • Automation • Data Privacy
Remote
United States
92 Employees
110K-130K Annually

Stripe Logo Stripe

Technical Writer

Payments • Software
Remote
US
5360 Employees

Identity Digital Logo Identity Digital

Senior Technical Writer

Consumer Web • eCommerce • Internet of Things
Remote or Hybrid
United States
240 Employees
130K-150K Annually
Remote
United States
135 Employees

Similar Companies Hiring

Sailor Health Thumbnail
Healthtech • Social Impact • Telehealth
New York City, NY
20 Employees
Granted Thumbnail
Mobile • Insurance • Healthtech • Financial Services • Artificial Intelligence
New York, New York
23 Employees
OneImaging Thumbnail
Healthtech
Miami, FL
62 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account