Technical Writer, Microbiology Quality Control

Medline Industries, LP; Mundelein (IL); On-site; USD 68,000 - 100,000; Full time

Job summary

An established industry player is seeking a Technical Writer to join their dynamic team. This role involves crafting essential Standard Operating Procedures (SOPs) and technical documents that ensure compliance and clarity across various teams. You will engage with subject matter experts to gather information and transform complex scientific concepts into accessible language. With opportunities for independent project management and collaboration, this position is perfect for those looking to make a significant impact in the medical equipment manufacturing sector. Join a company that values diversity and offers a competitive rewards package.

Benefits

Health Insurance

401(k) Contributions

Paid Time Off

Life and Disability Insurance

Employee Assistance Program

Qualifications

• 2+ years experience in medical or pharmaceutical writing.
• Skilled in creating SOPs and technical documentation.

Responsibilities

• Create and edit SOPs, change controls, and technical documents.
• Collaborate with teams to identify documentation needs.

Skills

Technical Writing

Regulatory Compliance

Document Management

Root Cause Analysis

Communication Skills

Education

Bachelor's Degree

Tools

Microsoft Word

Microsoft Excel

Adobe Acrobat Pro

Adobe InDesign

Microsoft Visio

Job description

Technical Writer, Microbiology Quality Control

2 weeks ago Be among the first 25 applicants

Job Summary

Write Standard Operating Procedures (SOPs), change controls, deviations, non-conforming material reports, and training materials based on validated processes. Responsible for determining root cause, authoring and corrective actions associated with deviations and non-conforming material reports (NCMRs). Design, develop, and implement customized technical documents for use across a variety of teams. Gather information about needs, objectives, functions, features, and requirements. Conducts work assignments of increasing complexity, under moderate supervision with latitude for independent judgment. Transform technical and scientific concepts into simple language so that average readers can easily understand

Job Summary

Write Standard Operating Procedures (SOPs), change controls, deviations, non-conforming material reports, and training materials based on validated processes. Responsible for determining root cause, authoring and corrective actions associated with deviations and non-conforming material reports (NCMRs). Design, develop, and implement customized technical documents for use across a variety of teams. Gather information about needs, objectives, functions, features, and requirements. Conducts work assignments of increasing complexity, under moderate supervision with latitude for independent judgment. Transform technical and scientific concepts into simple language so that average readers can easily understand

Responsibilities

Job Description

• Responsible for the creation, writing and/or editing of procedures, SOPs, deviations, non-conforming material reports, and change control documents. Responsible for coordinating deviation and non-conformance investigations. Work with subject matter experts to assign root cause and corrective actions for deviations and non-conforming material reports.
• Responsible for identifying documentation needs across maintenance, production, quality, and engineering teams.
• Design and manage independent projects, communicating project updates to key team members on a regular basis.
• Interview production, maintenance and engineering personnel to become familiar with product technologies and production methods. Observe production and experimental activities to determine work instructions, as well as what type of documentation may be needed for personnel training.
• Responsible for overseeing documents through the quality review process, ensuring reports are approved by key subject matter experts and regulatory personnel prior to final submission.
• Illustrate technical or scientific concepts using photographs, drawings, sketches, diagrams, and charts. Study drawings, specifications, and equipment in order to draft operating procedures, work instructions, or report justifications in detail.
• Identify trends in manufacturing process based on reports related to product quality (such as deviations and NCMRs). Collaborate with other teams to track key information and create trend reports as needed.
• Organize material and complete writing assignments according to set standards regarding clarity, conciseness, style, and terminology. Edit, standardize, or make changes to material prepared by others.
  
  

Minimum Qualifications

• At least two years’ experience in Medical, Pharmaceutical, Manufacturing, or other field under regulatory compliance. OR At least one year experience in Experience with Microsoft Excel and Microsoft Word.
• Experience with Adobe Acrobat Pro.
  
  

Preferred Qualifications

• Knowledge of FDA GMP compliant manufacturing is a plus.
• Experience with Adobe InDesign, Photoshop, and/or Illustrator is a plus. Experience with Microsoft Visio is a plus.
• Experience in training, teaching, or general instructional design is a plus.
  
  

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The Anticipated Salary Range For This Position

$68,640.00 - $99,320.00 Annual

The actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.

Every day, we’re focused on building a more diverse and inclusive company, one that recognizes, values and respects the differences we all bring to the workplace. From doing what’s right to delivering business results, together, we’re better. Explore our Diversity, Equity and Inclusion page here.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Marketing, Public Relations, and Writing/Editing

• Industries

  Medical Equipment Manufacturing

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