Integra LifeSciences

Technical Writer, Quality Compliance

Integra LifeSciences$94K — $129K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required.
  • 8+ years of technical writing experience or a Master's degree with 5+ years required.
  • Experience in medical device, pharmaceutical, or biotechnology industries required.
  • Familiarity with compliance frameworks like FDA, ISO 13485, and EU MDR is essential.
  • Advanced technical writing and presentation skills required.
  • Strong organizational and proofreading skills essential.
  • Demonstrated project management skills required.

Responsibilities

  • Draft future-state procedural documentation based on ECMP outputs and regulatory requirements.
  • Gather and review site-level procedural documentation.
  • Support in-person ECMP and WS-centric events.
  • Complete necessary ECMP forms to capture outputs and outcomes.
  • Review and verify accuracy and completeness of documents.
  • Coordinate and route ECMP documentation for approval.
  • Perform additional duties as assigned.

Benefits

  • Medical, dental, and vision insurance coverage.
  • Life insurance and disability coverage.
  • Business accident insurance and group legal insurance.
  • 401(k) savings plan.
  • Potential eligibility for bonuses, commissions, or equity.
Full Job Description
SUMMARY DESCRIPTION

The Technical Writer, Quality Compliance is a key member of the Enterprise Compliance Master Plan (ECMP) Team with responsibility to support the Workstream (WS) Leaders by drafting future-state procedural documentation based on the outputs from the applicable ECMP phases, events and regulatory requirements; gathering and reviewing site-level procedural documentation; supporting in-person ECMP and WS-centric events; completing any necessary ECMP forms to capture outputs and outcomes for applicable ECMP phases and meetings; coordinating and routing ECMP related and ECMP WS Output documentation for approval; and reviewing and verifying accuracy and completeness of documents.

ESSENTIAL DUTIES AND RESPONSIBILITIES

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily including their overarching responsibility of supporting the ECMP WS Leaders, including:
  • Drafting future-state procedural documentation based on the outputs from the applicable ECMP phases, events and regulatory requirements;
  • Gathering and reviewing site-level procedural documentation;
  • Supporting in-person ECMP and WS-centric events;
  • Completing any necessary ECMP forms to capture outputs and outcomes for applicable ECMP phases and meetings;
  • Reviewing and verifying accuracy and completeness of documents;
  • Coordinating and routing ECMP related and ECMP WS Output documentation for approval; and,
  • Other duties as assigned.


DESIRED MINIMUM QUALIFICATIONS

Education:
  • Bachelor's degree is required.


Skills/Knowledge:
  • 8+ years of experience in technical writing is required, or equivalent, i.e. Master's degree with 5+ years of experience.
  • Experience in medical device, pharmaceutical and / or biotechnology industries is required.
  • Experience in working within compliance frameworks such as FDA, ISO 13485, and EU MDR is required.
  • Advanced technical writing, presentation, bibliographic research and editorial skills are required.
  • Strong ability to interpret and disseminate relevant product information is required.
  • Strong organizational skills, attention to detail and proofreading skills are required.
  • Demonstrated project management skills are required.
  • The ability to produce procedures, reports and documents independently and evaluate the writing of others is required.
  • The ability to rapidly develop expertise in the company's internal document management system is required.
  • Experience with Electronic Documentation Management Systems and Electronic Approval Systems is required.
  • Being comfortable leading teams and educating team members as needed during process of document development is required.
  • Ability to travel up to 40% if needed based on ECMP Workstream needs.


PHYSICAL REQUIREMENTS

The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.

#LI-EM1

Salary Pay Range:

$94,300.00 - $129,950.00 USD Salary

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or trainingIn addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensationYour recruiter can share more about the specific salary range for your preferred location during the hiring process.

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences

Integra - Employer Branding from Integra LifeSciences on Vimeo

About Integra LifeSciences

Integra LifeSciences is an American company that develops, manufactures, and markets medical devices for use in neurosurgery, extremity reconstruction, orthopedics, and general surgery. The company's products include implants, devices, instruments, and systems used in neurosurgery, neuromonitoring, neurotrauma, and related critical care. Integra LifeSciences has its headquarters in Princeton, New Jersey.
Learn more about Integra LifeSciences
Size
3,800 employees
Market Cap
$4.6 billion
Industry
Net Income
$133.8 million
Founded
1989
5 Year Trend
+9.2%
Revenue
$1.3 billion
NASDAQ

Similar Jobs

More Jobs at Integra LifeSciences

More Pharmaceuticals & Biotech Jobs

Find similar Technical Writer, Quality Compliance jobs: