Senior Technical Writer

Biopharma Careers; New Jersey; On-site; USD 79,000 - 128,000; Full time

Benefits offered by this job

401(k) plan

Long-term incentive program

Paid time off

Job summary

Johnson & Johnson is seeking a Senior Technical Writer for the Titusville, NJ location to drive GMP documentation across QC investigations. You will write SOPs, validation reports, and CAPAs while ensuring compliance with FDA, GMP, and internal standards.

You will mentor junior investigators, lead writing activities, and coordinate with QA and lab teams to sustain regulatory readiness and process improvements.

Qualifications

• Detailed knowledge of analytical technologies used in QC lab (HPLC, Dissolution, IR, Karl Fischer).
• Experience in a QC laboratory as bench analyst.
• Advanced technical writing skills and GMP knowledge (cGMP, USP/EP/JP).
• Ability to lead investigations and mentor others in technical writing.

Responsibilities

• Lead writing of GMP documents and investigations in the NJ Stability Lab Operations.
• Plan, execute, and write investigations with root-cause analysis and corrective actions.
• Write and edit SOPs, validation protocols/reports, forms, and analytical documents from conception to utilization.
• Provide training and mentorship to new investigation writers and lab analysts.

Skills

Analytical reasoning

Problem solving

Technical writing

Communication

Cross-functional collaboration

Kepner-Tregoe / 5-Why analysis

MS Office

Quality systems awareness

Education

Bachelor's degree in life sciences or related field

Tools

TrackWise

COMET

DocSpace

TruVault

eLIMS

Job description

Johnson & JohnsonPosted October 20, 2026# Senior Technical WriterTitusville, United States Full timeQuality SeniorNotify me about similar jobsView Full Job & Apply at Johnson & JohnsonJohnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.## About this opportunityAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.comAs guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.**Job Function:**Quality**Job Sub Function:**Quality Control**Job Category:**Professional**All Job Posting Locations:**Titusville, New Jersey, United States of America**Job Description:**The Technical Writer is responsible for driving results in a fast-paced multi-faceted environment by leading the technical writing of GMP documents and investigations associated within the NJ Stability Lab Operations.Assignments are of varying complexity, where sound judgment and self-drive/initiative are required to resolve problems and make recommendations/decisions.This position requires technical writing and investigations to be completed in compliance with all applicable procedures, standards and GMP regulations as well as all local, state, federal and international regulations and guidelines (FDA, EPA, DEA, OSHA, etc.)• Plan, execute, and write laboratory investigations, in coordination with laboratory supervisors and QC Technical Leads, identifying immediate/root causes and determining effective corrective and preventative actions• Write and edit detailed SOPs, validation protocols/reports, forms, analytical and technical documents and reports from conception to utilization• Proofread documents for content and identify non-standard format or wording, and errors within documents• Review data where required pertaining to documents being drafted• Participate in gap assessments of technical documentation to ensure methods are up to current standards, and that processes investigated are present and functioning optimally. Provide recommendations/solutions to remediate any recognized gaps• Present authorship strategy to management to get pre-approval and endorsement• Build and maintain a progress-tracking matrix on document generation, qualification execution, document review and approval (Escalate any issue/delay to management as applicable)• Collect and trend historical data• Responsible for preparing technical documentation for highly complex issues (i.e. high impact investigations)• Make contributions to improved processes and templates as it relates to laboratory investigations• Provide training and mentorship for new investigation writers and lab analysts as it pertains to technical writing• Maintain individual training completion in a compliant state• Complete investigation records and CAPAs in a timely and compliant fashion• Provides information and support to escalations associated with laboratory investigations• Support as SME for Health Authority Inspections• Provide input to functional laboratory meetings• Make contributions to, and occasionally lead, continuous improvement teams• Provide leadership and insight as a member of global project teams**Required Knowledge, Skills and Abilities:**Detailed knowledge of analytical technologies used in the QC laboratory (HPLC, Dissolution, IR, Karl Fischer, etc.)Experience working in a QC laboratory as a bench analystDemonstrated use of root cause analysis tools such as Kepner-Tregoe, Fishbone, 5-Why, etc.Demonstrated written, verbal, and interpersonal communication skills with strong attention to detailKnowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratoryBasic knowledge of compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QCAdvanced technical writing skillsProficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint)Ability to complete investigations including identification of root causeAbility to work collaboratively and to lead and influence investigation team members to coordinate work based on priorities.Experience with Quality Systems such as Trackwise, COMET, Docspace, TruVault, eLIMS or equivalent requiredAble to communicate clearly at all levels of the organization requiredAbility to work independently on assignments with minimal oversight required**Required Skills:****Preferred Skills:**Analytical Reasoning, Business Behavior, Compliance Management, Controls Compliance, Cross-Functional Collaboration, Innovation, ISO 9001, Persistence and Tenacity, Problem Solving, Process Oriented, Quality Auditing, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Report Writing, Technologically Savvy**The anticipated base pay range for this position is :**$79,000.00 - $127,650.00Additional Description for Pay Transparency:Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).This position is eligible to participate in the Company’s long-term incentive program.Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:Vacation –120 hours per calendar yearSick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar yearHoliday pay, including Floating Holidays –13 days per calendar yearWork, Personal and Family Time - up to 40 hours per calendar yearParental Leave – 480 hours within one year of the birth/adoption/foster care of a childBereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar yearCaregiver Leave – 80 hours in a 52-week rolling period10 daysVolunteer Leave – 32 hours per calendar yearMilitary Spouse Time-Off – 80 hours per calendar yearFor additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits