Talent.com
Technical Writer Job at Bristol Myers Squibb in New Brunswick

Technical Writer Job at Bristol Myers Squibb in New Brunswick

MediabistroNew Brunswick, NJ, United States
job_description.job_card.variable_hours_ago
serp_jobs.job_preview.job_type
  • serp_jobs.job_card.full_time
job_description.job_card.job_description

Join to apply for the Technical Writer role at Bristol Myers Squibb

Direct message the job poster from Bristol Myers Squibb

Duration : 12 Months with Possible Extension

Pay Rate : $41.29 - $44.29 / hr on W2

50% onsite required

Work Schedule : Mon-Friday (normal business hours)

Job Description :

This individual will be responsible for delivering CMC documentation (dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application.

This role requires effective collaboration across technical functions to deliver on timelines for submissions. The position interfaces with experts in Process Development, Analytical Development, Cell Therapy Technical Ops, Quality and Regulatory Sciences. The successful candidate will work effectively in cross-functional project teams to accomplish company goals.

Primary Responsibilities :

  • Co-authors / authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports.
  • Plan and facilitate submission kick-off for clinical regulatory submissions across CTD pipeline assets.
  • Manage the logistical process and detailed timeline for regulatory submissions.
  • Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy.
  • Provide input and scientific oversight for content generation for Module 2.3 and 3.
  • Must possess a thorough understanding of the source documentation requirements needed for regulatory submissions and the correlation to the authoring process.
  • Review and adjudicate comments in collaboration with technical SMEs, facilitate comment resolution, revise draft sections.
  • Ensures content clarity / consistency in messaging across dossier.
  • Facilitate and manage the data verification process.
  • Assist with dossier creation and system compliance for regulatory submissions
  • Coordinate response authoring, review and data verification to queries from HA for submissions.
  • Track upcoming submissions and ongoing submission progress
  • Maintain submission content tracker for regulatory submissions and work with doc specialist / PM / Reg CMC to update tracker.
  • Represent Tech Writing and Document management in cross-functional CMC teams as required.
  • Collaborate and coordinate with CMC matrix team leaders to ensure timely submissions.
  • Collaborate with external suppliers as needed for CTD content and review.
  • Support and implement continuous process improvement ideas and initiatives.
  • Train others on procedures, systems access and best practices as appropriate.
  • Mentor and train employees on the document management process
  • Work independently under supervision and collaborate with other teams.

Qualifications :

  • Required Bachelors degree in Biology or related discipline with a minimum of 2 years experience
  • Familiarity and understanding of regulatory requirements and guidance pertaining to CMC documentation is preferred; Cell therapy CMC experience required.
  • Familiarity with eCTD structure for regulatory submissions is required; BLA experience is strongly preferred.
  • Outstanding verbal and writing communication skills, strong attention to detail, planning, organizational and negotiating skills, demonstrated ability for timely delivery.
  • Proficiency in commonly used Microsoft Office applications (Word, Excel, SharePoint, PPT) is required.
  • Experience with computer-assisted document preparation tools is preferred along with proficiency in compliance ready standards for final publication.
  • Experience in biotech / pharma end-to-end product development required. Must be capable of working in a fast-paced changing team environment, prioritizing multiple tasks to meet filing deadlines.
  • Take ownership of the section formatting, language check, connections to other sections / tables.
  • Works independently under supervision and collaborates with other team members from scientific functions, project management, document management in cell therapy.
  • Travel :

    Occasionally to other local NJ sites for larger team meetings (2-3 times a year).

    This posting is for a contract assignment with ASK Staffing DBA ASK Consulting to provide services to Bristol Myer-Squibb.

    The starting hourly compensation for this assignment is the following range ( $41.29 - $44.29 / hr ). While the final, individual compensation and any available benefits will be determined by your employer of record ASK Staffing, Inc (and not BMS), factors that will be included in making the final determination may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location where the job is performed. The starting hourly compensation may be subject to change.

    About ASK Consulting

    ASK Consulting is an award-winning, woman-owned staffing and recruitment solutions provider with over three decades of industry experience. We specialize in connecting businesses of all sizes—across IT, healthcare, engineering, finance, and more—with top-tier professionals. Backed by a global network and personalized service approach, our team is dedicated to building meaningful partnerships that drive organizational success and empower job seekers to excel in their careers.

    ASK Consulting provides comprehensive, ACA-compliant health coverage, along with dental, vision, Short- and Long-Term disability for eligible employees. We also offer commuter benefits, a 401(k) plan with no matching, and a referral bonus program. In addition, ASK Consulting offers unpaid leave and paid sick leave as required by law.

    Equal Opportunity Employer

    ASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws.

    California Applicant Notice

    ASK Consulting is committed to complying with the California Privacy Rights Act (CPRA), effective January 1, 2023, as well as all relevant data privacy laws in the jurisdictions where we recruit and hire. To learn more, please review our Notice to California Job Applicants Regarding the Collection of Personal Information on our website. Applicants with disabilities may request this notice in an alternative format by contacting HR@askconsulting.com.

    If you are selected for a position at ASK Consulting, your offer is contingent upon successfully meeting several requirements, which may include a criminal background check. In accordance with all applicable federal, state, and local “Fair Chance” ordinances and laws—such as the Los Angeles County Fair Chance Ordinance (FCO) and the California Fair Chance Act (FCA)—we consider qualified applicants with arrest or conviction records. The background check will evaluate whether any criminal history could reasonably pose a direct, negative impact on job-related safety, security, trust, regulatory compliance, or overall suitability for the role. Findings that raise concerns may result in withdrawal of a conditional job offer.

    To learn more about how ASK Consulting collects and uses personal information during the recruiting process, please review our Privacy Notice and CCPA Addendum. As part of our recruitment efforts, we may ask you to disclose various categories of personal information, including identifiers, professional details, commercial information, educational background, and other related data. ASK Consulting will use this information solely to facilitate the recruitment process.

    This posting does not constitute an offer of employment. All applicants seeking positions in the United States must be legally authorized to work in the United States. Submitting intentionally false or fraudulent information in response to this posting may disqualify you from consideration. Any eventual offer of employment will be considered “at will,” regardless of the expected assignment duration.

    Seniority level

  • Mid-Senior level
  • Employment type

  • Contract
  • Job function

  • Writing / Editing
  • Industries

  • Pharmaceutical Manufacturing and Biotechnology Research
  • Referrals increase your chances of interviewing at Bristol Myers Squibb by 2x

    Get notified about new Technical Writer jobs in New Brunswick, NJ .

    New Brunswick, NJ $43.00-$45.00 1 week ago

    New Brunswick, NJ $42.00-$44.29 1 week ago

    New Brunswick, NJ $40.00-$45.00 1 week ago

    Technical Writer - CMC Regulatory Submissions (Hybrid, New Brunswick)

    New Brunswick, NJ $72,800.00-$93,600.00 1 week ago

    Technical Writer - Operations Labeling Group

    Lab Instruments Software Validation Analyst / Technical Writers

    Holmdel, NJ $70,000.00-$85,000.00 19 hours ago

    Edison, NJ $59,020.00-$76,128.00 2 weeks ago

    Business Analyst Pipeline Strategy Execution

    Somerset, NJ $107,482.00-$141,070.00 1 week ago

    Product / Business Analyst with Expertise in OKTA & IAM (Identity and Access Management)

    Business Analyst, Cross Study Operations and Specimen Management Product Line, Global Development Operations IT

    Pennington, NJ $110,000.00-$125,000.00 1 month ago

    Morristown, NJ $68,000.00-$80,000.00 1 month ago

    Business Analyst with Pharma Background - Onsite

    We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

    #J-18808-Ljbffr

    serp_jobs.job_alerts.create_a_job

    Technical Writer • New Brunswick, NJ, United States

    Job_description.internal_linking.related_jobs
    Technical Writer Job at Integrated Resources in New Brunswick

    Technical Writer Job at Integrated Resources in New Brunswick

    MediabistroNew Brunswick, NJ, United States
    serp_jobs.job_card.full_time
    Location : New Brunswick, NJ - 50% Remote role.Duration : 12 Months+ (Possibility of Extension).The Technical Writer will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strat...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    Technical writer Job at Capgemini in Raritan

    Technical writer Job at Capgemini in Raritan

    MediabistroRaritan, NJ, United States
    serp_jobs.job_card.full_time
    E / E & Semiconductor Engineer - Technical writer.E / E & Semiconductor Engineer - Technical writer.Develop and document user and functional requirements, test cases, scripts, and validation protocols ...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    • serp_jobs.job_card.new
    Technical Writer Job at Jobs via Dice in New York

    Technical Writer Job at Jobs via Dice in New York

    MediabistroNew York, NY, United States
    serp_jobs.job_card.full_time +1
    We have a 6 month contract opportunity for a Technical Writer.This role is fully remote but must work CST business hours. We are seeking a detail-oriented Technical Writer to collaborate closely wit...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_hours
    • serp_jobs.job_card.new
    Technical Writer Job at Equiliem in New York

    Technical Writer Job at Equiliem in New York

    MediabistroNew York, NY, United States
    serp_jobs.job_card.full_time
    We are seeking a technical writer to assist in our specification transfer project.The applicant must possess excellent technical writing skills and have an understanding of steam or other process p...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_hours
    • serp_jobs.job_card.new
    Scientific Writer Job at NeoGenomics Laboratories in New York

    Scientific Writer Job at NeoGenomics Laboratories in New York

    MediabistroNew York, NY, United States
    serp_jobs.job_card.full_time
    NeoGenomics is looking for Technical Writer who wants to learn to continue to learn in order to allow our company to grow. This is a remote position, with a Monday – Friday day shift.NeoGenomics is ...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_hours
    • serp_jobs.job_card.new
    KBR, Inc. is hiring : Technical Writer in New York

    KBR, Inc. is hiring : Technical Writer in New York

    MediabistroNew York, NY, United States
    serp_jobs.job_card.full_time
    The successful candidate will be part of the KBR team supporting the Test Resource Management Center’s (TRMC) Big Data and Knowledge Management Team working on Big Data systems supporting DoD Test ...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_hours
    NESCO Inc is hiring : Technical Writer in New York

    NESCO Inc is hiring : Technical Writer in New York

    MediabistroNew York, NY, United States
    serp_jobs.job_card.full_time
    Nesco Resource, a national staffing company, has an immediate need for a Technical Writer with a leading energy client.We are seeking for a technical writer to assist in our specification transfer ...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    Technical Writer Job at Integrated Resources in Warren

    Technical Writer Job at Integrated Resources in Warren

    MediabistroWarren, NJ, United States
    serp_jobs.job_card.full_time
    Work Schedule : Mon - Fri, Business Hours.Purpose and product of position : .The Technical Writing Specialist supports the successful implementation of laboratory equipment and systems at multi-use si...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Technical Writer

    Technical Writer

    TradeJobsWorkForce10113 New York, NY, US
    serp_jobs.job_card.full_time
    Research, write, edit and proofread complex technical data.Create, maintain and update manuals, procedures, specifications and other documents. Create, maintain and update installation instructions,...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    • serp_jobs.job_card.promoted
    Technical Writer

    Technical Writer

    EquiLendNew York, NY, US
    serp_jobs.job_card.full_time
    We are a a global financial technology firm serving over 200 of the world's leading financial institutions, including asset owners, broker-dealers, hedge funds, and lending banks.Since launchin...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    ZipRecruiter is hiring : Technical Writer in New York

    ZipRecruiter is hiring : Technical Writer in New York

    MediabistroNew York, NY, United States
    serp_jobs.job_card.full_time
    Job DescriptionJob Description .Building Services 32BJ Benefit Funds.Funds”) is the umbrella organization responsible for administering Health, Pension, Retirement Savings, Training, and Legal Serv...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    • serp_jobs.job_card.new
    Tech Writer Job at Largeton Group in New York

    Tech Writer Job at Largeton Group in New York

    MediabistroNew York, NY, United States
    serp_jobs.job_card.full_time
    Technical Writer (SaaS) - Contract (25-30 hours per week).Location : EST Time Zone, Virtual, United States.Ensure all materials are accurate, current, and comply with agency standards and accessibil...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_hours
    • serp_jobs.job_card.promoted
    Technical Writer

    Technical Writer

    Building Service 32BJ Benefit FundsNew York, NY, US
    serp_jobs.job_card.full_time
    Building Services 32BJ Benefit Funds.Funds”) is the umbrella organization responsible for administering Health, Pension, Retirement Savings, Training, and Legal Services benefits to over 100,...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    Technical Writer Job at Eclaro in New Brunswick

    Technical Writer Job at Eclaro in New Brunswick

    MediabistroNew Brunswick, NJ, United States
    serp_jobs.job_card.full_time
    Be part of a company that delivers life-changing healthcare solutions.ECLARO's client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that mak...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    Technical Writer Job at Stellar Services in New York

    Technical Writer Job at Stellar Services in New York

    MediabistroNew York, NY, United States
    serp_jobs.job_card.full_time
    Salary Depends on Experience : $50,000 - $100,000.Primary role would be to assist the Board Agenda group.Review and edit procurement documents for the Board Directors. Prepare brief synopses of procu...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    Technical Writer Job at Macpower Digital Assets Edge in Jersey City

    Technical Writer Job at Macpower Digital Assets Edge in Jersey City

    MediabistroJersey City, NJ, United States
    serp_jobs.job_card.temporary
    The ideal candidate will be responsible creating, editing and maintain high-quality documentation that communicates complex technical information clearly and concisely to a variety of audiences.Thi...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    Technical Writer Job at TalentBurst, an Inc 5000 company in Branchburg

    Technical Writer Job at TalentBurst, an Inc 5000 company in Branchburg

    MediabistroBranchburg, NJ, United States
    serp_jobs.job_card.temporary
    Title : Technical Writer Med / Clin I.Duration : 12 months contract (High Chances of Extension).As a Technical Writer in the Operations Labeling Group, you will be responsible for creating, revising, a...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Technical Writer

    Technical Writer

    AmigoNew York, NY, US
    serp_jobs.job_card.full_time
    Amigo builds trust and safety infrastructure for AI in mission-critical environments.We partner with organizations in healthcare and other regulated sectors to deploy AI systems that operate reliab...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days