Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

QA Documentation Specialist

Kashiv BioSciences LLC

VISA SPONSORSHIP NOT AVAILABLE

Kashiv BioSciences is a fully integrated biosciences company with an expanded and dynamic platform for growth including advanced drug delivery technologies, biosimilars, prodrugs, and a large development pipeline. We are looking for a Documentation Specialist to join our Piscataway NJ Quality Management team. Job Type: Full-time Essential Responsibilities Perform Issuance, Archival and maintain of all GMP documents like SOP, Batch Record, Forms. Maintain OOS, Deviation, CCF, CAPA log Review Cross Functional departments SOP Perform batch related sampling Assist in batch record review To train cross functional team on GDP and cGMP To perform additional work assigned by supervisor as and when required Education BS or MS in a scientific discipline or equivalent and a minimum 3 years of related experience. Expert knowledge of scientific principles and concepts. Special Skills Ability to read and interpret all quality documents. Ability to understand GMP requirements. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Effective verbal and written communication and reporting writing skills Work Environment & Physical Demands General work environment and physical demands as required to successfully perform the essential functions of this job. Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines. Some travel may be involved. Kashiv BioSciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Kashiv BioSciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, and transfer, leaves of absence, compensation and training. #J-18808-Ljbffr Kashiv BioSciences LLC

Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the QA Documentation Specialist in Piscataway, NJ vacancy
  •  ...including advanced drug delivery technologies, biosimilars, prodrugs, and a large development pipeline. We are looking for a Documentation Specialist to join our Piscataway NJ Quality Management team. This is an exciting opportunity to work closely with Management on... 
    Suggested
    Local area
    Flexible hours

    Kashiv BioSciences LLC

    Piscataway, NJ
    21 hours ago
  • Kashiv BioSciences LLC is looking for a full-time Documentation Specialist to join its Quality Management team in Piscataway Township, NJ. The role involves managing GMP documents, including SOPs and batch records, as well as ensuring compliance with quality standards.... 
    Suggested
    Full time

    Kashiv BioSciences LLC

    Piscataway, NJ
    1 day ago
  • $70.67k - $92.76k

    QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating life‑threatening diseases. Headquartered in Somerset, New Jersey, we develop advanced cell therapies across multiple technology platforms. Role Overview The... 
    Suggested
    Work experience placement
    Flexible hours

    BioSpace

    Raritan, NJ
    2 days ago
  • A leading biotechnology firm in Raritan, New Jersey, is seeking a QA Document Control Specialist to support the document management process within its manufacturing facility. The ideal candidate will have a Bachelor's degree in a related field and at least 2 years of experience... 
    Suggested

    BioSpace

    Raritan, NJ
    3 days ago
  • SSUSA Job #1118: DOCUMENTATION SPECIALIST Job Description Documentation Specialist Job Summary We are seeking an enthusiastic and detail-oriented Documentation Specialist to develop, manage, and maintain our client’s internal and client-facing documentation. The employee... 
    Suggested
    Work at office

    Canon Solutions America

    Edison, NJ
    2 days ago
  • $38 - $41.8 per hour

    Documentation Analyst will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). This individual will be responsible for delivering CMC documentation (dossier and supporting documents... 
    Hourly pay
    Contract work
    Temporary work
    Work at office
    Local area

    Bristol Myers Squibb

    Piscataway, NJ
    2 days ago
  • A leading document solutions provider in Edison, New Jersey is seeking a Documentation Specialist to develop and manage internal and client-facing documentation. The ideal candidate will have a Bachelor's degree in a relevant field and strong proficiency in Microsoft Office... 
    Work at office

    Canon Solutions America

    Edison, NJ
    2 days ago
  • Join a forward-thinking company as a Quality Assurance Specialist, where you will oversee critical quality processes in a dynamic environment. This role involves managing CMO oversight, ensuring compliance with GMP standards, and preparing for regulatory audits. You will... 

    TechDigital Group

    New Brunswick, NJ
    21 hours ago
  • Summary The Quality Assurance Specialist II is a regular employee in a full-time exempt position...  ...involves reviewing and assembling batch documentation, issuing and tracking controlled...  ...completion. Direct experience in manufacturing QA support (sampling, room/line clearance,... 
    Full time
    Work at office
    Flexible hours

    Kashiv Biosciences LLC

    Piscataway, NJ
    12 hours ago
  • The Quality Assurance Specialist will provide Quality oversight to the CMO with the ability to...  ...site up to support Quality Reviews and QA Shop Floor manufacturing support. You will...  ...Records. Reviews executed Batch Records, GMP documents and prepares documentation for product... 

    TechDigital Group

    New Brunswick, NJ
    2 days ago
  • NeilMed Pharmaceuticals is seeking a hands-on Sr. QA Specialist for its South Plainfield location. The role involves managing batch review...  ...in manufacturing. Key responsibilities include reviewing documentation, leading investigations, and ensuring compliance with... 

    NeilMed Pharmaceuticals

    South Plainfield, NJ
    3 days ago
  • Kashiv BioSciences LLC in Piscataway Township, NJ is looking for a Quality Assurance Specialist responsible for ensuring compliance with cGMP regulations and quality event documentation. The role requires 0-5 years of experience in a pharmaceutical manufacturing... 
    Work at office

    Kashiv BioSciences LLC

    Piscataway, NJ
    1 day ago
  • A leading clinical trial supply organization is seeking an experienced Quality Assurance Specialist. In this role, you will oversee the quality and compliance of clinical trial materials, ensuring adherence to FDA and internal standards. You will conduct inspections, manage... 

    JUPITER RESEARCH SERVICES INC

    Edison, NJ
    4 days ago
  • Kashiv Biosciences LLC in Piscataway Township, New Jersey is seeking a Quality Assurance Specialist. This role involves inspecting, sampling, and testing incoming materials, ensuring compliance with cGMP regulations, and providing quality assurance oversight. The ideal... 
    Work at office

    Kashiv Biosciences LLC

    Piscataway, NJ
    21 hours ago
  •  ...seeking an experienced Quality Assurance Specialist to join our team. In this role, you will...  ..., and internal JRS standards. The QA Specialist ensures that all products and...  ...Review, approve, and maintain controlled documents including SOPs, Work Instructions, Forms... 
    Worldwide

    JUPITER RESEARCH SERVICES INC

    Edison, NJ
    6 days ago
  • $26 - $28 per hour

     ...The Fountain Group is a national staffing firm and we are currently seeking a Documentation Coordinator II for a prominent client of ours. This position is in Branchburg, NJ 08876. Details for the position are as follows: Job Description: ~$26 - $28/hour... 
    Work experience placement
    Work at office
    Monday to Friday

    The Fountain Group

    Somerville, NJ
    21 hours ago
  •  ...Document Controller New Brunswick, NJ, United States About the Job The Company develops, manufactures, and markets in-vitro diagnostics (IVD) tests. Responsibilities Develop and implement production processes related to document control and management... 
    Relocation package

    ISEE Careers

    New Brunswick, NJ
    2 days ago
  •  ...Job Description: Contractor: Document Controls Specialist Reporting to the Document Controls Manager, this position has overall responsibility to support all procedures, processes and systems of the administered plan for controlled documents and information management... 
    For contractors

    Crossfire Consulting

    South Plainfield, NJ
    21 hours ago
  •  ...Document Control Specialist Reporting to the Document Controls Manager, this position has overall responsibility to support all processes and...  ...as a backup to Documents Manager when needed Work with QA procedures to test and evaluate the system Help to develop... 
    For contractors
    Work at office

    PSG Global Solutions

    South Plainfield, NJ
    1 day ago
  •  ...QA Shop Floor Specialist II Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening...  ...forward for manufacturing quality issues. Review of all documentation, in accordance with Good Documentation Practices (GDP).... 
    Work experience placement
    Immediate start
    Worldwide
    Flexible hours
    Weekend work
    Day shift

    Legend Biotech

    Raritan, NJ
    1 day ago
  •  ...Documentation Specialist II Provide administrative support to multiple managers within the Contract Development department by submitting requests/entering key information into multiple applications and files, independently manage and maintain trackers, manage mail... 
    Contract work
    Work at office

    HireTalent

    Bridgewater, NJ
    4 days ago
  •  ...insurance, life insurance,short term and long term disability, and the Bank's 401k Plan. Position Summary: TheSenior Loan Documentation Specialist consistently provides exceptional outputwhen reviewing and generating in-house loan documents. Loan documents must... 
    Temporary work
    Immediate start

    FirstBank

    North Brunswick, NJ
    5 hours ago
  • Kashiv Biosciences LLC is seeking a Quality Assurance Specialist II in Piscataway, NJ. This full-time role involves supporting Quality Assurance management in reviewing and managing the quality system, ensuring compliance with cGMP requirements, and conducting quality... 
    Full time

    Kashiv Biosciences LLC

    Piscataway, NJ
    21 hours ago
  • A biotechnology company in New Jersey seeks a QA Change Control Specialist II responsible for quality oversight in a cell therapy manufacturing facility. Applicants should possess a Bachelor's degree in Science and a minimum of two years' experience within a cGMP environment... 

    Legend Biotech

    Raritan, NJ
    21 hours ago
  • $81.27k - $106.67k

     ...immunotherapy in the treatment of multiple myeloma. Position QA Change Control Specialist II - Quality team, Raritan, NJ Role Overview The QA...  ...requirements. Review change controls, SOPs, and other documentation. Require minimal direction to complete tasks and... 
    Permanent employment
    Contract work
    Temporary work
    Work experience placement
    Work at office
    Local area
    Worldwide
    Flexible hours
    Shift work

    Legend Biotech

    Raritan, NJ
    21 hours ago
  • $69.5k - $102.35k

    Johnson & Johnson, QA Specialist II (1 of 2) - Application via WayUp Join to apply for the Johnson & Johnson, QA Specialist II (1 of 2...  ...a cGMP manufacturing facility. Perform review of production documentation and provide guidance to resolve quality related manufacturing... 
    Contract work
    Temporary work
    Part time
    Local area
    Immediate start
    Afternoon shift

    WayUp

    Raritan, NJ
    21 hours ago
  • $75.97k - $99.71k

     ...multiple myeloma. Role Overview Legend Biotech is seeking a QA Shop Floor Specialist II/III as part of the Quality Operations team based in...  ...forward for manufacturing quality issues. Review of all documentation, in accordance with Good Documentation Practices (GDP).... 
    Work experience placement
    Immediate start
    Worldwide
    Flexible hours
    Weekend work

    Legend Biotech

    Raritan, NJ
    2 days ago
  • A healthcare service provider in East Brunswick Township is seeking a Quality Assurance Specialist to ensure compliance with Division of Developmental Disabilities standards. The role involves developing monitoring programs, conducting audits, and facilitating training... 

    APluscare Behavioral Health

    East Brunswick, NJ
    3 days ago
  • $65k - $104.65k

     ...Johnson is currently seeking three Quality Assurance Incoming Specialist II. This position will be located in Raritan, NJ! At Johnson...  ...record results to complete receipt process Review inspection documentation (C of A or other Material Certifications) for inbound... 
    Local area
    Immediate start
    Shift work
    Day shift

    Johnson & Johnson Innovative Medicine

    Raritan, NJ
    21 hours ago
  • Unipac (NeilMed Pharmaceuticals) is searching for a hands‑on Sr. QA Specialist to support a high‑volume pharmaceutical manufacturing...  ...make sound, risk‑based decisions and produce clear, defensible documentation. QUALIFICATIONS Bachelor’s degree in a scientific... 
    Immediate start

    NeilMed Pharmaceuticals

    South Plainfield, NJ
    3 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to QA Documentation Specialist. Be the first to apply!