QA Documentation Specialist
Kashiv BioSciences LLC
Description 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. This is an exciting opportunity to work closely with Management on all aspects of Quality related to our pharmaceutical manufacturing site. Will work as a member of the Quality team to ensure GMP documents & quality standards. 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 Requirements 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. This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization. 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 is seeking a Documentation Specialist to join our Quality Management team in Piscataway, NJ. This role involves ensuring compliance with GMP standards and maintaining various quality documents. The ideal candidate will have a BS or MS in a scientific...Suggested
- A pharmaceutical company in Newtown, PA is looking for a Senior QA Associate to enhance quality systems and compliance. The role requires 5-8 years of QA experience, with a Bachelor's degree in a scientific field and expertise in deviation management. Responsibilities...SuggestedFull time
$36.06 - $40.87 per hour
...Assists with the development of various documentation products in support of assigned program/project system. Collaborates with appropriate team members to develop required documentation materials (end-user manuals, technical documents, graphics, etc.). Ensures all developed...SuggestedContract workWork at office- divh2Job Title/h2pCapital Health is seeking a dedicated professional for a position that plays a crucial role in the efficient operation of our healthcare services./ph3Position Overview/h3pThe role involves retrieving and filing information, ensuring prompt and efficient...SuggestedTemporary workWork at officeImmediate start
- ...looking for a motivated Submarine Systems Quality Assurance Specialist to join our team in Philadelphia, PA . Founded in... ...style inspections) of manufactured equipment and components, documenting findings and reporting results to NAVY. Conduct on-site evaluations...SuggestedContract work
$60.97k - $103.64k
...Associate QA/QC Inspector Description Associate QA/QC Inspector Location: Newark, NJ - candidates must be located or willing to relocate to New Jersey to be considered Ready to make a difference? To support our growth, we are currently seeking an Associate Quality Assurance...Full timeContract workFor contractorsWork experience placementFor subcontractorLocal areaRemote workRelocationFlexible hours- Senior QA Associate KVK Tech is seeking a Senior QA Associate to join our team in Newtown, PA. The Senior QA Associate will serve... ...deviations, investigations, CAPAs, change controls, complaints, document control, and quality event trending. This role acts as a cross‑functional...Full timeFlexible hours
- A leading testing solutions provider located in Horsham, Pennsylvania, is searching for a Quality Assurance Specialist. This role focuses on ensuring compliance with regulations and quality systems, performing audits, and supporting quality improvement initiatives. Candidates...
- ...Job Description Job Description QA Batch Record Reviewer About KVK Tech KVK Tech is a U.S.-based generic and specialty... ...is responsible for ensuring that manufacturing and packaging documentation is complete, accurate, and compliant with cGMP standards, FDA data...Hourly payWork at officeDay shiftAfternoon shift
- ...KVK Tech, Inc. is looking for a 2nd Shift QA Batch Record Reviewer in Newtown, PA. This role involves reviewing packaging batch records to ensure accuracy and compliance with cGMP standards and internal quality protocols. The ideal candidate will have strong attention...Afternoon shift
- ...KVK Tech is seeking a 2nd Shift QA Batch Record Reviewer to join our team in Newtown, PA. The QA Batch Record Reviewer is responsible for reviewing executed packaging batch documentation to ensure accuracy, completeness, and compliance with cGMP requirements and internal...Work at officeFlexible hoursAfternoon shift
$23.47 - $38.62 per hour
Role Overview USPS is actively accepting applications for Mail Handler Assistants nationwide. This position is open to candidates of all experience levels, with comprehensive training provided to help you succeed. Join a dynamic work environment where you will interact...Hourly payFlexible hours- ...to our values - honesty, integrity, and accountability. *Hybrid Position* Provides administrative and operational support for document processing, records management, return mail handling, and data maintenance activities while ensuring accuracy, compliance, and...Work at officeLocal area
- Job Title Gentell is one of the largest vertically integrated wound care companies in the world. Based in Yardley, PA and with offices, distribution centers and manufacturing plants around the world, our purpose is to make a positive difference in the quality of life...Work at office
$15 - $18.32 per hour
Datavant is looking for an entry-level team member in Trenton, NJ to process medical record requests efficiently while ensuring patient confidentiality. You will manage health records and interact with customers while adhering to strict HIPAA regulations. The ideal candidate...Hourly pay$23.47 - $38.62 per hour
Role Overview USPS is accepting applications for PSE Mail Processing Clerks nationwide. This role is vital to ensuring the timely and accurate processing of mail. USPS provides comprehensive training to help you succeed, even if you have no prior experience. Position...Hourly pay- ...Quality Assurance Specialist If you're passionate about quality, compliance, and clinical... ...field. Master's degree and prior QA, data, or KPI experience preferred Minimum... ...(MHPA) Experience with clinical documentation review, audits, or quality improvement processes...Daily paidFull timeWork at officeFlexible hoursShift workNight shiftWeekend workWeekday work
- ...The Quality Assurance (QA) Specialist is responsible for analyzing the efficiency and effectiveness of individual case analysts. Key Responsibilities: The Quality Assurance (QA) Specialist is responsible for analyzing the efficiency and effectiveness of individual...Contract work
$95.5k - $149.2k
...reduction. We are seeking a Submarine Systems Quality Assurance Specialist to support multiple U.S. Navy submarine classes, ensuring... ...style inspections) of manufactured equipment and components, documenting findings and reporting results to NAVY. Conduct on-site...Full timeContract workPart timeLocal areaRemote work$52k - $70k
Job Posting Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients' lives through the manufacturing and distribution of high-quality pharmaceutical products. With a diverse portfolio of generic and branded pharmaceuticals, ANI ...- ...products from concept to patient. The Senior Associate, QA Operations is responsible for providing quality oversight of... ...presence on the manufacturing floor and review/approval of GMP documentation. This role ensures that manufacturing operations comply with cGMP...Local area
- ...takes care of your products from concept to patient. The Associate II, Quality Operations provides day-to-day QA oversight and documentation review to support GMP manufacturing of intermediates and drug substances. The role ensures production activities are executed...Local area
$39.13k
...Mail & Document Processor, Associate page is loaded## Mail & Document Processor, Associatelocations: NJM - Trentontime type: Full timeposted on: Posted Todayjob requisition id: R2007913The Document Processor, Associate is responsible for, but not limited to, handling...Full timeWork at office- ...Job Summary : The Proofreader/QA Specialist role is responsible for ensuring all marketing and brand materials, across print and digital, are accurate, polished, and error-free before release. You will serve as the final checkpoint in the creative process, helping maintain...Temporary workCasual workWork at office
- ...com. Job Description: We are seeking a Quality Assurance Specialist who will play an important role in ensuring compliance with... ...include: Maintain accurate quality records and documentation within QA systems. Perform internal audits to assess compliance with...Work experience placementMonday to Friday
$23.47 - $38.62 per hour
Role Overview USPS is accepting applications for Assistant Rural Carriers nationwide. In this role, you deliver and collect packages along designated suburban and rural routes, often using your personal vehicle. The position primarily involves working on weekends and...Hourly payWeekend work- Wolters Kluwer N.V. is seeking a Fulfillment Associate in Ewing, NJ. This entry-level position involves accurately processing and shipping customer orders. The ideal candidate will have 2+ years’ experience and strong attention to detail. The role includes opportunities...
$43.89k - $102.08k
Hispanic Alliance for Career Enhancement seeks a dedicated professional to provide consulting services to Plan Sponsors, focusing on accurate completion of plan contracts and certificates. Applicants should have over five years of relevant work experience and a high school...Work experience placement$55k - $62k
...gap between finance, legal, leasing, and property management to keep our operations moving smoothly. From managing critical leasing documents and updating marketing collateral to overseeing daily office operations and team scheduling, your efforts will directly impact our...Permanent employmentTemporary workWork experience placementWork at officeShift work- Unit Secretary With a commitment to patient- and family-centered care, performs a variety of clerical duties, including data entry into Hospital Information System to support the operations of the unit. They assist in overall unit flow including supporting patients ...Full timeImmediate startAfternoon shift
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to QA Documentation Specialist. Be the first to apply!



