Senior QA Specialist - Batch Release & Investigations
NeilMed Pharmaceuticals, Inc.
NeilMed Pharmaceuticals is seeking a hands-on Sr. QA Specialist for its South Plainfield location. The role involves managing batch review, investigations, and maintaining quality systems in a high-volume pharmaceutical environment. The ideal candidate should hold a Bachelor’s degree in a scientific discipline and possess 5–7+ years of QA experience in manufacturing. Key responsibilities include reviewing documentation, leading investigations, and ensuring compliance with regulatory standards. #J-18808-Ljbffr NeilMed Pharmaceuticals
- ...biopharmaceutical company in New Jersey is seeking a Quality Assurance Specialist to support cGMP quality operations. The role focuses on... ...regulatory standards through the review of controlled documents, batch records, and deviations. Candidates should have a degree in...SuggestedRemote work
- ...Pharmaceuticals) is searching for a hands‑on Sr. QA Specialist to support a high‑volume... ...capable of independently managing batch review, investigations, and quality systems with minimal training... .... RESPONSIBILITIES Batch Release & Operational QA Review executed batch...SeniorImmediate start
- ...are manufactured, tested and released according to established Client... ...and disposition executed batch records pertaining to the preparation... ...partners. Participates in investigations related to the areas of... ...and optimize or achieve the QA Department and Company goals....SuggestedContract workDay shift
- ...Quality Assurance Specialist will provide Quality... ...Reviews and QA Shop Floor manufacturing... ...and CMO product release. This position may... ...oversight for CMO Batch Production Records... ...quality problems to Senior Management in a... ...for Industry for Investigating OOS Results, Deviations...Suggested
- The Quality Assurance Specialist II is a full‑time exempt position at Kashiv... ...documentation supporting batch, laboratory, warehouse, metrology... .../quality monitoring and release of controlled systems and environments... ...experience with manufacturing QA support; document control and...SuggestedFull timeFlexible hours
- ...experienced Quality Assurance Specialist to join our team. In... ...JRS standards. The QA Specialist ensures... ...Instructions, Forms, Batch Records, Labeling Specs... ...documentation. Lead or support investigations for: temperature... ...to: clinical supply release; temperature‑...Worldwide
- ...standards Perform analysis coding unit testing and documentation for batch programs online transactions and interfaces running on the... ...corrections and validation support Participate in code reviews design reviews release planning and operational readiness activitiesSenior
$106.2k - $167.2k
MSD Malaysia seeks a Senior Specialist in Quality Assurance to oversee GMP activities and ensure compliance with quality standards. The role requires a Bachelor's degree in a related field and a minimum of five years of experience in the pharmaceutical industry. Strong...Senior- ...The Quality Assurance Specialist position plays a key role... ..., completed batch records, material disposition... ...role directly supports release of vector timeline... ...primary focus of the QA Specialist role will be... ...initiation of deviation investigations. • Review deviations,...
- 1 00% onsite Job Title: CTO QA Label Specialist Shift: This position is scheduled for Wed- Sat... ...control, product complaints, deviations, investigations and CAPA management. Performs... ...Manufacturing Operations, related to batch documentation to support the various Manufacturing...Shift work
- An established industry player is seeking an Associate Specialist for Quality Product Release-Disposition. This role is crucial for maintaining compliance... ...candidate will manage quality records, support batch record processing, and ensure efficient documentation practices...
$70k - $103.5k
Plymouth Rock Assurance in Port Reading, NJ, seeks a skilled insurance fraud investigator to join their team. The ideal candidate will have over 5 years of experience focusing on Personal Injury Protection (PIP) claims, conducting investigations into complex fraud cases...Senior- ...Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control... ...document change requests, troubleshooting and releasing documents to an effective state. • May... ...Reports to Jenna Walker - Associate Director, QA Training & Document Control Education:...
- Kashiv BioSciences LLC is seeking a full‑time Quality Assurance Specialist II in Piscataway, N.J. This role supports the Quality Assurance team with managing the quality system to ensure compliance with cGMP requirements and company policies. Key responsibilities include...Full time
- ...more exclusive features. Job Title :QA Label Specialist Location : Summit, NJ Hours/Schedule... ...control, product complaints, deviations, investigations and CAPA management. Performs... ...a 401(k) plan. Ref: #568-Clinical Seniority level Seniority level Entry level Employment...Contract workAfternoon shift
$85k - $130k
...ESIS ProClaim is seeking an experienced Senior Claims Representative. Reporting to the... ...is responsible for reviewing coverage, investigating third-party claims, securing evidence, assessing... ...professionals have secured appropriate releases, proofs of loss, or compensation...SeniorLocal area$100k - $120k
A global certification leader is seeking an experienced auditor to conduct third-party certification audits for AS9100/AS9120 standards. The ideal candidate will have a Bachelor's degree in Engineering and at least 4-5 years of experience in the aerospace industry. Responsibilities...SeniorRemote work$85k - $105k
...execution, calculate and report results. Actively participate in investigation of laboratory results. Review laboratory analysis data for... ...techniques, such as spectrophotometric, dissolution and drug release, chromatographic techniques and measuring physical parameters...SeniorTemporary workLocal areaFlexible hours- 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...
- ...Review laboratory instrument calibration/qualification records, standard qualification records and records associated with investigations Review Raw-material, Excipients, Finished Product for data integrity, compliance with Specifications, Methods and USP monographs...Senior
- ...stakeholders and design the implementation of new features. Investigate cyber security controls of processors and microcontrollers and... ...with CICD teams to add new capabilities to the build and release pipeline and customize pipeline for new projects. Collaborate...Long term contract
$120k - $140k
ANS, a civil engineering firm in New Jersey, is seeking a Senior Geotechnical Engineer. This role requires a Bachelor's degree in Civil... ...experience. Responsibilities include conducting geotechnical investigations, preparing technical reports, and collaborating with a high-...Senior- ...the purpose of generating early clinical development plans and Investigational New Drug applications* Developing clinical development... ...external opportunities* Must have experience in industry or as senior faculty in academia* Minimum of 3 years clinical medicine experience...SeniorLocal area
$87 - $88 per hour
...Senior Application Developer New York, New York, United States $ 87.00 - 88.00 (US Dollar) About the Job Senior Application Developer... .../reverse engineering reports built using SSRS Active Batch Familiarity with scheduling jobs on Active Batch Ability to...SeniorWork at office- ...I have an opportunity for "Senior Data Architect" _ (Piscataway, NJ - Hybrid )" and I am looking for a candidate who can join Immediately... .... • Experience in architecting & implementing Data pipelines (Batch and real-time) on Cloud. • Experience in Data Modeling for...SeniorImmediate start
- ...spectrophotometers, and Karl Fischer titrators. Responsibilities include documentation of methods and results, participation in investigations, and assisting with project work. Ideal for candidates with strong analytical skills and attention to detail. #J-18808-Ljbffr...Senior
- Hanover Insurance Company in Plainfield, NJ, is seeking a Senior Field Property Adjuster to manage complex field property claims. This role requires advanced investigation, negotiation skills, and collaboration with various stakeholders. The ideal candidate will have 5-...SeniorRemote jobFull timeWork at office
- ...services provided by suppliers Serves as the site single point of QA contact for BMS Direct and Indirect material suppliers.... ...to ensure proper and timely resolution of deviations, complaint investigations and CAPAs, ensuring proper documentation per BMS procedures. Supplier...SeniorWork at officeLocal areaWorldwideMonday to Friday2 days per week
- ...Quality Assurance Specialist Ready to proactively identify problems with products and goods? In manufacturing and industrial environments, that's what quality assurance specialists and technicians do best. If you have what it takes to report and verify defects, troubleshoot...Immediate start
$135k - $160k
...Role summary: The Senior HR Business Partner (Sr. HRBP) is a strategic advisor, trusted partner, and member of the Novatae Executive... ...equitable outcomes. Employee relations: Lead complex investigations and high-risk performance/behavior matters in partnership with...Senior
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