QA Associate Specialist GMP & FDA Compliance
$65.99k - $90.74kShiseido
Shiseido is seeking a Quality Assurance Associate Specialist in East Windsor Township, NJ. This role focuses on ensuring FDA compliance, reviewing GMP documentation, and releasing Finished Goods. The ideal candidate has a bachelor's degree in Engineering or Science and at least two years of quality assurance experience in the pharmaceutical sector. You will prepare the CARESS ACT list, conduct quality training, and manage batch records. A salary range of $65,992 to $90,739 per year is offered. #J-18808-Ljbffr
$92.04k - $147.26k
...we are In it for life. Guarantees cGMP compliance in all activities and systems related to... ...requires 3-5 years of relevant experience in a QA GMP environment within the Pharmaceutical... ...shared upon offer. Quality Assurance Specialist Compensation Range: $92,040 to $147,264...SuggestedContract workTemporary workWorldwide$81.04k
...Specialist I, QA QMS for Tris Pharma, Inc to work at our Monmouth Junction... ...Manufacturing Practices (cGMP), FDA standards + batch record... ...documentation, maintenance + tracking, compliance, + operations. May assist in... ...and 2 years of relevant GMP experience in the...Suggested$92.04k - $147.26k
...An independent pharmaceutical company in East Windsor Township seeks a Quality Assurance Specialist to manage quality activities and ensure compliance with cGMP standards. The successful candidate will possess a university qualification in a scientific field, 3-5 years...Suggested- ...supervision, the Quality Assurance Specialist III will ensure systems and processes are in a state of compliance with regard to internal,... ...training records, and other ISO/GMP-related items, as needed to... ...understanding of laboratory regulations (FDA, ISO, GLP, GMP). Experience...SuggestedFull timeContract workFor subcontractorMonday to Friday
- ...Summary: The Shipping/Receiving Pharma QA Specialist ensures compliance with regulatory requirements and... ...maintain Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP)... ...compliance with regulatory requirements (FDA, DEA, etc.). · Manage...Suggested
- ...and process changes/deviations before product release to ensure compliance with defined specifications. Address and resolve any... ...or chemical industries Knowledge of ISO 9001 and HACCP and GMP standards Proficiency in Microsoft Office and quality systems...Permanent employmentFull timeContract workWork at officeShift workDay shift
- ...documents. Provide guidance and training to other QA staff in quality assurance activities.... ...-5 years of QA/validation experience in an FDA-regulated industry. • Familiarity with... ...manufacturing processes and thorough understanding of GMP. • Strong technical writing skills and the...
$80k - $100k
...The Quality Systems Specialist supports the execution and... ...control, formatting and compliance review of records, and... ...System (eQMS). Support QA, production, warehouse,... ...environment. Experience of GMP document control... ...or working conditions associated with the job. It is intended...Contract workWork at officeWork from homeFlexible hours$72k
...and invoices. The role assists QA product managers with responsibilities... ...line with Acrotech SOPs. The Specialist will also help ensure that... ...responses. Review status updates to FDA. Perform additional duties as... ...Three years of experience in a GMP environment such as a...Temporary workFor contractorsWork at officeFlexible hours- ...Quality Assurance Specialist Monroe Township, New Jersey... ...- Support daily QA operations related to document... ..., and deviations in compliance with internal procedures... ...Quality Systems within a GMP or ISO 13485regulated... ...Knowledge of ISO 13485, FDA QSR, and GMP...Work at office
$63k - $93k
...hiring a Quality Assurance Documentation Specialist- Supplier Quality in our Cranbury, NJ location... .... They have a solid working knowledge of FDA regulations, FSMA, and GFSI standards,... ..., and Abilities Familiar with GFSI or NSF QA Standards and Auditing systems FSMA requirements...Work at officeLocal areaRemote work- ...Inprocess Quality Assurance Associate I Location: US-NJ-East Windsor High School Diploma or Equivalency. Up to 2 years of experience... .... Must be a team player able to effectively communicate with QA Supervisor, IPQA, Quality Control, Production, and Supply Chain...
- ...chemical industries. · Knowledge of ISO 9001 and HACCP and GMP standards. Tip 3 Skills: · Proficiency in... ...and process changes/deviations before product release to ensure compliance with defined specifications. Address and resolve any concerns or...Work at officeShift workDay shift
$94k - $151.8k
...of Companies, is recruiting for a Sr. Specialist, External Quality (Synthetics)! This position... ...that meet or exceed safety, regulatory compliance, and product standards. Key... ...inspections and audits; monitor and follow-up on associated responses and commitments. Provide...Local areaImmediate start- ...motivated Submarine Systems Quality Assurance Specialist to join our team in Philadelphia, PA.... ...Quality Evidence (OQE) to verify compliance with contract, drawing, and performance... ...navigation, or electromagnetic systems and associated equipment. EDUCATION: ~ Bachelor...Contract work
- ...Support Drug Product Complaint management; forwarding to respective drug product manufacturing site and coordinate with corporate QA for investigations. Support Drug Product recall/field alert management. Assist with review of Quality Agreements For applicable...Contract workWork at office
- Overview It’s a mix of relationship-building, problem-solving, and attention to detail—way more than just a typical sales role! It’s about understanding. It’s a mix of relationship-building, problem-solving, and attention to detail—way more than just a typical sales role...
- ...Made Scientific is seeking a QC Specialist II in Princeton, NJ, to support in-process and release testing for Cell Therapy products. This role requires a Master’s Degree and at least 2 years of GMP experience in microbiology and analytical methods. Key responsibilities...
- ...Scientific combines the agility of a specialist CDMO with the deep technical... ...translation and subsequent GMP Operations to be successful.... ...operations and inventory, ensuring compliance with company policies and... ...activities. Familiarity with FDA, EMEA, ICH, USP, GMP guidelines...Contract workFlexible hoursShift workDay shiftAfternoon shift
- ...Quality Control Specialist Monroe Township, New Jersey, United States About the Job Quality... ...Control or Quality Assurance within a GMP-regulated manufacturing environment. -... ...Working knowledge of ISO 13485, GMP, and FDA quality regulations is a plus. - Strong attention...Work at office
- .... We are rapidly expanding, and have an opportunity for a QA Specialist/Copyeditor to join our team in Princeton, New Jersey. THE... ...things in creating learning/training resources in scientific, compliance, and regulatory areas. BENEFITS Retirement Plan...
$57.4k - $99k
...Provides guidance and education to coding associates and leaders on established coding... ...Immediately provides reports related to compliance risks when requested .... ...Professional Coder) CCS-P (Certified Coding Specialist-Phys Based) CCS (Certified Coding Specialist...Temporary workWork at officeImmediate startRemote work$77.9k - $104.37k
...succeeds. Responsibilities: Conduct quarterly file audits for all lines of business against business process flows to determine compliance with regulatory standards according to NCQA, URAC and CMS. Analyze, prepare, and distribute quarterly audit outcomes including error...Full timeWork experience placementLive inLocal areaRemote work
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