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
- ...Quality Assurance (QA) Associate job at Strides. East Brunswick, NJ. Job Description Primary responsibilities of this role include the following... ...matters for disposition of product returns. Assist during FDA inspections and local regulatory inspections at Strides’ US corporate...SuggestedContract workWork at officeLocal area
- ...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...Suggested
$52k - $70k
...sample inspections and control finished product and raw material retain samples stored in the reserve sample room. • Monitor GMP areas for compliance with general GMP requirements such as proper gowning and cleanliness, per CFR21 Subpart A General Provisions to assure...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
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- ...combines the agility of a specialist CDMO with the deep... ...manufacturing, reviewing GMP documentation, and making... ...activities to ensure compliance with applicable quality... ...industry. 3-5 years of QA experience in a GMP-regulated... ..., and relevant ICH and FDA guidance....Contract workFlexible hoursShift workAfternoon shift
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$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- ...TreeHouse Foods is looking for an Associate Quality Specialist at their Princeton, KY facility. The role involves supporting food safety and quality compliance initiatives and contributing to audits and documentation efforts. Ideal candidates should have a Bachelor’s degree...Full time
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- ...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
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- ...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...Contract workFlexible hoursShift workNight shiftAfternoon shift
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- A leading fruit juice supplier based in New Jersey is looking for a detail-oriented Quality Group team member. This on-site role involves tracking customer technical requests, maintaining documentation, and supporting quality verification activities. Ideal candidates will...Work at office
- Scorpion Therapeutics is looking for a Specialist, Quality Document Control to manage documentation within the ZenQMS electronic quality... ...various functional groups. Ideal candidates should possess an Associate’s Degree in a science-related field and 3-5 years of quality...Work at office
$56k - $68k
...A biotechnology company is seeking a Specialist in Quality Document Control in Cranbury Township, NJ. This role involves managing documentation... ...accurate document handling. Applicants should have an Associate's degree and at least three years of experience in document management...$56k - $68k
...Rocket Pharma is seeking a Specialist, Quality Document Control in Cranbury Township, NJ. This role involves managing documentation within... ...paper-based records. Candidates should have a science-related Associates Degree and a minimum of three years in document control. The...- Wayfair in Cranbury Township seeks an IC Warehouse Associate to ensure inventory integrity and product quality within the fulfillment network. This full-time role requires meticulous attention to detail and the ability to operate material handling equipment safely. Responsibilities...Full time
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...Iron Mountain Incorporated is looking for a meticulous Digitizing Records Specialist to join their Global Digital Solutions team in Freehold, New Jersey. This role involves the end-to-end conversion of physical assets into digital records, managing high-capacity scanning...$65k - $75k
...seeking a professional dedicated to food safety and quality assurance. This role involves supporting daily operations, maintaining compliance with regulations, and implementing HACCP and SOPs. Candidates should have a Bachelor's degree in food science or related fields,...$70.35k - $87.94k
...Analytics below.Quality Product Safety Specialist page is loaded## Quality Product Safety... ...(onsite). Be part of a detail-oriented, compliance-driven, collaborative team where together... ...initiatives* Maintain accurate records for FDA and regulatory compliance* Interact...For contractors
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