We are currently hiring for an onsite QA Associate (IT) position based in Hauppauge, NY . This is a full-time, salaried opportunity within a regulated pharmaceutical manufacturing environment.
Role Details
The QA Associate (IT) will be responsible for reviewing Batch Production Records (BPRs) and associated documentation to ensure full compliance with GMP , regulatory requirements, and internal quality systems. This role plays a critical part in maintaining documentation accuracy, audit readiness, and overall product quality.
Key ResponsibilitiesReview Batch Production Records (BPRs), manufacturing instructions, protocols, and equipment logs for completeness and GMP compliance
Verify documentation accuracy, signatures, dates, and resolution of discrepancies prior to approval
Review, create, and revise BPRs, SOPs, and manufacturing-related documentation
Support internal and external regulatory audits (FDA, GMP inspections)
Review engineering and facility records (temperature/humidity data, calibration, preventive maintenance)
Conduct daily quality rounds on the shop floor to ensure GMP compliance
Escalate quality issues and discrepancies to QA management
Ensure assigned training completion and adherence to cGMP, SOPs, and safety requirements
Bachelor's degree in pharmacy, Life Sciences, Chemistry, or a related field
2 3 years of experience in pharmaceutical Quality Assurance , specifically Batch Record Review
Strong knowledge of GMP , FDA and EMA regulatory requirements
Experience with Electronic Document Management Systems (EDMS) (e.g., Master Control)
Audit and inspection readiness experience
Excellent attention to detail, documentation accuracy, and organizational skills
Pharmaceutical or regulated life sciences background is mandatory
US Citizen or Green Card Holder required
This position is onsite only (no remote or hybrid option)
Local candidates preferred
If this opportunity aligns with your background and career goals, please share your updated resume along with your availability to discuss further.
#QAJobs #PharmaJobs #QualityAssurance #GMP #cGMP #BatchRecordReview #BPR #PharmaceuticalManufacturing #FDACompliance #EMA #RegulatedIndustry #LifeSciencesJobs #OnsiteJobs #HauppaugeNY #MasterControl #EDMS #AuditReadiness #QualitySystems #USCitizensOnly #LocalCandidates
...Job Description Jackson Nurse Professionals is seeking a LPN / LVN for a travel job in Augusta, Georgia. Job Description & Requirements ~ Specialty: LPN / LVN ~ Discipline: LPN / LVN ~ Start Date: 01/05/2026~ Duration: 13 weeks ~40 hours per week...
...mentality where innovative and agile problem solving are part of our DNA along with competitive compensation and benefits The Security Manager partners and collaborates with Field Asset Protection and Field Operations management teams with physical security and safety...
...experiences that enrich their lives. Joining SAS Retail Services, an Advantage Solutions... ...this role, you will provide in-store merchandising support to Retailers to meet shoppers... ...maximize sales opportunities. This is a traveling position that requires regular travel...
...technical skills to systems development. Position requires 6+ years of programming and related experience as outlined above. Mainframe application skills and experience are required. Skills and tools include (but not limited to): COBOL, IMS, DB2, MFS, DLT0,...
...DWI/DUI) in past 5 years. Must be able to work at least 40 hours per week throughout the Summer Internship Program. Must have a minimum of three months experience in sales, customer service, management, or leadership. Must be authorized to work in the United States...