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QA/QC Specialist III

Integrated Resources, Inc

Cambridge, Massachusetts

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JOB DETAILS
JOB TYPE
Contractor
SKILLS
Asepsis, Biology, Biotech and Pharmaceutical, CMOS, Change Control, Chemistry, Clinical Data, Clinical Research, Clinical Support, Communication Skills, Contract Manufacturing, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Drug Products, Establish Priorities, External Audit, Information Technology & Information Systems, Interpersonal Skills, Manufacturing, Manufacturing Operations, Medical Equipment, Medical Products, Multitasking, Operational Support, Presentation/Verbal Skills, Product Development, Product Lifecycle, Quality Assurance, Quality Control, Quality Management, Regulations, Rehabilitation Nursing, Research & Development (R&D), Small Molecules, Standard Operating Procedures (SOP), Supply Chain Operations, Time Management, Validation Plan, Writing Skills
LOCATION
Cambridge, Massachusetts
POSTED
3 days ago
QA/QC Specialist IIIA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionJob SummaryThe individual will work in the External Quality Assurance Department. This unit oversees contract manufacturing (3rd party manufacturing) operations, supply chain operations and supplier quality functions. This position supports the execution of quality systems including the external audit program. This position is responsible for successful, timely completion of goals and objectives that strengthen the Quality organization.Responsibilities• Support of Clinical Operations including Drug Substance, Bulk Drug Product Manufacture, Clinical Packaging & Labeling and oversight of Clinical CMOs and Distributers• Reviewing QC data and COA approval.• Review and approval of clinical data for stability and applicable data for CMC submissions.• Liaison with Regulatory as needed to ensure business/regulatory timelines are met.• Provide QA guidance/review/approval for Product Development projects in Phase 1 to Phase 3.• Oversee appropriate Quality Systems appropriate for Clinical Phase Materials.• QA Contact for applicable Quality Systems related to R&D.• Review and approved: Master Batch Records, executed batch records, deviations, CAPA and change controls.• May lead investigations and nonconformance reviews.• Reviewing and approving specifications, SOPs, validation protocols/reports, investigations, CAPAs, and change controls.Education and Qualification:• Bachelor's degree in chemistry, biology or a related disciplineMinimum 5 years Quality Assurance experience supporting the manufacture of drugs, biologics, or devices.• Experience in applying phase appropriate cGMP's to Clinical Product Life Cycle.• Understanding of quality systems, cGMPS and Regulatory Agency guidance as applicable to drugs or biologics.• Excellent interpersonal and professional skills with the ability to communicate well orally and in writing.• Strong Quality Assurance knowledge, previous experience in QC a plus.• Must be able to prioritize and multitask in a dynamic environment.• Quality experience in parenteral biotech manufacturing (aseptic or sterile processing)• Experience working with contract manufacturers.• Experience with Quality Control.• Experience with packaging and labeling operations.• Experience with TrackWise.• Experience with Medical Device, Small Molecules and other pharmaceutical technologiesQualificationsMinimum 5 years Quality Assurance experience supporting the manufacture of drugs, biologics, or devices.• Experience in applying phase appropriate cGMP's to Clinical Product Life Cycle.• Understanding of quality systems, cGMPS and Regulatory Agency guidance as applicable to drugs or biologics.• Excellent interpersonal and professional skills with the ability to communicate well orally and in writing.• Strong Quality Assurance knowledge, previous experience in QC a plus.• Must be able to prioritize and multitask in a dynamic environment.• Quality experience in parenteral biotech manufacturing (aseptic or sterile processing)• Experience working with contract manufacturers.• Experience with Quality Control.• Experience with packaging and labeling operations.• Experience with TrackWise.• Experience with Medical Device, Small Molecules and other pharmaceutical technologiesAdditional InformationFeel free to forward my email to your friends/colleagues who might be availableWarm Regards,Jay KaushikClinical RecruiterIntegrated Resources, Inc

About the Company

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Integrated Resources, Inc