QA Training Specialist: GMP Training & Compliance Lead
RoslinCT
RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization. The QA Training Specialist role supports maintenance and ongoing management of the Training Program within the Quality Management System, on-site in Hopkinton, MA. You will implement and maintain the Learning Management System, review training content, administer users, and collaborate with cross-functional teams to ensure training compliance and continuous improvement. #J-18808-Ljbffr RoslinCT
- RoslinCT US is seeking an on-site QA Training Specialist to support the training program within the Quality Management System. You will... ...while collaborating with cross-functional teams to ensure compliance with GMP and QMS standards. Ideal candidates have 3-5 years of...SuggestedWork at office
- Replimune Group, Inc. in Massachusetts is seeking a Quality Assurance professional to support GMP compliance, batch release, and QA operations across departments. You will partner with Regulatory, Clinical, and Manufacturing to ensure readiness for inspections, maintain...Suggested
- ...Framingham, MA seeks a Principal Associate I/II, Quality Assurance to support GMP compliance and product disposition for BDS, DP, and FDP across internal and external facilities. You will collaborate with QA, QC, Regulatory, and Clinical teams, manage batch release,...Suggested
- ...WE ARE RoslinCT is a world-leading cell and gene therapy contract... ...YOUR FUTURE The QA Training Specialist is a position responsible for... ...performance indicators and compliance trends, and operational needs... ...refresher training such as GMP training, eQMS workflows training...SuggestedContract workWork at officeFlexible hours
- Replimune, headquartered in Massachusetts, seeks a Quality Assurance professional to support GMP compliance and QA operations. The role interacts with multiple departments to enhance quality processes in a GMP environment and improve readiness for inspections. You will...Suggested
- ...RoslinCT is seeking a QA Specialist I – Plant Operations to provide QA support for manufacturing operations and ensure compliance with cGMP/ICH. The role focuses on batch record creation and approval, documentation control, and improving QA processes to support product...
$38 - $40 per hour
...RoleWe are seeking a Supplier Quality Specialist to support supplier quality and compliance activities within a regulated... ...supplier performance management within a GMP-regulated environment.... ...QualificationsExperience participating in or leading supplier, internal, or external...Contract workTemporary work- RoslinCT in Hopkinton, MA is seeking a Quality Assurance Specialist - Supplier Quality to join a world-leading cell and gene therapy CDMO. You will oversee... ...change management, audits, and corrective actions in compliance with FDA regulations. The role requires a BS in...
- ...Quality Assurance Specialist Boston BioProducts is seeking... ...(QMS) and ensure compliance with applicable quality... ...regulatory requirements. The QA Specialist is... ...action within the scope of training. Preferably strong knowledge... ...ISO 13485, ISO 9001and GMP Have strong written...Work at officeLocal area
- ...RoslinCT is a world-leading cell and gene therapy... ...The Quality Assurance Specialist – Supplier Quality supports... ...Quality Management in compliance with FDA regulations... ...education, experience and training. Experience in cell... ...and guidance, GMP and GLP regulations....Contract workWork at officeFlexible hours
- ...RoslinCT is a world-leading cell and gene therapy... ...FUTURE The Senior QA Specialist – Plant Operations is... ...review and approval of GMP documentation including... ...testing records to ensure compliance with approved... ...implementations. · Develop training materials and deliver...Contract workWork at officeFlexible hours
- ...We at RoslinCT, are a world-leading cell and gene therapy contract... ...ACCELERATING YOUR FUTURE The QA Specialist I– Plant Operations is... ...documentation Review and approval of GMP documentation such as, EM... ...QA specific procedures for compliance and identify opportunities...Contract workFlexible hours
- ...GDP, and regulatory standards. You will collaborate with Manufacturing, Quality Control, and cross-functional teams to review records, guide on GMP requirements, and ensure compliant manufacturing activities are performed to high standards. #J-18808-Ljbffr Replimune-2
- ...Description Support of Commercial QA Compliance: Deviation Review and Trending, CAPA Review and Trending, Extension request review and trending; Support of data analysis and metrics for QMR, KPIs, and other reportable forums; Skills/Behaviors Proficiency with Microsoft...
$38 - $40 per hour
...Supplier Quality Specialist Location: Westborough, MA Schedule... ...support supplier quality and compliance activities within a regulated... ...management within a GMP-regulated environment. Responsibilities... ...participating in or leading supplier, internal, or external...Contract workTemporary workMonday to Friday$38 - $40 per hour
...Maintain supplier quality and compliance documentation, including... ...Skills vendor management, Gmp, Quality assurance, supplier... ...equivalent combination of education, training, and professional experience.... ...participating in or leading internal, external, or supplier...Contract workTemporary work- SCIEX, a Danaher operating company, seeks a Service Trainer to develop and deliver LC/MS training programs for the global field service workforce in Marlborough, MA. You will enable engineers in end-to-end workflows—from sample prep to data reporting—and improve troubleshooting...
- ...Substance, Drug Product, and QC testing to maintain cGMP and GDP compliance. This position requires collaboration across departments and on-... ...in Framingham. The ideal candidate has 5-7+ years in pharma QA/manufacturing, with strong communication and documentation skills...Afternoon shift
- RoslinCT in Hopkinton, MA, is seeking a Quality Assurance Specialist - Supplier Quality to strengthen our supplier ecosystem in a fast-... ...with Supply Chain, Purchasing, and Manufacturing to ensure cGMP compliance. The ideal candidate has a biology/engineering background, 3+...
- RoslinCT is seeking a QA Specialist I - Plant Operations to provide QA support across manufacturing operations, including batch review and lot disposition, with Cell and Gene Therapy experience preferred. The role requires 2-5 years in QA within pharma/biotech manufacturing...
- ...Quality Assurance to provide day-to-day quality oversight for Drug Substance, Drug Product, and Quality Control operations, ensuring compliance with cGMP and GDP. The role partners with Manufacturing, QC, and other teams to review batch records, deviations, and change...
- ...Job Description We're seeking a Training Coordinator to drive our employee development efforts and foster a culture of continuous learning... ...People & Skills, Process & Systems, and Culture. You'll lead initiatives ranging from onboarding and cross-training to leadership...Work at office
$55k - $60k
...Overview Salary: $55,000-60,000 The Training Specialist II facilitates trainings in core certifications and other areas of professional development; schedules and maintains a catalogue of trainings and facilitators and works in collaboration with the training and...Full timeWork at officeMonday to Friday$55k - $60k
...Advocates in Westborough, MA is seeking a Training Specialist II to deliver trainings, coordinate the training calendar, and maintain the Learning Management System to support a robust employee development program. This in-person role requires a Bachelor's Degree, 1–2...- ...Job Description Job Description We’re seeking a Training Coordinator to drive our employee development efforts and foster a culture of continuous... ...across People & Skills, Process & Systems, and Culture. You’ll lead initiatives ranging from onboarding and cross-training to...Work at officeWorldwideFlexible hours
$24 - $29 per hour
...seeking an entry-level Quality Assurance Specialist to support quality operations within a... ...product release support, and maintaining compliance with internal procedures and quality standards... ...in Quality Assurance within a GMP/cGMP environment. Qualifications Associate...Contract workMonday to Friday$38 - $40 per hour
...We are seeking a detail-oriented Supplier Quality Specialist to support supplier qualification, compliance, and quality management activities within a regulated... ...control processes. ~ Prior experience working within GMP, GxP, FDA-regulated, pharmaceutical, biotechnology,...Contract workTemporary work$22 per hour
A leading organic market located in Natick, Massachusetts, is seeking Produce Managers in Training to join their team. The ideal candidates will have a passion for team development, a strong focus on customer experience, and the ability to train others. This role offers...Hourly pay- ..., information and training, we’ll help you in... ...Quality Assurance Specialist, you will support... ...clinical trials. Assess compliance with study... ...improvement of Clinical QA processes, audit... ...Practice (GMP) and Good Documentation... ...-GCP or Certified Lead Internal Auditor....Hourly payLocal areaRelocationShift work3 days per week
$57.5k - $75k
...everything possible. Supplier Quality Operations Specialist is responsible for maintaining global... ...on-site role. What You Will Do Manage compliance of supplier qualification documentation... ...and regulations (i.e. ISO, CFR, GMP, etc.) Data analytics and report development...Hourly payNight shift
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