QA Specialist I: GMP Quality & Batch Release
PCI Pharma Services
PCI Pharma Services seeks a QA Specialist in Madison, Wisconsin, to ensure product quality and compliance with internal and external standards. The role focuses on batch documentation review, managing deviations, and driving quality system improvements. Ideal candidates will have a Bachelor's Degree in a relevant scientific field, 3-5 years of experience in the pharmaceutical industry, and strong knowledge of FDA regulations. This position offers a vital opportunity to contribute to life-changing therapies within a collaborative team environment. #J-18808-Ljbffr PCI Pharma Services
- Arrowhead Pharmaceuticals is looking for a Senior Specialist in Quality Assurance to support ongoing development programs for drug candidates. This... ...involves developing and maintaining quality systems within GMP regulations, reviewing documentation, and collaborating with...Quality
- ...recruitment firm in the pharmaceutical sector is seeking a QA Specialist in Madison, WI. This full-time, mid-senior level role... ...in a cGMP setting. The position involves providing quality assurance support, reviewing batch records, and ensuring proper documentation of...QualityFull time
$26 - $46 per hour
...Quality Assurance Senior Associate Work Your Magic with us!... ...: The Quality Assurance (QA) Senior Associate position at... ...team and will perform data and batch review and release and document control... ...support batch release. Ensure GMP documentation are completed...QualityHourly payImmediate startFlexible hours- Actalent is seeking a Quality Assurance Specialist for the 3rd shift in Madison, WI. This role involves providing quality oversight, performing production audits, and ensuring compliance with GMP and FDA standards. The ideal candidate will have 2+ years of quality assurance...QualityNight shift
- A leading non-profit stem cell services institute in Madison is seeking a Quality Assurance (QA) Specialist. This full-time, onsite role requires a minimum of 5 years' experience in GMP quality assurance. Responsibilities include managing quality events, conducting investigations...QualityFull time
$85k - $95k
...Responsibilities include : The On‑Site QA Specialist will be introduced to the on‑... ...the event. Reviews executed batch records. Perform inspection... .../or CAPAs. Performs shipping release procedures. Assists in the... ...type Full‑time Job function Quality Assurance and Manufacturing...QualityFull time- ...analytical and detail-oriented Quality Assurance (QA) Specialist to join our collaborative... ...and monitoring, batch record review, and supporting... ...qualification documents, etc.) Product release: Release of WiCell Stem... ...: A minimum of 5 years in GMP quality assurance or compliance...QualityFull timeVisa sponsorshipWork visa
- A leading pharmaceutical company located in Madison, Wisconsin, seeks a QA Specialist responsible for ensuring product quality and regulatory compliance. The role involves batch documentation review, CAPA administration, and quality system enhancements. Ideal candidates...Quality
- ...leading pharmaceutical services provider in Madison, WI is seeking a QA Specialist I to ensure product quality and compliance with internal procedures and external standards. The role involves batch record review, deviation evaluation, and quality oversight. Candidates...Quality
$62k - $90k
Job Title: Quality Assurance Specialist - 3rd Shift Job Description The Quality Assurance... ...Manufacturing Practice (GMP) and regulatory standards.... ...and CAPAs. Review executed batch records, cleaning records, and... ...and collaborate with QA and operations to drive continuous...QualityPermanent employmentFull timeTemporary workWork at officeFlexible hoursNight shift$62k - $72k
...Description Job Description Job Title: Quality Assurance Specialist Job Description The Quality... ...critical documentation, such as executed batch records, cleaning records, and... ...and mini audits to confirm adherence to GMP, FDA, ISO, and internal quality requirements...QualityPermanent employmentFull timeTemporary workWork at officeMonday to FridayFlexible hoursShift workNight shiftRotating shiftDay shift- ...together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're... ...lead deviation and CAPA activities, and oversee the review and release of final products. In this role, you will have the opportunity...QualityWorldwide
$70k - $85k
...of this position is to provide quality assurance support to programs utilizing... ...but not limited to, executed batch records, testing records,... ...verification/approval. Assist with QA duties as needed. Requirements... .... Working knowledge of GMP, GCP, and/or GLP regulations as...QualityFull timeContract workWork at office- ...Senior Associate I - Quality Assurance Operations Position... ...for execution of the QA on the Floor program.... ...for production, including Batch Production Records,... ...substance. Performs release of produced solutions and... ...equipment records in support of GMP operations....QualityLocal area
- PCI TRGR Penn Pharmaceutical Services Ltd is looking for a Quality Specialist I in Madison, WI. This position involves monitoring sterile manufacturing practices, ensuring compliance with aseptic techniques, and documenting significant activities. Candidates should have...Quality
- A leading biopharma services provider located in Madison, Wisconsin, seeks a Quality Specialist I - Aseptic Core Monitor to ensure compliance with aseptic operations and regulatory expectations. This role involves real-time oversight during sterile manufacturing processes...Quality
- Senior Associate I - Quality Assurance Operations (2nd shift... ...Execute the QA on the Floor program. Perform... ...for production, including Batch Production Records, Product... ...solutions and columns. Release produced solutions and... ...records to support GMP operations. Control and...QualityAfternoon shift
- Senior Associate I - Quality Assurance Operations (2nd shift... ...for execution of the QA on the Floor program.... ...for production, including Batch Production Records, Product... ...substance. Performs release of produced solutions and... ...records in support of GMP operations. Accountable...QualityAfternoon shift
- A global pharmaceutical manufacturer in Madison, WI seeks a Specialist I in Quality Assurance to ensure compliance with FDA regulations and internal quality systems. The successful candidate will manage supplier quality programs, conduct audits, and provide training. Applicants...Quality
- Cardinal Health is looking for a Sr. Specialist in Sales Performance Operations Quality Assurance to manage coding of USMPD accounts. This role partners with sales leaders and works with offshore teams, generating reports while ensuring the accuracy of territory coding...QualityRemote job
- Cardinal Health in Madison, Wisconsin is seeking a Senior Specialist in Quality Assurance to oversee quality programs and ensure compliance with regulatory standards. The role involves executing policies, supporting audits, and mentoring junior specialists. The ideal candidate...Quality
- ...our global network to pioneer and shape the future of PCI. The Quality Specialist I - Aseptic Core Monitor (ACM) at PCI Pharma Services is a... ...electronic quality systems (preferred). Prior experience in a QA or manufacturing oversight role at PCI or a similar aseptic operation...QualityWork at office
- ...located in Madison, WI, is seeking a Supervisor for Quality Assurance Internal Operations. The role involves leading QA teams in ensuring compliance with cGMP standards,... ...a BS in a scientific discipline and 5+ years of GMP experience. Opportunities for leadership and...Quality
- Catalent Pharma Solutions in Madison, Wisconsin, is seeking a Senior Associate I - Quality Assurance Operations (2nd shift) with a focus on executing quality assurance processes and supporting manufacturing operations. This role requires a Master's, Bachelor's, Associate...QualityAfternoon shift
$90k - $110k
...position within the Quality Assurance... ...Manufacturing Practices (GMP) within the organization. The Senior Specialist is expected to interact... ..., including master batch records, executed... ...records. Perform QA on the floor and manufacturing room release. Review and release...QualityShift workAfternoon shift- ...Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Fluctuating Temps hot/... ...Fisher's commitment to delivering high-quality biopharmaceutical therapies. Join us and... ...responses. * Drive timely resolution of QA audit findings, deviations, CAPAs, and effectiveness...QualityTemporary workWork at officeShift work
- Catalent in Madison, Wisconsin is looking for a Senior Associate I in Quality Assurance Operations (2nd shift) to ensure quality in manufacturing processes and documentation. This role requires a degree in a STEM discipline, with varying experience levels accepted. The...QualityAfternoon shift
- ## Quality Assurance AssociateApplylocations: New Lisbon, WItime type: Full timeposted on: Posted 8 Days Agojob requisition id: JR101910**Be Part of Something Bigger at Mill Haven Foods**At Mill Haven Foods, we don’t just make products—we help fuel performance, health,...QualityContract workLocal areaMonday to Friday
- The CMDO QA Supervisor is responsible for developing, implementing and maintaining the Quality System to support the integrity and compliance... ...process development, engineering batch production, clinical trials,... ...Responsibilities include Release raw materials, products (...Quality
- Position Overview The Quality Control Supervisor assists in the development... ...management with respect to GMP’s, allergens, food safety,... ...Performs pre-shipment reviews and release of finished product. Provides... ...experience. Experience in QA/QC or laboratory in a food...QualityHourly payDaily paidContract workFlexible hours
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