Senior QA Specialist, Biotech GMP & Vendor Documentation
Arrowhead Pharmaceuticals, Inc.
A biopharmaceutical company in Verona, Wisconsin is seeking a Quality Assurance professional to provide support for development and clinical programs. The ideal candidate will have at least 5 years of experience in a GMP-regulated environment and hold a BS/BA in a scientific field. Responsibilities include reviewing vendor documentation, collaborating with internal departments, and ensuring compliance with quality standards. Excellent communication skills are essential as you will work closely with multiple organizations to maintain quality assurance in the clinical pipeline. #J-18808-Ljbffr Arrowhead Pharmaceuticals, Inc.
- ...onsite role based at our GMP Lab in Middleton,... ...Quality and Compliance Specialist ensures that facilities... ...planned, executed, and documented in a state of control and... ...including resolution of QA audit findings, inspection... ...interact with outside vendors and internal...SuggestedContract workWork at officeRelocationRelocation package
- ...shape the future of PCI.The QA Specialist will work with other departments... ...:Perform review of batch documentation for release of internal and... ...support of batch release and GMP compliance Provide direction... ...years of pharmaceutical or biotech industry experience.2+ years...SuggestedFull timeFlexible hours
$25 - $39 per hour
...4th shift Scientist, Quality Associate Senior position is responsible for cGMP analytical... ...4+ years of experience in a GMP manufacturing or testing laboratory Understanding... ...and verbal communication skills and good documentation practices and attention to detail...SeniorHourly payLocal areaImmediate startShift work- Senior Engineer - Engineering, EquipmentPosition SummaryShift: Monday... ...service to pharma, biotech, and consumer health customers... ...continuous improvement in a GMP biologics manufacturing environment... ...stakeholdersAuthor and review technical documentation (batch records, protocols,...SeniorFull timeContract workLocal areaMonday to Friday
$86.7k - $173.3k
...Position OverviewThe Lead Clinical Lab QA Specialist is responsible for the development, implementation... ...best practice advocacy.Investigate, document, and resolve complex quality assurance... ...teams, enterprise teams, and 3rd party vendors.Utilize project management experience...SuggestedWork experience placementWork at officeShift work- ...or an alternative application process. QA Specialist FullTime Franksville, WI, US Quality Assurance... ...-quality products, accurate technical documentation, and exceptional service. You'll have... ...improvement. Develop and deliver GMP, GDP, Food Safety, and job-specific training...Full timeContract workWork at officeWorldwide
- ...organizations. The incumbent will review vendor documentation and perform lot disposition per... ...vendors and external organizations as the QA team representative. Other duties consistent... ...biochemistry Working knowledge of drug GMP regulations, as well as ICH/FDA guidance...SeniorContract workWork at office
- ...products. Review labels for accuracy and compliance. Assist with Document Management. Audit Records. Maintains a safety conscious... ...team management environment. Ability to negotiate with outside vendors. Experience with personal computers (spreadsheet, Word, E-mail)...
$23 per hour
...regulatory standards by reviewing batch documentation, maintaining quality records, supporting... ...quality records.Maintain Quality Assurance (QA) documentation and support Quality... ...documentation.Ensure compliance with applicable GMP, FDA, ISO, and internal quality...Contract workTemporary workWork at officeMonday to FridayDay shift- ...oriented Quality Assurance (QA) Specialist to join our... ...of validated systems Document control: Utilizing the... ...minimum of 5 years in GMP quality assurance or compliance... ...the pharmaceutical or biotech industries Education:... ...visa. Job details Seniority level: Mid-Senior level...Full timeVisa sponsorshipWork visa
- ...heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated... ...Creating and reviewing submission documents and eCRTs Communicating with and/or responding... ...trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or...SeniorRemote workFlexible hours
$99.3k - $198.7k
...not limited to, the following:Receive and document incoming customer communications.Work... ...Qualifications7+ years of experience in a Biotech/Medical Device field working in a regulated... ...environment, e.g., CAP, CLIA, ISO 13485, FDA GMP, or USDA.7+ years of experience working...SeniorWork at officeNight shift- ...as review and approve relevant documents. You will perform quality oversight of all validation for GMP including equipment, facility... ...lakes, parks, cultural richness, biotech leadership, and access to... ....Collaborate with clients and vendors to meet project and company objectives...
$75.2k - $112.8k
...range. The Supplier Quality Specialist works in the Supplier Quality... ...with raw material suppliers and vendors and is therefore expected to... ..., supplier development and document management. This position is... ...organizational skills. Understands GMP, HACCP, HARPC, FSMA, FSVP,...Remote workFlexible hours$125k - $140k
...to patients in need. The Position This Senior Scientist will be part of a team responsible... ...internally developed assays to external vendors.Effectively collaborate in a highly... ...a manager or mentor.Author and oversee documentation through all stages in GCLP-regulated clinical...Senior- ...provide accurate and effective analysis. Elicit, analyze, and document clear business requirements and translate them into functional... ...working closely with developers, project managers, and external vendors (limited). Demonstrated ability to quickly grasp business processes...Senior
$70k - $90k
...Our client is seeking to add a Senior Casualty Claims Adjuster to their team. This individual... ...with internal stakeholders, outside vendors, insurance partners, and legal counsel.... ..., and claim exposure while gathering documentation necessary to support claim decisions. Evaluate...SeniorWork at office- ...Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting,... ...etc.) Job Description Position: Senior Scientist Location: Middleton,... ...communication skills, particularly for technical documentation and scientific discussion. ~...SeniorRemote jobFull timeWork at officeRelocationRelocation package
$130k - $150k
...seeking a highly motivated and experienced Senior Scientist on Analytical Chemistry to lead... ..., investigations, and technical documents generated by external partners.Monitor project... ...analytical activities comply with applicable GMP, ICH, FDA, EMA, and other regulatory...SeniorContract work- Senior Scientist - Downstream Process Development, mRNAPosition Summary:Work Schedule:... ...suitability for intended use (development vs GMP release) preferred Ability to support... ...working in a cGMP environment Good documentation practices (GDP) Aseptic technique experience...SeniorFull timeLocal area
- ...refrigeration, cooking, and dishwashing specialists found in world’s most luxurious homes.... ...resources, Application Management Services vendors and business stakeholders to support... ...our ecosystemDevelop and maintain documentation related to SAP system administration best...SeniorFull time
$116k - $194k
...growing and seeking to hire an experienced Senior ERP Engineer to join our talented... ...to Workday.Creates and review technical documentation for new and existing processes, policies... ...and testing ERP integrations to external vendors or other parties.Detail oriented team player...SeniorFull timeRemote work- ...Location-Verona, WI Direct Hire A Senior Mechanical Design Engineer responsible... ...systems and creating detailed documentation using Autodesk Inventor. You will be involved... ...management. You'll collaborate with customers, vendors, and internal teams to deliver custom...SeniorWork at office
$78k - $156k
...than 160 countries.Position OverviewThe Senior Application Analyst- SAP Development will... ...challenges.Create and maintain system documentation.Lead the estimation of enhancement or support... ...systems stakeholders and software vendor’s implementation staff to ensure alignment...SeniorWork at officeLocal areaRelocation packageNight shift$78k - $156k
...than 160 countries.Position OverviewThe Senior Application Analyst will work on software... ...challenges.Create and maintain system documentation.Lead the estimation of enhancement or support... ...systems stakeholders and software vendor’s implementation staff to ensure alignment...SeniorWork at officeLocal areaRelocation packageNight shift- ...Senior Technical LeadWe are seeking an uncommon professional to join our team as a Senior... ...existing solutions (across publicly available, vendor packages, etc.) where appropriate.... ...support work.20% 3. Develop, test, implement, document and maintain high quality business...SeniorWork experience placement
- Senior Associate I - Quality Assurance Operations Position Summary:... ...implementation and maintenance, documentation management, site-wide systems... ...for execution of the QA on the Floor program.Performs... ...equipment records in support of GMP operations.Accountable for control...SeniorFull timeLocal area
$78k - $156k
...160 countries.Position OverviewThe SAP Senior Application Analyst will work on business... ...current challenges.Create and maintain system documentation.Lead the estimation of enhancement or... ...systems stakeholders and software vendor’s implementation staff to ensure alignment...SeniorWork experience placementWork at officeLocal areaRelocation packageNight shift$63.6k - $95.5k
...work in the US. Your Role The Operations Specialist, Quality Control position supports... ...technical reports, user requirements, and other documentation using the principles of ALCOA+.... ...Other duties as assigned. Adhere to the GMP requirements defined within 21 CFR parts...Work at officeShift work- ...Job Title: Senior Director Operations Location: Madison, WI (Onsite)... ...locations across North America listed in the documents. Job Summary : • The Senior... ...excellent business relationships with outside vendors and service providers, as well as...SeniorFull timeRelocation
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