✦ Luna Orbit — Engineering (Non-Software)

Quality Technical Specialist

at Avantor

📍 Remote, US Remote 💰 $62K – $100K USD / year Posted April 15, 2026
Salary $62K – $100K USD / year
Type Not Specified
Experience mid
Exp. Years Minimum of three (3) years of combined experience
Education BS/BA Degree in Biology, Biotechnology, Bio Engineering, Chemistry, Chemical Engineering, or related field required
Category Engineering (Non-Software)

This role supports quality assurance operations by ensuring compliance with standards and regulations and helping resolve quality issues through testing and process improvements. The specialist also manages customer Quality Agreements and prepares/maintains quality documentation to support audits and corrective actions.

  • Ensure compliance with standards and regulations
  • Support testing and process improvements for quality outcomes
  • Manage customer Quality Agreements with the legal team
  • Respond to customer technical and quality inquiries by phone and email
  • Develop and maintain quality documentation and update product/customer databases

You will operate in a pharmaceutical/chemical quality context, applying cGMP, FDA, ICH, and WHO requirements to support testing, audits, and corrective actions. The work includes technical inquiry response, researching product specifications and monographs, and maintaining quality documentation and customer quality agreement records using Microsoft Office and databases.

The ideal candidate has a BS/BA in a life science or chemical engineering field and 3+ years of combined experience in technical services, engineering, quality, or sales within a chemical or pharmaceutical environment. They understand cGMP, FDA, ICH, and WHO requirements and can support audits, corrective actions, testing, and the development/maintenance of quality documentation and customer Quality Agreements.

BS/BA Degree in BiologyBiotechnologyBio EngineeringChemistryChemical Engineeringor related fieldMinimum of three (3) years of combined experience in technical servicesengineeringquality or sales in chemical or pharmaceutical environmentSynthetic pharmaceutical & biopharmaceutical drug development and manufacturingUnderstanding of industry regulations (cGMPFDAICHand WHO)Quality and validationQuality and process engineering in a chemical or pharmaceutical environmentExcellent knowledge of Microsoft Office Suite
Hands-on experience in a laboratory or manufacturing environmentProject management experienceExperience in at least one of the following areas is highly desired
Microsoft Office Suitedatabases
Quality assurance operationscompliance with standards and regulationstestingprocess improvementsauditscorrective actionsMicrosoft Office SuitecGMPFDAICHWHOquality and validationquality documentationproduct databasescustomer databasesQuality Agreementslean principles
Microsoft Office Suitetechnical servicesengineeringquality assurance operationstestingprocess improvementsaudits and corrective actionscompliance with standards and regulationscGMPFDAICHWHOsynthetic pharmaceutical drug development and manufacturingbiopharmaceutical drug development and manufacturingquality and validationquality and process engineeringquality documentationproduct documentationproduct databasescustomer databasesQuality Agreements managementcustomer Quality Agreementslean principles reviewlaboratory environment experiencemanufacturing environment experienceproject management experience
collaborationcommunicationresearch and compiling informationresponding to technical inquiriescross-functional collaborationmanaging processes and documentationcustomer-facing partnershipcontinuous improvement mindsetproject execution
Industry Manufacturing
Job Function Provide technical quality support and manage compliance documentation and customer quality agreements for pharmaceutical and laboratory product offerings
Role Subtype Quality Engineer
Quality Technical SpecialistBS/BA DegreeBiologyBiotechnologyBio EngineeringChemistryChemical EngineeringcGMPFDAICHWHOquality and validationquality assurancetestingprocess improvementsauditscorrective actionsMicrosoft Office SuitedatabasesSynthetic pharmaceuticalbiopharmaceuticaldrug development and manufacturingQuality Agreementsquality documentationcustomer Quality Agreementslean principleslaboratory environmentmanufacturing environmentproject management

BS/BA Degree in Biology, Biotechnology, Bio Engineering, Chemistry, Chemical Engineering, or related field, Minimum of three (3) years of combined experience in technical services, engineering, quality or sales in chemical or pharmaceutical environment, Demonstrated knowledge of cGMP, FDA, ICH, and WHO

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