{"id":2108061,"url":"https://alion.io/job/qrcgroup-tstm-scientist","title":"TS/TM Scientist","company":{"id":4444,"name":"QRC Group","domain":"qrcgroup.com","url":"https://alion.io/company/qrcgroup","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SmartRecruiters","truth_index":null},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":"contractor","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Juncos, Puerto Rico"],"countries":["PR"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":74000,"max_usd":164000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":1203},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-10-08T20:23:11Z","employer_posted_date":"2026-10-08","last_verified_at":"2026-10-13T10:27:53Z","board_verified":true,"closed_at":null,"days_open":4,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":4},"description":"QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.\nLog on now to our website http://www.qrcgroup.com / to learn more about our services and solutions!\n We are seeking a highly skilled Scientist in Technical Services / Manufacturing Science (DRY-EM TS/MS) to provide scientific and technical support for spray dry dispersion (SDD), solid oral dosage manufacturing, technology transfer, process validation, continued process verification, deviation investigations, and manufacturing support activities performed by external manufacturing partners. This role requires strong technical expertise, regulatory knowledge, and the ability to collaborate with internal and external stakeholders to maintain a compliant and reliable supply of pharmaceutical products.\nKey Responsibilities\nProvide technical oversight for spray dry, solid dosage manufacturing and packagingprocesses, leveraging a strong technical foundation and previous experience supporting these processes.\n\nParticipate in resolution of technical issues, including those related to control strategy and manufacturing.\n Possess excellent technical writing capabilities, including authoring of deviations and change controls.\nEmploy excellent communication skills to manage internal and external relationships with external partners, site management, and cross-functional teams.\nBuild and maintain relationships with development and central technical organizations.\nEnsure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.\nUnderstand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.\nMaintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.\nSupport ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.\nSupport technical transfer and validation activities to external partners manufacturing and packaging sites.\nWork cross-functionally within the site and other functions to deliver on technical objectives.\nSome flexibility may be required to support 24/7 operations and issue resolutions with external partners across different time zones.\nBachelor's degree (minimum) in scientific disciplines of Chemistry, Pharmacy, or Engineering.\n5+ years of demonstrated hands-on working experience and proficiency with spray dry, solid dosage manufacturing and packaging.\nWorking knowledge of regulatory expectations (cGMPs and applicable global regulator guidance).\nStrong understanding of regulatory requirements and their application in a manufacturing environment.\nProficient in data management practices across manufacturing and packaging operations.\nProven ability to communicate effectively and influence across diverse technical and business teams.\nDemonstrated project management expertise with a track record of coordinating and executing multifaceted projects.\nDemonstrates adaptability, a collaborative mindset, and a positive attitude toward change.\nAvailable to support 24/7 operations and issue resolutions across multiple time zones as needed.\nFluent in English and Spanish, with the ability to communicate effectively across diverse teams and stakeholders\n All your information will be kept confidential according to EEO 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