{"id":4108113,"url":"https://alion.io/job/weil-group-inc-specialist-quality-control","title":"Specialist Quality Control","company":{"id":4465740,"name":"Weil Group, Inc","domain":"weilgroup.com","url":"https://alion.io/company/weilgroup","size_band":null,"is_staffing_agency":true,"employer_type":"agency","is_intermediary":false,"listed_via":null,"ats_vendor":"CATS","truth_index":null},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":null,"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":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GLP","optional":false},{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-11-11T22:52:27Z","employer_posted_date":"2026-11-11","last_verified_at":"2026-11-12T23:33:39Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"SUMMARYUnder general direction, functions as the technical specialist for testing & development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources.\nFUNCTIONS\n-Responsible for providing technical guidance, Provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise.\n-Resolve technical issues and troubleshoot for assays as necessary\n-Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety.\n-Manage existing and/or develop and implement new programs, processes and methodologies.\n-Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact.\n-Approve lab investigations, Lead audit teams\n-May serve as subject matter expert to develop technical training.\n-May perform routine work in a specific area of responsibility as necessary.\n-Represents the department/organization on various teams, Independently responsible for following through on multi-site action items.\n-May interact with regulatory agencies regarding area(s) of responsibility including written responses.\n-May resolve issues with outside resources.\n-Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements.\nEDUCATION\n-Doctorate OR -Masters + 2 years of directly related experience OR -Bachelors + 4 years of directly related experience OR -Associates + 8 years of directly related experience OR -High school/GED + 10 years of directly related experience.\nCOMPETENCIES/SKILLS\n-Understand, support and demonstrate the AMGEN values.\n-Excellent communication skills, facilitation and presentation skills.\n-Excellent technical writing skills.\n-Strong computer operation skills including work processing, presentation, database and spreadsheet application skills.\n-Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion.\n-Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities.\n-Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution.\n-Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility.\n-Knowledge of pharmaceutical processes.\n-Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products.\n-Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products.\n-Extensive knowledge and application of GMPs/CFRs.\n-Ability to evaluate compliance issues.\n-Skill in evaluating and documenting according to Company and various guidelines.\n-Proficient at maintenance, troubleshooting and operation of equipment in area of expertise.\n-Advanced scientific data analysis and interpretation skills.\n-Advanced skills in solving complex problems.\n-Advanced data trending and evaluation.\n-Strong skill in working independently and to effectively interact with various levels.\n-Ability to interact with regulatory agencies both orally and in writing.\n-Initiate, coordinate and lead cross functional teams.\n-Excellent skill in leading, motivating, influencing, and negotiating.\n*Weil Group is proud to be an Equal Employment Opportunity Employer.*","description_format":"text","description_chars":3724,"description_truncated":false,"requirements":{"experience_years_min":8,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"high_school","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":[],"lifecycle":[{"event":"open","at":"2026-11-11T22:52:27Z"}],"visa":[],"liveness":{"score":52,"band":"ok","label":"Likely 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