NewQuality Control Scientist II Zenith LifeScience, LLCQuality Control Scientist IIWestborough, MAThis role provides technical leadership across QC Microbiology and Manufacturing by ensuring effective microbiological testing, mentoring laboratory staff, supporting quality systems and delivering aseptic technique training to maintain compliance with GMP and contamination control requirements. The Scientist II QC Microbiology serves as senior technical subject matter expert responsible for overseeing microbiological testing programs supporting GMP operations.
Quality Control Inspection - DEFENSE The Structures Company, LLCQuality Control Inspection - DEFENSEChelmsford, MAAs trusted partners to major aerospace OEMs and Tier 1 suppliers, we connect professionals with opportunities to grow and excel in the aviation and aerospace industries. Perform all types of inspections to support all phases of assembly and manufacturing, including subcontracted and purchased parts.
NewQuality Control / Documentation Analyst Karwell TechnologiesQuality Control / Documentation AnalystLexington, MAJob Description: Assist in document authoring/ revision and approval (protocols, test methods, SOPs) and other routine laboratory activities supporting the lab as 079 activities are completed by the biochem team. This role supports the daily operations of the QC Raw Materials department, whose primary responsibility is the testing and release of raw materials for GMP use in manufacturing.
Associate Director, Quality Control Lab Automation ModernaTXAssociate Director, Quality Control Lab AutomationNorwood, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. The Associate Director, Quality Control Lab Automation Strategy & Digital Integration is responsible for leading the strategy, implementation, and lifecycle management of laboratory automation and digital integration across Moderna’s Quality Control laboratories.
Training Instructor /Quality Control Monitor - AIS AhtnaTraining Instructor /Quality Control Monitor - AISAndover, MassachusettsOutlines comprehensive documentation, QC measures, inspection programs, internal audits, personnel training, and master file of QC inspections (includes inspections scheduled and performed, results of completed inspections, and dates/details of any corrective actions taken). Complete and/or maintain an approved and accredited Principles of Instruction course or similar training (NRA, Police Academy, state POST Academy, FLETC, or military training course) certifying the individual as an instructor showing competency in the performance areas of: Presentation skills.
Asphalt Quality Control Tech Northeast PavingAsphalt Quality Control TechWestford, MAMust possess strong written and verbal communication skills and have the ability to interact with individuals at any level of the organization (i.e. plant production personnel, plant managers, contractors, and agency representatives). - Hubbard Construction Company - Northeast Paving - Sunmount Paving - Virginia Paving Company, are hereby referred to as Vinci Construction USAAccessibility: If you need an accommodation as part of the employment process please contact Human Resources atBlythe Construction, Inc.
Senior Scientist I, Quality Control Candel Therapeutics IncSenior Scientist I, Quality ControlNeedham, MAThis position collaborates with external manufacturing and tech transfer and is focused on Adenovirus and Herpesvirus vectors, associated cell-based potency assays, as well as performing training of new technical staff and troubleshooting and validation of new and established assays. A strong background in one or more analytical techniques such as various HPLC based methods, microplate UV/Vis/Luminescent assays, cell-based assays including virus quantification and potency, qPCR, electrophoresis, sizing techniques such as DLS, etc.
Scientist I, Analytical Development and Quality Control Kailera TherapeuticsScientist I, Analytical Development and Quality ControlWaltham, MassachusettsThe Scientist I, Analytical Development and Quality Control is an experienced scientist within the Analytical Development and Quality Control (AD/QC) organization, with a primary focus on analytical quality control, method validations, stability programs, and data integrity. Evaluate temperature excursions for stability and release samples, assessing potential impact on product quality using scientific judgment, stability data, and relevant regulatory/technical guidance.
Associate Director Quality Control, Microbiology Bristol-Myers Squibb CoAssociate Director Quality Control, MicrobiologyDevens, MA$173,280–$209,976 / yearThe Associate Director, Quality Control Microbiology Laboratory Operations is accountable for the strategic leadership, governance, and GMP-compliant execution of microbiological quality control activities supporting commercial and clinical biologics manufacturing at the Devens site. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Analyst II, Quality Control Molecular Biology The Steely GroupAnalyst II, Quality Control Molecular BiologyWoburn, MAThe QC Analyst II will perform analytical methods including but not limited GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed to support in-process, drug substance and drug product release, stability to support AAV-based gene therapy programs. Routine work includes release and stability testing, critical reagent qualification, method validation and transfer, critical reagent qualification, analyzing data, and authoring technical documents.
Quality control manager Integrated Resources, IncQuality control managerCambridge, MassachusettsContractorRESPONSIBILITIES:Method design (re-design) and validation (re-validation)Method performance monitoring (trending), control and troubleshootingMethods transfer working with internal and contract sitesAuthor analytical regulatory sections and response to questionsWork with interconnected departments and other groups in Pharmaceutical OperationsAnalytical expert for assay optimization, validation and transferPresent analytical issues and findings to senior managementQualificationsQUALIFICATIONS AND SKILLS NEEDED:• A bachelor's degree in analytical chemistry with 5+ years or a Master's with 3+ years of leadership and experience in a pharmaceutical/biotechnology industry.• Experience with regulatory writing of analytical sections and response to questions• Excellent communicator, author and creative thinker with extensive knowledge in the area of expertise• Specific techniques include chromatography, particle size, XRPD, Dissolution and Disintegration, ICP-MS, KF and compendia methods• Excellent project and people manager who can motivate, direct projects, and align scientificAdditional InformationRegardsPooja MishraClinical RecruiterIntegrated Resources, Inc.
Quality Control Analyst Integrated Resources, IncQuality Control AnalystLexington, MassachusettsContractorThis position is with my direct clientJob DescriptionPosition Details:Client Direct ClientLocation Lexington, MAJob Title Quality Control AnalystDuration 1 Year+Must have skill-set [Job Description] Responsibilities:Analyze samples using specific procedures and instrumentation. Quality Control AnalystA Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Sr. Director Global Quality Control Scholar Rock Holding CorpSr. Director Global Quality ControlCambridge, MA$245,000–$335,000 / yearProvide strategic oversight of stability programs, including protocol design, pull schedule governance, data review, and trending, shelf-life support, comparability assessments, and post-approval stability commitments. Lead the companys global QC function across a fully outsourced model with end-to-end oversight of external QC laboratories, CMOs, and other testing partners supporting clinical and commercial programs.
Quality Control Analyst III Integrated Resources, IncQuality Control Analyst IIILexington, MassachusettsContractorGMP and HPLC Experience 100% Necessary• At least 2 years in a QC Environment• Performing Analytical testing• Oversight of general QC Lab activity• Quality System experience a plus• Candidates need minimum of 2 yrs QC analytical HPLC experience.• Works under general supervision. Testing may include but not limited to samples from drug substance and drug product manufacturing, stability, raw materials and various protocol studies using test methods derived from the various compendial and non-compendial sources.•
Senior Scientist I, Quality Control Candel TherapeuticsSenior Scientist I, Quality ControlNeedham, MAThis position collaborates with external manufacturing and tech transfer and is focused on Adenovirus and Herpesvirus vectors, associated cell-based potency assays, as well as performing training of new technical staff and troubleshooting and validation of new and established assays. A strong background in one or more analytical techniques such as various HPLC based methods, microplate UV/Vis/Luminescent assays, cell-based assays including virus quantification and potency, qPCR, electrophoresis, sizing techniques such as DLS, etc. .
Head of Quality Control 3383 Shire Human Genetic TherapiesHead of Quality ControlLexington, MassachusettsThe actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. Working closely with Manufacturing and Quality partners, you will champion continuous improvement, employee development, and innovation while fostering an inclusive environment where diverse perspectives are valued and everyone is empowered to succeed.
HIM Quality Control Specialist Lahey Hospital and Medical CenterHIM Quality Control SpecialistBurlington, MA$20–$26.92 / hourUnder the supervision of the Director of Health Information Management, the Health Information Management Quality Control Specialist provides continuous quality review of electronic medical record functions to support Beth Israel Lahey Health's (BILH) clinical practice and Health Information Management (HIM) regulatory compliance. Actual compensation is determined based on several factors, that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other applicable factors permissible by law.
Quality Control Technician PhilipsQuality Control TechnicianBedford, MA$27.46–$43.94 / hourYou're the right fit if: You have a minimum of 2+ years experience in FDA/ISO 13485 regulated Medical Device manufacturing quality environments, with a focus on production controls, supporting validations, administering calibration, quality records, incoming/in-process/final Inspection, using hand tools and optical inspection systems. The Quality Control Technician is responsible for supporting highly complex quality control tasks to address manufacturing abnormalities, and coordinates quality control protocols while ensuring adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
Manager, Quality Control Operations Kiniksa Pharmaceuticals International PlcManager, Quality Control OperationsLexington, MA$129,000–$144,000 / yearReporting to the Associate Director, Quality Control Stability and Trending, the Manager, Quality Control Operations will be responsible for day-to-day oversight of routine batch testing at contract and internal Kiniksa testing laboratories. Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.
Director, Quality Control Dyne Therapeutics IncDirector, Quality ControlWaltham, MA$190,000–$230,000 / yearRole Summary: The Director, Quality Control leads global Quality Control activities, including oversight of external laboratories supporting analytical testing, release, and stability programs across clinical and commercial stages. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.