Quality Control Scientist

Belcan

Westborough, MA

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JOB DETAILS

SALARY

$55–$56.67 Per Hour

SKILLS

Asepsis, Assays, Change Control, Cleanroom, Communication Skills, Cross-Functional, Current Good Manufacturing Practice (cGMP), Environmental Monitoring, GMP (Good Manufacturing Practices), Interpersonal Skills, Investigative Reports, Laboratory, Laboratory Operations, Legal, Maintain Compliance, Manufacturing, Manufacturing Operations, Mentoring, Microbiology, Operational Audit, Operational Support, Operations Processes, Process Improvement, Project/Program Management, Quality Assurance, Quality Control, Regulations, Risk Analysis, Standard Operating Procedures (SOP), Team Player, Technical Leadership, Technical Operations, Technical Training, Technical Writing, Test Lab, Test Program, Training/Teaching, Validation Plan, Writing Skills

LOCATION

Westborough, MA

POSTED

2 days ago

Job Title: Quality Control Scientist Location: Westborough, MA Zip Code: 01581 Duration: 6 Months Pay Rate: $55 - $56.67/hr. Keyword's: #Westboroughjobs; #QualityControlScientistjobs. Start Date: Immediate We provide a competitive pay and benefits package. This position is offering a pay range of $55 - $56.67/hr. however, Belcan considers several factors when extending an offer, including but not limited to education, experience, geographic location, and discipline. Benefits offered may include health care, dental, vision, life insurance; 401(k); education assistance; paid time off including PTO, holidays, and any other paid leave required by law. Job Description: The Scientist II QC Microbiology serves as senior technical subject matter expert responsible for overseeing microbiological testing programs supporting GMP operations. This 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. Responsibilities: * Serve as subject matter expert for microbiological testing programs including environmental monitoring, sterility, endotoxin, mycoplasma, microbial identification, and contamination control. * Support QC Microbiology Senior Manager in oversight of laboratory operations, technical initiatives, and microbiological program execution. * Develop and deliver aseptic technique and contamination control training for manufacturing and QC personnel to maintain compliance with GMP and cleanroom practices. * Track and support quality system activities including deviations, investigations, CAPAs, Change Control and trending associated with QC microbiology operations. * Review and approve microbiological data, protocols, quarterly reports , SOPs and other technical documentation. * Lead data trending and interpretation of environmental monitoring and microbiological data to identify risks and support contamination control strategy. * Provide technical leadership and mentorship to microbiologists and junior scientist within QC microbiology laboratory. * Author and review SOPs, protocols, validation reports, investigation reports and technical documents in accordance with GMP requirements. * Lead or support method qualification, validation, and technology implementation for microbiological assays. * Collaborate cross-functionally with Manufacturing, QA , Facilities and other teams to support manufacturing operations and process improvements. * Support regulatory inspections, audits and responses by providing technical justification and documentation. Required Qualifications * BS degree in Biology/Microbiology with 10+ years or M.S. with 6+ years of relevant experience in a GMP QC microbiology laboratory. * Demonstrated advanced expertise in microbiological testing including environmental monitoring, bioburden, endotoxin, sterility, mycoplasma and microbial identification. * Experience supporting aseptic manufacturing environments and cleanroom operations. * Demonstrated experience mentoring laboratory staff and providing technical training. * Strong knowledge of cGMP regulations and microbiological control strategies. * Excellent technical writing and communication skills. * Strong interpersonal skills, highly collaborative within a multi-disciplinary team and contributes to a supportive and positive work environment. * This role is scheduled to work during day shift (8 am to 5 pm) Monday to Friday. * Flexibility to work weekend hours may be required to support GMP Operations. Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, colour, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

About the Company

Belcan

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