469 Qa Auditor Biotechnology Research jobs in Worcester,MA

Adecco

Ayer, MA 01432

Quality Assurance Bulk Technician
Location: Ayer, MA
Shift: 1st Shift
Pay: $24/hour
Perform quality inspections and testing on bulk oil products
Collect product samples and document results accurately
Monitor production processes and report quality or safety concerns
Maintain quality records, logs, and related documentation
Verify product specifications, labeling, and compliance standards
Support GMP, HACCP, sanitation, and food safety procedures
Assist with inventory tracking and product traceability
Maintain a clean and organized work area
Collaborate with production and warehouse teams as needed
Previous quality assurance, manufacturing, or food production experience preferred
Strong attention to detail and organizational skills
Ability to follow written and verbal instructions
Basic computer and data entry skills
Comfortable working in a warehouse or manufacturing environment
Ability to stand, walk, bend, and lift throughout the shift
Knowledge of GMP, HACCP, or food safety standards is a plus

Animal Outpatient Specialty Network

Boxborough, MA 01719

Hoerbiger

Worcester, MA 01605

Adecco

Devens, MA 01434

Associate degree required
Minimum 2+ years of experience in Quality Assurance, preferably in a supervisory role
Familiarity with ISO 9001 and quality management systems
Understanding of risk-based quality techniques and their impact on product fit, form, and function
Excellent communication skills with the ability to work independently and in team settings
Strong analytical, organizational, and problem-solving skills
Experience working with cross-functional teams to resolve quality issues
Authorize product release and enforce established quality standards
Develop and manage incoming material inspection processes
Establish QC procedures, inspection criteria, and controlled documentation
Lead, mentor, and train QA/QC team members, including resource planning
Maintain audit readiness and represent Quality during internal and customer audits
Oversee non-conformance investigations and ensure effective CAPA implementation
Monitor cleanroom bioburden and particulate levels, escalating deviations as needed
Track and report QC metrics, inspection results, and trend analysis
Collaborate cross-functionally with manufacturing, engineering, logistics, and supply chain

Genmab

South Grafton, MA 01560

PhD, Pharm D, MS, Bachelor's or equivalent degree preferably within the medical, biological, pharmaceutical science or related discipline
Minimum requirement: 6+ years of experience in clinical research with at least 3 or more years of drug development experience (preferably in oncology)
Experience working in a project-oriented matrixed team environment
Extensive knowledge and understanding of GCP
Proven experience working in teams
Ability to work successfully under pressure in a fast-paced environment and with tight timelines
Extensive knowledge and understanding of Clinical Research
A team player with demonstrated ability to collaborate with a diverse group of internal and external stakeholders (e.g. Scientists, Trial Managers, Data Managers, Clinicians, vendors labs) to support product development strategy
Strong communication skills - both oral and written