Supervisor Quality Control, Analytical Laboratory

TEI BIOSCIENCES INC; Braintree (MA); On-site; USD 81,000 - 113,000; Full time

Benefits offered by this job

medical

dental

vision

life insurance

short- and long-term disability

business accident insurance

group legal insurance

savings plan (401(k))

Job summary

Integra LifeSciences in Massachusetts seeks a Supervisor, QC Analytical Laboratory to provide technical and operational leadership for the QC Analytical Lab. The role ensures compliant testing of raw materials, in‑process, finished products and stability samples, with data integrity and regulatory readiness.

You will supervise daily lab operations, oversee method performance and instrument status, mentor staff, review records, manage external contract testing, and drive continuous improvement

Qualifications

• GMP/GLP laboratory experience in FDA-regulated industry.
• Experience with analytical method validation/verification/transfer.
• Leadership experience supervising laboratory personnel.

Responsibilities

• Supervise daily operations of the QC Analytical Laboratory.
• Oversee analytical testing of materials and products for release.
• Provide oversight of method performance and instrument status.
• Lead investigations (OOS/OOT/NC) and CAPA activities.
• Ensure data integrity and regulatory compliance.

Skills

GMP/GLP

QMSR

OOS/OOT

CAPA

LIMS

Data integrity

Analytical instrumentation

Leadership

Communication

Education

Bachelor's degree in Chemistry or related

Tools

LIMS

Job description

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

Position Summary Description

The Supervisor, QC Analytical Laboratory provides technical and operational leadership of the QC Analytical Laboratory. Responsible for analytical testing supporting raw material, in-process, validation, stability and finished product release activities. Ensures compliant laboratory operations, data integrity, testing execution, inventory control, personnel development, and inspection readiness while partnering with Manufacturing, QA, Engineering, Product Development, and external laboratories. The role ensures compliance with applicable FDA regulations, ISO 13485 requirements, GMP/GLP standards, and company quality system procedures while fostering a culture of quality, compliance, and continuous improvement.

Job Description

• Supervise daily operations of the Quality Control Analytical Laboratory and ensure testing activities are completed accurately and on schedule.
• Oversee and coordinate analytical testing of raw materials, in-process materials, finished products, validation samples, stability samples, and special studies in support of manufacturing operations and product release.
• Provide technical oversight of analytical chemistry and mechanical testing systems, including method performance, instrument suitability, troubleshooting, and data review activities.
• Provide leadership, coaching, mentoring, and performance management for laboratory personnel.
• Assign laboratory workload and establish testing priorities to support manufacturing schedules and business objectives.
• Ensure laboratory testing is performed in accordance with approved procedures, specifications, GMP, GLP, GDP, and applicable regulatory requirements.
• Review, approve, and ensure the accuracy of laboratory data, testing records, logbooks, protocols, reports, and other quality records.
• Manage analytical testing performed by qualified external contract laboratories, including sample submission, testing requirements, data review, and vendor communications.
• Maintain laboratory documentation, logbooks, controlled records, and electronic data in accordance with GDP and data integrity requirements.
• Lead or support analytical Test Method Validation (TMV), method transfer, implementation, lifecycle management, and continuous improvement activities.
• Support process validation, cleaning validation, equipment qualification, product transfer, and product development activities requiring analytical laboratory support.
• Collaborate with Research & Development, Product Development, Manufacturing, Engineering, and Quality Assurance to support product lifecycle activities.
• Lead or support Laboratory Error, Out-of-Specification (OOS), Out-of-Trend (OOT), Nonconformance (NC), CAPA, and data integrity investigations and associated corrective actions.
• Prepare, review, analyze, and communicate laboratory performance data, quality metrics, adverse trends, and management reports.
• Ensure laboratory equipment, computerized systems, and associated software are qualified, calibrated, maintained, secured, and operating within validated parameters in accordance with data integrity requirements.
• Manage and procure laboratory materials including reagents, reference standards, consumables, laboratory supplies, and PPE.
• Develop, review, revise, and approve laboratory procedures, test methods, work instructions, forms, specifications, and related controlled documents.
• Participate in FDA inspections, ISO certification audits, surveillance audits, internal audits, customer audits, and regulatory inspections as a subject matter expert.
• Ensure laboratory personnel complete required training and maintain competency for assigned responsibilities.
• Identify and implement continuous improvement initiatives to improve laboratory efficiency, compliance, data integrity, and overall laboratory performance.
• Maintain compliance with company safety policies, hazardous material handling procedures, and environmental requirements.
• Perform additional duties and special projects as assigned.

Job Requirements

• Bachelor's degree or higher in Chemistry, Biochemistry, Biology, Engineering, or a related scientific or engineering discipline.
• Minimum seven (7) years of GMP/GLP laboratory experience within the medical device, pharmaceutical, biotechnology, or other FDA-regulated industry.
• Minimum two (2) years of supervisory or technical leadership experience.
• Strong working knowledge of FDA Quality Management System Regulation (QMSR), 21 CFR Part 820, ISO 13485, and applicable quality-system requirements.
• Experience with analytical method validation, verification, transfer and investigations.
• Extensive hands-on experience with material characterization instrumentation, mechanical testing systems, and physical/chemical wet chemistry techniques within a regulated cGMP environment.
• Demonstrated experience managing product stability programs, validation protocol execution, physical testing operations, and analytical instrument calibration and system suitability activities.
• Experience with OOS/OOT, NC, CAPA and root cause investigations.
• Strong understanding of laboratory data integrity principles and documentation practices.
• Excellent communication, technical writing, organizational, leadership, and problem-solving skills.
• Proficiency with Microsoft Office applications and laboratory information management systems (LIMS) or equivalent electronic systems preferred.

Supervisory Responsibilities

• Directly supervises Quality Control Analytical Laboratory personnel.
• Identify resource needs; recruit, onboard, schedule, and train personnel.
• Performance evaluations, coaching, corrective actions, and employee development.
• Manage laboratory priorities and resource allocations to meet operational objectives.
• Provide cross-functional technical leadership.

Salary Pay Range: $81,650.00 - $112,700.00 USD

Benefits

• medical
• dental
• vision
• life insurance
• short- and long-term disability
• business accident insurance
• group legal insurance
• savings plan (401(k))

In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation.

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

This site is governed solely by applicable U.S. laws and governmental regulations.

Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA.