EHS Specialist

TEI BIOSCIENCES INC; Braintree (MA); On-site; USD 85,000 - 120,000; Full time

Job summary

TEI BIOSCIENCES INC in Massachusetts seeks an experienced Environmental Health & Safety professional to lead cleanroom safety programs in ISO7/8 environments and ensure regulatory compliance.

You will collaborate with Quality and Manufacturing, manage chemical handling and waste, support internal and FDA inspections, and drive continuous safety improvements. GMP experience and OSHA 30-hour certification are preferred; on-site work in Braintree may be required.

Qualifications

• Bachelor’s degree in Environmental Health & Safety, Industrial Hygiene, Environmental Science, or related field.
• 2–5 years of EHS experience in cleanroom manufacturing (medical device, pharma, biotech preferred).
• Experience working in GMP/FDA-regulated environments required.
• Strong understanding of OSHA safety regulations, MassDEP hazardous waste regulations, MWRA wastewater permitting requirements, chemical hygiene in controlled environments.

Responsibilities

• Develop and maintain EHS programs for ISO7/8 cleanrooms.
• Ensure regulatory compliance with OSHA, FDA cGMP, ISO13485 & ISO14644.
• Manage chemicals, hazardous waste, SDS, and safe handling.
• Support audits and regulatory inspections including FDA.
• Lead incident investigations and drive safety improvements.

Skills

Cross-functional collaboration

Incident investigation

Training delivery

Contamination control

Education

Bachelor’s degree in Environmental Health & Safety

2–5 years of EHS experience in cleanroom manufacturing

Experience in GMP/FDA-regulated environments

OSHA 30-hour certification

RCRA/DOT certification

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.

Key Responsibilities

Cleanroom Safety & Contamination Control

Develop and maintain EHS programs specific to ISO‑classified cleanroom environments (ISO7/8). Evaluate safety risks while ensuring they do not compromise product sterility or cleanroom integrity.

Regulatory Compliance & Quality Integration

• Ensure compliance with OSHA (29 CFR1910), FDA cGMP requirements (21CFRPart820), ISO13485 & ISO14644 cleanroom standards, EPA and MassDEP environmental regulations.
• Partner with Quality to ensure EHS programs align with validated processes, change control, and audit readiness.
• Support internal, customer, and regulatory audits, including FDA inspections.

Chemical & Hazardous Material Management

• Manage chemicals used in cleanroom environments (e.g., disinfectants, solvents, sterilants).
• Ensure compliance with cleanroom‑compatible chemical handling, labeling, and storage requirements.
• Oversee hazardous waste segregation and disposal, ensuring no cross‑contamination risks.
• Maintain Safety Data Sheets (SDS) and ensure compatibility with clean manufacturing processes.

Environmental Monitoring & Industrial Hygiene

• Partner with consulting firms on industrial hygiene assessments related to airborne contaminants, cleanroom disinfectants and chemical exposure, ventilation effectiveness (HEPA systems awareness).
• Ensure safe interaction with HVAC systems, HEPA filtration, and pressurization controls.

Safety Risk Management in Controlled Environments

• Perform Job Hazard Analyses (JHAs) tailored to cleanroom tasks (e.g., assembly, inspection, sterilization prep).
• Evaluate ergonomic risks associated with repetitive motion under cleanroom constraints, extended gowning periods.
• Lead incident investigations with a focus on personnel safety and potential product impact (non‑conformance linkage).

Training & Cleanroom Behavior Compliance

• Develop and deliver EHS training integrated with chemical safety in controlled environments and emergency response in cleanroom settings.
• Reinforce human performance and contamination control behaviors (movement, material handling, PPE compliance).
• Collaborate with Quality to ensure training supports GMP compliance and documentation requirements.

Emergency Preparedness & Response (Cleanroom‑Specific)

• Develop emergency procedures that account for cleanroom constraints, including controlled evacuation protocols, chemical spill response inside cleanrooms, fire safety without compromising product safety.
• Serve on the Emergency Response Team (ERT) with training in cleanroom shutdown procedures.
• Coordinate with Facilities for HVAC isolation if needed, and document responses.

Documentation & Continuous Improvement

• Maintain EHS documentation in compliance with GMP document control standards.
• Track and trend safety metrics (TRIR, near misses), environmental data, and cleanroom‑related incidents.
• Drive continuous improvement initiatives that balance safety compliance and product quality.

Qualifications

Education & Experience

• Bachelor’s degree in Environmental Health & Safety, Industrial Hygiene, Environmental Science, or related field.
• 2–5 years of EHS experience in cleanroom manufacturing (medical device, pharma, biotech preferred).
• Experience working in GMP/FDA‑regulated environments required.

Technical Knowledge

• Strong understanding of OSHA safety regulations, MassDEP hazardous waste regulations, MWRA wastewater permitting requirements, chemical hygiene in controlled environments.
• Familiarity with environmental monitoring programs, HVAC/HEPA systems, and cleanroom pressurization concepts, pH neutralization wastewater systems.

Skills

• Ability to balance safety requirements with strict contamination control standards.
• Strong cross‑functional collaboration with Quality and Manufacturing teams.
• Effective incident investigation and root cause analysis.
• Clear communication and training delivery in regulated environments.
• Actively support Safety Committee goals and objectives.

Certifications (Preferred)

• OSHA 30‑hour certification
• RCRA/DOT

Working Conditions

• Regular work within ISO‑classified cleanrooms requiring full gowning.
• Exposure to disinfectants and other chemical agents; controlled temperature and humidity environments.
• Must follow strict gowning, hygiene, and behavioral protocols.
• Occasional off‑shift support for manufacturing or environmental monitoring activities.

Success Measures

• Zero significant EHS‑related audit findings.
• Reduction in safety incidents without impacting product quality.