Location
Confidential Location
Description
To assist a pharmaceutical manufacturer prepare for its OSHA Voluntary Protection Program inspection, HRP was retained to complete an OSHA Compliance audit. Specifically, HRP reviewed the facility and compliance related documentation for compliance with the following OSHA topics:
Subject |
OSHA General Industry Standard |
---|---|
Confined Space |
29 CFR 1910.146 |
Materials Handling (Lifting Weights) |
General Duty |
Powered Industrial Trucks (Forklifts) |
29 CFR 1910.176 |
Personal Protective Equipment (PPE) |
29 CFR 1910.132-139 |
Lockout/Tagout |
29 CFR 1910.147 |
Exit/Egress (Proper maintenance of) |
29 CFR 1910.35-38 |
Industrial Hygiene and Air Contaminants |
29 CFR 1910.94, 29 CFR 1910.1000-1052 |
Hazard Communication |
29 CFR 1910.1200 |
Machine Guarding* |
29 CFR 1910.211-219 |
Cranes/Slings |
29 CFR 1910.179-184 |
Noise Exposure/Protection |
29 CFR 1910.95 |
Walking & Working Surfaces |
29 CFR 1910.21-30 |
Hazardous Materials |
29 CFR Subpart H |
Welding/Cutting/Brazing |
29 CFR 1910.251-255 |
First Aid/Bloodborne Pathogens |
29 CFR 1910.151, 29 CFR 1910.1030 |
Flammable Liquids |
29 CFR 1910.106 |
Emergency Action Plans/Fire Prevention Plans |
29 CFR 1910.38 |
Electrical Safety* |
29 CFR 1910 Subpart S |
Fire Protection |
29 CFR Subpart L |
Welding and Brazing |
29 CFR Subpart Q |
General Safety (Observation of unsafe acts or conditions) |
General Duty |
To complete audit, HRP conducted:
- A two day site walkthrough;
- Interviewed representative facility personnel; and
- Reviewed provided safety related Health, Safety, Environmental & Business Continuity Procedures, OSHA compliance plans, training records, and industrial hygiene reports.
The information collected was utilized to evaluate if manufacturing operations are consistent with respect to the OSHA regulations contained in 29 CFR 1910 and general safety practices. The remainder of HRP’s letter-report summarized our findings and recommendations. Also, tables specifically outlining deficiencies and other “non violation” findings that may be potential safety concerns, as well as, recommended actions are included at the end of our letter-report. The report specifically included recommendations for facility modifications or operational/work practice changes recommended to ensure consistency with existing and/or proposed regulations. Lastly, HRP assisted in the prioritization of the corrective actions to ensure that the pharmaceutical manufacturer was prepared for this VPP inspection.
OSHA has recommended the company for VPP Star status and acknowledged the company's risk portfolio methodology and business continuity planning to be Areas of Excellence.