Deputy Process Safety Manager
Aarti Pharmalabs · Mumbai · onsite · Posted 57d ago
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About this role
Key Responsibilities:
1. PSM System Development & Implementation:
Develop, implement, and continuously enhance the corporate PSM framework, aligning it
with OSHA PSM, EPA, ISO 45001 and industry best practices.
Establish standardized policies, procedures, and guidelines for hazard identification, risk
assessment, and mitigation.
Integrate PSM principles with overall EHS and quality management systems.
2. Hazard Identification & Risk Management:
Lead Process Hazard Analysis (PHA) activities, including HAZOP, FMEA, What-If, and
LOPA studies across manufacturing sites.
Oversee Management of Change (MOC) processes to evaluate and mitigate risks
associated with process modifications.
Conduct comprehensive risk assessments for chemical processes, storage, handling, and
utilities.
Identify potential catastrophic hazards and implement effective control measures.
Job Description
3. Compliance & Regulatory Oversight:
Ensure strict compliance with local, national, and international PSM regulations and
standards (e.g., OSHA PSM, Indian Factories Act, CPCB guidelines).
Prepare for and provide support during regulatory inspections and audits.
Track and report compliance metrics and key performance indicators (KPIs) related to
process safety.
4. Incident Investigation & Root Cause Analysis:
Lead investigations of process safety incidents, near misses, and non-conformances.
Apply established methodologies such as RCA, and 5-Whys to determine root causes.
Develop and monitor the implementation of corrective and preventive action plans across
all sites.
5. Training, Awareness & Culture:
Design and implement corporate-level PSM training programs for site operations,
engineering, and management teams.
Promote a strong process safety culture, encouraging proactive hazard identification and
adherence to safe work practices.
Conduct PSM audits, workshops, and drills to reinforce awareness and preparedness.
6. Performance Monitoring & Continuous Improvement:
Develop and maintain process safety performance metrics, dashboards, and reporting
mechanisms.
Benchmark corporate PSM practices against global best practices and recommend
strategic improvements.
Drive continuous improvement initiatives across sites to reduce incident rates,
environmental releases, and near misses.
7. Cross-Functional Collaboration:
Collaborate effectively with Production, Engineering, Quality, EHS, and R&D teams to
integrate PSM into design, scale-up, and operational processes.
Support engineering teams in implementing inherently safer designs for processes,
storage, and utilities.
Facilitate cross-site sharing of lessons learned, best practices, and process safety
innovations.
Job Description
8. Documentation & Reporting:
Ensure thorough documentation of all PSM processes, PHAs, MOCs, SOPs, incident
investigations, and safety audits.
Prepare corporate-level process safety reports for senior management, regulators, and
internal stakeholders.
9. Key Competencies:
Strong knowledge of chemical and pharmaceutical processes.
Expertise in PSM frameworks, hazard analysis techniques, and risk assessment tools.
Excellent analytical, leadership, and communication skills.
Ability to drive a strong safety culture and influence cross-functional teams effectively.
Proficiency in data analysis, reporting, and safety management systems software.
10. Qualifications:
Bachelors/Master’s degree in Chemical Engineering, Process Engineering, or a related
field.
Professional certification in PSM, Risk Management, or Safety (preferred: CFPS,
NEBOSH, or equivalent).
8–12 years of experience in chemical / pharmaceutical manufacturing with significant
exposure to process safety management, hazard analysis, and regulatory compliance.
Sourced from naukri
Skills
About Aarti Pharmalabs

Aarti Pharmalabs
Pharma
2.0k+
employees
Mumbai
India
₹6.6L PA avg
Avg at Aarti Pharmalabs
About
Aarti Pharmalabs Limited (APL) is a leading Indian manufacturer of Pharmaceuticals and Nutraceuticals with a global footprint. We deliver process chemistry expertise, with a scale-up engineering competence, regulatory support and long-term supply by maintaining quality and timely delivery to create a sustainable future.
Over the last two decades, APL serving global clients with top notch scientific knowledge, industry experts, state-of-the-art R&D and USFDA, EUGMP, EDQM, KFDA inspected manufacturing facilities. We manufacture Generic APIs, Intermediates and Xanthine derivatives. We offer CDMO services for small molecules drug substances (API/NCE/RSM/Intermediate) process development and manufacturing focusing on Ph-I/II/III, launch and commercial phase projects for Innovator Pharmaceutical and Biotech companies. We have been helping our clients to bring their molecules to market quickly and efficiently from clinical development through commercial stage manufacturing.
We have dedicated facilities to manufacture HPAPIs, Corticosteroids, Cytotoxic and Oncology products.
We are one of the preferred partner for Beverages and Nutraceuticals Industries for our flagship product ‘Caffeine’.
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