EHS Specialist

Job Title Sr. EHS Specialist Job Description Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : Key accountabilities With limited supervision, assist and support the Associate Director of EHS with the development, implementation, and continuous improvement of all EHS management systems and programs. Support business plan KRAs/goals and develop and monitor to ensure goals are achieved. Develop implement, document, and periodically review Company training programs related to EHS to protect workers and satisfy regulatory and site requirements. Develop, review, approve and implement SOPs, Work Instructions, and all other EHS documents. Support site management with incident investigations, root cause analyses, and assignment & tracking of CAPAs as needed. Partner closely with internal cross-functional stakeholders to communicate, secure support, and inform the facility of EHS compliance risks and gain alignment on EHS initiatives and priorities. Ensure that the site complies with applicable EHS regulations and Company requirements, guidelines, and policies and takes the necessary steps to prevent non-conformances. Ensure that all EHS reporting, both internally and externally, is conducted timely and accurately. Assist with safety evaluations and risk assessments (JHA, PHAs, HAZOPs, FMEAs, PSSRs, etc.) of new products, processes, facilities, and equipment and recommend CAPAs to improve safety performance. Provide technical support for EHS programs (LOTOTO, Hazcom, Respiratory Protection, Chemical Hygiene, etc.) Assist with the development of annual EHS KRAs, goals, plans, objectives, and budget as directed by the AD. Complete requisite environmental reporting (Tier 2, biennial hazardous waste, air emissions, TRI, and stormwater) as directed by AD. Reporting injury/illness data electronically to OSHA & generating and posting requisite site reports Assigning and managing EHS education and training using MasterControl software system. Conducing new hire orientation (NHO) safety training and education as needed. Maintain and control site SDSs for RMs, SMs, IPs, and FPs per Hazcom Standards. Conduct qualitative/quantitative exposure assessments for hazardous materials and HPAPIs. Assessing site compliance with corporate policies/guidelines and federal, state, and local regulations through periodic workplace audits and walkthroughs (Gemba walks). Responsible for guiding Site Safety Committee (SSC) activities and initiatives. Work closely with Facilities, Engineering, Manufacturing, and Laboratory teams to ensure contractors and subcontractors work in compliance with all site EHS requirements (Safe Work Permits, PRCS entries, LOTOTO, hot work, etc.) Education / Experience Bachelor's degree in EHS, Engineering, Chemistry, Industrial Hygiene, or similar degree required. Master's degree in EHS or related field preferred. Minimum of 5 years of EHS experience in a pharmaceutical manufacturing environment preferred. EHS Certifications are a plus (CSP, CIH, QEP, CHMM). Sustainability & ESG experience are a plus. SDS authoring HPAPI containment and isolation equipment and practices. Job Competencies Excellent organizational and planning skills. Strong leadership and ability to influence all levels of employees. Strong problem solving/troubleshooting skills. Strong auditing and risk-assessment skills. Ability to self-lead work tasks to completion. Proficient in MS Office (Word, Visio, PowerPoint, & Excel), Emission Master, SAP, and Smartsheet. Strong written, verbal, and interpersonal communication skills. Excellent presentation and adult learning skills. Ability to develop, perform, evaluate, and troubleshoot within a scientific discipline. Self-motivated and detail oriented. About the Company Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group. Equal Employment Opportunity Statement PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions. #J-18808-Ljbffr