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Full-time
bachelor degree, postgraduate degree
Competitive Compensation, Exposure To International Pharmaceutical Operations, Flexible Work Arrangements, Travel Support
Posted 4h ago
~40 hrs/week
Responsibilities
The Mid-Level EHS Expert is responsible for managing EHS compliance programs and driving operational excellence across assigned sites. Key duties include leading incident investigations, conducting risk assessments, and training staff on regulatory obligations.
Requirements
Candidates must have a degree in EHS, Public Health, or Engineering with 5 to 15 years of progressive experience, preferably in pharma or biotech. Fluency in Spanish is required, and proficiency in EHS software platforms is highly desired.
Full job description
PharmEng / Efor is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our dedication to quality, safety, and excellence in everything we do. As we continue to grow, we are looking for a highly qualified and motivated EHS Expert to join our team.
Position Title: Mid-Level EHS Expert
Location: Madrid
Type of Contract: Full-Time / On site
Position Summary
The Mid-Level EHS Manager is a seasoned professional responsible for independently managing EHS program areas and driving operational excellence across assigned sites. This role includes ownership of compliance programs, training delivery, and leadership in risk management and continuous improvement initiatives.
Candidates must be fluent in Spanish, fluency in English is a plus.
Lead incident investigations using root cause analysis tools and issue corrective/preventive actions (CAPAs).
Conduct risk assessments and ensure appropriate controls are implemented and maintained.
Coordinate permitting and reporting activities with internal and external stakeholders.
Train staff on site-specific hazards, emergency response, and regulatory obligations.
Interface with regulators and participate in inspections/audits.
Lead cross-functional EHS meetings and safety committees.
Mentor junior EHS professionals and support contractor safety oversight.
Qualifications:
Bachelors or Masters degree in EHS, Public Health, Engineering, or equivalent.
5 - 15 years of progressive experience in EHS program management, preferably in pharma or biotech sectors.
Strong knowledge of OSHA, EPA, DOT, and applicable local/state regulations.
Demonstrated leadership in EHS audits, incident management, and training.
Hands-on experience leading incident investigations, root cause analysis, and corrective/preventive action planning.
Experience collaborating with cross-functional teams (Operations, Quality, Engineering, R&D) to embed a strong EHS culture.
Proficient in EHS software platforms and reporting systems (e.g., Gensuite, VelocityEHS).
Strong interpersonal, coaching, and communication skills.
Fluent in Spanish and English (advanced or native level required).
What We Offer
Competitive compensation based on experience and project scope.
Exposure to international pharmaceutical operations and regulatory environments.
Opportunity to lead high-impact injectable validation programs.
Flexible work arrangements and travel support.
Collaborative and technically driven work culture.
Join us: If you are a dedicated and highly motivated individual with a passion for ensuring the highest standards of EHS in the Pharmaceutical Industry, we encourage you to apply. PharmEng / Efor offers a dynamic and inclusive work environment, competitive compensation, and opportunities for professional growth. Be part of our team and contribute to the success of our industry-leading solutions.
PharmEng / Efor is an equal opportunity employer and welcomes applicants from all backgrounds.
Thank you for your consideration and application! We review all resumes and submissions, however, due to the high volume of applications we receive, only approved candidates will be contacted.
Related keywords
EHSRCRAHAZCOMBiosafetyLOTOOSHAEPADOTGensuiteVelocityEHSPharmaceuticalBiotechRoot Cause AnalysisCAPARisk ManagementSafety Committees
Now part of the Efor Group | Committed To Excellence
Industry
Pharmaceutical Manufacturing
Company size
201-500 employees
Headquarters
Toronto, Ontario
LinkedIn followers
41,286
PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.
As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.
Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.
At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.
Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).
Offices: 23 Lesmill Road, Suite 410, Toronto, Ontario M3B 3P6, CA · 2475 Northwinds Parkway, Suite 200, Alpharetta, Georgia 30009, US · 2500 Regency Pkwy, Cary, North Carolina 27518, US · 866 Yuhangtang Road, Hangzhou, CN · 116c 2F Quang Trung Street, Haoni City, VN
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