QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA
Responsibilities:
- Provide technical expertise for the management of Environmental Health & Safety programs at client.
- Under minimal supervision, perform EH&S duties for program design, development and implementation.
- Ensure compliance with EH&S federal, state and local regulations.
- Evaluate existing and new regulations
- Develops new programs and implement changes as necessary.
- Interface with EH&S regulatory agencies.
- Be recognized as a program liaison to external agencies.
- Prepare for and conduct inspections with agency representatives present.
- Prepare reports, responses to inquiries and conduct monitoring.
- Design, develop and implement EH&S programs.
- Maintain & continuously improve EH&S programs to support.
- Assess EH&S practices to management term liability for planning, acquisitions, etc.
- Design, develop and implement training programs.
- Implement & document procedures/policies.
- Determine impact of new operations/processes/capital projects upon the EH&S programs.
- Developing program changes necessary to support business objectives.
- Analyze existing and future processes to identify cost-effective solutions to reduce EH&S impacts.
- Design and implement programs for conducting periodic audits/inspections.
Qualifications:
- Bachelor’s or master’s degree in Engineering or Safety
- Two (2) years of Previous Experience
- Knowledge and experience in: Process Safety, Process Safety Management (PSM), High Risk Processes, Hazardous Gases, Combustible Dust, Risk Assessments, JHAs, and Machine Safeguards.
- Must be proficient in Microsoft Office and other computer software systems.
- Must have good technical & business writing skills and good communication and team skills.
- Advancement requires increased independent actions, responsibilities, program development and project management
- Experience in pharma manufacturing environment.
- Availability for administrative shift
- Shift: M-F 8:00-5:00 pm (special support for 3rd shift may be required)
What We Do
The Quality Consulting Group is a pharmaceutical, biotechnology, food and medical device specialty consultant that supports the manufacturing industry; services are provided in multiple areas including: Regulatory Compliance, Quality Operations, Validation, Manufacturing, Training and Technical Support. Starting, as individual services provider since 2002, Quality Consulting Group has supported clients implementing the latest standards such as Validation Guidance, ICH Guidelines, and Process Excellence and Risk Management tools.
Quality Consulting Group has provided expertise in such areas as: business, operational, quality, regulatory and manufacturing strategies; organizational structures; management controls; manufacturing and quality systems methodologies and practices; compliance programs; and accuracy reviews; FDA, EMEA and other regulatory matter
