EHS Specialist

2 days ago

Cape Town, South Africa Morpheus Recruitment Full time

Our client is looking for a **EHS Specialist (GMP)** to join a leading pharmaceutical organisation **in Lesotho on a 2 year contract.**

The objective is to produce Dronabinol API under EU-GMP conditions for distribution in Germany, Poland and the UK.

Role Responsibilities
- Must possess strong communication skills and demonstrate integrity and cooperation in working with diverse colleagues/groups.
- To monitor and analyze manufacturing facility Environmental Monitoring System (EMS) data.
- To maintain proper control of GMP facility with regard to EMS and facility issues.
- Assure environmental control in the facilities in adherence to cGMP requirements, Quality Standards, SOP’s and other regulatory requirements.
- Work responsibly, safely, with oversight of leadership.
- Strong teamwork and technical skills required.
- Will troubleshoot and solve problems with processes of equipment already in operation.
- Requires understanding of compliance, pharmaceutical, pharmacological, biological, and microbiological factors.
- Responsible for identifying and implementing efficiency, safety, quality and cost improvements on equipment and processes.
- Possesses the ability to critically analyze processes for trends, root cause failures, and investigations of day to day operations.
- Requires developing strategies and systems to improve.
- Ability to work in cross-functional teams with focus on deliverables, timelines, and meeting customer expectations and requirements.
- The EMS Specialist position supports multiple operating teams that serves as support to all for Environmental Monitoring System (EMS) and facility related issues.
- Supports the development and implementation of training programs, curricula, procedures and pertinent documents to address the skills & behaviors required to ensure that the aseptic area(s) operate in compliance.
- Serves as ongoing technical resource, overseeing that production lots are manufactured under required environmental conditions and practices as well as EHS and/or GMP requirements.
- Provides/assists in training as necessary, presents information to large groups in some cases.
- Works within the site change control systems to update compliance documents.
- Gathers, collects, and records data.
- Suggests/drives improvements in systems, equipment, and processes to improve compliance and/or efficiency.
- Ensures documentation is kept up to date and is updated within required periodic review requirements.
**Qualifications**

**Must-Have**
- 3+ years of experience in manufacturing
- HS diploma (equivalent) and 5+ years related experience in manufacturing operations or warehousing
- Demonstrated ability to interact effectively with all levels of the organization.
- Flexibility to respond to constantly changing conditions and priorities.
**Nice-to-Have**
- Pharmaceutical experience in Operations, Engineering
**Physical / Mental requirements**
- An aptitude for understanding process technology and equipment, aseptic processing, proven leadership ability, decision making ability, and excellent oral and written communication skills are essential.
- Demonstrated ability to interact effectively with all levels of the organization.

**Job Types**: Full-time, Temporary
Contract length: 24 months

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