Offers “Gsk”

Expires soon Gsk

Process Engineer

  • Zebulon (Wake County)
  • Design / Civil engineering / Industrial engineering

Job description

Details:
To provide support of technical and scientific activities including implementation of Product Control Strategies, technology transfer, product investigations, change management, and continuous
improvement projects.

Key Responsibilities:
- Support technical activities related to new and existing products, process optimization,
process and equipment troubleshooting and process validation.
- Manage, analyze and identify trends in data.
- Support activities relating to change of processes, components and raw materials utilizing
Change Control Procedures.
- Support investigations relating to manufacturing issues, product release performance and or
customer complaints.
- Support Technology Transfer activities for new products into the facility.
- Support Operational Excellence by identifying projects to improve yield, lower costs and
improve efficiency.
- Draft documents including Batch Documentation, Validation Protocols, Evaluation
Protocols/Reports, Investigation Reports and SOPs.
- Write simple evaluation reports.
- Support multiple process engineering projects and process validation initiatives.
- Participate in project teams to execute project goals and assignments.
- Support internal and external auditors and regulatory agencies as needed during inspections.
- Provide data gathering and analysis as needed to support technical projects.

Contact information:
You may apply for this position online by selecting the Apply now button.

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GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

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jobDetails

Desired profile

Basic qualifications:
BS in Engineering/ Pharmaceutical Science/Life Science

Preferred qualifications:
- Knowledgeable in cGMP's and regulatory requirements.
- Strong written and verbal communication skills.
- Working knowledge of pharmaceutical equipment and processes.
- Experienced with the investigational techniques and tools for process investigations and Technical Risk Assessment.
- Knowledgeable in the principles of cleaning validation, process validation and packaging validation.
- Proficient with Microsoft Project, Word and Excel.
- Statistical knowledge and use of Statistica, JMP, SAS or other data analysis software.

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