What are the responsibilities and job description for the Technical Specialist position at Clear Point Consultants?
Our client is seeking a Technical Specialist to support to analyze process data using statistical analysis software. The ideal candidate will have a strong understanding of drug product manufacturing and experience with data analysis, technical writing, and pharmaceutical development.
Key Responsibilities:
- Perform data analysis of commercial drug product processes using statistical analysis software.
- Collaborate with cross-functional teams to ensure compliance with regulatory and quality standards.
- Assist in the development of technical reports, protocols, and presentations.
- Utilize MS Word and Excel for documentation and data management.
- Apply knowledge of pharmaceutical manufacturing processes to assess process performance.
- Contribute to technical writing for process validation and regulatory documentation.
Qualifications & Skills:
- B.S. (or equivalent degree) in a relevant scientific or engineering discipline.
- 1-3 years of experience in pharmaceutical development, manufacturing, or a related field.
- Skilled in MS Word and Excel; experience with Matlab, R, or JMP is a plus.
- Strong analytical skills with the ability to interpret complex process data.
- Experience with technical writing and documentation in a regulated environment.
- Knowledge of pharmaceutical development and manufacturing processes is highly preferred.
This role is ideal for individuals who have a passion for data-driven decision-making in pharmaceutical manufacturing and are looking to grow their expertise in process analytics and CPV.
