If you are looking to move up in your pharmaceutical career, this position could be the opportunity for you! Our client is looking to expand their manufacturing capabilities and this newly created position would help build and oversee a team of chemist for the weekend shift.

Apply here to learn more about this exciting opportunity!

This position is onsite Friday- Sunday from 6am-6 : 30pm.

Responsibilities

• Write, revise, develop, evaluate, and review Standard Operational Procedures.
• Identify areas of improvement and implement efficient solutions that increase compliance, data integrity, efficiency and reduce chance of errors.
• Provide training and assistance to Quality Control group members. Formulate development plan for group members and develop succession plan.
• Assess equipment needs with regards to new technologies and capacity needs. Identify opportunities for out-sourcing of testing to optimize cost and efficiency.
• Manage and maintain project timelines and provide leadership supporting method improvements and development / validation activities.
• Perform data analyses and present findings and recommendations both verbally and in writing.
• Improve and develop analytical methods primarily utilizing HPLC, GC, and Wet Chemical methods of analysis.

Requirements :

• Bachelor’s degree
• 5 years of pharmaceutical experience in a laboratory environment required
• 3 years of experience in a supervisory role.
• Must have a comprehensive knowledge of cGMPs, DEA and FDA requirements.

Last updated : 2024-05-19