Summary of Key Responsibilities : Operate manufacturing equipment and instruments. Complete assigned tasks in a timely manner.
Conduct daily activities in an organized, efficient manner. Perform simple, routine, complex, and critical operations. Troubleshoot equipment issues, when necessary.
Ensure process equipment is appropriately maintained for operation. Perform and document operations in accordance with cGMP’s.
Execute equipment qualification protocols and validation protocols. Routinely draft and revise standard operating procedures and master batch records.
Recognize and initiate process deviations. Support continuous improvement initiatives by identifying areas needing improvement, recommending strategies for improvement, and implementing those strategies once approved.
Communicate effectively, both in written and verbal formats. Maintain training compliance. Ensure a safe working environment for all staff.
Required Qualifications and Skills : A.A.S. in a scientific discipline, or equivalent experience preferred. 3-5 years’ experience in a cGMP manufacturing environment is required.
Experience with semi-solids, creams, and gels is highly preferred Experience training / mentoring staff is a MUST! No direct reports.
Must be able to work within and adapt to electronic systems. Able to work in an intense, fast-paced work environment. Able to function, with guidance, in a rapidly changing environment while balancing multiple priorities simultaneously.
Able to work independently and as part of a team. Must be able to read, write and converse in English. Must have a good working knowledge of MS Office (Outlook, Word and Excel). Powered by JazzHR
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