Responsibilities include:

	Managing and performing scale-up, optimization and validation batches for current and newly developed pharmaceutical and OTC products.
	Providing scientific and technical support for the transfer of technology from product development to production.
	Evaluating current products and production methods and recommending and participating in continuous process improvement.
	Preparing and executing protocols for process optimization and validation batches.
	Coordinating inter-departmental resources in product development and production, including staff, equipment, facilities and supplies.
	Providing scientific and technical support for non-conformance investigations.
	Developing and maintaining accurate documentation as required in a cGMP regulated pharmaceutical environment.

Qualifications and key competencies include:

	Bachelor’s degree or higher in Chemistry, Chemical Engineering and/or Pharmaceutical Science.
	Five or more years related industry experience in manufacturing, process development and/or process validation of semi-solid and liquid pharmaceutical and/or OTC products.
	Excellent writing and PC skills required to develop batch records and validation protocols, along with the verbal communication skills necessary to work effectively with other departments.
	Must be familiar with equipment commonly used in a manufacturing environment.
	Flexibility to work overtime and alternate shifts, when required.

How To Apply