Senior Formulations Scientist

sciAre you ready to join a growing, global drug development and manufacturing organization that puts people first?  Come to Adare!  We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world.  Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success.  With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!

Join our mission at Adare!

What can Adare offer you?


* Medical/dental/vision/life – low employee premiums


* 401k with a highly competitive match


* Generous PTO, including floating holidays


* Career growth and internal opportunities


* Tuition reimbursement


* Relocation assistance


* Performance-based bonus


* Employee Recognition Programs

 

We are seeking to hire a Senior Formulation Scientist to join our Pharmaceutical Development Team…

 

If any of the below describes you, we would love to meet you! 

JOB SUMMARY

The Senior Formulations Scientist will report to the Associate Director of Formulations, and will be expected to develop pharmaceutical dosage forms with an emphasis on immediate and modified-release solid oral dosage forms.  This is a client-facing role providing a career path to advancement within Pharmaceutical Development. 

 

RESPONSIBILITIES AND LEARNING OPPORTUNITIES


* Design and perform formulation development studies on immediate and modified release oral solid dosage forms defined by management/customer and assume the responsibility needed to meet the product specific objectives.


* Develop new products utilizing existing and new technologies available within the industry from pre-formulation to manufacturing stage.


* At times, interact directly with Adare’s clients in project update meetings; provide technical expertise, presentation of data


* Write development and cGMP batch records, stability study protocols, in-process and finished product specifications and product development reports


* Assist both Manufacturing and Quality Assurance departments in scale-up and production trouble-shooting


* Perform technology transfer to customer production sites and train/assist customer personnel in scale-up and production.


* Develop and/or locate new technologies that will be of interest to the Company’s product development objectives.


* Supervise/train formulation scientists and ensure their activities comply with CGMP regulations.


* Conducts and manage development projects with manager’s guidance and ensure the successful scale-up of a new product and/or process.


* Comply with all regulations as specified by OSHA, EPA, FDA, DEA, etc., and as defined in the Corporate Hygiene plan.


* Assist in writing and preparation of ...