Are 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 and commercial manufacturing 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 Technical Services Scientist to lead our Validation and Technical Services Team…

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

　　JOB SUMMARY

　　In this position, the Scientist will focus on supporting commercial products. The main activities will be scale-up, technology transfer, process development, process optimization, troubleshooting, deviations, failure investigations, and technical writing. The Scientist will also participate in Lean Manufacturing and Operational Excellence projects.

　　RESPONSIBILITIES AND LEARNING OPPORTUNITIES

　　Manage scale-up, technology transfer, and process development of commercial products, manufacturing feasibility batches, writing batch records, and summarizing results for both internal and 3rd party manufacturing.

　　Develop and execute studies for process, equipment, and activities related to bulk drug delivery and finished dosage formulations developed by Research and Development (R&D) and products currently in commercial production to Adare, customer, and regulatory (domestic and foreign) requirements.

　　Support Manufacturing through process optimization, trouble-shooting, deviations and failure investigations, batch record revisions, and report writing. Supports Manufacturing, Quality Assurance, and Regulatory Affairs in technical issues.

　　Provide product impact assessments for deviations and investigations to QA and Regulatory Affairs.

　　Technical writing. Experimental protocols, experimental reports, batch records, deviations, investigations.

　　A main contributor and practitioner of Lean Manufacturing and Op Ex programs within the facility.

　　Technical experience and/or expertise in the operation of pharmaceutical equipment including but not limited to tablet presses, blenders, fluid beds, roller compactors, pan coaters, mixers, ovens, capsule fillers, packaging equipment, and other pharmaceutical equipment.

　　Operate independently and provide feedback and solutions to technical issues for both internal projects and projects at 3rd party sites.

　　Provide technical training and support to departments supported by the Technical Services department (Third party GSQ, Manufacturing, etc.).

　　Upholds Company policies, including the Professional Conduct Policy and Prohibition Against Harassment Policy, and the Business Ethics and Conduct Code.

　　Works in a cooperative manner with managers, supervisors, coworkers, customers, and the public.

　　Works effectively under deadlines.

　　Requirements

　　REQUIRED SKILLS AND QUALIFICATIONS

　　BS/BA degree from a four-year accredited university or college in Biology, Chemistry, Engineering, or related field; plus 5-8 years of related experience required.

　　Ability to continually learn on the job: new equipment, new manufacturing technologies, new raw materials, etc.

　　Problem solving and trouble-shooting abilities. Ability to determine the root causes of failures and problems.

　　Capable of scientific observation of processes; has ability to accurately record observations and draw conclusions from them.

　　Technical writing ability. Ability to explain scientific and technical issues to a non-specialist audience.

　　Good working knowledge of “Good Manufacturing Practices”.

　　Excellent interpersonal written and oral communication skills.

　　Proficient in Microsoft Office – Word, Excel, PowerPoint, Visio. Statistical software such as JMP.

　　Ability to coordinate, contribute to, and work within cross-functional teams.

　　Able to prioritize duties and work on multiple projects with minimal supervision.

　　Possesses good attention to detail and excellent organizational skills.

　　Benefits

　　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