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New Haven, CT 06510

Posted: 07/31/2024 Job Number: 72889 Pay Rate: Pay Rate: $22.76/Hr.

Job Description

Associate Scientist Pharmaceutical
New Haven CT
Contract -1st Shift
Pay Rate: $22.76/Hr.
Benefits: medical, dental, vision, 401k

Requirements: Associate Scientist Pharmaceutical

US Citizenship
BS or MS degree in Biochemistry, Pharmaceutical Science, Chemical Engineering, or relevant field with 0 to 2 years relevant work experience with a pharmaceutical or biotechnology company
Solid understanding of protein stability, thermodynamics, and mechanism of protein degradation.
Experience of working with H/UPLC’s, imaged capillary electrophoresis (iCE/Maurice), Ion Exchange Chromatography (IEX), Micro-flow imaging (MFI), light obscuration (LO), DLS, NanoTemper and DSC is desirable.
Ability to execute experiments with minimal supervision is required.
The individual must be able to work in a collaborative setting and has ability to adhere to timelines is essential.
Excellent interpersonal, collaborative and communication skills
Experience with various software packages like MS Office programs, including Word, Excel, Outlook, and PowerPoint
The duties of this role are conducted in a lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video and electronic messaging; engage in problem solving and non-linear thought, analysis and dialogue; collaborate with others; maintain general avail

Job Description: Associate Scientist Pharmaceutical The position is required to join Injectable Drug Product Development group of our clients Rare Disease Pharmaceuticals Pharmaceutical Development and Clinical Supply (PDCS) department. The job entails experimental work on various aspects of drug product characterization, including formulation development, in use compatibility studies for intravenous and subcutaneous administration, process development to support drug product manufacturing support, and particulates testing. The ability to work with minimal supervision as well as part of the team is essential. The position entails execution of the studies, data processing and compiling to generate development reports as well as other required documentation.
Responsibilities: Associate Scientist Pharmaceutical

With some supervision, design and execute development studies for Alexion pharmaceuticals’ clinical drug candidates and commercial products, characterizing protein drug conformational and colloidal stability using industry standard methodology (e.g., circular dichroism, differential scanning fluorimetry, analytical ultracentrifugation, size-exclusion chromatography, etc.)
Can prioritize multiple assigned tasks and projects. The ability to work independently as well as part of the team is essential.
Execute drug development studies including physico-chemical characterization, particulates testing, and stability studies for the client's rare disease pharmaceuticals’ drug candidates and commercial products
Assist in preparation of internal technical reports on the executed studies with minimal supervision
Participate in cross-functional development teams

Preferred Experience & Skills: Associate Scientist Pharmaceutical

Experience of working with sub-visible particulates characterization and testing
Experience of working with biophysical testing and analytical testing
Familiarity with regulatory guidelines.
High level proficiency in MS Office software including Word, Excel, Outlook, and PowerPoint.
Experience with electronic record keeping software, like ELN, EndNote, e-logbooks; maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade, etc.) will be a plus.
Ability to take initiative in problem solving and finding solutions to scientific challenges.
The individual must be able to work in a collaborative setting and ability to adhere to timelines is essential.
Excellent people skills are required, as is the strong ability to communicate effectively

72889

EEO Statement Apollo Professional Solutions, Inc. is an equal opportunity employer. We provide equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, marital status, age, national origin, ancestry, disability status, medical condition, pregnancy, genetic information, protected veteran status, gender, sexual orientation, gender identity or expression, or any other status or characteristic protected under federal, state, or local law.

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