Analytical Scientist

Analytical Scientist

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

• Title: Analytical Scientist
• Location: Somerset, NJ
• Industry: Pharmaceutical
• Shift: Monday-Friday: 8:30AM-5:00PM
• Salary: $47/ hour paid weekly with benefits options
• Employment Type: Contract through April 2025

Environment: This client is a worldwide leading generic pharmaceutical company and one of the top 15 companies in the industry. With over 45,000 employees in 60 countries worldwide, they are proud to say that our employees are the reason for our success . They believe in empowering employees, presenting them with new challenges and letting them grow and develop professionally.

Job Scope:

• The primary responsibilities of this position are to provide analytical support for the Analytical Development team in the development, validation and transfer of analytical methods, with limited supervision.
• The Scientist will also perform routine analysis of APIs, excipients and finished product using laboratory techniques and instrumentation.
• Hands-on method development, method improvement, and validation, including but not limited to HPLC, GC, Dissolution, UV-Vis Spectroscopy, FTIR, Microscopy, PSD etc.
• Assists in complex experiments and tasks such as unknown impurity identification and excipient compatibility studies.
• Prioritizes activities to provide timely analytical support to product development.
• Anticipates analytical issues early in the R&D development process and provides long term planning for analytical method development and improvement.
• Supports formulation development and transfer activities for assigned projects.
• Supports the investigations of method performance, reliability and conducts optimizations studies, as needed.
• Participates in the preparation of technical documents, including validation protocols and reports, reference standard qualification reports and analytical test procedures.

Job Requirements:

• BS, MS in Chemistry, Biochemistry or related discipline with 4+ years (BS), 2+ years (MS) of experience in pharmaceutical industry.
• Prior experience in Analytical R&D is preferred
• Working knowledge of GXP, regulatory (ICH) and compendial (USP/EP/JP) requirements.
• Ability to multi-task and demonstrate diplomatic skills.
• Proficient (excellent) in English verbal and written communication skills to convey and receive ideas and instructions to/from others within and outside the organization.
• Strong organizational skills.
• Proficient skills in Microsoft Office applications (Word, Excel, PowerPoint).
• Ability to work effectively under pressure to meet deadlines.

EOE/ADA

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