Job Information
Actalent Research Associate I in Norwich, New York
Research Associate I
Job Description
The Method Development and Analytical Services (MDAS) Research Associate II is an experienced professional responsible for performing sample testing and validating methods to support the development and commercialization of pharmaceutical products. This role involves bench chemistry testing for new products, incoming transfer of existing products, and analytical support throughout the product life cycle. The Research Associate II will also assist with method development, transfer, validation, and verification of methods related to raw materials, semi-finished/finished products, and stability. Additionally, active participation as the analytical chemistry expert on work teams and customer communication may be required.
Responsibilities
Perform hands-on laboratory bench work and sample testing to support pharmaceutical product development, including assays, related compounds testing, dissolution, and uniformity tests.
Develop, optimize, and troubleshoot analytical methods for testing raw materials and products.
Validate analytical methods necessary for pharmaceutical product commercialization, including evaluating requirements, equipment acquisition, reference standards, drafting protocols, and training.
Author and review method validation, verification, and transfer protocols and reports compliant with cGMP regulations and industry standards.
Conduct laboratory testing with high accuracy and precision, including quantitative weighing, sample handling, instrumental analysis using HPLC, GC, dissolution, UV-visible spectrophotometry, and other techniques.
Evaluate data for conformance with specifications and investigate unexpected results.
Peer review experimental documentation, calculations, and results for scientific integrity.
Contribute to troubleshooting, method development, and validation alongside senior staff.
Address method installation issues efficiently, determining root causes and solutions.
Provide training and guidance to junior staff on specific techniques.
Interact with project teams to influence decisions and drive projects forward as the analytical expert.
Work efficiently to meet deadlines and provide regular progress reports to leadership.
Ensure compliance with US and international regulatory agencies and analytical testing requirements.
Maintain laboratory equipment and perform housekeeping duties.
Travel to external laboratories for training or to provide training, including potential international travel.
Essential Skills
BS in Chemistry or related science with 2 years of experience in a pharmaceutical development or QC laboratory (or equivalent education and experience, such as a PhD with analytical laboratory experience).
Familiarity with GMP regulations and ICH guidelines.
Expertise in HPLC, GC, dissolution, UV-Vis, X-ray Diffraction, IR, PSD, wet chemistry, and USP/EP compendial test procedures.
Experience with chromatographic data acquisition systems (e.g., Empower, ChemStation).
Strong analytical skills and ability to apply scientific theory and techniques to problem-solving.
Advanced proficiency in Microsoft Word and Excel.
Excellent written and verbal communication and presentation skills.
Strong organizational skills and the ability to manage and complete projects on time.
Additional Skills & Qualifications
- Experience with Empower software is highly preferred.
Work Environment
This role is based in a laboratory environment. The position may require travel to external laboratories for training purposes, which could include international travel. The work involves handling various laboratory equipment and ensuring compliance with regulatory standards. The dress code is typical for a laboratory setting, including the use of personal protective equipment as necessary.
Pay and Benefits
The pay range for this position is $62000.00 - $65000.00/yr.
Company Benefits• Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Norwich,NY.
Application Deadline
This position is anticipated to close on Mar 4, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
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