Research Associate I

Job Description

The Method Development and Analytical Services (MDAS) Research Associate I is a technical resource performing the analytical testing necessary to support the development and commercialization of new pharmaceutical products. The MDAS Research Associate I is responsible for performing bench chemistry testing for release, stability, and product characterization. The MDAS Research Associate I performs laboratory work independently commensurate with their training and experience.

Responsibilities

• Perform hands-on laboratory bench work and sample testing to support the development of pharmaceutical products, including assays, related compounds testing, dissolution, uniformity, and other tests.
• Develop, optimize, and troubleshoot analytical methods for testing raw materials and products under the guidance of staff.
• Conduct laboratory work for method validation, verification, transfer, equipment maintenance, calibration, reference standards qualification, drafting methods/reports, and training.
• Carry out laboratory testing with a high degree of accuracy and precision using techniques such as HPLC, GC, dissolution, UV-visible spectrophotometry, and more.
• Provide training and guidance to junior staff on specific techniques as directed by management.
• Process sample data to determine reported results and ensure results are appropriately documented in computerized systems or directly reported to stakeholders.
• Evaluate data for conformance with specifications, expectations, and trends, and investigate unexpected results.
• Peer review experimental documentation, calculations, and results generated by other staff for adherence to established procedures and scientific integrity.
• Comply with laboratory procedures and SOPs, following written and verbal instructions from staff with minimal supervision.
• Perform administrative functions, materials sourcing, vendor inquiries, and exploration of new technologies to ensure project progression.
• Work efficiently, manage time to meet deadlines, and provide regular progress reports to leadership and during team meetings.
• Ensure compliance with all US and international regulatory agencies and compliance requirements related to analytical testing.
• Maintain laboratory equipment and facility, performing laboratory housekeeping duties as necessary.

Essential Skills

• BS in Chemistry or related science plus 2 years of experience in a pharmaceutical analytical laboratory.
• Familiarity with GMP concepts related to pharmaceutical quality control.
• Practical hands-on experience with HPLC, GC, UV-Vis spectroscopy, dissolution, titration, FTIR, wet chemistry, and USP/EP compendial test procedures.
• Strong analytical aptitude and ability to apply knowledge and experience to solve problems.
• Advanced computer skills, specifically in Microsoft Word and Excel.
• Refined written and verbal communication and presentation skills.
• Strong organizational skills and the ability to manage and complete assigned projects on time.

Additional Skills & Qualifications

• Experience with method validation and development.
• Ability to work independently with minimal supervision.
• Experience in training and guiding junior staff.

Work Environment

The work environment includes performing laboratory bench work with various analytical techniques such as HPLC, GC, UV-Vis spectroscopy, dissolution, and more. The role requires compliance with US and international regulatory agencies and GMP standards. The position offers room for growth and benefits, including PTO

Pay and Benefits

The pay range for this position is $60500.00 - $60500.00/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 Syracuse,NY.

Application Deadline

This position is anticipated to close on Mar 10, 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 for other accommodation options.

Salary : $60,500