Scientist, Analytical Sciences & Technology

Net2Source

East Syracuse, NY

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JOB DETAILS

SALARY

$34.46–$40 Per Hour

SKILLS

Agile Programming Methodologies, Analysis Skills, Analytical Method Development, Assays, Biology, Biotech and Pharmaceutical, Calibration, Cell Cultures, Chemistry, Clinical Support, Communication Skills, Continuous Improvement, Delivery Management, Drug Products, Entrepreneurship, Establish Priorities, GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), Housekeeping/Cleaning, ICH Regulations, Identify Issues, Industry/Trade Analysis, Instrumentation, Interpersonal Skills, Laboratory Management, Leadership, Manufacturing, Mass Spectrometry, Operational Audit, Order Supplies, Presentation/Verbal Skills, Problem Solving Skills, Procedure Development, Process Development, Process Improvement, Quality Assurance Methodology, Quality Control, Real-time PCR (qPCR), Regulations, Regulatory Submissions, Risk, Safety/Work Safety, Scientific Publications, Specimens/Samples, Standard Operating Procedures (SOP), Team Player, Technical Writing, Testing, Time Management, UV/VIS (Ultraviolet-Visible Spectroscopy), Writing Skills

LOCATION

East Syracuse, NY

POSTED

30+ days ago

Join a Global Leader in Workforce Solutions Net2Source Inc.

Who We Are
Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision Right Talent. Right Time. Right Place. Right Price.

PN: This is a temporary position that will be filled for 8 months, however, may be extended based on employee performance and planned workload.

POSITION SUMMARY
The Contractor Scientist within the Analytical Science and Technology team is responsible for supporting analytical method lifecycle activities including method development, qualification, validation, and technical transfer of methods for the testing of biologics drug substance and drug product samples. The candidate will execute non-GMP testing, non-GMP stability testing, reference standard qualification, and comparability studies to support clinical and/or commercial GMP manufacturing.

Duties/Responsibilities:
" Develop, author, and peer review standard operating procedures, analytical methods, protocols, reports, and other associated scientific technical documents.
" Perform testing of study samples to support upstream and downstream process development, characterization, and process improvements.
" Document and evaluate experimental results and perform data verification and trending.
" Provide technical expertise and guidance to support investigations and help troubleshoot analytical operational issues.
" Identify new analytical technologies and opportunities for technical advancements.
" Support the preparation and review of regulatory submissions related to analytical procedures, method development and validation, specifications, reference standards, extended characterization, and product stability/ shelf-life.
" Support regulatory inspections, third-party audits, and customer audits through participating in inspection readiness and addressing inspectional findings.
" Perform routine laboratory activities including sample management, instrument maintenance and calibration, inventory and ordering of supplies, general housekeeping, and other related activities.
" Work in a diverse group environment while focusing on inclusivity and safety to produce high quality, compliant results.

Quals--
Education/Experience/ Licenses/Certifications:
" B.S in Biology, Chemistry, Biotechnology, or equivalent area of related study, with 2-5 yrs. industry experience in biologic/protein analytics or M.S./Ph.D. with 0-5 yrs. experience.
" Experience across the analytical method lifecycle in protein biotherapeutics for a variety of methodologies and instrumentation used in the testing and characterization of raw materials, excipients, in-process, drug substance, and drug product samples including HPLC/UPLC methods and various other analytical techniques (i.e., qPCR, ELISA, CE-SDS, iCIEF, SDS-PAGE, UV-VIS, western blotting, mass spectrometry, and cell-based assays) is preferred.
" Working knowledge and experience in the biopharmaceutical development process, GMP, PAT, CMC and regulatory guidance, ICH guidelines, and compendial requirements is desired.
" Experience authoring, validating, and coordinating timely transfer of test methods with and to Quality Control laboratories is desired.

QUALIFICATIONS
Specific Knowledge, Skills, Abilities, etc:
" Strong written, verbal, presentation, and interpersonal communication skills.
" Detail oriented with good organization skills.
" Ability to prioritize, independently manage and complete deliverables within given timelines.
" Ability to problem solve and apply risk-based critical thinking in a technical environment.
" Demonstrated history of continuous improvement is desired

Physical Demands:
" The role is a combination of laboratory and office-based work.
" The laboratory work requires appropriate levels of personal protective equipment (PPE). The role may require contact with
biohazardous materials such as live cell cultures and other hazardous chemicals including methotrexate, acids, and caustics.
Powdered materials and high temperature liquids and solids may also be handled. Use of a respirator may be required.
" Frequent repeated motions such as pipetting, lifting, bending, twisting, squatting, crouching, sitting, kneeling, climbing on stepstools, and reaching may be required. Repetitive use of arms/hands/wrists and grasping may be required.
" The role may require unassisted lifting (not to exceed 50 lbs.).

Work Environment:
" Position is primarily laboratory and office based with occasional work in a classified GMP manufacturing environment.
" Dynamic, fast-paced, interactive, and entrepreneurial environment.
" Position is a team and project-based position that may require occasional shift work, weekends, and holidays.

Why Work With Us?
We believe in more than just jobs we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter.
Our Commitment to Inclusion & Equity

Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.

Awards & Recognition
" America's Most Honored Businesses (Top 10%)
" Fastest-Growing Staffing Firm by Staffing Industry Analysts
" INC 5000 List for Eight Consecutive Years
" Top 100 by Dallas Business Journal
" Spirit of Alliance Award by Agile1
Ready to Level Up Your Career?
Click Apply Now and let's make it happen.

About the Company

Net2Source

Net2Source Inc. is a Global Workforce Management Solutions Company, headquartered in New Brunswick, NJ with its local offices in Texas, California, Florida, Illinois, Colorado and Michigan and its global operations in Canada, UK, Europe, UAE, Malaysia, Australia, China, Singapore and India. Net2Source offers a wide gamut of consulting solutions customized to specific client needs including but not limited to Application Development, Workforce Management and Project Consulting. Whether it’s a Fortune client, whether it’s a System Implementer or whether it is a Start -up, our recipe to success – Exceed expectations! Under promise, over deliver.

COMPANY SIZE

50 to 99 employees

INDUSTRY

Other/Not Classified

WEBSITE

http://www.net2source.com

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