Highlights
This role provides a combination of analytical laboratory testing and non-laboratory support to the QC Product Technical Support department in support of product lifecycle management. In Chemistry, Biology or related scientific discipline with a minimum of 5 years of applicable laboratory experience or M.S with a minimum of 3 years of relevant experience.
Numbers & Facts
| Location | Andover, MA |
| Industry | Staffing/Employment Agencies |
| Salary | $50 |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
Description
ROLE SUMMARY
This role provides a combination of analytical laboratory testing and non-laboratory support to the QC Product Technical Support department in support of product lifecycle management. The scope includes analysis of biological products as well as authoring documentation to support lifecycle activities. Responsibilities include analytical method optimization, method validation, comparability assessments, and the evaluation of new technologies. The role requires a solid understanding of scientific principles underlying test methods, method validation requirements, data analysis, and cGMP requirements.
ROLE RESPONSIBILITIES
Provide technical support for new or established analytical methods, troubleshooting methods and method improvements.
Analyze and interpret results with a solid scientific understanding, ensuring accuracy, completeness, and compliance.
Author test methods, validation protocols and reports, as well as supporting technical documentation for product lifecycle management.
Identify technical issues, method performance issues, instrument malfunctions and methodology problems and participate in necessary investigations.
Maintain all related data and records in compliance with cGMPs and quality procedures.
Track timelines and deliverables, and communicate effectively across teams to ensure alignment and timely execution.
BASIC QUALIFICATIONS
B.S. In Chemistry, Biology or related scientific discipline with a minimum of 5 years of applicable laboratory experience or M.S with a minimum of 3 years of relevant experience.
Knowledge and practical application of relevant analytical techniques
Experience within the biopharmaceutical industry, including knowledge and experience relevant to biopharmaceutical unity operations and/or laboratory operations.
Experience in method troubleshooting and laboratory investigations
Experience in validation of analytical methods
Experience with cGMPs and regulatory guidance
Experience with HPLC, Client, gel, spectroscopy
This role provides a combination of analytical laboratory testing and non-laboratory support to the QC Product Technical Support department in support of product lifecycle management. The scope includes analysis of biological products as well as authoring documentation to support lifecycle activities. Responsibilities include analytical method optimization, method validation, comparability assessments, and the evaluation of new technologies. The role requires a solid understanding of scientific principles underlying test methods, method validation requirements, data analysis, and cGMP requirements.
ROLE RESPONSIBILITIES
Provide technical support for new or established analytical methods, troubleshooting methods and method improvements.
Analyze and interpret results with a solid scientific understanding, ensuring accuracy, completeness, and compliance.
Author test methods, validation protocols and reports, as well as supporting technical documentation for product lifecycle management.
Identify technical issues, method performance issues, instrument malfunctions and methodology problems and participate in necessary investigations.
Maintain all related data and records in compliance with cGMPs and quality procedures.
Track timelines and deliverables, and communicate effectively across teams to ensure alignment and timely execution.
BASIC QUALIFICATIONS
B.S. In Chemistry, Biology or related scientific discipline with a minimum of 5 years of applicable laboratory experience or M.S with a minimum of 3 years of relevant experience.
Knowledge and practical application of relevant analytical techniques
Experience within the biopharmaceutical industry, including knowledge and experience relevant to biopharmaceutical unity operations and/or laboratory operations.
Experience in method troubleshooting and laboratory investigations
Experience in validation of analytical methods
Experience with cGMPs and regulatory guidance
Experience with HPLC, Client, gel, spectroscopy
About Company
We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.