Scientific Associate II - Analytical

Employer
CSL Behring
Location
Holly Springs, North Carolina
Posted
Jan 21, 2021
Ref
R-127828
Required Education
Bachelors Degree
Position Type
Full time
About CSL

With operations in 35+ nations and ~27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is one of the largest influenza vaccine companies in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

Job Description

Responsibilities:
  • Performs qualitative and quantitative analysis of viral vaccine candidates and standards under limited supervision/guidance.
  • Executes analytical UPLC and HPLC assays following SOPs in support of vaccine process and product development programs.
  • He/she will contribute to analytical assay development, optimization, qualification, and in-process control to support product and process development, stability, release and characterization of Tox and CTM.
  • Provides support on reviewing documentation in notebooks and reviewing data in LIMS for specific lab based processes.
  • Able to work under tight deadlines.
  • Ensures all experimental procedures and documentation are compliant with highest quality and regulatory standards.
  • Partners with diverse team members from various functions, countries and members at various levels in the organization.
  • Authors study protocols, characterization reports, and/or scientific manuscripts for external publication and patent application
  • Uses scientific and statistical knowledge to support product, process and testing related investigations and deviations including complaint, deviation, OOE and OOS investigations that require support for development work


Qualifications:
• BS with a minimum of 3 years of laboratory experience, specifically with HPLC or UPLC systems

• Experience in biotech or pharmaceutical development in one or more of various disciplines including (but not limited to) Analytical Chemistry, Biochemistry, Biomolecular Sciences, etc. Hands on experience required for LC method development on large and/or small molecule analysis

• Hands on experience with RNA analysis is highly desired

• Experience on CE is beneficial

• Data collection and reporting with knowledge of GLP/GMP environments preferred

• Good verbal & written & presentation communication skills in a cross functional environment