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Sr. Scientist, Technical Operations

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Job Details
Job Order Number
JC141231570
Company Name
CSL Behring
Physical Address

Kankakee, IL 60901
Job Description

Sr. Scientist, Technical OperationsUnited States of AmericaR-0930832010 CSL Behring L.L.C.

About CSL

With operations in 35+ nations and ~ 22,000 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 the second largest influenza vaccine company 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

Responsible for leading and executing PPD R&D process improvement activities in support of local manufacturing operations related to CSL Behring’s commercially licensed products and intermediates. Supports other CSL Behring global manufacturing sites producing plasma products or intermediates. Works closely with the data analytics team to exploit historical process data and interpret data analytics results to trouble shoot process challenges and identify improvement opportunities, particularly related to yield, cost, and robustness. Follows methodical process optimization and scale-up/down approaches to generate results; adheres to GMP compliant procedure to implement new process changes. Responsible for ensuring that studies are executed according to the site priorities using representative and qualified scale-down and pilot scale models per existing policies. Displays team work and global perspective while collaborating with other global PPD R&D groups in alignment with CSL Behring’s PPD strategic objectives.

Position Purpose:

The Sr. Scientist, Plasma Product Development (PPD) Technical Operations-II (TO-II) is responsible for leading and executing PPD R&D process improvement activities in support of local manufacturing operations related to CSL Behring’s commercially licensed products and intermediates. Support activities can also extend out to other CSL Behring global manufacturing sites producing plasma products or intermediates. The scope of the role includes process improvements (e.g., yield, robustness, and cost), work closely with the data analytics team to exploit historical process data and interpret data analytics results to trouble shoot process challenges and identify improvement opportunities. Follow methodical process optimization and scale-up/down approaches to generate results, and follow GMP compliant procedure to implement new process changes. The incumbent is responsible for ensuring that studies are executed according to the site priorities using representative and qualified scale-down and pilot scale models per existing policies. The incumbent will display team work and global perspective while collaborating with other global PPD R&D groups in alignment with CSL Behring’s PPD strategic objectives.

The Sr. Scientist, PPD TO-II will be expected to keep abreast of new technologies and approaches and strategically employs these into the improvement and optimization of protein separation/purification processes in order to increase safety, compliance, and/or commercial profitability.

Main Responsibilities and Accountabilities:

As a Sr. Scientist, TO II, s/he focuses on short to long term activities. Areas of responsibilities include:

+ Ensuring agreed targets for quality, timelines, costs, and user requirements are met

+ Planning project plans with clear goals, timelines, and resources.

+ Effective partnership with Manufacturing, PD, BTT, TO-I and Data-Analytics functions to identify feasible process improvement opportunities.

+ Leading and executing protocol-driven Process improvement studies through effective utilization of DoE methodology.

+ Scale up from bench, to macro (kilo scale), and pilot scale.

+ Technical transfer to pilot scale and commercial scale.

+ Process characterization and support for validation activities.

+ Aligning functional outputs with developments in Regulatory and Quality guidances (e.g. ICH Q8/9/10/11 and FDA/EMEA process validation guidance).

+ Implementing best practices in bioprocess support (e.g. application of DOE methods, use of numerical risk assessments, application of principles of Quality by Design (QbD), implementation of value-added new technologies.

+ Full documentation of Process Improvement activities according to appropriate Quality standards and in support of IP.

+ Ensuring data integrity and scientific rigor in TO experiments

+ Support of regulatory filings and regulatory audits as appropriate.

Maintains awareness of cGXPs, good scientific practices, follow and promote lab and office safety.

Provides effective and transparent communications to customers and stakeholders such as but not limited to, Quality, Operations, and Global and local R&D and site senior management.

Position Qualifications and Experience Requirements:

Combination of academic qualification and appropriate * experience in biotech industry.

+ e.g., B. Sc. in Bioprocess Engineering or Biological Sciences +5 years.

+ e.g., M.Sc. in Bioprocess Engineering or Biological Sciences +3 years.

+ e.g., Ph.D. in Bioprocess Engineering or Biological Sciences +2 years.

**_*_** Appropriate: A combination of protein purification, plasma fractionation or bioprocess R&D manufacturing technical support experience .

Essential Skills, Knowledge and Experience:

+ Technical knowledge of product life cycle management, process change management, biological licensure, and plant operations,

+ Experience in regulatory and quality audits and generation of documentation to support quality assessments and for submission to regulatory agencies is required,

+ Demonstrated implementing innovative solutions,

+ Experience with project management,

+ Functional knowledge of CMC and equipment/facilities requirements,

+ Plasma fractionation experience is highly preferred. In-depth knowledge and hands-on experience with Protein separation/Purification process optimization and scale-up/down are required.

+ Proven knowledge or expertise of DoE/statistical analysis.

Strategic Skills

+ Business Acumen

+ Creativity

+ Decision Quality

+ Problem Solving

Energy and Drive

+ Drive for Results

Organizational Positioning Skills

+ Organizational Agility

+ Presentation Skills

+ Written Communications

Operating Skills

+ Informing

+ Managerial Courage

+ Managing and Measuring Work

+ Organizing

+ Planning

+ Priority Setting

+ Time Management

+ Results driven

Personal and Interpersonal Skills

+ Customer Focus

+ Ethics and Values

+ Integrity and Trust

+ Motivating Others

+ Negotiating

+ Peer Relationships

+ Team Player

+ Positive spirit

Share:

State/Province : Illinois

City : Kankakee

Street Address : 1201 N. Kinzie

Primary Location : CSL Behring Kankakee

Full Time/Part Time : Full Time

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please click be


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