A PHP Error was encountered

Severity: Notice

Message: MemcachePool::get(): Server 127.0.0.1 (tcp 11211, udp 0) failed with: Connection refused (111)

Filename: drivers/Cache_memcached.php

Line Number: 142

Backtrace:

File: /home/theinjobs/public_html/application/controllers/Indeed.php
Line: 536
Function: get

File: /home/theinjobs/public_html/application/controllers/Indeed.php
Line: 863
Function: indeed_job_details

File: /home/theinjobs/public_html/index.php
Line: 316
Function: require_once

QC ASSOCIATE - METHOD Job In Cytovance Biologics At Oklahoma

QC ASSOCIATE - METHOD VALIDATION Details

QC ASSOCIATE - METHOD VALIDATION

Cytovance Biologics - Oklahoma City, OK

Employment Type : Full-Time

WHY CYTOVANCE?


At Cytovance, we are on the cutting-edge and we are committed to providing a work environment that fosters creativity and success while giving our employees the ability to achieve their full potential. We believe that as our industry grows, so will our employees.

WHAT CYTOVANCE HAS TO OFFER:

A Meaningful Career- Forward-thinking individuals working together to explore and create state of the art medicines that change the lives of people around the world.

An Energetic Community – Headquartered in Downtown Oklahoma City, offering everything you look for in a modern metropolitan community. An abundance of arts, quality health care, excellence in education and more. It is a distinctly livable city where you can chase your dreams and still enjoy a rich quality of life. Visit abetterlifeokc.com

A Competitive Benefit Package – Cytovance offers a competitive 401k match, medical benefits, Professional Development and Tuition Reimbursement, Paid Holidays, and a generous amount of paid time away from your job.

HOW WILL YOU MAKE AN IMPACT?

http://schemas.microsoft.com/office/2004/12/omml" xmlns:st1="urn:schemas-microsoft-com:office:smarttags" xmlns="http://www.w3.org/TR/REC-html40">

The QC Associate I- Method Validation will participate in the assay performance, qualification/validation of assays and laboratory equipment, and transfer of standard protein characterization methods. Duties will be carried out in accordance with quality standards and procedures set by the company and applicable government agencies.

Essential Duties and Responsibilities:

  • Participate in qualification/validation of analytical methods.
  • Assist in preparation of method qualification/ validation protocols, reports and test method SOPs.
  • Author / execute method transfer protocols for various analytical methods for the characterization of biopharmaceutical protein products.
  • Work on developing and improving assays for various projects as needed.
  • Work under general supervision of QC scientist / manager to meet project goals in a timely manner.
  • Specify and source new analytical equipment as required to expand the testing capabilities of the QC Analytical Laboratory.
  • Assist with the overall maintenance and calibration of the QC laboratory analytical equipment as needed.
  • Analyze laboratory data for trending.
  • Support the training of new and existing laboratory personnel
  • Evaluates technology transfers associated with new products or processes.
  • Other duties as assigned.

Job Requirements:


  • B.S. in Life Sciences/Chemistry
  • 0-1 year of industry experience is expected. However, successful academic research experience will also be considered.
  • Working experience with a range of protein analytical/bioanalytical techniques including ELISA, HPLC, UPLC, enzymatic, and electrophoretic (SDS-PAGE, Western blots, IEF and CE) procedures.
  • Experience in a GMP Laboratory / environment is plus.
  • Organizational, multitasking, problem-solving, math, statistical, interpersonal, written and oral communication skills. Detail-oriented and ability to prioritize work.
  • Must be able to work within multifunctional teams.
  • Ability to function well in a fast-paced multiple project environment.
  • Communicates openly with development, production & quality personnel to resolve problems before or as they arise.


Physical Demands:

While performing the duties of this job, the employee is frequently required to stand; sit and talk or hear. The employee is occasionally required to walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance and stoop, kneel, crouch, or crawl.

Work Environment:

While performing the duties of this Job, the employee is occasionally exposed to fumes or airborne particles and toxic or caustic chemicals. The noise level in the work environment is usually moderate.

Cytovance Biologics acknowledges that Providers may be a valuable resource for identifying and recruiting Candidates for employment. However, we require that all Recruiters engage directly with Cytovance Biologic’s Human Resource Team and comply with Cytovance Biologic’s requirements prior to transmitting any Resumes/CV’s or introducing any Candidates to Cytovance Biologics. Cytovance Biologic’s Human Resource Team is the only function within the Company that can enter contractual relationships with external Recruiters and Recruiting Agencies.


We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

Posted on : 2 years ago
 Apply Now