Manufacturing Technician II Buffer - Whiptail

Posté 12 oct. 2021

Carlsbad, California - United States

Demander un identifiant 231236

Détails

 

A career with MilliporeSigma is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.


Your Role

The Fill/Finish Manufacturing Technician 2 position will work in a cleanroom environment and follow cGMP batch records and SOPs to manufacture viral vector products (may include cell culture, buffer and medium preparation, membrane clarification, membrane concentration, and buffer exchange, column purification, terminal filtration, Fill and Finish, stocking supplies and raw materials, and cleaning process equipment). Employees will support projects in conjunction with other GMP Manufacturing personnel (Leads, Supervisors, Managers). Employees will prepare suites for manufacturing, to document deviations, and to operate in a safe and compliant manner. The employee must be self-motivated, work well in a group, and communicate well with all levels of the operations team.

 

The primary responsibility of the Fill/Finish Technician 2 will be to participate in the execution of all phases and facets of drug product formulation, fill, visual inspection, and labeling. This will include requesting materials, setup, preparation, final filtration, and formulation, filling vials inside a Grade A isolator with an automated filling machine, labeling, visual inspection, document review, and documentation of any events. This role may also assist with any manufacturing role as needed including buffer/media prep, cell culture, downstream operations.

 

Who You Are:

 

Basic Qualifications:

  • Bachelor of Science degree
  • 1+ years of experience in a cGMP cleanroom environment performing aseptic manufacturing operations
  • 1+ years of experience operating in a cGMP/GDP environment
  • 1+ years of experience with aseptic operations in a BSC/LFH (biosafety cabinet, laminar flow hood)

 OR

  • HS Diploma/GED
  • 5+ years’ work experience in a cGMP cleanroom environment performing aseptic manufacturing operations
  • 1+ years of experience operating in a cGMP/GDP environment
  • 1+ years of experience with aseptic operations in a BSC/LFH (biosafety cabinet, laminar flow hood)

 

Preferred Qualifications:

  • Experience with automated fill in an isolator
  • Experience with sterile filtration and fill of media, buffers, and drug products
  • Experience with filtration, TFF (UF/DF), column chromatography, sterile final filtration, media and buffer preparation operations

RSRMS

 


 

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

 

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