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11190
Contract

cGMP Manufacturing Associate (1st Shift)

Location: Norwood, Massachusetts

Connexion strives to be the unrivaled staffing solution for both job seekers and hiring organizations by expertly connecting talent with opportunity. We build world class teams for our customers, and better the lives of our candidates by providing them with fulfilling careers.

 

Connexion would like to provide you with details about this new opportunity as we are seeking individuals with the following skills:

 

cGMP Manufacturing Associate - BioMed

Description:

We are seeking a first shift (Tuesday-Saturday) cGMP Manufacturing Associate for mRNA Manufacturing of Personalized Cancer Vaccines. The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based personalized cancer vaccines for evaluation in human clinical trials. He/she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. The anticipated time frame for this role is six months.

What You'll Do:

  • Produce mRNA Personalized Cancer Vaccines
  • Execute manufacturing operations using disposable technologies, automation and Manufacturing Execution Systems (MES)
  • Develop batch records, SOPs and training materials
  • Closely partner with QA peers for rapid disposition of personalized cancer vaccines
  • Demonstrate general knowledge of standard manufacturing practices and equipment.
  • Strict adherence to current good manufacturing practices, standard operating procedures, and manufacturing documentation
  • Establish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions, and of process data
  • Monitor process operations to ensure compliance with specifications
  • Assist in the investigation of procedural deviations.
  • Practice safe work habits and adhere to our safety procedures and guidelines
  • Utilize knowledge to improve operational efficiency
  • Adhere to gowning procedures and maintain a clean general operating area
  • Adhere to documented waste handling procedures to respect environmental regulations

Here's What You'll Bring to the Table:

  • 3 years of experience in a GMP manufacturing environment
  • Bachelor's Degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical engineering, Biochemistry or related field, Associates with 3 years related experience or 5 years of related GMP experience
  • Proven track record of success in a fast-paced production environment at a biotech/pharmaceutical company preferably in GMP or GLP
  • Ability to collaborate fluidly with peers, supervisors and cross functional support groups required
  • Exceptional written, oral communication, and organizational skills required

 

Date Posted: 3/11/2020

Hiring Organization: Connexion Systems & Engineering

Job Title: cGMP Manufacturing Associate

Industry: BioMed

Location: Norwood, MA     

Employment Type: Full Time, Contract

Pay Range:  30-33/hr.

Duration: 6 months

Job #: bh11190

 

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If you are active in a job search but this job is not for you, please reach out to jobpostings@csetalent.com. We would be glad to help you find the perfect job!

ConneXion Systems & Engineering

490 Boston Post Road

Sudbury, MA 01776