Pharma Manufacturing Associate - 1st Shift

Randstad
Norwood, Massachusetts
$32-$34 an hour
Full-time

job summary : Responsibilities :

Responsibilities :

What You Will Be Doing :

  • Execute manufacturing operations using disposable technologies, automation, and Manufacturing Execution Systems (MES) to produce mRNA
  • Closely partner with QA peers for rapid disposition of mRNA
  • 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 Moderna’s 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.

Qualifications :

  • Bachelor's degree (please no Masters or PhD candidates) in Biotechnology, Biochemistry, Molecular Biology, or related field.
  • Familiarity with cGMP regulations and industry standards for biopharmaceutical manufacturing.

Why Join Us :

  • Supportive management invested in your success
  • Opportunity to learn new skills and grow your career
  • Experience at a brand name, highly recognizable global organization

Skills : GMP, mRNA, Laboratory / Sciences Experience : Entry Level2 year(s)

responsibilities :

What You Will Be Doing :

  • Execute manufacturing operations using disposable technologies, automation, and Manufacturing Execution Systems (MES) to produce mRNA
  • Closely partner with QA peers for rapid disposition of mRNA
  • 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 Moderna’s 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.

Qualifications :

  • Bachelor's degree (please no Masters or PhD candidates) in Biotechnology, Biochemistry, Molecular Biology, or related field.
  • Familiarity with cGMP regulations and industry standards for biopharmaceutical manufacturing.

Why Join Us :

  • Supportive management invested in your success
  • Opportunity to learn new skills and grow your career
  • Experience at a brand name, highly recognizable global organization

The essential functions of this role include :

working weekends

qualifications : Experience

Experience

  • Entry Level
  • 2 years

Education

  • Bachelors (required)
  • skills :
  • mRNA
  • mRNA
  • Laboratory / Sciences
  • 30+ days ago
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