Manufacturing Associate

Manufacturing Associate
  • $30 - $37 per Hour
    HOUR
  • Temporary
  • Norwood MA, US Norwood NORFOLK US 02062
Job Ref: JO000127743
Sector: Light Industrial / Assembly
Sub-sector: Light Industrial
Date Added: 14 January 2022

Manufacturing Associate

6 Month Contract with possible renewable

Description:

Moderna is seeking a cGMP Manufacturing Associate I for mRNA Manufacturing within Drug Product Fill-Finish. This position is located at our new GMP Manufacturing site in Norwood, MA. This role will be a 1st shift Monday through Friday for the first few weeks and then move to Sun-Wed 1st shift.
The individual in this role will be part of a cohesive team responsible for supporting GMP mRNA-based medicines for evaluation in human clinical trials focusing primarily in Fill-Finish (both automated and manual filling lines). 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.
Here’s 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 for startup of the Norwood Facility
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 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.
Here’s What You’ll Bring to the Table:
0-2 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 4+ 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

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SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

SRGTalent
14/02/2022 12:00:00
USD 30.00 37.00 Hour
Contact Consultant:
Katherina Ramirez

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