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Manufacturing Associate - Sun-Thurs 2nd shift

Westwood, MA

Posted: 12/20/2022 Industry: Scientific and Life Sciences Job Number: 15167

Job Description

Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services while treating candidates with the professionalism and respect they deserve.

Title: Manufacturing Associate
Hiring Organization: Connexion Systems & Engineering
  • Duration: Temp to Perm
  • Pay rate: $26-35/hr
  • Job Location: Westwood, MA
  • Job# 15167

Seeking a cGMP Manufacturing Associate for mRNA Manufacturing of Personalized Cancer Vaccines based at our GMP Manufacturing site in MA. These are shift positions within PVU Manufacturing.
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.

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 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:
  • Bachelor’s Degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical engineering, Biochemistry or related field with 0-2 years, Associates with 2-4 years related experience or 5+ years of related GMP experience and/or 2-3 years’ in a GMP environment.
  • 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


Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you immediately.
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Meet Your Recruiter

Emily Donahue
Regional Recruiting Manager

  • Directthe recruitment efforts for both the Quincy, MA and Providence, RI branches. 
  • Manages a distributed team of recruiting leads, individual contributor recruiters and account managers. 
  • Responsible for leading the fulfillment and execution of sourcing, recruiting, sales and business development practices across the region. 
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