You are viewing a preview of this job. Log in or register to view more details about this job.

Biology/Microbiology Career Starter - Moderna in Norwood, MA - Excellent Opportunity

How passionate are you about your work? This is an opportunity to connect your work to passionate contributions in the pharmaceutical and biotech industry. This could be a great match for you!
 
Your quality skills and experience could contribute to producing cutting-edge vaccine technologies based on messenger RNA
 
Manufacturing Associate I - Manufacturing Operations - Norwood, MA
 
This position is located at our new GMP Manufacturing site in Norwood, MA (relocation is not provided). The shifts for this position will be Day shift: 6 AM - 6 PM; Night shift: 6:00 PM - 6:00 AM (night shift please add a 25% shift differential!)

You will work 3 days on a constant rotational shift. Will discuss schedule during a phone call.

Pay: $32 - $35/hour

Moderna is seeking a cGMP Manufacturing Associate for mRNA Manufacturing. This position is located at our new GMP Manufacturing site in Norwood, MA.
 
The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based medicines 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 assignment is six months.
 
Here’s What You’ll Do:
·       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.
 
 
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
Quality Control experience in a cGMP organization with a focus in Microbiology Familiarity with relevant and current FDA, EU, USP, ICH guidelines and regulations (nice to have)
 
Apply today to move forward with an opportunity to improve your career, while contributing to improving health.
FOR MORE IMMEDIATE CONSIDERATION, email a current resume to iris.levy@randstadusa.com
TXT: Your name and mRNA to 954-361-4744.

Share this opportunity with your similarly-skilled colleagues!