Lead Manufacturing Associate Position Available In Wake, North Carolina
Tallo's Job Summary: Our client, a leader in therapeutics, seeks an Associate Manufacturing Engineer. Pay is $40-42/hr for a 6-month contract with potential extension. Responsibilities include producing clinical material, supporting testing, and updating SOPs. Requirements: Bachelor's degree or equivalent experience, 2+ years in cGMP environment, and ability to lift 25-50lbs. Apply with relevant skills.
Job Description
Lead Manufacturing Associate Astrix Technology Group – 3.5 Morrisville, NC Job Details Contract $40 – $42 an hour 16 hours ago Qualifications CGMP Management Bachelor of Science GMP Mid-level High school diploma or GED Bachelor’s degree 1 year Manufacturing Full Job Description Our esteemed client, a leader in therapeutics, renowned for their expertise in creating and manufacturing lifesaving therapies, is in search of an exceptional Associate Manufacturing Engineer to join their dynamic team.
Pay:
$40-42/hr.
Terms:
6 month contract with potential for extension or conversion What you will be doing: Use of MBRs and SOPs to produce clinical material from cell expansion through downstream processing in non-GMP and GMP settings. Support Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) as well as equipment commissioning and validation, including associated reports and protocols. Assess incoming products against existing Manufacturing Ecosystem and work as part of Tech Transfer to ensure successful scale-up and process implementation. Work with Supply Chain and MSAT to maintain operational readiness for a variety of processing scales by identifying preferred materials for unit operations as well as acceptable substitute items. Update and maintain Standard Operating Procedures (SOPs) and Master Batch Records (MBRs) for process execution and equipment operations in partnership with MSAT and QA. Participate in investigations to determine a root cause for process deviations and author investigation reports. Support troubleshooting for process operations in the event of batch processing issues. What you bring to the company: Bachelor of Science Degree (Engineering, Life Sciences, or related technical field) OR Associates/High School Diploma with equivalent industry experience 2+ years experience with AKTA and Unicorn with Downstream Processing in a cGMP environment 1-3 years’ experience in cGMP batch documentation and lifecycle management experience Ability to life, or move 25-50lbs on occasion •This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you•#LI-DNP INDBH
