A leading contract development and manufacturing organization is seeking an Upstream Manufacturing Associate III to support bioproduction efforts. Candidates should have at least 4-6 years of relevant experience, with strong knowledge of CGMP manufacturing processes and equipment. Responsibilities include monitoring production, training new employees, and leading continuous improvement efforts. The position requires adherence to safety and hygiene standards. Join a collaborative team dedicated to advancing medicine.
Qualifications
6+ years of related experience or an Associate’s Degree in Life Sciences/Engineering for high school diploma holders.
4+ years of related experience for bachelor’s degree holders.
Familiar with standard troubleshooting approaches including root cause analysis.
Responsibilities
Perform operations applicable to commercial scale production.
Train employees and serve as a subject-matter expert.
Monitor and record batch parameters following GDP/GMP guidelines.
Lead Continuous Improvement Teams and facilitate cross-department discussions.
Skills
Knowledge of CGMP manufacturing
Ability to read and follow detailed instructions
Good verbal/written communication skills
Good computer skills: Microsoft Word, Excel
Good interpersonal skills
Education
High school diploma or Associate’s Degree in Life Sciences/Engineering
Bachelor’s Degree
Tools
Laboratory and pharmaceutical production equipment
Job description
A leading contract development and manufacturing organization is seeking an Upstream Manufacturing Associate III to support bioproduction efforts. Candidates should have at least 4-6 years of relevant experience, with strong knowledge of CGMP manufacturing processes and equipment. Responsibilities include monitoring production, training new employees, and leading continuous improvement efforts. The position requires adherence to safety and hygiene standards. Join a collaborative team dedicated to advancing medicine.