JT998 - ASSOCIATE MANUFACTURING PROCESS TECHNICIAN

Quality Consulting Group, LLC; New Albany (OH); On-site; USD 40,000 - 70,000; Full time

Job summary

An established industry player in the pharmaceutical and biotech sectors is seeking a motivated individual to join their dynamic team. In this role, you will be involved in complex manufacturing processes, contributing to the production of high-quality biotech solutions. The position offers a unique opportunity to work in a world-class environment, where your contributions will directly impact the efficiency and quality of operations. If you are passionate about the biotech industry and eager to grow your career in a supportive team, this role is perfect for you. Join a company that values innovation and excellence in manufacturing.

Qualifications

• Associate degree or equivalent experience in biotech or related field.
• Basic understanding of GMP and material handling processes.

Responsibilities

• Perform complex processes according to Standard Operating Procedures.
• Handle materials and prepare large scale solutions.

Skills

Biotech DS manufacturing experience

Basic GMP knowledge

Material Handling

Understanding of measurements and calculations

Ability to stand for prolonged periods

Education

Associate degree

High school/GED + 1 year of related work experience

Tools

Electric Batch Records

DeltaV

LIMS

Job description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated, and enthusiastic individual to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Routinely perform moderately-complex to complex processes according to Standard Operating Procedure (SOP).
• Specific responsibilities include moving totes, large scale solution prep batching, cleaning equipment, steaming equipment, and prepping equipment.
• Material Handling.

Qualifications:

• Associate degree or High school/GED + 1 year of related work experience.
• Biotech DS manufacturing experience, preferably solution prep; understanding of measurements, calculations, and the metric system.
• Basic GMP knowledge.
• Understanding of Electric Batch Records, DeltaV, and LIMS.
• Warehousing, assembly, and packaging experience.
• Must be willing to stand for prolonged periods.
• 12 hr. shift 6am - 6pm; this role will transition towards the end of the year to night shift.
• 5 days per week 8hr shift after July 2025 from 10:30pm - 7am.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.