JT004 - MANUFACTURING PROCESS TECHNICIAN NS

Quality Consulting Group, LLC; Ohio; On-site; USD 35,000 - 55,000; 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 integral to manufacturing processes, ensuring compliance with Standard Operating Procedures while collaborating on continuous improvement initiatives. Your expertise will help train and guide operators, draft essential documentation, and troubleshoot equipment issues. This position offers a unique opportunity to contribute to a world-class manufacturing environment, where your skills and dedication will drive operational excellence and innovation. If you thrive in a fast-paced setting and are eager to make a significant impact, this role is perfect for you.

Qualifications

• 1-3 years of manufacturing experience in an FDA-regulated environment.
• Strong documentation and communication skills are essential.

Responsibilities

• Perform manufacturing processes and review batch records.
• Train staff and support continuous improvement projects.

Skills

Manufacturing Processes

Documentation Skills

Problem Solving

Communication Skills

GMP Knowledge

Education

High School Diploma

Tools

SAP

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 to a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

1. Perform manufacturing processes according to Standard Operating Procedures with minimal supervision.
2. Review manufacturing procedures and batch records.
3. Train Manufacturing Operators and Associate Manufacturing staff on process theory.
4. Draft and revise documents such as MPs, SOPs, technical reports, validation documents, and investigation reports.
5. Audit critical records.
6. Propose corrective actions for Quality incidents.
7. Plan and assist with routine process improvements.
8. Collaborate with other departments to implement improvements.
9. Identify and propose solutions to complex problems.
10. Analyze data (e.g., SPC, CPV) on critical process parameters.
11. Serve as a lead for equipment and process operations.
12. Support the generation and review of manufacturing documentation.
13. Troubleshoot processes and monitor performance.
14. Support training activities.
15. Participate in NC CAPA processes, including process assessments, cross-functional investigations, defining/implementing CAPAs, and trend reporting.
16. Assist in generating, reviewing, and executing process validation protocols.
17. Support new product introductions and product lifecycle activities.
18. Manage Level 1 and Level 2 Change Control records.
19. Handle material loading and movement through SAP.
20. Operate equipment and document issues or exceptions.
21. Support continuous improvement projects.
22. Perform equipment cleaning.

Qualifications:

• High School diploma with relevant experience.
• 1 to 3 years of manufacturing experience, preferably in an FDA-regulated environment.
• Pharma experience is a plus.
• Ability to stand for prolonged periods when necessary.
• Knowledge of Operations/GMP.
• Ability to operate advanced equipment safely.
• Strong documentation and communication skills.
• Availability for night shift: 2:30 pm - 11:00 pm, Monday - Friday (may vary).

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.