GMP Associate I - 2nd shift at Techtrueup

Clinton, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

03 May, 26

Salary

0.0

Posted On

03 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP, GDP, Equipment Operation, Packaging, HMI, Cleanroom Protocols, Documentation, In-Process Checks, FDA Standards, ISO 13485, Safety Procedures, Lean Initiatives, 5S, Kaizen, Attention To Detail, Medical Device Manufacturing

Industry

Human Resources Services

Description

Company Description Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE-certified Healthcare Staffing and Engineering Services provider supporting industries including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food & Beverage, and Automotive. We proudly partner with 120+ clients such as Johnson & Johnson, Haemonetics, Delta, Caterpillar, Artisan Chef, Baxter, and many more. Our wide network of consultants and contract-to-hire engineers brings deep expertise across Engineering, Technical, Administrative, Healthcare, Life Sciences, Blue Collar, Skilled Trades, IT, Software Development, Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software's enabling us to source and screen top talent within hours. This ensures rapid response times, high-quality matches, and virtually zero attrition. Job Description Job Title : GMP Associate I - 2nd shift Duration : 6 Months Location : Clinton, PA Summary: The GMP Associate I supports the manufacturing of high-quality medical devices by operating equipment, packing finished products, loading automatic hoppers, and resolving basic equipment faults through HMI (Human-Machine Interface) screens. This role requires adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and cleanroom standards while contributing to a safe, lean, and team-oriented environment. Key Responsibilities 1. Safety • Follow all safety procedures, including the proper use of PPE. • Report hazards, malfunctions, and incidents promptly. 2. Quality • Adhere to cleanroom protocols and gowning requirements. • Maintain accurate, compliant documentation (batch records, logs, GDP). • Perform in-process checks and follow GMP, FDA, and ISO 13485 standards. 3. Manufacturing & Delivery • Load hoppers and monitor material levels to avoid interruptions. • Assemble components and subassemblies per work instructions. • Execute activities in molding such as proper packaging and completion of GDP paperwork. • Operate production equipment and resolve basic HMI faults, escalating as needed. • Perform routine cleaning and sanitization of equipment and workspace. 4. Continuous Improvement • Participate in lean initiatives (5S, Kaizen, QEK). • Complete required lean curriculum for associate level. 5. Company Values • Collaborate with Quality, Engineering, and other teams to achieve production goals. • Uphold company values and policies with professionalism. • Stand for extended periods; perform repetitive tasks. • Lift/move up to 25 lbs as needed. • Wear cleanroom attire (gown, mask, gloves) for prolonged periods. Qualifications • High school diploma or equivalent. • Prior manufacturing or production experience preferred. • Basic knowledge of HMI systems and cleanroom procedures a plus. • Strong attention to detail and commitment to quality. • Ability to stand for long periods and perform repetitive tasks. • Willingness to wear full cleanroom PPE. Physical Requirements • Stand for extended periods; perform repetitive motions. • Lift/move up to 25 lbs as needed. • Wear cleanroom attire (gown, mask, gloves) for prolonged periods. Additional Information All your information will be kept confidential according to EEO guidelines.

Responsibilities

The GMP Associate I supports medical device manufacturing by operating equipment, packing products, loading hoppers, and resolving basic equipment faults using HMI screens. This role strictly requires adherence to GMP, GDP, and cleanroom standards while contributing to a safe and team-oriented environment.