Sr. Manufacturing Technician

Integrated Resources Inc.; SOUTH PLAINFIELD (NJ); On-site; USD 70,000 - 100,000; Full time

Job summary

A leading staffing firm seeks a Sr. Manufacturing Technician in South Plainfield, NJ. This role involves performing key manufacturing operations including set-up, calibration, and leading technical issues in a GMP-compliant environment. The successful candidate will bring substantial experience, particularly in downstream purification and aseptic processes.

Qualifications

• Minimum of 5 years related experience required.
• Experience in downstream purification and buffer prep.
• Knowledge in GMP document generation.

Responsibilities

• Perform set-up and calibration of manufacturing operations.
• Lead operations in a Single-use technology facility.
• Write routine production and quality documents.

Skills

Problem Solving

Technical Issue Resolution

Communication

Education

College degree

Tools

GMP Documentation

Chromatography Equipment

Job description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Job Title: Sr. Manufacturing Technician

Location: South Plainfield, NJ

Duration: Contract to hire

Job Summary

• The Manufacturing Technician will report to the Supervisor of Manufacturing.
• The Manufacturing Technician performs or leads functions associated with Manufacturing operations, including set-up and calibration tasks, aseptic processing and sampling operations, single-use component set up and operations, buffer formulation and transfer, TFF, depth filtration, polishing and sterile grade filtration, viral removal operations, column chromatography, and final fill operations..

Essential Duties and Responsibilities:

• Assists or leads with resolving technical issues
• Performs and leads operations in a Single-use technology facility
• Experience working in GMP manufacturing
• Writes routine reports, quality documents (SOPs, batch records, deviations, change controls), and shift exchange summaries
• Trains and mentors other technicians
• Leads operations or projects as assigned by Management
• Applies concepts of basic algebra and geometry in everyday activities

Supervisory Responsibilities:

• This position will serve as the primary technician in support of the Manufacturing Supervisor.
• Management training may be assigned as part of a progression plan.
• Leadership responsibilities in support of or in lieu of the Manufacturing Supervisor will be assigned and/or expected

Language, Mathematical, and/or Reasoning Ability:

• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedures
• Ability to speak effectively in a group setting
• Ability to present data and information slide shows in front of a group
• Ability to interpret a variety of instructions provided in written, oral, diagram, or schedule format

Physical Demands:

• While performing the duties of this job, the employee is required to move frequently and sit or stand as the job requires
• The employee may frequently lift and/or move up to 25 pounds and occasionally lift or move up to 50 pounds
• The employee may frequently move large mobile vessels across a room or from one room to another
• Must be willing to work longer than 8 hours (or shift hours) during processing
• Must be flexible with scheduling and working hours to accommodate a staggering or 2nd/3rd shift

Qualifications

Education and/or Experience:

• College degree and/or a minimum of 5 years of related experience required .
• Downstream purification experience with specific attention towardsTFFat either bench scale or large scale.
• Experience with chromatography and buffer prep is a plus
• Experiencewith fill/finish, final fill equipment, and filling isolators
• Experience working withprocess automation
• Experience working in anaseptic or clean room environment
• Experience authoring standard operating procedures, batch records and working in GMP document generation/life cycle management

Additional Information

Kind Regards,

Clinical Recruiter

Integrated Resources, Inc.

Gold Seal JCAHO Certified for Health Care Staffing

“INC 5 0 0 0 ’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)