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Sr Manufacturing Process Technician (JP9679)
Albany, OH · Biotech/PharmaceuticalJob Title: Sr Manufacturing Process Technician (JP9679)
Location: Albany, OH 43054
Employment Type: Contract
Duration: 2 years with likely extensions
Job posting date: 1/19/2022
Note: Temporarily Remote
3 Key Consulting is hiring a Specialist IS Analyst for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
Job Summary:
Top Must have Skill Sets:
Day-To-Day Responsibilities:
Employee Value Proposition:
The worker in this role will have an opportunity to work at a new location.
Red Flags:
Engineers, Scientists, PhD, Doctorate Degrees not required for this role.
Interview Process:
Phone panel interview
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
Location: Albany, OH 43054
Employment Type: Contract
Duration: 2 years with likely extensions
Job posting date: 1/19/2022
Note: Temporarily Remote
3 Key Consulting is hiring a Specialist IS Analyst for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
Job Summary:
- Responsible for operating an automated and sophisticated manufacturing equipment necessary for the packaging operations of our products.
- This individual will be trained and cross-trained to both operate and troubleshoot issues (in the event of faults and machine stops) across a variety of equipment such as: automated, assembly, labeling, printing and robotic automation.
- In addition to equipment operation and troubleshooting, this individual will be responsible for the product quality as a result of the performance of the equipment.
- This position requires mechanical aptitude for machine troubleshooting and problem-solving skills, and the willingness to work in a fast-paced manufacturing environment.
The Basic Qualifications are: - Associate’s degree and 4 years of related experience in Pharmaceutical, Medical Device, or Packaging environment Or
- High school diploma and 6 years of related experience in Pharmaceutical, Medical Device, or Packaging environment
Top Must have Skill Sets:
- Capability to follow written procedures
- Capability to diagnose malfunctions, and perform necessary equipment setup
- Educational Background in Mechanical, Electronic Engineering Technology or Industrial Mechanics
Day-To-Day Responsibilities:
- Perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency. These tasks must be completed under minimal supervision.
- Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment.
- Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions.
- Assist in the review of documentation for assigned areas (i.e procedures, job plans, logs, area audits and batch records).
- Assist as training resource on manufacturing tasks and equipment use.
- Utilize human machine interfaces (HMIs) to identify alarms and correct line stoppages.
- Ensures components and products are available for a continuous operation.
- Executes equipment inspections and generates emergency, corrective, or preventative work orders as needed in the Maximo system.
- Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes.
- Communicate with cross-functional teams to help drive improvement opportunities.
- Able to utilize computer systems to support material inventory system (SAP transactions) and electronic batch records.
- Execution of equipment/process validation protocols under minimal supervision.
- Safely follow standard operating procedures including but not limited to material handling, record keeping, assembly and packaging. Must follow Good Manufacturing Practices (GMPs)
- Notifies Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained.
- Train fellow staff on the manufacturing processes, equipment, and general skills.
- Perform other duties as required
Employee Value Proposition:
The worker in this role will have an opportunity to work at a new location.
Red Flags:
Engineers, Scientists, PhD, Doctorate Degrees not required for this role.
Interview Process:
Phone panel interview
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
Regards,
3KC Talent Acquisition Team