Jt364 - Associate Manufacturing

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic 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:    

• Perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency.
• 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
• Use human machine interfaces (HMIs) to identify alarms and correct line stoppages.
• Ensures components and products are available for a continuous operation.
• Carries out 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.
• Partner with cross-functional teams to help drive improvement opportunities.
• Able to use computer systems to support material inventory system (SAP transactions) and
• electronic batch records.
• Oversight of equipment/process validation protocols independently.
• Safely follow standardized operating procedures including material handling, record keeping,
• assembly and packaging. Must follow Good Manufacturing Practices (GMPs).
• Reports to 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.

Qualifications:

• Associate degree or High school/GED + 1 year of related work experience
• 0 to 1 year of experience in a manufacturing or distribution environment where following procedures was essential.
• Proficiency with basic technology such as laptops and tablets (including iPads) are required.
• Prior exposure to GMP-regulated industries, electronic batch records, DeltaV, or LIMS is a plus but not required, as training will be provided.
• Candidates must be open to starting on a day shift and later transitioning to a rotating 12-hour schedule as part of a 24/7 operation.
• This entry-level role involves material handling and preparation of drug product for processing and requires standing for prolonged periods.
• Reliability, punctuality, strong attention to detail, and a consistent work ethic are essential for success in this position.
• Shift: 6am - 6:30pm
  3 days week 1 Mon, Thurs, Friday - 4 days week 2 Tues, Wed, Sat, Sun
  Must work every other weekend
• Workers may be assigned to either AM or PM shift. Candidates must be prepped to take any shift.
• No prior manufacturing experience is required but would be a plus.

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.