Quality Consulting Group, LLC

JT353 - MANUFACTURING ASSOCIATE

Quality Consulting Group, LLC  •  Thousand Oaks, CA (Onsite)  •  5 days ago
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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 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:

  • Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs)
  • Hands-on operations: set-up, operation, and cleaning of various manufacturing equipment
  • Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
  • Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
  • Performing and monitoring critical processes with the ability to perform basic troubleshooting
  • Performing in-process sampling of equipment and operating analytical equipment
  • Performing washroom activities: clean small and large scale equipment used in production activities
  • Maintaining an organized and clean workspace
  • Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
  • Drafting and revising documents (SOPs, MPs)
  • Identifying, recommending, and implementing improvements related to routine functions
  • Assisting in the review of documentation for assigned functions (equipment logs, batch records)

Qualifications:

  • Bachelor’s Degree in Biology and/or Life Sciences preferred
  • Mechanically inclined (understanding of repairs, etc.)
  • Manufacturing /Operations experience
  • Able to work in teams to complete operational tasks safely and accurately
  • Able to take direction well, follow documents and policies at all times (SOP)
  • Able to take initiative
  • Will start on days Rotating Shift: Days: 6am-5pm: Sunday-Wednesday or Wednesday-Saturday AND Swings: 1pm-12am: Sunday-Wednesday or Wednesday-Saturday (3 month rotation)
  • Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule.

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.

Quality Consulting Group, LLC

About Quality Consulting Group, LLC

The Quality Consulting Group is a pharmaceutical, biotechnology, food and medical device specialty consultant that supports the manufacturing industry; services are provided in multiple areas including: Regulatory Compliance, Quality Operations, Validation, Manufacturing, Training and Technical Support. Starting, as individual services provider since 2002, Quality Consulting Group has supported clients implementing the latest standards such as Validation Guidance, ICH Guidelines, and Process Excellence and Risk Management tools.

Quality Consulting Group has provided expertise in such areas as: business, operational, quality, regulatory and manufacturing strategies; organizational structures; management controls; manufacturing and quality systems methodologies and practices; compliance programs; and accuracy reviews; FDA, EMEA and other regulatory matters.

Industry
Consulting & Advisory
Company Size
11-50 employees
Headquarters
San Juan, PR
Year Founded
2011
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