Quality Control Inspector with GMP Manufacturing background Position Available In Palm Beach, Florida
Tallo's Job Summary: The Quality Control Inspector with GMP Manufacturing background at Keystaff, Inc. in West Palm Beach, FL, will provide oversight of manufacturing and packaging operations, ensuring adherence to procedures and regulations. Responsibilities include inspections, documentation, and escalation of issues. This full-time position offers a pay rate of $18.00 - $21.00 per hour with benefits such as dental, health, and vision insurance.
Job Description
Quality Control Inspector with GMP Manufacturing background Keystaff, Inc. West Palm Beach, FL 33404
Location:
Riviera Beach, FL Pay Rate:
$22.00-$25.00 hourly
Working Schedule:
Monday- Friday 7am-3pm Purpose The Quality Assurance (QA) Line Inspector will provide quality oversight of all manufacturing and packaging operations as trained and assigned. The QA Line Inspector will work collaboratively with the site operations and management to assure adherence to procedures, regulations, guidelines and standards. Duties and Responsibilities Provide quality oversight of all manufacturing operations including line clearance, in-process inspections, label inspections and control, raw material release, environmental monitoring and sample retention. Follows and completes training according to the assigned training curricula. Only performs activities for which the Line Inspector I has been trained. Performs GMP inspections and attribute inspections of materials, intermediates, and product according to the batch record, packaging record, specifications and procedures. Monitors all aspects of manufacturing, processing, and packaging operations, documenting inspection results by completing records and logs as required by procedures. Maintains safe and healthy work environment by following written standards and procedures; complying with applicable regulatory requirements. Escalates potential issues and concerns immediately to QA and Operations management. Accomplishes quality and organization mission by completing related activities as assigned, thoroughly and in a timely manner. Performs any other duties which may be properly assigned to this position Knowledge, Skills and Abilities Basic knowledge and understanding of current Good Manufacturing Practices (cGMPs), as well as ICH and other regulatory requirements/ guidelines, especially as they relate to pharmaceuticals. Must have the ability to handle multiple priorities, maintain confidentiality and interface with individuals from other departments. Ability to establish sound positive working relationships and interact with different types of people on all levels of skill, background and position are essential. Excellent verbal and written communication skills. Proficiency in English usage, spelling, grammar and punctuation. Requires flexibility and ability to multi-task. Must be flexible to work overtime as needed with little to no advanced notice. #GEN1
Job Type:
Full-time Pay:
$18.00 – $21.00 per hour
Benefits:
Dental insurance Health insurance Vision insurance
Schedule:
8 hour shift Day shift Monday to
Friday Overtime Experience:
GMP:
2 years (Preferred) Shift availability: Day Shift (Preferred)
Work Location:
In person