Quality Supervisor

If you have an interest in being part of one of the fastest growing industries in the nation in you may consider wanting to work for Trulieve! If you have a desire to help others in need through your efforts, this may be the role for you! At Trulieve, we strive to bring our patients the relief they need in a product they can trust. Our plants are hand-grown in an environment specially designed to reduce unwanted chemicals and pests, keeping the process as natural as possible at every turn. Our products are designed to alleviate seizures, severe and persistent muscle spasms, pain, nausea, loss of appetite, and other symptoms associated with serious medical conditions such as cancer. Our specially trained staff works hand-in-hand with physicians to provide the right products and the correct dosage to ensure patients get the compassionate care they need. To learn more about our company, please visit our website; https://www.trulieve.com

Requisition ID:

19921

Remote Work Available:

 No 

Job Title:

 Quality Assurance Supervisor

Department:

 Quality Assurance Reports to: QA Manager

FLSA Status:

 Exempt/Salary

Location:

Quincy, FL

POSITION SUMMARY

The Quality Assurance Supervisor - Processing will be responsible for the coordination and effective scheduling of workers to meet targets and quality standards. Responsibilities will include the training of staff in production methods, safety, policies, and procedures, as well as the identification and correction of potential work problems, health, and safety issues.

KEY DUTIES AND RESPONSIBILITIES

Approves incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials Approves in-process production by confirming specifications; conducting visual and measurement tests; communicating required adjustments to the production supervisor Approves finished products by confirming specifications; conducting visual and measurement tests; returning products for re-work; confirming re-work Documents inspection results by completing reports and logs; summarizing re-work and waste; inputting data into a quality database Maintains a safe and healthy work environment by following standards and procedures, complying with legal regulations Overseeing and coordinating daily prioritization of QC testing Manage and direct activities and resources of the quality department to meet the company objective of producing the highest quality product Ensure product is manufactured in accordance with the proper Standard Operating Procedure's (SOP) Continuous Improvement to maximize product quality and minimize costs. Participating on teams as the Quality Control Liaison as required Provide feedback and evaluations as needed Approving or rejecting raw materials, in-process, and finished goods according to company specifications Train employees as required Monitor training plan and matrix as required ensuring ongoing compliance and staff proficiency Assist with management of critical programs such as stability program, reduced testing program, environmental services, retained samples, etc. Maintain and improve the level of quality by managing and implementing inspection criteria and procedures of quality control inspections in manufacturing and job sites consistent with all applicable standards and specifications Take an active role in investigating and resolving problems related to quality, including sourcing substitute materials and/or suppliers Analyze statistical data to determine trends and implement corrective actions as required Communicate and coordinate objectives with manufacturing personnel and departments to improve the manufacturing process to be more cost-effective by maintaining continuous high standards of quality to minimize rejection of product Ensure product is manufactured in accordance with established best practices, procedures, to meet customer/contractual obligations and in compliance with regulatory codes and standards Staff selection/development - ensures staff has appropriate qualifications, knowledge to meet objectives Assist in the development of statistical data and product specifications to determine present standards and establish proposed quality and reliability expectancy of finished product Review test results and confirm compliance with specifications Ensure goods and products comply with company standards, GMP, and any other regulatory agencies Assist team members in Investigations, Root Cause Analysis procedures and implementation of effective CAPAs Assist in the investigation and tracking of customer complaints regarding quality Communicate quality and/or compliance concerns with urgency Identify possible areas for improvement in quality control processes Facilitate change management. Monitor and facilitate third party compliance testing. Performs other duties as required

SKILLS AND QUALIFICATIONS

Pharmaceutical or food manufacturing experience is preferred Strong computer skills, including Microsoft Office Suite, database management and manufacturing management systems Familiarity with Quality System Practices, such as Document Control, Auditing, Investigations, and CAPAs Possess solid root cause analysis and problem-solving capability Independent self-starter with decision-making ability Strong attention to detail Excellent oral and written communication skills, with proven ability to share information effectively with all levels Ability to keep calm under pressure Ability to prioritize activities under tight deadlines Understanding of test equipment Excellent organizational skills Ability to work at multiple locations

Desired:

Knowledge of cGMP requirements and HACCP Ability to create and review technical documentation, including project plans, test procedures, and design documents Able to develop, review, and maintain metrics and quality audits Strong problem identification and problem resolution skills A well-defined sense of diplomacy, including solid negotiation, conflict resolution, and people management skills Strong work ethic and positive team attitude Well-developed problem-solving skills and ability to develop conceptual alternatives Able to find new methods and principles and ability to incorporate them into existing practices as needed High degree of resourcefulness, flexibility, and adaptability. Must have the ability to plan, organize, develop, implement, and interpret programs, goals, objectives, policies, procedures, etc. Strong negotiation and prioritization skills Experience with MS Office (Excel, Word, Outlook, and Access) and be able to handle working with multiple programs. Ability to read/write English at a proficient level

ADDITIONAL

 MINIMUM

QUALIFICATIONS

Must be able to pass a Level 2 background screening Must be at least 21 years of age (State Law)

PHYSICAL REQUIREMENTS

Must be able to push, pull, move, and/or lift a minimum of 40lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistance Must be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stopping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasks Must be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater) Must have visual acuity with/without job aids to perform activities such as reading, viewing a computer terminal, visual inspection involving small parts/details. Clarity of vision at 20 ft or more in day and night/dark conditions Must be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc. (Moderate noise)

WORK SCHEDULE

40+ hours weekly with flexible hours depending on department needs. Must be available to work occasional evenings, weekends, and holidays. Equal Opportunity Employer - Trulieve Supports a Drug Free WorkplaceSalary will be commensurate with experience. A comprehensive benefits package including paid time off is offered with this position. Trulieve provides equal employment opportunities to all employees and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, pregnancy or any other characteristic protected by federal, state or local laws.