Good quality Assurance Manager, Lake Wales – Discover Sativa

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GrowHealthy is looking for a Good quality Assurance/Good quality Manage (QA/QC) Specialist to join our processing and manufacturing facility in Lake Wales, FL.

 

Job Description

As a GrowHealthy QA/QC Specialist, you will be accountable for assisting with excellent-connected activities connected with sampling and inspection of completed goods, customer complaints, item investigations, and Corrective and Preventive Action (CAPA). The goods contain cannabis oil, cannabis flower, cannabis-infused goods such as lotion, capsules, vape pens, edibles, and cartridges). This position is also accountable for assisting make sure goods are created in a manner that meets all specifications and GrowHealthy brand consistency. As a QA/QC Specialist, you will help in identifying possible excellent dangers and functioning with compliance, operations and manufacturing personnel to create improvement possibilities.

 

Responsibilities contain, but are not restricted to:

·       Build new processes or modify and increase present processes by setting up clear and definite excellent systems and SOPs and document final results of new procedures just after implementation to show excellent improvements.

·       Comprehend processes such as Good quality Systems such as Deviations, Corrective and Preventive Action (CAPAs), Adjust Controls, Out of Specifications (OOS), and 1st-In, 1st-Out and create CAPA plans and lead continuous improvement initiatives and handle on-time closure of CAPAs and assigned deviations.

·       Execute actions for item quarantine, destruction, rework, withdrawal/recall.

·       Active participation in the evaluation, implementation, and upkeep of electronic systems made use of inside the organization to gather, shop, analyze, and/or report details in help of GxP activities such as Fantastic Manufacturing Practices (GMPs), Fantastic Agricultural Practices (GAPs), and Fantastic Laboratory Practices (GLPs).

·       Implementation, monitoring, and common oversight of GxP electronic systems made use of to help document management, education applications, essential excellent management systems, labeling of goods, and other GxP connected activities.

·       Execute oversight and inspections of active production and manufacturing locations to resolve complications and to make sure compliance with SOPs and policies.

·       Analyze excellent inspection information to determine all kinds of excellent complications and carry out root trigger evaluation.

·       Execute completed item sampling and inspection and carry out gear and item line clearances ahead of production runs.

·       Help in implementing essential QA/QC methods for manufacturing, cultivation and retail per suitable techniques and accountable for complaint handling and problems-shooting root-trigger.

·       Participate in multi-function group activities, help and sustain Good quality Systems and carry out other assignments as directed by Director.

 

Qualifications / Necessary Knowledge, Education, and Abilities

 

  •        five+ years of practical experience functioning in a pharmaceutical, dietary supplement, and/or meals manufacturing facility focused on the Good quality function.
  •        Pharmaceutical and/or Meals and Drug Administration (FDA) practical experience preferred.
  •        Bachelor’s degree (B.S.) degree in Engineering or Science from an accredited institution with at least one particular (1) year of clinical trials, pharmaceutical business or auditing practical experience.
  •        Knowledge with Good quality Systems, Auditing, Root Lead to Evaluation, CAPA.
  •        Knowledge with Meals Security Plans/HACCP.
  •        Need to be proficient with Computer applications. i.e, Microsoft Workplace (Word, Excel, PowerPoint, SharePoint).
  •        Knowledge in establishing ISO 9001:2015.
  •        Knowledge in education, calibration, and preventive upkeep systems.
  •        Expertise and understanding of GxP and regulatory compliance as defined in government regulations such as 21 CFR Components 11, 111, 210, and 211.
  •        Preventive Controls Certified Person Certification, SQF practitioner, and ISO practical experience preferred.
  •        Great organizational expertise and interest to detail are critical.
  •        Great communication expertise each verbal and written across all levels of management.
  •        Sustain a powerful interest to detail to sustain Audit Records and Audit Reports.
  •        Sturdy interpersonal and collaboration expertise.
  •        Need to have the potential to adapt ad take-on further tasks as requested.
  •        Need to possess a higher degree of integrity and potential to sustain confidentiality with sensitive matters.
  •        Could be essential to travel to other facilities to carry out education and/or help with excellent challenges.



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