Quality Control Supervisor

ProCaps Labs•Henderson, NV

8d•Hybrid

About The Position

The Quality Control Supervisor is responsible for overseeing the coordination, training, and supervision of the daily tasks of Quality Control personnel. In addition, the role entails providing support to Quality Control employees to ensure the precise and effective completion of departmental duties and functions. Facilitating communication with management and other departments is also essential to ensure the fulfillment of quality production requirements.

Requirements

Associates degree or equivalent experience commensurate to the industry
Minimum of five years’ experience in the area of Quality Assurance and/or Quality Control in a Pharmaceutical, Dietary Supplement, Cosmetics, or Food manufacturing environment; to include a minimum of three years in a laboratory environment in a Supervisory capacity
Experience in wet chemistry (chemical identification; sample extraction; titration) and use of other analytical equipment; e.g., HPLC, FT IR, GC, and Spectroscopy
Familiarity with troubleshooting of various laboratory instrumentations
Knowledge of cGMP and GLP required
Familiarity with FDA regulations
Must possess the computer skills to be proficient in Microsoft Office
Strong written and verbal communication skills, to include the ability to communicate effectively with employees and management
Detail and quality oriented

Nice To Haves

Experience in Microbiological and Stability testing a plus

Responsibilities

Oversee the analysis process for physical and/or chemical requirement to meet turnaround requirements
Assist in audits as requested
Ensure the highest quality product is produced by continually striving to improve and create company and department SOP
Ensure that products meet cGMP specifications for Identity, Purity, Strength, and Composition
Generate and distribute department reports
Prepare for and attend company and department meetings as required
Train all QC personnel on all current QC laboratory procedures
Train all QC personnel in cGMPs and GLP regulatory requirements
Develop, train, and implement the use of laboratory notebooks and Analytical Worksheets
Provide support for developing test methods for finished goods and raw materials
Provide support for developing test methods for current QC laboratory equipment and train QC personnel on current methods
Implement testing of raw materials using created specifications and current QC lab equipment
Research and submit proposal for additional laboratory equipment
Create, review, and revise QC SOPs
Work with QA Supervisor regarding compliance and problem-resolution issues, as well as laboratory development
Complete daily report listing completed projects, current issues, and projects pending completion
Contributes to a working environment that allows all employees equal opportunities for development, growth, and advancement
Conducts business in compliance with the Company’s Code of Business Conduct
Provides effective leadership and directs the work of subordinates
Carries out supervisory responsibilities in accordance with the organization's policies and procedures
Participates in staff selection, coaches performance, and provides ongoing and timely communication regarding performance, training, and development opportunities
Perform other duties and responsibilities, as assigned

Benefits

Competitive salary
Top-Tier Medical, Dental & Vision Coverage - $0 when you qualify for the Wellness Program!
Paid Time Off
Eight (8) Company Holidays
401(k) with Company Match – up to 4.5%
100% Company Life Coverage
100% Short Term Disability Coverage
Gym Membership Reimbursement
Vitamin Allowance + Discounts
Company-Funded Health Savings Account ($1,600/year)
Cash Reward Employee Referral Program
Pet Insurance