Job Details

ID #52740424
Estado Missouri
Ciudad Saintlouis
Full-time
Salario USD TBD TBD
Fuente SSM Health
Showed 2024-10-21
Fecha 2024-10-22
Fecha tope 2024-12-20
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Quality Assurance Specialist Pharmaceutical Compounding

Missouri, Saintlouis, 63101 Saintlouis USA
Aplica ya

It's more than a career, it's a calling.MO-SSM Health Mission HillWorker Type:RegularJob Highlights:

Department: Pharmacy Quality Assurance

Schedule: Full Time, Day Shift, Mon-Fri – hours of operation are 8am-4:30pm – some flexibility with start and end times.

Starting Pay: 23.86 minimum (Offers are based on years of experience and equity for this role.)

Shift Differentials: N/A

Location: Mission Hill Office – St. Louis, Missouri

Experience in Pharmacy/Sterile Compounding preferred

Job Summary:Responsible for quality assurance and regulatory compliance with pharmaceutical compounding at the organization. Ensures site operations and processes are well integrated, meeting all regulatory requirements including Federal Drug Administration (FDA), Drug Enforcement Administration (DEA), United States Postal Service (USPS) and the Board of Pharmacy requirements and industry best practices. Acts as a communicator, facilitator, and translator of the organizational quality expectations. Ensures pharmacy staff have the knowledge to effectively accomplish an engaged quality workforce.Job Responsibilities and Requirements:PRIMARY RESPONSIBILITIES

Drives and maintains regulatory compliance under relevant regulatory areas for pharmaceutical compounding and outsourcing, including 503b and other regulations.

Maintains all pharmaceutical compounding quality systems and ensure compliance with Current Good Manufacturing practices (cGMPs). Ensure each lot of compounded sterile products remains quarantined until sample testing has been completed/released and suspends operations if not in compliance.

Establishes compliance monitoring system designed to prevent, track and trend compliance related issues. Drafts and reviews quality-related documents (e.g., standard operating procedures, forms, logs, training records, audits, deviations, etc.).

Maintains product retains and label control, maintains stock, prints labels for production, conducts label reconciliation, and verifies materials issued for packaging.

Performs Acceptable Quality Level (AQL) inspection for in-process and finished product. Responsible for inspection, documentation, and acceptance/rejection status.

Reviews and brings concerns to leadership of any changes or need for change that impacts product quality. Ensures that quality related complaints, deviations, and events are investigated and resolved.

Ensures all samples are appropriately analyzed and the results are reported. Maintains all quality related records. Ensure a program of continuous quality improvement is in place. 

Coordinates communication as necessary with federal and state regulatory agencies (DEA, FDA, applicable state agencies) regarding regulatory requirements pertaining to pharmaceutical compounding.

Works in a constant state of alertness and safe manner.

Performs other duties as assigned.

EDUCATION

High School diploma/GED or 10 years of work experience

EXPERIENCE

Three years' industry experience, with one year in quality assurance or control

PHYSICAL REQUIREMENTS

Frequent lifting/carrying and pushing/pulling objects weighing 0-25 lbs.

Frequent sitting, standing, walking, reaching and repetitive foot/leg and hand/arm movements.

Frequent use of vision and depth perception for distances near (20 inches or less) and far (20 feet or more) and to identify and distinguish colors.

Frequent use of hearing and speech to share information through oral communication. Ability to hear alarms, malfunctioning machinery, etc.

Frequent keyboard use/data entry.

Occasional bending, stooping, kneeling, squatting, twisting and gripping.

Occasional lifting/carrying and pushing/pulling objects weighing 25-50 lbs.

Rare climbing.

REQUIRED PROFESSIONAL LICENSE AND/OR CERTIFICATIONS

None

Department:3955000214 Pharm 503B OutsourcingWork Shift:Day Shift (United States of America)Scheduled Weekly Hours:40SSM Health is an equal opportunity employer. SSM Health does not discriminate on the basis of race, color, religion, national origin, age, disability, sex, sexual orientation, gender identity, pregnancy, veteran status , or any other characteristic protected by applicable law. Click here to learn more. (https://www.ssmhealth.com/privacy-notices-terms-of-use/non-discrimination?ga=2.205881493.704955970.1667719643-240470506.1667719643)

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