A natural match if you have 2+ years of QA experience in the pharmaceuticals industry.
Derived from job-description analysis by Serendipath's career intelligence engine.
Original posting from Nordic Naturals via Greenhouse
Location - Vista, CA
Salary - $21/hr
POSITION SUMMARY
The Quality Assurance Warehouse Inspector performs inspection of raw materials, packaging components, intermediates, 3rd party bulks and finished goods for compliance to our established Acceptable Quality Limits (AQL). Pulling samples from each lot of materials for testing and retention. Adherence to applicable standard operating procedures (SOP), Good Documentation Practices (GDP) and Common Good Manufacturing Practices (cGMP) as applicable to individual tasks. Maintains Master Incoming Inspection Tracker, a shared business tool, to ensure visibility of all material status’ throughout their release cycle period
ESSENTIAL FUNCTIONS
Reasonable Accommodations Statement
To accomplish this job successfully, an individual must be able to perform, with or without reasonable accommodation, each essential function satisfactorily. Reasonable accommodations may be made to help enable qualified individuals with disabilities to perform the essential functions.
Essential Function Statements
Performs inspection of raw materials, packaging components, labels, intermediates, 3rd party bulks and Finished Goods; pulling the required samples (per the Sampling paperwork) for testing, in the time limit and priority specified
Prints and/or completes all required documentation in the applicable sampling specification report and on an Inventory Card. Documents any quality-related product findings on the sampling and/or inspection report
Affix disposition placards on all pallet on all lot of material that has been inspected by QA and or by the QC Lab (when appropriate) and the same disposition on the Inventory Card
Updates and maintains the Master Incoming Inspection Tracker for the inspection results, date and inspection reports (where applicable)
Reports any general safety hazards to Materials and Compliance Specialist, QA Manager, QA Director
Performs any other duties assigned by Supervisor or Manager, to include and not limited to, retrieving retention samples, or pulling extra samples, as per management’s request, in the time frame and priority requested
Performs weekly and monthly tasks that include and are not limited to, replacing chart recorders, settling plates, destruction of raw materials… as needed.
Performs other duties as assigned.
POSITION QUALIFICATIONS
Competency Statements
Positive – Ability to view all situations with a positive attitude
Willingness – Possesses willingness to learn new skills and use new tools and methods
Innovative – Ability to look beyond the standard solutions and “think outside the box”
Detail Oriented – Ability to pay attention to the minute details of a project or task
Enthusiastic – Ability to bring energy to the performance of a task
Friendly – Ability to exhibit a cheerful demeanor toward others
Initiative – Ability to make decisions or take actions to solve a problem or reach a goal
Organized – Possessing the trait of being organized or following a systematic method of performing a task
Reliability – The trait of being dependable and trustworthy
SKILLS & ABILITIES
Education:
High school diploma or GED required.
Experience:
Experience in the pharmaceuticals industry is highly preferred but not required
Experience Required: 2+ years
Able to lift, bend, climb and reach
Effective communication skills, including ability to read and write in English (Bi-lingual language skills in Spanish, helpful but not required)
Previous QA experience highly preferred
Flexibility in work hours preferred
Team player, excellent work ethics and able to multitask, attention to details as well as flexibility to changing priorities
Computer Skills:
Analytical, computer and mathematical skills.