QA Incoming Inspector - Shift Hrs 10:00 to 6:00 Customer Service & Call Center - Magna, UT at Geebo

QA Incoming Inspector - Shift Hrs 10:00 to 6:00

QA Incoming Inspector - Shift Hrs 10:
00 to 6:
00 page is loaded QA Incoming Inspector - Shift Hrs 10:
00 to 6:
00 Apply locations Conshohocken time type Full time posted on Posted 8 Days Ago job requisition id JR29783 SUMMARY Responsibilities include both visual and physical inspection of packaging components and bulk product related to contract packaging.
Additionally, participation in internal, external or regulatory audits will be required at the discretion of senior management.
The impact of the quality inspection process directly impacts company compliance to regulatory requirements and customer satisfaction.
ESSENTIAL DUTIES AND
Responsibilities:
The following is a list of responsibilities related to inspection.
Other duties may also be assigned.
Assure that you are properly garbed prior to performing inspection according to the Sharp requirements.
Verify all documentation (CoA, CoC, Bill of Lading, etc.
) matches the material labeling and item specification.
Responsible for the execution of the sampling and inspection of the components and bulk product assuring that they meet the item specification and documenting the results on the applicable inspection form.
Operate a variety of testing equipment (FT-IR, Keyence, Magna-Mike, UV-Vis and Global Vision) and documenting the results on the applicable inspection form.
Ability to use and read calipers and rulers.
Work in electronics system for inventory, training, and documentation storage.
Responsible for participating in internal, customer, and regulatory audits at the discretion of senior management.
Responsible for training of designated peers at management request.
Assist with receiving, transfer and shipping of controlled substances.
SUPERVISORY
Responsibilities:
None
Qualifications:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed below are representative of the knowledge, skill, and/or ability required.
The individual must pass a colorblindness test to assure they can detect if a color is out of specification.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
REQUIREMENTS:
Due to the nature of our work, all employees must be over the age of 18 and will be required to undergo a pre-employment drug test and background check.
EDUCATION and/or
Experience:
High School diploma, or equivalentPreferred Skills/Abilities:
Two (2) years of quality or manufacturing experience in a regulated environment Knowledge of cGMP (21CFR 210, 211, 820) and/or DEA regulations for controlled substances Knowledge of DEA regulations for controlled substances.
Attention to detail.
Strong communication skills (verbal and written), interpersonal skills, team building and organizational skills.
Ability to read, write and speak the English language and follow verbal and written instructions.
Skill and ability to perform work in a thorough and accurate manner.
Ability to use a wide variety of test and measurement equipment.
Ability to follow and comply with procedures.
Ability to develop and produce reports and documentation.
Ability to work overtime (weekend - Saturday and/or Sundays) MATHEMATICAL SKILLS:
Ability to apply moderately complex mathematical operations to assigned tasks.
This includes an understanding of statistical sampling plans.
LANGUAGE SKILLS:
Ability to effectively communicate (either written or verbally) with the following groups:
Internal:
Daily contact with Quality and Warehouse Departments for information on quality inspection issues and cGMP issues.
REASONING ABILITY:
A thorough understanding of each aspect of the job is required.
Ability to make rational decisions pertaining to quality compliance.
Ability to resolve problems effectively and efficiently.
COMPUTER SKILLS:
Basic Windows applications including Microsoft Office Suite (Outlook, Word, Excel, etc.
).
Experience with electronic systems (Veeva and QAD) desired.
PHYSICAL DEMANDS:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The employee frequently will sit to complete paperwork.
The employee is occasionally required to stand, walk, and reach with hands and arms.
The employee must occasionally lift and/or move up to 50 pounds.
Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus.
The ability to see color and assure it matches the specification is also a necessity.
WORK ENVIRONMENT:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is normally required to sit at a desk or periodically go onto the shop floor.
The working environment is clean and not normally subject to hazardous environment or conditions.
The noise level in the work environment is usually moderate.
About Us Sharp Packaging Services works across the world to create unique commercial and clinical packaging solutions for the pharmaceutical and biotechnology industry.
We are made up of two dynamic international divisions, Sharp Packaging Solutions and Sharp Clinical Services.
Together our 1,600-strong team works from state-of-the-art facilities in the United States, United Kingdom, Belgium and the Netherlands.
We've built an exceptional global reputation for the design, serialisation and production of innovative, cost-effective compliance packaging for even the most complex products.
Our extensive range includes blister packs, bottles, pouches and stick packs, but our expertise goes far beyond, enabling us to support your product through every stage of design, development, manufacture and delivery.
Our clinical services division is one of the world's leading providers of innovative clinical supply chain services, with a talented and highly experienced team that can handle every aspect of your supply chain.
Our work spans everything from drug development and manufacturing to clinical supplies packaging, labelling, distribution, Qualified Person auditing and comparator sourcing.
#J-18808-Ljbffr Recommended Skills Attention To Detail Auditing Communication Coordinating Customer Satisfaction Electronics Apply to this job.
Think you're the perfect candidate? Apply on company site $('.
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