176282 - Quality Assurance Inspector - PA
Industry
MAN
Region
PA-Pennsylvania
City
Allentown
State
PA
Rate
Up to $21.00 DOE
Duration
6 Months
Description
Chipton-Ross is seeking a Quality Assurance Inspector for an opening in Allentown, PA.

RESPONSIBILITIES:
Applies Good Manufacturing Practices (cGMP) in all areas of responsibility.
Demonstrates and promotes the company vision.
Performs approval of specifications and incoming inspections on material (i.e. drug, components) and distribution shipments.
Performs process inspections, samplings, and audits as required.
Participates in continuous improvement initiatives and assists with root cause investigations for nonconforming issues.
Author’s, revises, and complies with all relevant SOP’s and Work Instructions and properly documents activities when necessary.
Follows all Client Standard Operating Procedures.
Performs all activities in a safe and efficient manner.
Assures that issues potentially affecting product quality/compliance are escalated to the attention of the Team Leader and/or Management.
Assures that issues are resolved in a timely manner and corrective actions are implemented accordingly.
Other duties may be assigned to meet business needs.

REQUIRED EXPERIENCE:
A minimum of 1 year of experience in Pharmaceutical or of a related, regulated industry and at least 2 years supervisory experience required.
Experience with Quality Systems (Change Control, deviations, complaint management, documentation management, among others).
Must be able to work in a refrigerated environment (35F to 46F) with provided protective wear.
Must be able to work in a freezer environment with provided protective wear.
Must be able to work in potent compound suites with provided protective wear (PPE).
Good reasoning and problem-solving skills, basic math skills, good communication skills, basic computer skills.
Must be willing to work various shifts and overtime depending on business needs.
Must be able to work independently.
Must not be allergic to penicillin or cephalosporin products.
Extensive standing and walking on packaging floor in order to monitor room activities.
The employee must occasionally lift and/or move up to 20 pounds.

PREFERRED EXPERIENCE:
Bachelor’s degree
Proficient in Microsoft Office including Word, Excel, Access, and Outlook.Knowledge or prior experience with Current Good Manufacturing Practices (cGMP) for pharmaceutical products .

EDUCATION:
Accredited Associate’s degree

WORK HOURS:
2nd Shift, Monday through Friday, 8 hours per day. Additional overtime and weekend (Saturday or Sunday) work may be required.
Full-Time

Contact
Tyler Harrell at tharrell@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293

Phone: (310) 414-7800 x342 or (800) 927-9318 x342

Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.

Employment will be contingent on candidate clearing pre-employment drug screen and background check.

Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.