Quality Auditor - Fixed Term Contract
Role Overview
The role is essential in ensuring in-process and finished products meet customer specifications.
This role provides total manufacturing quality inspection services including quality inspection, quality control, sampling inspection, documentation and record keeping.
Adhering to Good Documentation Process (GDP) is essential to maintain all documentation necessary to ensure conformity to specifications and traceability of records.
Essential Duties and Responsibilities Perform sampling, inspections, and testing of in-process and finished goods products per applicable procedures and AQL plans, utilizing both visual means as well as calibrated test equipment.
Release acceptable in-process and finished goods product for further processing and/or shipping.
Understand and follow applicable ISO standards requirements.
Perform review of inspection records to assure product conforms to specifications and proper documentation practices.
Retains sample of finished products and maintains all applicable documents to form batch records and ensures appropriate batch records disposition (i.e. filing, scanning etc.) as necessary.
Print documents from Master Control, shopfloor or other software program and manages documents related to the Quality System.
Segregate nonconforming product and handle quarantined product and raw materials as applicable by site.
Generate rejection and deviation reports as directed by site.
Perform trace back investigation of nonconforming raw material and product as directed by site.
Promotes and supports a Lean environment.
Conforms with and abides by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules.
Exhibits regular, reliable, punctual and predictable attendance.
Other duties as assigned.
Additional Responsibilities Provide a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
Maintain a clean, orderly, and safe workstation and environment at all times.
Conform with and abide by all regulations, policies, work procedures, instruction, and safety rules.
Exhibit regular, reliable, and punctual attendance.
Perform other duties as assigned based on business needs.
Keep current with new GMP compliance guidance and internal QA procedures.
Support new GMP compliance guidance and Data Integrity initiatives.
Full Job Posting
Additional Requirements
- Ability to learn, understand, and remember normal tasks. Ability to hear, speak, and understand conversation in English. Must maintain the ability to work well with others in a variety of situations. Must be able to multi-task, work under time constraints, problem solve, and prioritize. Read and interpret data, information and documents Work under deadlines with constant interruptions West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to [email protected] . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening. #LI-ME1
Preferred Qualifications
- 1 year of manufacturing experience preferred Preferred Knowledge, Skills and Abilities Able to be aware of all relevant standard operating procedures as per Company policy. Support and contribute to Lean Sigma programs and activities towards delivery of the set target. Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude. Willingness to learn new and review new analytical techniques. Meet individual and departmental goals as required. Physical Requirements Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects. Additional Requirements Ability to learn, understand, and remember normal tasks. Ability to hear, speak, and understand conversation in English. Must maintain the ability to work well with others in a variety of situations. Must be able to multi-task, work under time constraints, problem solve, and prioritize. Read and interpret data, information and documents Work under deadlines with constant interruptions West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to [email protected] . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening. #LI-ME1
About West Pharmaceutical Services
Manufacturer of injectable pharmaceutical packaging and delivery systems.
Visit company websiteJobs and hiring trendsApply for this job in 1 click
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
More jobs at West Pharmaceutical Services
Inventory & Logistics Analyst
, USA
Technical Support, R&D, Pilot Plant
, USA
Technikumsmitarbeiter RD
, USA
Operations Assistant (m/f/d)
, USA
Fachbereichsassistenz Operations (m/w/d)
, USA
Production Operator (m/f/d)
, USA
Maintenance Mechanic (m/f/d) 1
, USA
Manufacturing Quality Engineer
, USA