Quality yst
Quality yst
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Job Description
Role: Quality yst Senior
Pay Rate: $35/hr on W2
Position Type: Contract 1 year with possibility of extension
Location: Exton PA United States
Description:
100% onsite
We are seeking a highly sed Raw Material Expert with extensive knowledge and handson experience in Raman spectroscopy. The successful candidate will be responsible for the ysis and characterization of raw materials ensuring their quality and suitability for production processes. This role involves working closely with crossfunctional teams to develop and implement testing protocols trouble material issues and support continuous improvement initiatives.
Essential Functions:
Conduct detailed ysis of raw materials using Raman spectroscopy and other ytical techniques.
Develop and validate testing ods to ensure the accuracy and reliability of material characterization.
Collaborate with R&D quality urance and production teams to address materialrelated challenges.
Maintain accurate records of all yses and prepare comprehensive reports.
Stay updated with the latest advancements in Raman spectroscopy and material science.
Requirements
Education and Experience
Bachelors or Masters degree in Chemistry Material Science or a related field.
Proven experience in using Raman spectroscopy for material ysis.
Strong understanding of material properties and their impact on production processes.
Excellent problemsolving ss and attention to detail.
Ability to work effectively in a teamoriented environment.
Training within a regulated Pharmaceutical/biotech/medical device environment.
Understanding and application of cGMPs (EP JP USP).
Detailed knowledge and application with electronic Quality Systems and Data Integrity.
Technical
Strong attention to detail as demonstrated through consistent quality of work.
Excellent written and verbal communication ss.
Computer proficiency in MS Word and Excel MS Access required.
Demonstrates process orientationthinks through required steps and sequencing to ensure quality work output.
Ability to anticipate potential problems and take proactive action to avoid/minimize impact. Function as change agent to ensure accurate and timely facilitation of global and department GMP etc. changes.
Anticipates consequences of actions and how they impact other areas.
Ability to utilize project management ss to independently prioritize plan and schedule workflow.
Timely follow up to ensure satisfactory resolution to issues.
Knowledge of CGMPs (relevant laws guidance directives and industry practice) and demonstrated ability to apply learnings appropriately in a controlled environment.
Ability to interpret and apply GMPs relevant laws guidances and directives to extremely complex pharmaceutical situations.
Ability to work and coordinate activities across multiple functional groups with a sense of professionalism and urgency.
Ability to work collaboratively with internal and external team members and customers/contacts.
Selfmotivated; able to work with minimal supervision. Exercises independent judgment in evaluating compliance.
Employment Type
Full Time
