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Quality Control Analyst
6 days ago
Insight Global Malvern, United StatesTitle: QC Lab Services Analyst - External Sample Management/Raw Material Release Specialist · Duration: 2 year contract · Hours: Monday – Friday, 8 or 9am start time (typical 40 hour work week) · Pay: $28-35/hr · Interview Process: 1 and done-for next week · Requirements: · -A m ...
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Quality Control Analyst
3 weeks ago
Insight Global Malvern, United StatesRequired Skills and Experience: · -Minimum of a Bachelor Degree in science or equivalent technical field · -Minimum of two years of experience working within biological or pharmaceutical system management · -Experience in a Quality Control setting. · -Skilled in basic and advance ...
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Laboratory Quality Control
4 weeks ago
Pyramid Consulting, Inc Malvern, United StatesImmediate need for a talented Laboratory Quality Control. This is a 08+ Months contract opportunity with long-term potential and is located in Malvern, PA (Onsite). Please review the job description below and contact me ASAP if you are interested. · Job ID: · · Pay Range: $ ...
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Quality Control Inspector
3 days ago
ZEISS Group Chester, United States Full timeHow many companies can say they've been in business for over 177 years? · Here at ZEISS, we certainly can As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEIS ...
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Quality Control Inspector
4 weeks ago
Active Staffing Services Exton, United StatesJob Description · Job DescriptionA diversified international avionics supplier to civil, military, business and commercial aircraft parts and instruments is expanding its team of skilled Electronics Technicians. Company located in Exton, PA offers excellent career opportunities f ...
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Quality Control Laboratory Technician
6 days ago
Integration International Inc. Exton, United StatesJob Details: · Title: QC Lab Technician I · Location: Exton, PA 19341 · Duration: 03 months (Possible extension or conversion) · Job Description: · Key Responsibilities: · Conduct laboratory tests and inspections on raw materials, in-process, and finished products. · Analyze and ...
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Quality Control Manager
1 week ago
Piper Companies Wayne, United StatesPiper Companies · is currently seeking a · Quality Control Manager · for an opportunity in · Wayne, Pennsylvania (PA), · to join a contract research organization conducting Next Generation Sequencing-based QC testing for the development of biotherapies. · Responsibilities of the ...
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Quality Control Manager
1 week ago
Piper Companies Wayne, United StatesPiper Health and Sciences is currently seeking a Quality Control Manager to support an innovative and reputable Biologics Quality Control Testing company in Wayne, PA.Responsibilities for the Quality Control Manager · •Serve as lead scientist and SME for new and ongoing NGS assa ...
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Ocugen Malvern, United StatesJob Details · Job Location: Main Corporate Office - Malvern, PA · Salary Range: Undisclosed · Description · Job Purpose · The Senior Manager/Associate Director of QC is a strategic leadership role responsible for fostering a culture of quality, efficiency, and excellence, en ...
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Quality Control Associate
2 weeks ago
Teva Pharmaceutical Industries West Chester, United StatesWho we are · Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Wor ...
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Quality Control Manager
2 days ago
Ecolab King Of Prussia, United StatesAs a Quality Control Manager with Purolite an Ecolab Company, you will establish quality control guidelines and testing procedures. You will ensure that raw material and finished product quality and reliability are in compliance with engineering and product specifications. Will r ...
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Quality Control Associate
2 weeks ago
Teva Pharmaceuticals West Chester, United StatesQuality Control Associate - Bioassay & Potency, GMP (On-site) · Date: May 14, 2024 · Location: · West Chester, United States, Pennsylvania, 19380 · Company: Teva Pharmaceuticals · Job Id: 55397 · **Who we are** · Together, we're on a mission to make good health more affordable an ...
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Quality Control Laboratory Manager
4 weeks ago
System One Holdings, LLC Exton, United StatesTitle: · Quality Control Laboratory Manager · Location: · Exton, PA · Type: · Contract to hire · Schedule: · Monday - Friday 8AM-5PM · Overview: · Growing Biopharmaceutical Company is looking for a hands on manager to lead and oversee their QC Lab in operational activities a ...
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Quality Control Microbiologist
6 days ago
ClinLab Staffing Norristown, United StatesAnalyst II, Quality Control (QC) Microbiology – East Norriton, PA · General Company Description · My client is a first-of-its-kind manufacturing and technology company dedicated to broadening access to complex medicines and protecting biopharmaceutical supply chains against disru ...
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Quality Control
3 weeks ago
Finish Tech Corp Warminster, United StatesJob Description · Job DescriptionFor printing / laminating / converting business · We are looking for a full-time Quality Control/Lab Technician for our manufacturing plant in Warminster, PA. Finish Tech is in the laminating/printing/converting business. Knowledge or experience i ...
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Quality Control Inspector
3 weeks ago
GOGcG Collegeville, United States Full timeOverview · Allied Wire and Cable (AWC), a GCG Company, is currently seeking a Quality Control Inspector to join our team in Collegeville, PA · You'll be part of a team that values precision and accountability, where your efforts have a direct impact on our product quality and cus ...
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Quality Control
3 days ago
Satin Fine Foods Inc. Chester, United StatesThis Quality Control / Food Safety Position is responsible for working closely with the Quality Control Team to manage all resources related to quality. This includes reviewing, developing, implementing, and maintaining programs to improve product quality, food safety or technolo ...
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Quality Control Scientist
3 weeks ago
Beacon Hill Exton, United StatesGeneral Responsibilities: · Performs testing in support of product manufacturing, employing manual and automated analytical equipment for a variety of molecular, protein and cell based assays, such as PCR, ELISA, and flow cytometry. · Responsibilities: · Execute Analytical Test M ...
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Quality Control Analyst
1 week ago
NEUROVUE Philadelphia, United StatesNEUROVUE is disrupting the Life Sciences consulting paradigm with a proprietary approach to talent attraction and retention. With focus and extensive investment, NEUROVUE has created an unparalleled employment experience that attracts industry top minds for our clients' project n ...
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Quality Control Technologist
2 weeks ago
InsideHigherEd Philadelphia, United States· Quality Control Technologist (Center for Cellular Immunotherapy) · University Overview · The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistent ...
Associate Director, Quality Control - Malvern, United States - VenatoRx Pharmaceuticals, Inc.
3 weeks ago
Description
The Associate Director, Quality Control has responsibility for actively overseeing cGMP quality control activities associated with development and commercialization of the company's small-molecule assets.
This function operates within a virtual (100% outsourced) business model and the incumbent will be responsible for oversight of Quality Control activities of drug substance, drug product, intermediates.
The individual must be knowledgeable of US government regulations (ICH, GMP, GLP, etc. A thorough understanding of the drug development process as related to methods development, validation, and transfer is also required.An in-depth knowledge of release/stability testing, specification setting, reference standard maintenance and quality assurance/regulatory practices is also necessary to fulfill the requirements the requirements for this position.
Duties and responsibilitiesResponsibilities include:
Understand test methods, validations and stability testing for raw materials, excipients, drug substance and drug products. Contribute to the development, improvement and optimization of methods for release and stability.
Practical understanding of pharmaceutical drug development and GxP requirements is essential.
Extensive experience in chromatographic (HPLC/UPLC, GC, IC) data review is required.
Working knowledge of other GMP testing including but not limited to microbiological, wet chemical techniques and metals analyses is required.
Manage and support method transfer and validation activities to external sites. Provide review and approval of related documentation.Identify, write, and revise standard operating procedures, work instructions, and laboratory policies, procedures and standard practices. Review methods, protocols, reports, IND and NDA sections as appropriate.
Initiate and/or support change controls, laboratory investigations, CAPAs and deviations as appropriate. Participate with external laboratory investigations.
Responsible for working with external partners for analytical method validation life-cycle management and process improvement.
Participate in CMC technical meetings as support for QC and analytical functions.
Contribute as author/reviewer of appropriate analytical IND and NDA sections.
Support reference standard program through tracking of standard testing data and issuance of CoAs and retest memos.
Serve as CMC team member and project contact with internal and external entities including quality assurance and regulatory.
Maintain up-to-date knowledge of government regulations and Venatorx policies and procedures.
Other projects and duties as required/assigned.
Qualifications
Candidate requirements:
PhD (or BS/MS with experience) individual contributor position with extensive experience in quality control operations.
(PhD with 6+, MA with 8, and BA with 10) years of experience in analytical chemistry or related life sciences discipline.
Work experience should include a combination of data management and quality control experience in pharmaceutical product developmentHands-on experience and/or familiarity with HPLC/UPLC, GC, KF, spectroscopy (UV, FTIR, etc.), dissolution and other common analytical techniques used for small molecule drug substance and solid oral dosage drug product testing.
Advanced working knowledge of cGMP compliance requirements for pharmaceutical analytical development and quality control laboratories.Preferred Qualifications:
CDMO management employing cross-functional collaboration skills.
Small molecule pharmaceutical development for solid oral dosage forms and parenteral
Experience in a virtual (100% outsourced)development business model is preferred
This is a representative description of the job and is not intended to be all-inclusive. Employee may perform other related duties as required to meet the ongoing needs of the organization. Duties, responsibilities, and activities may change at any time with or without notice.
Venatorx is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, national origin, age, marital status, protected veteran status, disability status, or any other status protected by federal, state, or local law.
For more information, please check out our website:#J-18808-Ljbffr
Associate Director, Quality Control professionals in Malvern
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Farukh Naqvi
Manufacturing Business Partner