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Validation Specialist
1 week ago
PharmaLex Jersey City, United StatesJOIN OUR TEAM · PharmaLex is a highly successful and growing consulting company for the Healthcare industry. PharmaLex offers professional development, training, competitive compensation, plus a stimulating and collaborative work environment. We are committed in providing exciti ...
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Validation Specialist I
3 weeks ago
PSG Global Solutions New York, United StatesWe're looking for a · Validation Specialist I , working in · Pharmaceuticals · and · Medical Products · industry in · 55 Corporate Drive, Bridgewater, New Jersey, 08807, United States . · Job description: · Manages system documentation review, storage, versioning and sign ...
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Computer System Validation Specialist
2 weeks ago
Ask Staffing New York, United StatesJob Title: Computer System Validation Specialist · Duration: 11 Months · Pay: $53- $55.57 · Location: Syracuse NY · This is not a remote position. We require MINIMUM on site in Syracuse 50%. · Qualifications: · ÂÂÂÂÂ Experience in Computer System Validation · ÂÂÂÂÂ Able to ...
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Product Validation Specialist
1 week ago
CHUBB Jersey City, United States Regular - Full timeChubb's North American Digital Consumer Division brings together the digital products and services of Chubb's North American consumer businesses. We are a diverse, dynamic, and nimble team that uses technology, smarts, and a customer-centric focus to build and digitally distribut ...
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Brillio New York, United StatesJob Title: · Translation Validation Specialist with Localization Expertise · Location: USA and US PST Time zone (onshore/nearshore) · Year of relevant expertise – 3-5 years of handsome experience on similar role · Job Description: · We are seeking a skilled Translation Validati ...
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Validation Specialist
3 weeks ago
TSR Consulting Summit, United StatesTSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading Pharmaceutical company is hiring a MES Validation Specialist. · Rate type: W2 only · Comments · Minimum 50% onsite required every week(Candidate is supposed to ali ...
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Validation Specialist
2 weeks ago
Lynkx Staffing LLC Saddle Brook, United StatesJob Description · Job Description · Validation Specialist · Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device IT & Human Resources disciplines in New Jersey. The Validation Specialist performs validation ac ...
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Validation Specialist
3 weeks ago
Ferring Pharmaceuticals Inc. Parsippany, United StatesDay to Day: · Insight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full time position. This position will be 5 days a week onsite, in Parsippany, NJ. This individual will play a crucial role in ensuring quality ...
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Validation Specialist
3 weeks ago
Insight Global Parsippany, United StatesInsight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full-time position. This position will be 5 days a week onsite, in Parsippany, NJ. This individual will play a crucial role in ensuring quality and compliance ...
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Validation Specialist
1 week ago
Artech Summit, United StatesVALIDATION SPECIALIST · SUMMIT NJ · Hybrid Role · The pay ranges between $ $57.60 an hour · Required Skills: Bachelor's degree in a life sciences, engineering or technology discipline required . · Minimum of 2+ years relevant work experience required preferably in a pharmaceut ...
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Validation Specialist
1 day ago
On-Board Companies Summit, United StatesOn-Board Services is hiring a Validation Specialist · in Summit, NJ · For immediate consideration please send your resume to · Subject Line: Position Title and State you are Located. · About Us: · On-Board Services, Incorporated is an on-site contract service provider for a loca ...
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Validation Specialist
6 days ago
Ferring Pharmaceuticals Inc. Parsippany, United StatesDay to Day: · Insight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full time position. This position will be 5 days a week onsite, in Parsippany, NJ. This individual will play a crucial role in ensuring quality a ...
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Validation Specialist
2 weeks ago
Ferring Pharmaceuticals Inc. Parsippany, United StatesDay to Day: · Make your application after reading the following skill and qualification requirements for this position. · Insight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full time position. This position w ...
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Validation Specialist
2 days ago
Insight Global Parsippany, United StatesInsight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full-time position. This position will be 5 days a week onsite, in Parsippany, NJ. This individual will play a crucial role in ensuring quality and compliance ...
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Validation Specialist
1 week ago
Lynkx Staffing LLC Saddle Brook, United StatesJob Description · Job DescriptionValidation Specialist Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device IT & Human Resources disciplines in New Jersey. The Validation Specialist performs validation activities ...
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Validation Specialist
3 weeks ago
Dover Brook Associates Port Chester, United StatesJob Description · Job Description · We are looking for a bright, energetic, and committed professional to work as a research associate in our New York Facility. Dover Brook Associates will provide support and extensive training for the activities related to the exciting project ...
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Validation Specialist
3 weeks ago
Dover Brook Associates Mahwah, United StatesJob Description · Job Description · We are looking for a bright, energetic, and committed professional to work as a research associate in our New York Facility. Dover Brook Associates will provide support and extensive training for the activities related to the exciting project ...
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Validation Specialist
2 weeks ago
Katalyst Healthcares and Life Sciences South Plainfield, United StatesResponsibilitiesPerforms validation document generation, program management, and protocol execution activities. · Interface with Engineering, and end user groups to support development of life cycle documents and system requirements. · Design the validation approach with techni ...
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Validation Specialist
2 weeks ago
Dover Brook Associates Mahwah, United StatesJob DescriptionJob DescriptionWe are looking for a bright, energetic, and committed professional to work as a research associate in our New York Facility. Dover Brook Associates will provide support and extensive training for the activities related to the exciting projects. This ...
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Technical Validation Specialist
1 week ago
Cross River Fort Lee, United StatesWho We Are · Cross River is a highly profitable, fast-growing financial technology company powering the future of financial services. Our comprehensive suite of innovative and scalable embedded payments, cards, and lending products deliver financial services for millions of busi ...
Quality Validation Specialist - New York, United States - INCOG BioPharma Services
Description
Quality Validation SpecialistWHO?
INCOG BioPharma is looking for a Quality Validation Specialist to join their QA team This individual will be working closely with the Manager of QA, and will be instrumental in ensuring site compliance and reviewing and approving various organizational documentation.
Having recently been voted as one of the Best Places To Work in Indiana for the second year in a row, INCOG is the perfect place to continue building your career.
WHAT?
Review documentation for compliance and Quality approval, including but not limited to: commissioning, IQ/OQ/PQ protocols and reports, validation lifecycle documents, cleaning validation protocols and reports, and process validation protocols and reports.
Use technical skills and applied statistics to analyze and track deviations and to identify sources of variability and error site processes.
YOU
The ideal candidate will have a Bachelor's Degree (Chemistry, Biology, Biochemistry, Microbiology etc.).
They will also have at least 2 years of biopharma industry experience with increasing responsibilities in Commissioning, Qualification, and Validation.
Experience with CQV activities for aseptic manufacturing facilities or clean utilities (e.g. Water for Injection, Clean Steam, etc.) is preferred but not required.Don't meet all the requirements? Don't sweat We're always looking for an excuse to discuss your next opportunity. You might just surprise yourself...
Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.