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- ...Associate Validation Specialist Position Summary Typical working hours are Monday - Friday 8 AM - 5 PM. This position is 100% on... ...agency audits. Other duties as required in support of Catalent Pharma Solutions high performance The Candidate HS Diploma...SuggestedWork at officeLocal areaMonday to Friday
Catalent Inc
Winchester, KY5 days ago - ...Position Title : Validation Engineer Work Location : Tucson, AZ 85755 Assignment Duration : 12 months Work Arrangement : Onsite... ...experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive...SuggestedLocal area
SPECTRAFORCE
Tucson, AZ10 hours ago $60 - $65 per hour
...message the job poster from Talent Groups We are looking for a Validation Associate with 7+ years of experience in Computer System Validation... ..., United States $60.00-$65.00 16 hours ago Validation Lead - Pharma/Biotech/Medical Device Thousand Oaks, CA $36.60-$38.90 16 hours...Suggested16 hoursFull timeContract workTalent Groups
New York, NY3 days ago- ...Creative Solutions Services, LLC is looking for validation consultants for a 9-month project in South Carolina. The consultants will support validation execution and assessments tied to equipment qualification and product-specific needs. Ideal candidates will have a Bachelor...Suggested
Creative Solutions Services, LLC
Lafayette, IN5 days ago - A leading validation services provider is offering a Validation Intern position in Maryland. The role involves supporting the validation team in documentation preparation, equipment qualification, and project collaboration in a regulated environment. Ideal candidates should...SuggestedInternship
$85k - $100k
...PSC Biotech in Los Angeles is seeking experienced Validation Engineers responsible for commissioning, qualification, and validation in the pharmaceutical industry. This role requires a Bachelor’s degree in Engineering or Life Sciences and 2-7 years of relevant experience...SuggestedPSC Biotech
Los Angeles, CA5 days ago- ...PSC Biotech in St. Louis is hiring a motivated CQV Engineer I responsible for commissioning, qualification, and validation of facilities in the pharmaceutical sector. The role includes developing and executing important validation protocols while adhering to regulatory...Suggested
PSC Biotech
Saint Louis, MO5 days ago $84.3k - $134.9k
...Jubilant HollisterStier is proudly part of the global, Jubilant Pharma family. established force in the pharmaceutical and... ...and ideas - you belong here. Job Description: The Validation Specialist serves on project teams in support of complex capital...SuggestedFull timeContract workTemporary workImmediate startWorldwideFlexible hoursShift workAfternoon shiftWeekday workJubilant HollisterStier Spokane
Spokane, WA13 days ago- ...chemical analyses using HPLC, GC, UV-Vis, FTIR, titration, and other analytical techniques. Conduct stability testing and method validations according to ICH guidelines. Prepare and standardize laboratory reagents and solutions. Accurately document test results in accordance...SuggestedWork at office
Harba
Indianapolis, IN4 days ago - ...join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client...Suggested
CAI
Italian Republic4 days ago - ...Creative Solutions Services, LLC in Raritan, NJ seeks a candidate experienced in Computer System Validation (CSV) within the Pharmaceutical, Biotechnology, or Medical Device industry. The role involves managing the end-to-end validation lifecycle, ensuring compliance...Suggested
Creative Solutions Services, LLC
Raritan, NJ4 days ago - ...Qualification activities within pharmaceutical manufacturing. The role requires over 5 years of experience in Equipment and Computer System Validation, strong knowledge of cGMP, and bilingual capabilities in English and Spanish. Responsibilities include developing documentation,...Suggested
Mentor Technical Group
New York, NY3 days ago - ...Unither Pharma is looking for a Validation Specialist in Rochester, NY, to manage validation projects in a regulated environment. Key duties include developing protocols, executing validation, and collaborating with cross-functional teams. Ideal candidates have a Bachelor...Suggested
Unither Pharma
Rochester, NY5 days ago - ...Experic, LLC is seeking a Validation Specialist for their Cranbury, NJ office. This role involves supporting validation activities for manufacturing and computerized systems in line with cGMP guidelines. Key responsibilities include preparing and reviewing validation...SuggestedWork at office
Experic
New York, NY5 days ago $128.6k - $193k
...A leading engineering consulting firm in Hauppauge is seeking an experienced Commissioning/Validation Specialist. In this role, you’ll develop and implement project commissioning plans for bio-pharmaceutical facilities, ensuring compliance with design and regulatory standards...SuggestedStantec Consulting International Ltd.
Hauppauge, NY4 days ago- ...pharmaceutical company in Los Angeles is seeking a CQV Engineer for a 12-month project. This onsite position requires 3-10 years of Validation Engineering experience, particularly in pharmaceutical environments. The role involves managing project documentation, conducting...Shift work
- A leading IT staffing company in Zebulon, North Carolina, seeks an experienced validation specialist. This role involves ensuring compliance with regulatory requirements, overseeing the commissioning and validation of manufacturing processes in the Pharmaceutical industry...
$65k - $75k
...Job Title Validation - Engineer II When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with... ...of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx / OpEx project management and/or...Full timeWork experience placementWork visaPerkinElmer
Elkhart, IN4 days ago- ...Integrated Resources, Inc. is seeking a Quality Control Validation Specialist in Durham, NC. The ideal candidate must have expertise in validating laboratory instruments in a pharmaceutical setting, with a thorough understanding of FDA regulations and cGMP standards....
Integrated Resources
Durham, NC5 days ago - ...Job Title Validation - Engineer III/Lead When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions... ...of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx / OpEx project management and/or...Full timeWork experience placementWork visa
PerkinElmer
Elkhart, IN1 day ago - ...Validation Area Specialist (Durham, NC) About the Department For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Being part of Novo Nordisk allows our employees to...Work at officeLocal area
Payfuture Technologies
Durham, NC4 days ago $36.54 - $41.1 per hour
...PCI Pharma Services in San Diego is seeking a Validation Associate III to perform complex validation activities for drug product manufacturing processes. The ideal candidate will have a Bachelor's degree and a strong understanding of GMP compliance, along with experience...Hourly payFull timePCI Pharma Services
Nacogdoches, TX4 days ago$45 per hour
...Greetings, I'm seeking to fill a remote six-plus-month contract role for one of my pharma clients. I am seeking a validation analyst with 5+ years of experience providing support to software systems and laboratory instrumentation. Must have strong PQ validation experience...Hourly payContract workRemote workAnveta
United States2 days ago- ...Edmond Pharma S.R.L. is seeking a highly skilled CQV Engineer based in Watertown, MA. This role leads commissioning, qualification, and validation (CQV) activities for GMP equipment and systems. You'll collaborate with various departments to ensure compliance with cGMP...
Edmond Pharma S.R.L.
Oklahoma City, OK1 day ago - ...Avion Pharmaceuticals, LLC is seeking a Technical Services Scientist to lead qualification and validation activities in Fort Worth, Texas. Responsibilities include developing protocols, performing validation testing, and ensuring compliance with industry standards. The...Full timeFlexible hours
Avion Pharmaceuticals
Fort Worth, TX5 days ago - ...Catalent Pharma Solutions in Kansas City is looking for a Biologics Validation Specialist to serve as a validation representative for laboratory activities. Responsibilities include generating validation documentation, leading validation efforts, and coordinating with...
Catalent Inc
Kansas City, MO4 days ago $52 per hour
...Maxonic maintains a close and long-term relationship with our direct client. In support of their needs, we are looking for a Senior Validation Quality Engineer Job Description: Job Title: Senior Validation Quality Engineer Job Type: Contract...Contract workLocal areaMaxonic
Sturtevant, WI1 day ago- ...Validation Specialist Reporting to the Validation Manager, the Validation Specialist is responsible for supporting and executing validation and qualification activities for manufacturing processes, equipment, utilities, and facilities in a regulated environment. This...Hourly payFor contractorsInternshipWork at officeShift work
Unither Pharma
Rochester, NY4 days ago - ...Pharmaceuticals, LLC. in Fort Worth is looking for a Technical Services Scientist responsible for developing and leading qualification and validation activities. This full-time role requires extensive collaboration with departments to ensure compliance with GMP/Validation...Full time
$85k - $100k
PSC Biotech® Corporation in Los Angeles is seeking experienced validation engineers to oversee the commissioning, qualification, and validation in the pharmaceutical and biotech sectors. The role emphasizes compliance with regulatory standards while ensuring documentation...
