Get new jobs by email
$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, NY2 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
- ...industry. About the Role We are seeking an experienced Principal Validation Engineer with 10+ years' experience to lead validation strategy... ...Seeded defect studies AQL sampling and acceptance criteria Pharma / Inspection Science Sterile injectable or parenteral...SuggestedFor contractorsVisa sponsorshipWork visaFlexible hours
$140k
PD Validation Engineer page is loaded## PD Validation Engineerlocations: Irvine, Californiatime type: Full timeposted on: Posted Yesterdayjob... ...of experience in validation, quality, or engineering within pharma, biopharma, medical device, or related industries • Experience...SuggestedWork at office- ...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, NY2 days ago - Intellectt Inc is seeking an experienced CSV Consultant to manage validation tasks across projects, including SAS Studio and data migration. This role involves owning validation deliverables, working with cross-functional teams, and ensuring system compliance. The ideal...Suggested
$120k - $150k
JobRx, Inc. is looking for a Sr. CQV Manager/Lead based in Portland, OR, to oversee commissioning, qualification, and validation for pharmaceutical projects. The ideal candidate will have at least 8-12 years of experience and strong skills in managing large-scale projects...Suggested- ...pharmaceutical environment. The ideal candidate will have over 5 years of experience in CQV and a strong background in equipment validation. Responsibilities include evaluating vendors, leading commissioning and qualification processes, and ensuring equipment readiness...Suggested
- 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...Suggested
- ...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...SuggestedShift work
$36.54 - $41.1 per hour
Validation Associate III page is loaded## Validation Associate IIIlocations: San Diego, CA, USAtime type: Full timeposted on: Posted Todayjob... ...with the company’s policies and practices.* Embodies PCI Pharma Services cultural values and aligns daily actions with department...SuggestedFull timeWork at officeFlexible hours- Ipro Networks Pte. Ltd. is looking for a Sr. Validation & Compliance Engineer in Kansas City. This role involves developing and executing validation protocols, coordinating closely with engineering and operations teams throughout the C&Q lifecycle, and supporting technology...Suggested
$100k - $115k
...California's Scientific community. We are currently looking for a Validation Engineer to work for a leading Greater Los Angeles area... ...validation engineering or a closely related field in a cGMP-regulated pharma or biotech environment. ~ Strong working knowledge of process...SuggestedContract workBioPhase Solutions
Los Angeles, CA15 days ago- ...Csv Specialist The CSV Specialist is responsible for planning, coordinating, and executing validation activities for computer systems to ensure compliance with regulatory requirements. This role involves working closely with IT, Quality Assurance, and business stakeholders...SuggestedWork experience placement
Katalyst HealthCares & Life Sciences
Raritan, NJ1 day 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 with...Suggested
- PSC Biotech in Saint Louis is searching for a CQV Engineer I. The role involves the commissioning, qualification, and validation of facilities and equipment in the pharmaceutical sector. You'll collaborate with cross-functional teams to ensure compliance with regulatory...
- A leading pharmaceutical company in Indianapolis is seeking a Validation Lead to oversee the site's validation strategy, ensuring compliance with regulatory standards. The role involves developing validation plans and collaborating with various departments for successful...Relocation package
$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...- ...developing documentation, and ensuring compliance with cGMP. Ideal candidates will have over 5 years of experience in equipment validation and be fluent in English and Spanish. This position offers an opportunity to contribute to safety and efficacy standards in life...
Mentor Technical Group
New York, NY2 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...- 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...
- ...In this role, you will conduct routine analysis of pharmaceutical dosages and raw materials, design method transfer protocols, and validate analytical methods. The ideal candidate has a Bachelor's or Master's degree in Chemistry and 6-10 years of relevant industry...Contract work
$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...$80k - $100k
...LHH Recruitment Solutions has partnered with a growing organization, and they are seeking a motivated Validation Engineer -- Medical Device / Pharmaceutical Manufacturing to join their team. This is a high-impact role supporting critical manufacturing and quality systems...Permanent employmentWork at officeLHH
Mundelein, IL1 day ago- ...Job Description Job Description Validation Engineer Tucson, AZ 12 Months Description: ***We are seeking a proactive Validation... ...in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive...Permanent employmentContract work
TalentBurst, Inc.
Tucson, AZ15 days ago - ...Computer Systems Validation Engineer This role is for a validation engineer coming out from a pharma/biotech space. They will be configuring and qualifying lab equipment and systems onsite within the labs. Must understand GMP. Must have worked with different lab equipments...
Samprasoft
Norwood, MA2 days ago $76k - $103k
A prominent pharmaceutical company in Fall River, Massachusetts, is seeking a Project Lead for Validation (Supervisor). This role involves designing and approving protocols for pharmaceutical drug production, ensuring compliance with regulatory standards, and leading engineering...- 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. This...
$87.15k - $94.6k
...Wisconsin is seeking a qualified professional for CQV activities. This role involves performing Commissioning, Qualification, and Validation tasks with a focus on safety. Candidates should possess a Bachelor's degree in Engineering, Chemistry, or Life Sciences with at...$90k - $115k
Anika is seeking a Validation Engineer II based in Bedford, MA, responsible for managing validation processes for pharmaceutical and medical device manufacturing. The ideal candidate has 3-5 years of validation experience and a strong understanding of cGMP regulations....Full time
