Average salary: $140,560 /yearly
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$140.77k - $215.7k
...all in-vitro diagnostics products manufactured at Quest. Provide oversight of engineering activities associated with equipment and process validations, improvement projects, packaging designs, technology transfers, and shared services. Lead product development activities...Suggested$80k - $100k
...with a growing organization, and they are seeking a motivated Validation Engineer -- Medical Device / Pharmaceutical Manufacturing to... ...Responsibilities: Lead validation efforts for manufacturing equipment, processes, and systems, ensuring compliance with regulatory...SuggestedPermanent employmentWork at office- ...supporting critical Production and Development semi-automated equipment with troubleshooting (Root Cause Analysis), complex repairs, maintenance... ...of equipment. Support Equipment Qualifications and Validations, where necessary Requirements ~ BS/BA degree or...Suggested
- ...resolution. Collaborate with peers for review of task direction, validation, and verification activities. Key Responsibilities: Support line capacity expansion activities Perform equipment qualification and process validation Execute existing...SuggestedTemporary workInternshipWork at officeFlexible hoursShift work
$112k - $149k
...optimize manufacturing processes. Candidates should possess a Bachelor's degree in engineering, with extensive experience in equipment validation and process improvement in the medical device or pharmaceutical industry. This role involves designing manufacturing...Suggested- ...Qualification (C&Q) activities geared towards pharmaceutical manufacturing. Candidates should have over 5 years of experience in equipment validation and a strong understanding of cGMP regulations. Bilingual candidates fluent in English and Spanish are preferred. This role...Suggested
- ...Position: Validation Process Engineer Duration: 12+ months / contract to hire Location: Tarboro, NC 27886 - this is onsite daily... ...pharmaceutical manufacturing operations that are focused on process and equipment validation, process improvements, manufacturing readiness, and...SuggestedContract workLocal area
$20 - $22 per hour
...the Job? Maintain a sterile environment in the cleanroom by garbing, cleaning, and following CGMP guidelines. Clean and validate equipment daily, ensuring all validations are current. Oversee techniques and practices of co-workers, including product assembly,...SuggestedShift work$40k - $46k
...PhaseI andII clinical trials. Responsibilities Prepare materials, equipment, and manufacturing suites for production. Conduct GMP... ...ensuring accurate documentation. Assist engineering with equipment validations, preventative maintenance, and cleaning verifications. Complete...SuggestedMonday to FridayFlexible hoursAfternoon shift- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who... ...are seeking a Validation Engineer with experience in upstream equipment to join our team. The Validation Engineer will be responsible...SuggestedWeekend work
- ...GxP requirements. This position will be responsible for authoring and enforcing SOPs to meet GMP guidelines, onboarding and validating new equipment, maintaining compliance of existing systems, and driving the implementation of new IT GxP solutions such as Data Historian...SuggestedTemporary workWork at officeLocal area
$65k - $85k
...Validation Specialist / Calibration Technician (CQV, GMP, Life Sciences) Location: Texas Salary: $65-85K + Bonus + Benefits... ...Qualification) protocols Work on validation of lab systems, equipment, and utilities Partner with engineering, validation teams,...Suggested$70k - $80k
...Job description: Job Summary: The Validation Engineer will be responsible for executing and supporting validation activities within... ...on, shop-floor–focused role requiring direct involvement with equipment, processes, and systems to ensure compliance with regulatory standards...Suggested$109k - $174.8k
...Key responsibilities include leading quality projects, reviewing compliance documentation, and providing oversight for equipment and process validations. The position is full-time and fully on-site, with an anticipated salary range of $109,000 - $174,800. #J-18808-Ljbffr...SuggestedFull time- ...QRC Group is seeking a Validation / Commissioning Specialist for a project in Manati, Puerto Rico. This role involves supporting the validation of load cells in a pharmaceutical environment. Key responsibilities include executing commissioning activities, ensuring compliance...Suggested
- ...Scientist responsible for developing and leading qualification and validation activities. This full-time role requires extensive... ...minimum 3 years' experience in pharmaceuticals, and expertise in equipment operations and validation principles. #J-18808-Ljbffr Alora Pharmaceuticals...Full time
- Creative Solutions Services, LLC in Marietta, Georgia is seeking a Manufacturing Engineer to support equipment and process validation for a medical device production facility. This full-time onsite role requires strong knowledge of regulatory standards and collaboration...Full time
- August Bioservices, based in Nashville, TN, is looking for a dedicated Validation Engineer to perform various validation tasks ensuring compliance with cGMPs. The role involves preparing validation protocols, overseeing validation studies, and developing acceptance criteria...
- ...Root Cause Analysis) Statistical tools (DOE, SPC, basic data analysis) Knowledge of GMP, FDA, and ISO regulations Equipment validation (IQ/OQ/PQ) and process validation Upon completion of waiting period consultants are eligible for: ~ Medical and Prescription...Weekly payContract workTemporary workFlexible hours
- ...Executing laboratory tests for method development, optimization, validation, and transfer while maintaining accurate and timely... ...responsibility for the operation and upkeep of assigned laboratory equipment. Ensuring all work processes consistently meet established data...
- ...and 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...
- Kindeva Drug Delivery is looking for a Floater Validation Engineer II in St. Louis, Missouri. This role will provide validation engineering... ...manufacturing facilities. Responsibilities include equipment qualification, cleaning validation, and process validation. Candidates...
- ...seeking a Manufacturing Test Engineer to support testing and validation within a regulated manufacturing environment. The ideal candidate... ...strong knowledge in manufacturing engineering support and equipment validation. The role includes setting up test configurations,...
$20 per hour
...support facility readiness by maintaining cleanroom environments, equipment, and documentation systems while contributing to continuous... ...startup activities including equipment qualification, process validation, and implementation of new procedures. Clean, disinfect, and...Hourly payPermanent employmentFull timeMonday to Friday- ...of the Engineering Department supporting product development, validation, and regulatory compliance. The ideal candidate will demonstrate... ...validation projects for existing products, new processes, and equipment, ensuring adherence to FDA, GMP, ISO 13485, and ISO 14971...Weekly payTemporary workFlexible hours
- ...Manufacturing Engineer Designs, specifies and installs new equipment and provides engineering technical support and troubleshooting... ...Develops and supports equipment commissioning and qualification (validation) activities. • Maintains personal training, goal development...For contractorsShift workRotating shiftWeekend work
$74k - $82k
...Maintenance Specialist II support pharmaceutical manufacturing plant, equipment, and utilities, and maintain compliance with all state and... ...equipment, utilities, and systems to maintain operations and validation Supports maintenance programs consistent with cGMP engineering...Flexible hours$96k - $132k
...Conduct engineering studies and process improvements to support process validation and contribute to maximizing production performance. Provide engineering support for production assembly equipment, methods and process validation of new and existing equipment. Performs...Temporary workFor contractorsWork at officeWork visaFlexible hours- ...sustaining effective and compliant processes, procedures, and equipment. Your responsibilities will include: Investigating and resolving... ...equipment efficiency. Develop, execute, and review IQ/OQ/PQ validation protocols of in-process machines, equipment, and utilities. Collaborating...
$80k - $120k
...develop, and continuously improve complex manufacturing processes, equipment, and technologies Act as the technical subject matter expert... ...both internal and external audits Lead process and equipment validation activities, including IQ/OQ/PQ Drive new product introduction...Local areaRelocation



