Quality Complaints, Senior Associate, GMP/Medical Device (JP10448)
3key Consulting, Inc.
Job Title: Quality Complaints, Senior Associate, GMP/Medical Device(JP10448) Location: Thousand Oaks, CA. Employment Type: Contract Business Unit: Product Complaints & Surveillance Duration: 1+ years with likely extensions or conversion to FTE Notes: 100% onsite Posting Date: 06/16/2022 3 Key Consulting is hiring Quality Complaint Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: Requirements: Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operation according to company guidelines. Be self-motivated, attentive to details and able to prioritize and meet deadlines. Basic statistical mathematical skills including the ability to trend data. Basic project management skills. Independently understand, follow and implement instructions. Written and verbal communication & collaboration skills. Strong word processing, database and spreadsheet application Skills: Strong organizational skills with the ability to manage multiple projects or assignments. Role may involve periods of prolonged sitting and standing. Role may involve lifting boxes and storage containers of up to 50lbs. Role may involve transporting samples to different buildings across campus. Top Must-Have Skill Sets: Attention to detail in lab environment Proficient in MS office Strong written and verbal communication skills Understanding GMP Background in quality inspection high plus Day to Day Responsibilities: Receive, clean, evaluate, and file/store returned samples Operate equipment such as cameras, biosafety cabinets, xrays Manage inventory of consumables Interface with complaint owners and cross functional team members Prepare samples for shipment to other locations Employee Value Proposition: Career growth/ opportunity Red Flags: Candidate needs to have strong attention to details Interview process: 2 WebEx interviews & 1 Onsite interview We invite qualified candidates to sendyour resume to View email address on click.appcast.io . Ifyou decide that you’re not interested in pursuing this position, please feel free to take a look at the other positions on our website . You are welcome to also sharethis opportunity withanyone you think might be interested in applying for this role. #J-18808-Ljbffr 3key Consulting, Inc.
- ...in Life Sciences and at least 1 year of related experience in quality assurance or manufacturing within the GMP pharmaceutical or medical device industry. Responsibilities include evaluating product complaint samples, managing inventory, and preparing shipments. Ideal...QualitySeniorComplaintsMedical device
- ...Thousand Oaks, California, focused on evaluating product complaint return samples. The role involves interaction with... ...related field, with at least 1 year of experience in quality assurance or manufacturing in a GMP environment. Strong attention to detail, project management...QualitySeniorComplaintsMedical device
- ...seeking a dedicated and detail-oriented Quality Complaints Senior Associate to join a dynamic team focused on... ...standards in life sciences and medical device quality assurance. The successful candidate... ...initiatives, all in a fast‑paced GMP environment. Key Responsibilities...QualitySeniorComplaintsMedical device
- ...have: documentation practices, GMP, previous lab experience.... ...clean, and evaluate product complaint return samples. This includes... ...Typically 1 plus years of related quality assurance or manufacturing... ...experience in a GMP pharmaceutical or medical device industry. Tasks and...QualitySeniorComplaintsMedical deviceSummer workLocal areaRelocationFlexible hoursShift work
$22 - $32 per hour
...Responsibilities Receive, clean, and evaluate product complaint return samples. This includes but is not... .... Typically 1 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Tasks and Expectations Evaluate...QualitySeniorComplaintsMedical deviceSummer work- The Steely Group is looking for a dedicated Quality Complaints Senior Associate located in Thousand Oaks, California. This role involves managing product... ...and ensuring accurate documentation in a fast-paced GMP environment. The ideal candidate should have a Bachelor's...QualitySeniorComplaints
$27 - $29 per hour
...: Receive, clean, and evaluate product complaint return samples. This includes but is not limited... .... Typically 1 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Top 3 Must Have Skill Sets...QualitySeniorComplaintsMedical deviceHourly payFull timeLocal areaFlexible hours$27 - $29 per hour
Responsibilities Receive, clean, and evaluate product complaint return samples, including photographs, x-... ...experience. Typically 1+ years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Top 3 Must Have Skill Sets...QualitySeniorComplaintsMedical deviceHourly payFull timeLocal areaFlexible hours- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented,... .... Draft, revise and ensure GMP manufacturing documents (SOPs... ...technologies. Qualifications Associate degree in engineering or...QualitySeniorMedical deviceShift workWeekend workDay shift
- Senior Device Engineer - Electromechanical Combination Products... ...systems, or medical devices, a background... ...and compliance. Lead complaint investigations by performing... ...collaboration with quality, manufacturing, and... ...of experience OR Associates degree and 8 years of...QualitySeniorComplaintsMedical devicePermanent employmentContract work
- Job Title: Engineer Senior, Combination Device Life Cycle Change Management... ..., Drug Delivery Medical Devices for a... ...Manufacturing, Regulatory, and Quality colleagues .... ...functional assessment of complaint record . What we... ...of experience OR Associate degree and 10 years...QualitySeniorComplaintsMedical deviceContract workWork at office
- ...Engineer, Medical Device - GMP Test Methods The Engineer will work under... ...Position involves support of senior staff in the initiation,... ...Network with manufacturing, quality and regulatory organizations... ...project status and risks associated with integrated timelines to...QualityMedical deviceFor contractorsWork experience placement
- ...the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to help... ...functional areas such as Manufacturing, Quality, Process Engineering, Validation, and... ...protocols. Generate, review, and approve GMP Lifecycle Documents (e.g., risk...QualitySeniorMedical device
- ...Downstream) and rotate every 6 months. This position will start on day shift and transition to NS after training approximately 1 month after starting. The ideal candidate will have 1-2+ years of hands-on experience in a regulated GMP environment. #J-18808-Ljbffr Neier Inc.QualitySeniorFlexible hoursNight shiftRotating shiftDay shift
- ...Job Title: MCS Senior Associate Quality Assurance Duration: 12 Months (Possibility of Extension) Location: 91320, Thousand Oaks, CA Must be flexible... ...will have hands-on QA or manufacturing experience in a GMP environment (preferably within biotech or Client) with strong...QualitySeniorWork experience placementFlexible hoursShift workRotating shiftDay shiftAfternoon shift
- ...Job Title: Engineer, GMP Drug Delivery Medical Device (JP13357T) Location: Cambridge... ...involves support of senior staff in the initiation,... ...Network with manufacturing and quality organizations internal to... ...project status and risks associated with integrated timelines...QualityMedical devicePermanent employmentContract work
$30 - $32 per hour
...candidates will have hands-on QA or manufacturing experience in a GMP environment, with strong critical thinking skills prioritized... ...record review and approve SOP revisions and work orders. Provide quality approval of minor deviations and evaluate compliance issues. Represent...QualitySeniorDay shiftAfternoon shift- Job Title: MCS Senior Associate Quality Assurance Duration: 12 Months, Possibility of Extension Location: Thousand Oaks, CA Shift Details Day... ...operations, and reviews quality documentation. This is a hands‑on, GMP‑focused QA support role that requires individuals who are...QualitySeniorTemporary workWork experience placementShift workNight shiftDay shift
$28 per hour
...seeking a discerning, detail-oriented Quality Complaints Senior Associate to join the Product Complaint &... ...with Good Manufacturing Practices (GMP) and Good Documentation Practices (... ...a GMP-regulated pharmaceutical or medical device environment. Technical Skills:...QualitySeniorComplaintsMedical deviceHourly payContract workTemporary workWork experience placementSummer workLocal areaShift work- Job Title: Engineer, GMP Test Methods Medical Device - (JP10960 / 11088) Location: Thousand Oaks, CA. 91... ...or equipment introduction to improve quality and reliability and reduce cost.... ...communicate project status and risks associated with integrated timelines to leadership...QualityMedical devicePermanent employmentContract workFor contractorsLocal area
- Senior Associate Quality Assurance The Sr. Associate QA will be a member of the Amgen Thousand Oaks Clinical... ...QA team, responsible for ensuring GMP compliance of all final drug product... ...retirement and savings plans, group medical, dental, vision, life and disability insurance...QualitySeniorFlexible hours
$44 - $48.5 per hour
3key Consulting, Inc. is seeking a Senior Device Engineer specializing in electromechanical combination... ...in design control and testing for medical devices. This contract position involves lifecycle management, complaint investigations, and cross-functional collaboration...SeniorComplaintsMedical deviceContract work$29 - $31 per hour
...routing supporting documents, performing quality checks of templated information to confirm... ...'s degree in science or engineering GMP experience Pay Transparency: The typical... ...benefits packages. Packages may include medical, dental, lifeion benefits, health savings...QualitySeniorHourly payFull timeLocal areaFlexible hours- Job Title: Engineer, GMP Test Methods Medical Device - (JP10960) Location: Thousand... ...Position involves support of senior staff in the initiation,... ...Network with manufacturing, quality and regulatory... ...project status and risks associated with integrated timelines...QualityMedical devicePermanent employmentContract workFor contractorsWork experience placement
- A prominent technology firm in California seeks an experienced MCS Senior Associate Quality Assurance to oversee Drug Substance manufacturing adherence to GMP standards. Responsibilities include providing PQA support, reviewing batch records, and ensuring compliance with...QualitySenior
- ACL Digital is looking for an Engineer - Complaints Technical Investigator in Thousand Oaks, CA, for a hybrid role requiring 2-3 days... ...5 years in complaints handling and failure analysis in medical devices. A bachelor's degree in engineering or relevant sciences is...SeniorComplaintsMedical device
- Senior Associate Quality Assurance The Sr. Associate Quality Assurance position supports Amgen’s Quality... .... Electronic batch record review GMP Document (SOPs/FORMs) revision review/... ...generous company contributions, group medical, dental and vision coverage, life and...QualitySeniorFlexible hoursShift workAfternoon shift
- US Tech Solutions is seeking a Senior Associate, Quality Assurance to provide onsite QA support at their Thousand Oaks location. The role involves... ...ideal candidate will have QA or manufacturing experience in a GMP environment, strong critical thinking skills, and a relevant...QualitySeniorRotating shiftDay shiftAfternoon shift
- Senior Associate Manufacturing What you will do Let’s do this! Let’s change... ...assignments within operations Quality systems (Deviations/CAPA/CAPA... ...Technical writing capability GMP knowledge with ability to... ...company contributions, group medical, dental and vision coverage,...QualitySeniorFlexible hours
$40 - $46 per hour
3key Consulting, Inc. is seeking an Engineer, Complaints Technical Investigator for drug delivery medical devices in Thousand Oaks, CA. This role involves evaluating... ...technical investigations, and ensuring quality compliance. Candidates should have a Master's or...QualityComplaintsMedical deviceContract work
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