Current jobs related to Validation Engineer – Laboratory Instruments - Rocky Mount, Virginia - Pfizer

  • Manufacturing Process Engineer

    1 week ago

    Rocky Mount, Virginia, United States Jobot Full time

    About the Role This position is hosted by Jobot. Overview: We are in search of a skilled and knowledgeable Process Engineer to enhance our operations. As a Process Engineer, your primary focus will be on the design, development, and implementation of control systems that optimize our manufacturing processes. You will collaborate with various teams to ensure...

  • Manufacturing Process Engineer

    1 week ago

    Rocky Mount, Virginia, United States Jobot Full time

    About the Role This position is hosted by Jobot. Overview: We are looking for a skilled and knowledgeable Process Engineer to enhance our operations. In this role, you will focus on the design, development, and execution of control systems tailored for our manufacturing processes. Collaborating with various teams will be essential to guarantee the smooth and...

  • Rocky Mount Site Quality Head

    2 months ago

    Rocky Mount, Virginia, United States Pfizer Full time

    Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through...

  • Process Validation Engineer

    2 weeks ago

    Rocky Mount, United States Technical Source Full time

    Job DescriptionJob DescriptionTechnical Source is currently in search of a Process Validation Engineer for a pharmaceutical client located in Eastern, NC area. The qualified candidate will have experience as a process validation engineer supporting activities in support of cGMP pharmaceutical manufacturing facilities. These activities include working with...

  • Process Validation Engineer

    3 months ago

    Rocky Mount, United States Katalyst Healthcares and Life Sciences Full time

    Responsibilities: uthor and Execute Process Validation Protocols. Conduct Troubleshooting of Manufacturing Equipment (Formulation/Filling/Packaging). Provide Oversight to Technicians and Operators. Bachelor's degree in engineering. 3+ Years of Relevant Work Experience in a GMP Environment. Knowledge of the Pharmaceutical Industry and Aseptic...

  • QC Laboratory Tech

    2 weeks ago

    Rocky Mount, United States Experis Full time

    Our client, in Pharmaceutical Manufacturing is seeking to fill a QC Laboratory Tech position.  Title: QC Lab Tech (nights) Location Rocky Mount, NC Shifts: 3rd shift 11-7a Payrate: $30-35/hr on W2 What's the Job? Perform testing for raw materials, in process, finished products, and/or TSR/validation/investigational testing in a safe, compliant, and...

  • Electrical and Instrumentation Engineer

    2 weeks ago

    Mount Clemens, United States Embakire Full time

    Job DescriptionJob DescriptionDescription-Qualifications:Bachelor's degree in electrical engineering or related engineering field.7 years professional work experience3 years or more of work experience in Electrical Instrumentation designProficient with AutoCADUnderstanding of OSHA, NFPA, NEC, engineering standardsWorking knowledge of controls systems...

  • Process Validation Engineer for Contract @Rocky mount wilson, NC

    4 days ago

    Rocky Mount, United States Abidi Solutions Full time

    Job DescriptionJob DescriptionJob Title: Process Validation EngineerLocation: Rocky Mount-Wilson, NC (onsite)Duration: Long term Responsibilities of the Process Validation Engineer include:Author and Execute Process Validation ProtocolsEfficiently Take Samples and Deliver to Labs for TestingProvide Oversight to Technicians and OperatorsQualifications of the...

  • Laboratory Technician

    3 days ago

    Rocky Hill, Connecticut, United States Zobility Full time

    Job OverviewThe Laboratory Technician at Zobility plays a crucial role in supporting various laboratory functions and experiments.Key Responsibilities:Work under the guidance of a Senior Technician or Chemist, demonstrating a proactive and independent approach.Prepare and conduct tests on adhesives, sealants, and coatings.Collect, evaluate, and document...

  • Laboratory Specialist

    11 hours ago

    Rocky Hill, Connecticut, United States zobility Full time

    Job SummaryZobility is seeking a highly motivated and detail-oriented Laboratory Technician to join our team. As a Laboratory Technician, you will be responsible for performing various laboratory tasks, including preparing and testing adhesives, sealants, and coatings.Key ResponsibilitiesExperimental Procedures: Conduct experiments using established...

  • QIS Instrument Interface Developer

    5 days ago

    Mount Laurel, New Jersey, United States ClinDCast LLC Full time

    ClinDCast LLC is seeking a highly skilled QIS Instrument Interface Developer to join our team. As a key member of our development team, you will be responsible for designing, developing, and implementing interfaces between medical devices and laboratory information systems.Key Responsibilities:Develop and maintain interfaces with medical devices and...

  • Laboratory Specialist

    1 week ago

    Rocky Hill, Connecticut, United States LanceSoft, Inc. Full time

    Position: Laboratory TechnicianLocation: Rocky Hill, CT (Onsite)Contract Duration: 6+ Months (Potential for Extension or Hire)Compensation: $ /hr on W2Work Schedule: 1st Shift 8am to 4pm Onsite Overview: The Laboratory Technician will play a crucial role in supporting laboratory operations by conducting various tasks under the guidance of senior staff. This...

  • Laboratory Technician

    1 week ago

    Rocky Hill, Connecticut, United States zobility Full time

    Position Overview:The Laboratory Technician will operate under the guidance of a Senior Technician or Chemist, taking on a variety of essential tasks with a strong sense of initiative and autonomy.Key Responsibilities:Preparation and evaluation of adhesives, sealants, and coatings.Collection, assessment, and documentation of experimental data.Engagement in...

  • Laboratory Technician

    1 week ago

    Rocky Hill, Connecticut, United States zobility Full time

    Position Overview:The Laboratory Technician will operate under the guidance of a Senior Technician or Chemist, taking on various responsibilities with a strong sense of initiative and autonomy.Key Responsibilities:Preparation and evaluation of adhesives, sealants, and coatings.Data collection, assessment, and documentation.Engagement in organizing and...

  • Laboratory Technician

    3 weeks ago

    Rocky Hill, United States LanceSoft, Inc. Full time

    Role: Lab TechnicianLocation: Rocky Hill, CT 06067 United States (Onsite)Duration: 6+ Months (Contract to Extension/Hire)Pay Rate: $20-25.00/hr on W2Shift hour: 1st Shift 8am to 4pm Onsite. Job Description: Qualifications: 0~3 years of demonstrated laboratory experience - Computer literate in Microsoft Office products - word, excel and PowerPoint. - Ability...

  • Laboratory Specialist

    1 week ago

    Rocky Hill, Connecticut, United States LanceSoft, Inc. Full time

    Position: Laboratory TechnicianLocation: Rocky Hill, CT 06067 United States (Onsite)Contract Duration: 6+ Months (Potential for Extension or Hire)Compensation: $ /hr on W2Work Schedule: 1st Shift 8am to 4pm Onsite. Job Overview: Required Qualifications:- 0 to 3 years of relevant laboratory experience.- Proficient in Microsoft Office Suite including Word,...

  • Laboratory Technician

    1 week ago

    Mount Clemens, United States Umanist Staffing LLC Full time

    Job DescriptionJob DescriptionESSENTIAL DUTIES AND RESPONSIBILITIES:? Operators are trained annually (TLM or orientation) to properly manage and dispose of hazardous and non-hazardous waste they generate. Site AOP SAF_A023 outlines how to properly handle and label hazardous and non-hazardous waste materials for our site. PLT_A003 is our site Spill Procedure...

  • Technical Sales Specialist in Analytical Chemistry

    1 week ago

    Rocky Mount, North Carolina, United States Diedre Moire Corp. Full time

    Sales Role in Analytical Chemistry InstrumentsRemote OpportunityWe are seeking a knowledgeable and driven Technical Sales Specialist to manage territory sales within the analytical chemistry instrumentation sector. This position offers a lucrative compensation structure with potential earnings exceeding $250,000.Key Responsibilities:Promote and sell advanced...

  • Laboratory Technician

    2 weeks ago

    Mount Clemens, United States MASHPOINT LLC Full time

    Job DescriptionJob DescriptionJob Title: Laboratory TechnicianDuration: 12 Months (Possible ext)Location: Mount Clemens, MI 48043Pay: $19/hourSummary:Operators are trained annually (TLM or orientation) to properly manage and dispose of hazardous and non-hazardous waste they generate. Site AOP SAF_A023 outlines how to properly handle and label hazardous and...

  • Laboratory Operations Manager

    1 week ago

    Mount Juliet, Tennessee, United States Pace® Analytical Services Full time

    About UsPace Analytical Services is dedicated to enhancing the safety and health of our environment. We are committed to advancing the scientific capabilities of businesses, industries, consulting firms, government agencies, and more. With a robust national laboratory network, we provide local-level services, ensuring the safety of our air, water, soil, and...

  • QIS Instrument Interface Developer

    2 months ago

    Mount Laurel Township, United States ClinDCast LLC Full time

    ClinDCast is looking for QIS Instrument Interface Developer· Minimum of 5 years of experience with Intersystems Cache development· Minimum of 5 years of experience interfacing medical devices/instruments to laboratory information systems.· Extensive experience with standard interface communication protocols such as ASTM and HL7· Solid, judgement,...

  • Quality Engineer

    3 months ago

    Rocky Mount, United States Prysmian Group Full time

    The Quality Engineer (SQE) will drive the Quality Management System and support all Elevator BU North American locations.  This includes drawing on experience, technical skills, and knowledge of manufacturing to work with customer care, production, and engineers to improve products, processes and services to customers.  SQE will led customer quality...

  • Laboratory Technician/ Lab Technician

    4 days ago

    Rocky Hill, United States Zobility Full time

    Responsibilities:Under the supervision of a Senior Technician or Chemist, the Technician will be expected to perform the following functions with a high level of initiative and independencePreparing and testing of adhesives, sealants, coatings.Evaluate, collect and record data.Participates in organizing and performing experiments using established procedures...

Validation Engineer – Laboratory Instruments

2 months ago

Rocky Mount, Virginia, United States Pfizer Full time
  • Why Patients Need You
    Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients. Role Summary The position of Validation Engineer – Laboratory Instruments is an individual contributor role which, under the guidance of a more senior Validation Engineer or Manager, is responsible for the validation lifecycle of laboratory instruments within the Quality Laboratories at the Pfizer, Inc. sterile injectable manufacturing facility located in Rocky Mount, North Carolina, USA. As a Validation Engineer – Laboratory Instruments, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues. It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe. Role Responsibilities
    • Serves as the validation representative for laboratory instruments and partnering with the laboratories, Quality System Administrators, Digital, Instrumentation and Quality Engineering on implementing new instruments at the site.
    • Initiates and leads risk assessment, gap analysis and deviation management for commissioning of, changes to, or decommissioning of laboratory instruments and associated instrument control software where applicable within the Quality Control laboratories.
    • Authors cGMP risk assessments, user requirements & functional specifications, validation plans, protocols (i.e. IQ, OQ, PQ), traceability matrices, reports, addendums, decommissioning plans and other validation deliverables as required by the site validation SOPs.
    • Ensures lab instrument's adherence to national and international regulatory guidelines on Electronic Records and Electronic Signatures and Data Integrity, cGMP, FDA 21 CFR Part 11/210/211, EU Annex 11, MHRA guidelines. Authors protocol to challenge the main aspects of these requirements during validation to demonstrate adherence. For systems found unable to fully comply, formulate workarounds/strategies with core stake holders to mitigate the gaps.
    • Assists the system owner with evaluating and recommending the appropriate user roles and privileges for data integrity (where applicable), writing instrument operation instructions and setting up preventive maintenance plans.
    • Performs periodic reviews of laboratory instruments and associated instrument control softwarewith focus on change control, deviation investigations and CAPA to ensure compliance and validated state of the instrument.
    • All other duties as assigned.
    QualificationsMust-Have
    • Applicant must have a High School Diploma (or equivalent) and 6 years of relevant experience OR an associate's degree with 4 years of relevant experience OR a bachelor's degree with 0+ years of relevant experience.
      Note: Relevant experience refers to validation of instruments including those with computerized systems (e.g. AA, DNA Sequencer, FT-IR, IC, ICP-MS, Keyence Instant Measurement, Particle Counter, SmartScope, TOC, UV_Vis, dimensional measurement systems) in a cGMP environment.
    • Excellent attention to detail and knowledgeable of FDA Regulations/Guidance, and Good Manufacturing Practices.
    • Demonstrated understanding of global regulations on data integrity, FDA 21 CFR Part 11 and validation/qualification requirements.
    • Ability to manage multiple activities and constantly change priorities.
    • Exposure to lab operations and scientific processes associated as well as familiarity with a variety of laboratory instruments within various areas (Biological, Chemical, Environmental Monitoring, Micro, etc.).
    • Ability to work both independently and in partnership with others; proven ability to use initiative and drive to achieve results.
    • Proven ability to follow a variety of instructions furnished in written, oral, diagram, or schedule form.
    • Good communication skills, oral and written, and attention to detail.
    • Mastery of core computer software/systems (Word, Excel, Sharepoint, Teams, etc.).
    • Excellent organizational skills, and ability to manage multiple activities and constantly changing deadlines.
    Nice-to-Have
    • 2+ years' experience in validation of instruments including those with computerized systems (e.g. AA,DNA Sequencer, FT-IR, IC, ICP-MS, Keyence Instant Measurement, Particle Counter, SmartScope, TOC, UV_Vis, dimensional measurement systems) strongly preferred.
    • Experience in a biotechnology or pharmaceutical cGMP manufacturing environment preferred.
    • 1+ years' experience in performing periodic review of laboratory instruments including those with computerized systems.
    • Experience with Trackwise/Veeva Vault CR/PR/CAPA systems.
    • Strong critical thinking and problem-solving skills.

PHYSICAL/MENTAL REQUIREMENTS

  • Mathematical and scientific reasoning ability.
  • Occasionally lift a computer system and/or instrument up to 50 pounds.
  • Use a computer terminal for up to 8 hours per shift, work around moving equipment, work with chemical and biological materials.
  • Stand for up to 8 hours, sit for up to 8 hours, walking, climbing stairs, responding to visual warning indicators, respond to audible warning indicators, respond to color or special visual indicators, wear specialized protective.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

  • Primary work schedule is Day shift ( M-F, 8 hours) , but evenings, weekends and holidays will be required as needed to support laboratory processes at the Rocky Mount site.
  • Must be able to wear proper gowning and PPE in laboratory and manufacturing areas as required to meet GMP and/or OSHA requirements.
  • Work safely in laboratory areas where biological and chemical hazards are present.

Work Location Assignment:On Premise

The annual base salary for this position ranges from $64,600.00 to $104, In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits ). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

Quality Assurance and Control

#LI-PFE


To help us track our recruitment effort, please indicate in your email – cover/motivation letter where ) you saw this job posting.