5,188 Laboratory Engineer jobs in the United States

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.
**Job Location (Full Address):**
250 East River Rd, Rochester, New York, United States of America, 14623
**Opening:**
Worker Subtype:
Regular
Time Type:
Full time
Scheduled Weekly Hours:
40
Department:
250548 LLE-Laboratory for Laser Energ
Work Shift:
UR - Day (United States of America)
Range:
UR URG 109
Compensation Range:
$55,955.00 - $78,336.00
_The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._
**Responsibilities:**
GENERAL PURPOSE
The Experimental Division is seeking an early career Laboratory Engineer to help design and build laboratory set-ups and conduct experiments exploring and diagnosing laser-material interactions. A successful candidate will be challenged by the wide range of electrical, mechanical and optical technologies used to conduct these experiments.
**RESPONSIBLITIES** :
+ Design, build, and trouble-shoot experimental systems that include lasers, vacuum systems, and imaging and interferometric diagnostics
+ Support the operation of existing and newly acquired equipment and instrumentation for laser physics experiments.
+ Develop system controls and interfaces.
+ Work in an environment with a visible and audible laser operating at both single shot and constant 10 Hz rep rates.
**QUALIFICATIONS** :
+ Bachelor's Degree and 1-year relevant experience required.
+ Degree in Mechanical or Electrical Engineering preferred.
+ Or equivalent combination of education and experience required.
+ US Citizenship preferred.
+ Ability to obtain a security clearance preferred.
**ESESSENTIAL SKILLS** :
+ Experience designing mechanical and electrical systems
+ Experience with electrical, controls, and vacuum systems
+ Proficiency in Microsoft Office and ability to learn additional software operation
+ Programming skills
+ Ability to lift up to 50 lbs. and navigate stairs/ladders
+ Excellent verbal and written communication
+ Work both independently and as a part of a multidisciplinary team
**PREFERRED SKILLS**
+ Experience with programming language such as Python or C++ Experience with CAD software such as NX or SolidWorks
+ Technical writing experience and documentation skills
+ Attention to detail
The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University's Mission to Learn, Discover, Heal, Create - and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.
Notice: If you are a **Current** **Employee,** please **log into myURHR** to search for and apply to jobs using the Jobs Hub. Your application, if submitted using this portal, cannot be moved forward.
**Learn. Discover. Heal. Create.**
Located in western New York, Rochester is our namesake and our home. One of the world's leading research universities, Rochester has a long tradition of breaking boundaries-always pushing and questioning, learning and unlearning. We transform ideas into enterprises that create value and make the world ever better.
If you're looking for a career in higher education or health care, the University of Rochester may offer the perfect opportunity for your background and goals
At the University of Rochester, we are committed to fostering, cultivating, and preserving an inclusive and welcoming culture and are united by a strong commitment to be ever better-Meliora. It is an ideal that informs our shared mission to ensure all members of our community feel safe, respected, included, and valued.

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.
**Job Location (Full Address):**
250 East River Rd, Rochester, New York, United States of America, 14623
**Opening:**
Worker Subtype:
Regular
Time Type:
Full time
Scheduled Weekly Hours:
40
Department:
250548 LLE-Laboratory for Laser Energ
Work Shift:
UR - Day (United States of America)
Range:
UR URG 109
Compensation Range:
$55,955.00 - $78,336.00
_The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._
**Responsibilities:**
GENERAL PURPOSE:
The Laboratory for Laser Energetics (LLE) of the University of Rochester is a unique national resource for research and education in science and technology focusing on using lasers to initiate fusion and high energy density physics. LLE is currently seeking a technical associate in the Experimental Operations group. Candidates are sought to install, maintain, operate and troubleshoot a variety of equipment in a cleanroom environment.
**RESPONSIBILITIES**
+ Support the operation of various equipment and diagnostics related to laser physics experiments
+ Troubleshoot mechanical, electrical and optical issues
+ Perform regular preventative maintenance
+ Support mechanical, electrical and optical engineers with design and installation of new equipment
+ Maintain complex vacuum systems
+ Handling of radiation materials. Will be required to qualify as a NYS Radiation Worker
+ Some second shift work is required
**QUALIFICATIONS**
+ Bachelor's degree in a Science, Technology, Engineering or Mathematics field or equivalent experience
+ Ability to obtain a security clearance
**REQUIRED SKILLS**
+ Well versed in engineering fundamentals including basic mechanics, geometry, calculus, reading mechanical drawings, and CAD proficiency
+ Ability to work in a cleanroom environment
+ Ability to lift up to 50 lbs. and climb stairs
+ Excellent verbal and written communication
+ Strong interpersonal skills working in a team-based environment
+ Proficiency in Microsoft Office and ability to learn additional software as needed
**DESIRED SKILLS**
+ Experience with electrical and vacuum systems
+ Experience with radiological materials
+ Technical writing experience
+ Proficiency reading and interpreting electrical schematics
+ Technical writing experience
The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University's Mission to Learn, Discover, Heal, Create - and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.
Notice: If you are a **Current** **Employee,** please **log into myURHR** to search for and apply to jobs using the Jobs Hub. Your application, if submitted using this portal, cannot be moved forward.
**Learn. Discover. Heal. Create.**
Located in western New York, Rochester is our namesake and our home. One of the world's leading research universities, Rochester has a long tradition of breaking boundaries-always pushing and questioning, learning and unlearning. We transform ideas into enterprises that create value and make the world ever better.
If you're looking for a career in higher education or health care, the University of Rochester may offer the perfect opportunity for your background and goals
At the University of Rochester, we are committed to fostering, cultivating, and preserving an inclusive and welcoming culture and are united by a strong commitment to be ever better-Meliora. It is an ideal that informs our shared mission to ensure all members of our community feel safe, respected, included, and valued.

**Job Description Summary**
The Thin film lab Engineer will be responsible for thin film lab maintenance and projects execution, designing and deploying novel applications for GE's future of flight tests. You will be working hands-on in a collaborative team to learn and apply thin film design expertise and integrate thin film sensor systems into next-generation engines. You will be working closely with engineers, interns and laboratory personnel to ensure on-time customer delivery of projects.
**Job Description**
**Roles and Responsibilities**
+ Design and execute the thin film sensor applications for Aerospace engines and aircrafts testing.
+ Support thin film sensor system integration to engine/rig and support testing and data post-processing.
+ Support thin film sensor process improvement and update the process documents.
+ Maintain thin film lab facilities and update their operational procedures.
+ Adhere to business standards, practices, procedures, & product requirements.
+ Review designs and consult with senior technical leaders for evaluation of work.
+ Develop strong internal and external customer relationships by serving as an interface point within GE Aerospace.
**Required Qualifications**
+ Bachelor's degree from an accredited university or college
+ Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.
**Desired Characteristics**
+ Strong oral and written communication skills.
+ Ability to document, plan, market, and execute programs.
_This role requires access to U.S. export-controlled information. Therefore, for applicants who are not U.S. lawful permanent residents, U.S. Citizens, or have been granted asylee or refugee status (i.e., not a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3), otherwise known as a U.S. Person), employment will be contingent on the ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government._
**Additional Information**
GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer ( . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
**Relocation Assistance Provided:** Yes
GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Take your career to the next level as a **Laboratory** **Services Engineer** on our Toxicology instrument team in **Raritan, NJ** ! Labcorp's work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide.
The Laboratory Services Engineer is responsible for performing preventive maintenance and diagnostic instrument repairs on UPC-MS/MS instrumentation and robotic liquid handlers. The instrument specialist works collaboratively within a decentralized group sharing responsibilities for on-site instrumentation as well as remote support responsibilities. The instrument group works in close collaboration with the MedTox Research and Development department. The position also includes project-based process improvement assignments.
***Pay Range:** $31.00 - $45.00 per hour
All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data
**Work Schedule: Monday - Friday (7:00am - 3:30pm)**
**Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here ( **.**
**Job Responsibilities**
+ Maintain, calibrate, and clean laboratory instrumentation
+ Perform scheduled/routine maintenance and critical function checks on all equipment
+ Diagnose and repair issues occurring with the analytical equipment
+ Recognize significant changes in instrument function and troubleshoot as indicated
+ Resolve issues quickly and efficiently to reduce overall down time of testing and/or instrument production
+ Maintain accurate records and documentation for all laboratory equipment
+ Schedule preventative maintenance and repairs
+ Work with external service vendors when needed
+ Consult with laboratory staff to ascertain that equipment functions properly and safely
+ Demonstrate and explain correct operation of equipment to laboratory personnel
+ Provide troubleshooting assistance to laboratory personnel
+ Document and communicate equipment status to lab supervisors
**Requirements**
+ Bachelor's degree in a chemical, physical, biological, clinical laboratory science or medical technology.
+ 4 years of experience in a laboratory setting including some instrumental analysis, specifically LC-MS.
+ Proficiency in Analyst, Sciex OS and Waters Acquity software is preferred
+ Strong mechanical skills and understanding of instrumental analysis
+ Ability to perform diagnosis of instrumentation errors
+ Strong communication skills; both written and verbal
+ Excellent problem solving, multitasking and prioritization skills
+ High level of attention to detail with strong organizational skills
+ Ability to work independently and within a team environment
**If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!**
**Labcorp is proud to be an Equal Opportunity Employer:**
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
**We encourage all to apply**
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site ( or contact us at Labcorp Accessibility. ( ) For more information about how we collect and store your personal data, please see our Privacy Statement ( .

Position Summary:

The Manager, QC Laboratory Systems Engineer is responsible for supporting laboratory instrumentation and computerized systems within a GMP-regulated environment, with a strong focus on data integrity. This role acts as a subject matter expert (SME) and system administrator for instruments and systems used in QC testing, Analytical and Microbiological Analysis (GMA) instruments. The engineer provides technical oversight, manages qualification activities, and ensures regulatory compliance and data reliability throughout system lifecycles.

Essential Duties & Responsibilities:

* Serve as SME and system administrator for QC laboratory instruments and computerized systems, including GMA equipment.
* Ensure all computerized systems are implemented and maintained in compliance with data integrity principles, GMP regulations, and internal policies.
* Manage qualification, validation, and periodic review activities for laboratory instruments and computerized systems.
* Troubleshoot instrumentation/system issues and coordinate resolution with internal teams (IT, Engineering) or external vendors.
* Author and review documentation including SOPs, user requirements, system specifications, and validation protocols.
* Collaborate with IT, Validation, and QC personnel on change controls, deviations, investigations, and CAPAs.
* Serve as key laboratory resource for audit/inspection readiness activities; presenting data integrity and system management processes during regulatory inspections.
* Lead and participate in risk assessments and continuous improvement initiatives to enhance system reliability and compliance.
* Provide training to QC staff on the operation and administration of laboratory computerized systems.
* Maintain current knowledge of regulatory expectations and best practices related to data integrity and computerized system validation.

Secondary Responsibilities and Functions

* Foster effective working relationships with internal and external stakeholders.
* Ensure all laboratory activities are conducted in full compliance with cGMP and applicable quality system requirements.
* Implement and maintain robust data backup and disaster recovery strategies for critical laboratory systems.
* Contribute to regulatory inspection readiness through proactive compliance and documentation practices.
* Ensure continued GxP compliance of QC laboratory computer systems and software.
* Perform additional duties and projects as assigned by management.

Minimum Qualifications:

* Education/Training:
* Bachelor's degree in Engineering, Life Sciences, Computer Science, or a related field is required. Master's degree preferred.
* Strong understanding of data integrity principles and ALCOA+.
* Strong understanding of FDA 21 CFR Part 11, EU Annex 11, and GAMP 5.

Experience:

* Minimum 5 years of experience in a GMP-regulated QC laboratory, preferably within the biopharmaceutical industry.
* Experience managing laboratory systems in a GxP environment.
* Hands-on experience with instrument qualification, computerized system validation, and administration.
* Prior experience supporting QC instrumentation.
* Experience with platforms such as LIMs, MODA, LabX, or equivalent.
* Experience with regulatory submissions (IND/BLA) and GMP inspections is a plus.

Skills:

* Strong verbal and written communication skills.
* Excellent organizational, planning, and time management abilities.
* Proficiency in software systems, data analysis, and project coordination.
* Demonstrated problem-solving and critical thinking skills.
* Ability to manage multiple priorities and meet deadlines in a dynamic environment.
* Ability to work effectively across functional teams and manage stakeholder relationships.
* Demonstrated ability to apply logical reasoning and sound decision-making.
* Expected to stay informed on evolving regulatory guidance for data integrity and computerized systems compliance

ProKidney is an Equal Opportunity Employer. All applicants are considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. We are committed to the principles of equal employment opportunity for all employees with a work environment free of discrimination and harassment.

Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.

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Position Summary:

The Manager, QC Laboratory Systems Engineer is responsible for supporting laboratory instrumentation and computerized systems within a GMP-regulated environment, with a strong focus on data integrity. This role acts as a subject matter expert (SME) and system administrator for instruments and systems used in QC testing, Analytical and Microbiological Analysis (GMA) instruments. The engineer provides technical oversight, manages qualification activities, and ensures regulatory compliance and data reliability throughout system lifecycles.

Essential Duties & Responsibilities:

• Serve as SME and system administrator for QC laboratory instruments and computerized systems, including GMA equipment.
• Ensure all computerized systems are implemented and maintained in compliance with data integrity principles, GMP regulations, and internal policies.
• Manage qualification, validation, and periodic review activities for laboratory instruments and computerized systems.
• Troubleshoot instrumentation/system issues and coordinate resolution with internal teams (IT, Engineering) or external vendors.
• Author and review documentation including SOPs, user requirements, system specifications, and validation protocols.
• Collaborate with IT, Validation, and QC personnel on change controls, deviations, investigations, and CAPAs.
• Serve as key laboratory resource for audit/inspection readiness activities; presenting data integrity and system management processes during regulatory inspections.
• Lead and participate in risk assessments and continuous improvement initiatives to enhance system reliability and compliance.
• Provide training to QC staff on the operation and administration of laboratory computerized systems.
• Maintain current knowledge of regulatory expectations and best practices related to data integrity and computerized system validation.

Secondary Responsibilities and Functions

• Foster effective working relationships with internal and external stakeholders.
• Ensure all laboratory activities are conducted in full compliance with cGMP and applicable quality system requirements.
• Implement and maintain robust data backup and disaster recovery strategies for critical laboratory systems.
• Contribute to regulatory inspection readiness through proactive compliance and documentation practices.
• Ensure continued GxP compliance of QC laboratory computer systems and software.
• Perform additional duties and projects as assigned by management.

Minimum Qualifications:

• Education/Training:
• Bachelor's degree in Engineering, Life Sciences, Computer Science, or a related field is required. Master's degree preferred.
• Strong understanding of data integrity principles and ALCOA+.
• Strong understanding of FDA 21 CFR Part 11, EU Annex 11, and GAMP 5.

Experience:

• Minimum 5 years of experience in a GMP-regulated QC laboratory, preferably within the biopharmaceutical industry.
• Experience managing laboratory systems in a GxP environment.
• Hands-on experience with instrument qualification, computerized system validation, and administration.
• Prior experience supporting QC instrumentation.
• Experience with platforms such as LIMs, MODA, LabX, or equivalent.
• Experience with regulatory submissions (IND/BLA) and GMP inspections is a plus.

Skills:

• Strong verbal and written communication skills.
• Excellent organizational, planning, and time management abilities.
• Proficiency in software systems, data analysis, and project coordination.
• Demonstrated problem-solving and critical thinking skills.
• Ability to manage multiple priorities and meet deadlines in a dynamic environment.
• Ability to work effectively across functional teams and manage stakeholder relationships.
• Demonstrated ability to apply logical reasoning and sound decision-making.
• Expected to stay informed on evolving regulatory guidance for data integrity and computerized systems compliance

ProKidney is an Equal Opportunity Employer. All applicants are considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. We are committed to the principles of equal employment opportunity for all employees with a work environment free of discrimination and harassment.

Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.

**Use Your Power for Purpose**
At Pfizer, our purpose is to deliver breakthroughs that change patients' lives. Central to this mission is our Research and Development team, which strives to translate advanced science and innovative technologies into impactful therapies and vaccines. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, your role is crucial. You will leverage cutting-edge design and process development capabilities to accelerate the delivery of best-in-class medicines to patients globally.
**What You Will Achieve**
A Senior Laboratory Automation Engineer within the Analytical Technologies and Compound Management (ATCM) Liquid Store team plays an important role in the stewardship of the Pfizer liquid compound collection by specializing in the design, implementation, and maintenance of leading-edge automated platforms that support Compound Management workflows. These workflows facilitate order fulfillment operations resulting in the delivery of compounds in our corporate collection to research screening initiatives at Pfizer. The successful candidate will leverage engineering principles to develop robust automation solutions that increase throughput, efficiency, reproducibility, and data integrity within our laboratory operations. This hands-on role requires expertise across many disciplines including engineering, laboratory automation, robotics, project management, instrument protocol & method development, hardware & software troubleshooting, liquid handling, instrument quality control and workflow development & validation. The candidate will also collaborate with Discovery Biology and Pharmacology (DBP), hit follow-up, lead optimization, External Research Solutions, and Medicinal Chemistry stakeholders to ensure timely, high-quality access to the Pfizer compound collection. Partnerships with facility engineering & logistics teams, Digital, Contract Research Organizations, and external software & hardware vendors are also a key aspect of the role. As a senior member of the ATCM team, the successful candidate will have significant input in defining plans and strategies to support future demands on compound management.
**How You Will Achieve It**
+ Provide expert level knowledge and hands on experience in the operation, troubleshooting, and resolving issues encountered with laboratory automation hardware and associated vendor software to support daily production and screening campaigns providing near and assay ready plates.
+ Provide daily technical subject-matter-expertise, writing instrument protocols, troubleshooting assistance and guidance supporting the compound management workflows, automation infrastructure, and applications.
+ Collaborate with team members and partners to design and continuously improve workflows to increase capacity and throughput to ensure on-time delivery of requests.
+ Collaborate with the Pfizer Digital and ATCM Data support team to develop enterprise level solutions that address processed orders data analysis, storage, and curation, including the ability to mine data for insights that support decision making.
+ Contribute to the strategic direction by identifying and championing new ideas and technological strategies that will enable innovation, continuous improvement, and capability enhancements in workflows and operations within Compound Management.
+ The candidate should possess strong collaborative and written/verbal communication skills, and have an enthusiastic, optimistic attitude.
+ Interact and coordinate efforts with external vendors to drive workflows and support project delivery.
+ Lead & participate in project teams as a key contributor by providing insight & expertise on laboratory automation & material logistics to solve issues of significant complexity and improve the efficiency of operations in Compound Management.
+ Design and implement quality control experiments to evaluate hardware and software systems along with consumables and compound deliverables to drive innovation and continuously improve the efficiency and quality of deliverables to support screening campaigns.
+ Produce high-quality and detailed documentation for implemented solutions, including workflow & data diagrams, description of requirements, use cases, design, tests, users guides & standard operating procedures (SoP).
+ Present technological advancements & solutions internally to Compound Management stakeholders and externally to industry peers.
+ Mentor junior team members by modeling courage & excellence in your work and contributing to an environment of equity and joy that promotes active engagement & learning.
**Qualifications**
+ MSc/BSc degree in Engineering, Biochemistry, Biology, Pharmacology, Chemistry, Computer Science, or equivalent with 6-8 years relevant laboratory experience, or PhD degree with 1-3 years' experience.
+ Prior experience working in areas of compound management, or pharmaceutical laboratory automation. Hands-on experience working with automated tube & plate handling instrumentation, robotics, custom workflow design and/or protocol development and implementation.
+ Demonstrated expertise in the use of Beckman, Hamilton, Azenta Storage, and HighRes automation systems including strong familiarity with Cellario scheduling software and Acoustic technologies.
+ Strong problem-solving skills and the ability to apply novel and innovative approaches.
+ Demonstrated ability to develop innovative and creative solutions for complex issues that apply lean principles to solve daily production issues which streamline workflows and minimize risks for errors.
+ Demonstrated experience collaborating with stakeholders and external hardware & software vendors.
+ Demonstration of excellent verbal and written communication skills.
+ Understanding of primary pharmacology assay development and compound screening is a plus.
+ Demonstrated ability to develop strong collaborative relationships within and outside Pfizer and across multiple cultures: academic, industrial, and CROs.
+ Experience in working with multi-functional, cross line teams is preferred.
+ Proficiency with personal computers, including a working knowledge of Microsoft Office applications and relevant scientific software.
+ A commitment to timely delivery and quality of the work product.
+ Well organized with ability to multi-task and adjust to changing priorities.
+ Demonstration of ability to present in the form of internal and external posters, papers and presentations.
+ Strong leadership and mentoring skills.
+ Familiarity with cloud-based data analysis platforms and architecture is preferred.
**PHYSICAL/MENTAL REQUIREMENTS**
+ Position will require working in the lab, operating automated equipment, lifting, sitting, standing, walking, bending and the ability to solve complex technical problems.
**NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS**
+ Candidate may be asked to travel to other Pfizer sites to meet project team members.
+ Candidate must comply with laboratory safety practices and wear personal protection as required.
Relocation assistance may be available
Work Location Assignment: On Premise
The annual base salary for this position ranges from $90,900.00 to $151,500.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. 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 | (uscandidates.mypfizerbenefits.com). 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. This position requires permanent work authorization in the United States.
Pfizer endeavors to make accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
Research and Development
#LI-PFE

Job Summary:
The Biomedical Engineer plans, trains others, and installs, maintains and repairs sophisticated medical equipment and systems utilized in the diagnosis treatment and monitoring of patients.
Essential Responsibilities:
+ Working under the supervision of a manager or designee, perform all phases of scheduled and corrective repairs of biomedical equipment and medical systems.
+ Perform pre-issue and asset accounting, equipment installation and de-installation of related equipment as needed.
+ Performs scheduled and unscheduled inspections, maintenance and electrical safety tests of biomedical equipment where applicable to maintain code compliance.
+ Responsible for documenting the results of all inspections, maintenance and tests.
+ Must work collaboratively with all other biomedical engineers specialties (Instrumentation, X-Ray, CT/MR, Diagnostic Ultrasound, Nuclear Med, Clinical Laboratory, RT/Anesthesia, Ophthalmology/Lasers, and Clinical Systems Integrations), KPIT, Business Partners, and Original Equipment Manufacturer (OEM) representatives.
+ Individual is required to complete applicable documentation of all work performed, in a timely manner.
+ Frequent travel will be required for the Shared Services/Support biomed engineers to provide service support.
+ Occasional travel will be required for the Stationary Service Area Support biomed engineers to provide service support to other sites.
+ All biomed engineers will be required to travel to attend technical training.
+ Afterhours work may be required on a scheduled and nonscheduled basis to complete required work.
+ Will be assigned to weekday and weekend on-call schedule to perform emergency service.
+ Communication devices will be supplied and will need to be kept ON during duty hours.
Basic Qualifications:
Experience
Minimum four (4) years experience of formal and/or on the job training.
Clinical Laboratory - Must have a minimum of four years of service experience and formal OEM training on the various Instruments used in the Regional and Clinical Laboratory departments. Strong working knowledge and experience supporting large automated pre and post specimen processing systems.
Education
+ High School Diploma or General Education Develompment (GED)
License, Certification, Registration
+ Driver's License (California)
Additional Requirements:
+ Must have good driving record.
+ Must have experience and working knowledge of the medical equipment and systems in general instrumentation or the specialty area assigned and identified above.
+ Must be willing to work extended hours.
+ Must be proficient operating PCs with Windows operating systems.
Preferred Qualifications:
+ Associates degree or equivalent in electronics, physics or related science degree preferred.
COMPANY: KAISER
TITLE: Biomedical Engineer, Laboratory
LOCATION: Berkeley, California
REQNUMBER: 1372481
External hires must pass a background check/drug screen. Qualified applicants with arrest and/or conviction records will be considered for employment in a manner consistent with Federal, state and local laws, including but not limited to the San Francisco Fair Chance Ordinance. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, protected veteran, or disability status.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
**We are PCI.**
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
**What You'll Be Doing**
As an Instrumentation Systems Engineer, you'll serve as the go-to expert in QC for analytical and microbiology lab equipment. You'll ensure that all systems are compliant, qualified, and ready to meet the demands of a cGMP-regulated environment.
**Key Responsibilities:**
+ Own the full lifecycle of QC testing instrumentation: induction, qualification, validation, decommissioning, and beyond
+ Serve as the main point of contact for QC equipment inquiries, coordinating with vendors and internal teams
+ Support multiple QC functions including Analytical, Microbiology, Analytical Development, and Sample Management
+ Manage quality records (deviations, investigations, CAPAs, MOCs) from initiation to closure
+ Coordinate with validation, calibration, and metrology teams to ensure equipment is always audit-ready
+ Evaluate instrument performance and lead efforts for repair, replacement, or upgrades
+ Author and maintain SOPs, and ensure alignment with global, local, and regulatory standards
+ Drive improvements in method optimization and equipment functionality
+ Support internal and external audit preparation, and stay updated on USP, EP, JP, and FDA regulations
**What You Bring to the Role**
+ Bachelor's degree in a science, engineering, or related technical field
+ Up to **5 years of experience** in a regulated GMP laboratory or manufacturing environment
+ Solid understanding of **cGMP, GAMP, GxP, SDLC** , and **21 CFR Part 11**
+ Hands-on experience troubleshooting complex analytical or microbiology equipment
+ Familiarity with computer systems validation and equipment software
+ Excellent organizational and technical writing skills
+ Strong cross-functional collaboration and communication abilities
+ Experience with database systems and Microsoft Office Suite
+ Ability to prioritize, manage multiple tasks, and lead small to mid-sized projects
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Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled