Senior Specialist - Laboratory Operation Job at BioMarin Pharmaceutical (Novato)

Research Specialist I

Work independently with only occasional suggestions to modify, vary or adapt sta...

Location

United States of America , Rochester

Salary:

26.90 - 37.66 USD / Hour

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor’s Degree required
1 year of related work experience involving direct assistance to researchers or equivalent combination of education and experience required
Operational understanding of basic laboratory equipment, including the ability to make solutions, use centrifuges, and accurately operate micropipettes required
Mathematical skills including basic algebra and the ability to use scientific notation required
Familiarity with Microsoft Office programs (Word, PowerPoint, Excel) required
Ability to generate and organize large sets of data, strains, and plasmids, and familiarity with all aspects of a laboratory to effectively help organize the lab required
Ability to troubleshoot and repair equipment as needed required
Excellent organizational skills to help coordinate a number of projects, skills to help train inexperienced personnel, ability to use common sense, and attention to detail required
Must be able to work some evenings and weekends to conduct experiments required

Job Responsibility

Serve as Research Specialist I for a Principal Investigator in the Department of Environmental Medicine
Conduct and oversee processing and analysis of collected specimens for immunohistological, biochemical, and molecular techniques including microscopy analysis, immunohistochemistry, histological analysis, Western blotting, ELISA, neurotransmitter quantification, and other techniques
Train other laboratory members on these techniques
Oversee the tissue processing for mass spectrometry
Develop and optimize new laboratory techniques including writing laboratory SOPs and training other technical staff and students on such SOPs
Perform scientific literature searches and utilize such literature to develop SOPs and advise the principal investigator
Independently supervise and oversee large colonies of rodent breeding and maintenance
Oversee set up and conduct rodent inhalation exposures
Plan and oversee non-survival specimen collections from rodents
Supervise and train other members of the laboratory

Fulltime

Senior Research Specialist

The Senior Research Specialist provides direct research support at the senior pr...

Location

United States of America , Rochester

Salary:

63815.00 - 95723.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree required
Master's degree preferred
5 years of related experience
or an equivalent
or a combination of education and experience required
Applicants should be self-motivated and capable of working independently as well as in a collaborative setting required
Strong interpersonal and communication skills, including written communication required
Ability to readily learn new experimental techniques required
Strong analytical, communication, organizational and computer skills required

Job Responsibility

Collaborates with investigators in writing protocols for the conduct of research
Organizes research activities in accordance with approved protocols
Informs staff of their responsibilities in the project
Develops and installs operating procedures for the laboratory
Ensures that health and safety practices are maintained
Analyzes and evaluates experimental data and interprets results
Prepares written reports and presentations on all on-going projects
Keeps abreast of trends in field of interest
Independently operates histological-related equipment and microscopes
Maintains contact with outside research laboratories, vendors and technical representatives

Fulltime

Technical & Quality Centre Quality Product Analysis Specialist

The Quality Product Analysis Specialist plays a critical role within the Technic...

Location

United Kingdom , Rotherham

Salary:

Not provided

NAPA Auto Parts

Expiration Date

Until further notice

Requirements

Proven Experience: Ideally 3–5 years as a senior technician or diagnostic specialist in a high-volume garage, remanufacturing environment, or warranty inspection role
Certification: Level 3 Automotive Technician qualification or equivalent (e.g., IMI or City & Guilds)
Failure Analysis Training. Warranty Training: Experience or formal training related to warranty claim evaluation and processing preferred
Multi-System Mastery: Deep mechanical knowledge of modern vehicle and electronic systems
Electrical Proficiency: Ability to read electrical schematics and use multimeters or oscilloscopes to test rotating electrics and electronic sensors
Software Literacy: Comfortable with PC-based diagnostic software, CRM portals, warranty management systems, and standard office tools (e.g., Microsoft Word/Excel)
Precision Measurement: Skilled with precision tools such as micrometers, vernier calipers, and dial indicators for checking tolerances and shaft play
Warranty & Compliance Knowledge: Understanding of warranty policies, claim processing procedures, and applicable regulatory standards
Analytical Thinking: Logical, detective-like mindset adept at solving complex diagnostic puzzles that other technicians may overlook
Attention to Detail: Precision in inspecting fracture surfaces, wear patterns, and minute electrical deviations

Job Responsibility

Component Inspection: Conduct detailed physical and functional inspections on a wide range of components including turbos, braking systems, suspension units, clutches, and rotating electrics (alternators/starters)
Diagnostic Testing: Operate specialised test equipment (e.g., vacuum testers, electronic actuator testers, battery/alternator analysers, brake DTV machines, and brake caliper testers) to verify part performance against factory specifications
Root Cause Analysis: Investigate and determine the underlying cause of failure (e.g., carbon buildup, oil starvation, electrical surges, installation errors) to support warranty claim evaluations
Warranty Claim Assessment: Review and assess warranty claims in accordance with company policies, determining validity and identifying potential manufacturing or usage defects
Digital Reporting & Documentation: Utilise computer systems to log findings, upload digital photos of defects, generate professional inspection and warranty evaluation reports, and maintain accurate records for claim processing
Quality & Compliance: Maintain a clean, organised laboratory/testing environment ensuring all test equipment is in safe and calibrated working order. Ensure inspections comply with company standards and relevant regulatory requirements
Cross-Functional Communication: Collaborate closely with warranty administration, customer service, and re manufacturing teams to share findings, explain technical details, and support timely claim resolution

What we offer

We offer comprehensive benefit plans and programs designed to support your health and wellness, provide income protection and build financial security for your retirement

Biomedical Scientist – Microbiology

We are excited to present an excellent opportunity for a Biomedical Scientist to...

Location

United Kingdom , Central London

Salary:

35000.00 - 50000.00 GBP / Year

Hunter Gatherer AHP

Expiration Date

Until further notice

Requirements

HCPC-registered Biomedical Scientist (Microbiology discipline)
Demonstrable post-registration experience in a UKAS-accredited Microbiology laboratory
Strong technical skills in clinical bacteriology, virology, or related disciplines
Experience using LIMS systems and handling sensitive patient data
Committed to teamwork, service excellence, and continuous improvement

Job Responsibility

Conduct routine and specialist diagnostic microbiology tests, including bacteriology, virology, parasitology, and mycology
Process a wide variety of clinical samples accurately and efficiently
Operate and maintain a range of microbiological laboratory equipment after competency training
Participate actively in internal and external quality assurance schemes
Support stock control, equipment evaluations, and method development initiatives
Adhere to laboratory policies, procedures, and UKAS accreditation requirements
Work collaboratively with senior biomedical scientists and multidisciplinary teams

What we offer

Contributory pension scheme (up to 20% total contribution)
Private medical healthcare
33 days annual leave (inclusive of bank holidays)
Season ticket loan and family-friendly benefits
Access to retail and service discounts
Clear career development pathways and training support

Fulltime

Compound Management Application & Data Support Lab Head

Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. At the...

Location

United States , Groton

Salary:

120800.00 - 201400.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

13+ years of industry experience with a bachelor’s degree, 11+ years of experience with a Master’s degree or 8+ years of experience with a Ph.D in Computer Science, Software Engineering, Data Science, Information Science or related field
Demonstrated breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, senior leadership, stakeholders, external partners, and to develop, mentor and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
Demonstrated 5+ years of software engineering project management experience
Track record of leading cross functional/multi-disciplinary matrix teams to successful delivery of project objectives
Expert knowledge in the software engineering discipline and the importance of adhering to a software development lifecycle process to ensure high-quality software solutions
Expert technologist with practical experience in designing & developing software solutions to solve complex problems leveraging Agile methodologies
Demonstrated ability in performing business analysis and workflow/process design & development
Expert knowledge in troubleshooting highly technical, and complex software issues and identifying potential root causes
Excellent communication skills and a demonstrated ability to create and strongly contribute to and provide technical expertise to research initiatives and project teams
Recognized as an expert in identifying and developing technical strategies to support mid- and long-term goals for the department

Job Responsibility

Provide oversight & strategic management of the development, acquisition, implementation, operation, troubleshooting, maintenance and support of software solutions within the Groton sample management laboratories that manage the receipt, storage, solubilization, aliquoting, and preparation of samples for assays in an automated, efficient manner ensuring high-quality access to the Pfizer compound collection for drug discovery teams
Lead, mentor, and develop a group of Data & Computer Scientists that develop & support lab-based software solutions & collaborate with Digital teams on the development & support of enterprise-level software solutions in use within the Compound Management workflows
Play a key role in meeting financial targets by co-managing Digital project and Compound Management operational budgets by managing purchase orders, invoices and project spend, assisting in the preparation of funding requests, Request for Proposals, Statements of Work (SOWs) and Master Service Agreements (MSAs) and negotiating purchase & sustain software costs with vendors and internal procurement teams
Collaborate with Compound Management lab heads, Laboratory Automation specialists, Digital technologists, Hit-to-Lead and Lead Optimization scientific teams & stakeholders to drive the strategic direction for the portfolio of applications
Lead cross-functional teams to drive the implementation of enhancements to the software & hardware portfolio within ATCM
Leverage technical subject matter expertise & insight into the design & development of innovative solutions & algorithms to solve complex software, automation, and workflow needs within Compound Management
Align with Digital development & security requirements on infrastructure, technologies, software engineering best practices, development lifecycles, configuration management and software quality assurance
Contribute to the strategy of ATCM and Structure, Analytical, & Molecular Sciences (SAMS) groups as a member of the ATCM & SAMS Leadership Teams

What we offer

Relocation support available
Eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary
Eligibility to participate in our share based long term incentive program
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
Health benefits to include medical, prescription drug, dental and vision coverage

Fulltime

Metrologist Senior

Founded in 1985, ATS is a company with a presence in the United States, Mexico a...

Location

United States , Peoria

Salary:

93609.08 - 119717.75 USD / Year

Advanced Technology Products

Expiration Date

Until further notice

Requirements

Bachelor's degree in Engineering, Physics, or related field and five years metrology, engineering or operation and maintenance experience
or equivalent combination of education and experience
At least five years previous experience working in an industry related to calibration and/or M&TE
Experience performing data collection and calculations for measurement uncertainties
Expert knowledge in areas of metrology, including Flow, Electrical, Dimensional, and Physical
Ability to formulate policies and procedures relevant to program areas based on information of a conceptual nature from varied and complex sources
Demonstrated success gaining an internationally recognized accreditation in calibration and/or testing, including ISO17025, Z540

Job Responsibility

Identifies magnitude of error sources contributing to uncertainty of results through root cause analysis to determine reliability of measurement process in quantitative terms
Redesigns or adjusts measurement capability to minimize errors
Develops and/or validates calibration methods, techniques, and procedures based on principles of measurement science, technical analysis of measurement problems, and accuracy and precision requirements
Creates documentation and reporting to adhere to national and/or international testing standards, including ISO17025
Provides leadership, direction and technical guidance to calibration specialists, technicians and administrative staff
Provides high-level technical expertise, oversight and project management support for the operations of the Standards Laboratory, Measuring & Test Equipment (M&TE) related services, and Quality Assurance (QA) requirements for internal and external customers

What we offer

Medical, Dental and Vision plans
PTO
a 401k retirement plans with employer matching
tuition reimbursement

Fulltime

Senior Clinical Research Specialist

As a community, the University of Rochester is defined by a deep commitment to M...

Location

United States of America , Rochester

Salary:

60431.00 - 84603.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree and 3 years of relevant experience required
Ability to effectively manage complex research protocols/procedures required
Fully adheres to applicable safety and/or infection control standards
Proficiency in medical terminology, the clinical research process, and applicable regulatory guidelines, standards preferred
Proficiency in managing multiple and competing priorities/demands
Thorough knowledge of and established track record in assuring GCP, Responsible Conduct of Research standards, applicable safety standards, and OSHA guidelines throughout study implementation
Exceptional interpersonal, organizational, and time management skills
highly collaborative, promotes teamwork
Ability to build collaboration among research team members, laboratory staff, patients, and families, clinical services (requires tact, sensitivity, clarity, flexibility, empathy for patients)
Proficient in MS Office (e.g., Word, Excel, and PowerPoint), email, and internet

Job Responsibility

Provides leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols
Manages the day-to-day operations of multiple studies, carrying out study coordination duties from protocol development and initiation through to study close-out in accordance with regulatory/sponsor guidelines
Monitors and maximizes adherence to research standards, regulatory guidelines, and approved operational procedures
Works closely with study team members and other study sites to ensure the safety and adherence of study participants to the study protocol
Manages study-related administrative and human resources tasks and facilitates across-the-board flow of information, orchestrating study activities and personnel
Coordinates enrollment of participants
Oversees and facilitates eligibility screening and study recruitment activities
Plans study timelines and schedules appointments and study visits
Manages and organizes case report forms, source documents, and research records
Enters research data into data collection forms and/or study databases

Fulltime

Senior Embryologist

Performs unsupervised laboratory procedures associated with human in-vitro ferti...

Location

United States , Winston Salem

Salary:

47.50 - 71.25 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Biology or related field
Typically requires 5 years of clinical experience in in-vitro fertilization and sterile technique
Must possess the ability for accuracy and attention to detail when working
Strong communication and organizational skills to interact with patients, physicians, nurses and other employees
Must be able to handle stressful situations in a calm and professional manner
Ability to work a flexible schedule including weekends and holidays
Exposure to biological and chemical hazards and body fluids requires observation of universal precautions
protective clothing and following Material Safety Data Sheets (MSDS) suggested safety measures
Frequently lifts up to 10 lbs. Will occasionally be required to lift up to 50 lbs
Must be able to sit, stand and walk for the majority of the workday

Job Responsibility

Performs all aspects of assisted reproductive procedures including: sperm wash, media preparation, egg insemination/fertilization, egg clean-up/score of fertilization, embryo culture, grading, assisted hatching, Intracytoplasmic Sperm Injection (ICSI), sperm identification from epididymal aspirated or testicular biopsy, embryo transfer, embryo freeze, embryo thaw, and embryo biopsy
Performs egg freeze and egg thaw that results in a high survival rate
Orders, receives, inspects and stores culture media. Performs all initial quality control testing following outlined procedures before release of media, for use in embryology procedures
Performs identification and isolation of human oocytes from follicular fluid at the time of aspiration
Maintains proper operation of permanent specialized equipment such as the incubator, pH meter, osmometer, microscopes, centrifuge, hoods, ICSI equipment, freezing equipment and monitoring systems
Prepares and forwards the Embryology Laboratory Charges Report to the billing specialists at the end of each IVF procedure. Maintains all inventories of cryopreserved embryos by maintaining Cryopreserved Embryo Logs, AMG Cryopreserved Embryo Inventory Cards and Cryopreserved Embryo Billing Inventory Reports. Maintains and updates all patient files and paperwork concerning IVF procedures. Counsels patients, obtain patient consent to different procedures and answer their questions regarding the laboratory aspects of IVF care
Enters patient and cycle information into appropriate database and electronically transmits data to Society for Advanced Reproductive Technology (SART) in a timely manner. Enters data into the infertility data system (IDS) and maintains up to date electronic records of all aspects of the IDS
Assists in preparing for the College of American Pathologists (CAP) inspections
Acts as a lab and department resource and role model to employees, which includes training/orienting and providing day-to-day work direction. Assigns, monitors, and reviews progress and accuracy of work, monitors productivity, maintains appropriate staffing levels, directs efforts, and provides guidance on more complex issues
Maintains current knowledge of applicable policies, procedures and regulatory, compliance and scope of practice guidelines

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program

Fulltime

Senior Specialist - Laboratory Operation

BioMarin Pharmaceutical

Location:
United States , Novato

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 01, 2026

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