Laboratory Analyst (Medical Technologist)

Pfizer, S.A. de C.V; New Haven (CT); On-site; USD 69,000 - 114,000; Full time

Benefits offered by this job

401(k) matching contributions

Pfizer Retirement Savings Contribution

Paid vacation

Paid holidays

Personal days

Medical, dental, vision benefits

Job summary

Pfizer Laboratory is seeking a Laboratory Analyst (Medical Technologist) to perform routine and specialized clinical laboratory tests across hematology, chemistry, and urinalysis. You will ensure quality control, assist in assay validation, and support training and data documentation.

The role requires an Associate’s degree in Medical Technology with MT/MLT certification and at least 2 years’ lab experience in pharma, hospital, or research settings.

Qualifications

• Associate's degree in Medical Technology and MLT/MT certification is required.
• Minimum 2 years of relevant laboratory work experience in pharmaceutical, hospital, or medical research environment.
• Hands-on experience with computers and laboratory data handling acquisition systems.

Responsibilities

• Perform routine and special clinical chemistry, hematology, coagulation, urinalysis, immunological and other tests per SOPs.
• Perform quality control checks and maintain calibration data.
• Maintain inventory of laboratory supplies and notify for upcoming needs.
• Data entry and monitor Laboratory Information System (LIS).
• Be flexible with schedules to cover off-hours and specimen processing as needed.

Skills

Communication skills

Laboratory data management

Microsoft Word

Quality control

Education

Associate's degree in Medical Technology and MLT or MT certification

Tools

LIS software

Cerner

PIMS

Job description

Laboratory Analyst (Medical Technologist)

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

Pfizer Research & Development serves as the beating heart of Pfizer’s trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Working independently, you will beresponsible forperforming routine and special clinical laboratory testing using automated, semi-automated and/or manual methods and equipment,andcoordinating and organizing assigned laboratory sections (including Hematology, Chemistry, Urinalysis, Immunoassay, Coagulation and Biomarkers).Your responsibilitieswill also include quality control, assistingin the validation of newassays/instrumentation, new employee training/mentoring, documentation of data collection and other experiments, servingas a back-up to instrument key operators, performinginstrument calibrations, maintenance, reagent inventory and sample processing.You willserve as a back-up for pharmacokinetic biospecimen processing and sample shipping asrequired.

KEY RESPONSIBILITIES

Performs routine and special clinical chemistry, hematological, coagulation, urinalysis,immunologicaland other tests according to the Standard Operating Procedures.

Performs all quality control checks (monitor trends) on instruments, reagents, and techniques,maintainsquality control and calibration data.

Maintains the inventory of and order laboratory supplies including notifying instrument key operators of upcoming reagent/supply needs.

Perform data entry andmonitorlaboratory informationsystem (LIS).

Be flexible with the schedule to cover inadvertent times that subjects/volunteers arrive for visits, check-ins, and discharges late.

Utilize PIMS, Cerner and/or electronic notebooks for processing samples.

Assist the Laboratory Quality Coordinator with preparation for Internal audits and CLIA, COLA or CAP audits.

MaycoveroffhoursPK sample processing as needed.

RotatethroughSpecimenProcessor functions as needed.

MINIMUM QUALIFICATIONS

Associate's degree in Medical TechnologyandMLT or MT certification

Minimum of 2 years of relevantlaboratorywork experience inapharmaceutical, hospital, or medical researchenvironment

Hands-on experience with computers and laboratory data handling acquisition systems and knowledge of associated issues/risks

ProficientwithWord applications.

Strongcustomer facingcommunication skills

PREFERRED QUALIFICATIONS

Bachelor’s degree inachemical,physicalor biological sciencewith the followingeducationalrequirementsthatmeet CLIA 88 standards for high complexity laboratories:

---16 semester hours of biology courses, which are pertinent to medical sciences.

---16 semester hours of chemistry (at least 6 hours of Inorganic Chemistry)

--- 3 semester hours of math

Knowledge of pharmaceutical clinical researchoperations/trialsor experience in a clinicaltrialsenvironment.

Working knowledge ofGxP, GCP,CAPand CLIA regulations

PHYSICAL/MENTAL REQUIREMENTS

May require long period of standing.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

May require coverage during off hours in specimen processing.

POSITION SUMMARY

Working independently, you will beresponsible forperforming routine and special clinical laboratory testing using automated, semi-automated and/or manual methods and equipment,andcoordinating and organizing assigned laboratory sections (including Hematology, Chemistry, Urinalysis, Immunoassay, Coagulation and Biomarkers).Your responsibilitieswill also include quality control, assistingin the validation of newassays/instrumentation, new employee training/mentoring, documentation of data collection and other experiments, servingas a back-up to instrument key operators, performinginstrument calibrations, maintenance, reagent inventory and sample processing.You willserve as a back-up for pharmacokinetic biospecimen processing and sample shipping asrequired.

KEY RESPONSIBILITIES

• Performs routine and special clinical chemistry, hematological, coagulation, urinalysis,immunologicaland other tests according to the Standard Operating Procedures.
• Performs all quality control checks (monitor trends) on instruments, reagents, and techniques,maintains quality control and calibration data.
• Maintains the inventory of and order laboratory supplies including notifying instrument key operators of upcoming reagent/supply needs.
• Perform data entry and monitor laboratory information system (LIS).
• Be flexible with the schedule to cover inadvertent times that subjects/volunteers arrive for visits, check-ins, and discharges late.
• Utilize PIMS, Cerner and/or electronic notebooks for processing samples.
• Assist the Laboratory Quality Coordinator with preparation for Internal audits and CLIA, COLA or CAP audits.
• May cover off hours PK sample processing as needed.
• Rotate through Specimen Processor functions as needed.

MINIMUM QUALIFICATIONS

• Associate's degree in Medical TechnologyandMLT or MT certification
• Minimum of 2 years of relevant laboratory work experience in a pharmaceutical, hospital, or medical research environment
• Hands-on experience with computers and laboratory data handling acquisition systems and knowledge of associated issues/risks
• Proficient with Word applications.
• Strong customer facing communication skills

PREFERRED QUALIFICATIONS

• Bachelor’s degree in a chemical, physical or biological science with the following educational requirements that meet CLIA 88 standards for high complexity laboratories:

---16 semester hours of biology courses, which are pertinent to medical sciences.

---16 semester hours of chemistry (at least 6 hours of Inorganic Chemistry)

--- 3 semester hours of math

• Knowledge of pharmaceutical clinical research operations/trials or experience in a clinical trials environment.
• Working knowledge of GxP, GCP, CAP and CLIA regulations

PHYSICAL/MENTAL REQUIREMENTS

May require long period of standing.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

May require coverage during off hours in specimen processing.

Work Location:

On Premise

The annual base salary for this position ranges from $68,600.00 to $114,300.00. 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 | (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.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

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 www.pfizer.com/careers 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 [e-mail]. 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.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.