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QO Technical Associate II (3rd Shift)
QO Technical Associate II (3rd Shift)-May 2024
Kalamazoo
May 7, 2025
ABOUT PFIZER
Pfizer is a pharmaceuticals and biotechnology company.
10,000+ employees
Biotechnology, Manufacturing
VIEW COMPANY PROFILE >>
About QO Technical Associate II (3rd Shift)

  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.

  What You Will Achieve

  You will be a team member who is relied on to have a good understanding of procedures, techniques, tools, materials and equipment. Your decision making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. You will contribute to the team's success by sharing your previously acquired knowledge.

  It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.

  Using standardized procedures, the candidate will conduct a variety of microbiological environmental sampling in aseptic /classified processing areas. The sampling performed supports high through-put pharmaceutical manufacturing.

  In addition to performance of routine environmental sampling, the candidate will assist in the overall operation of the microbiology laboratory including:

  Incubation of samples

  Read out of sample results and entry of results into an electronic database

  Completion of training activities

  Maintenance of records, equipment, basic lab supplies, and reagents in accordance with current good manufacturing requirements.

  Second checks records and assists in training others.

  How You Will Achieve It

  Manage own time, professional development and be accountable for own results.

  Interpret and evaluate data in terms of accuracy, precision, trends, and potential Good Manufacturing Practices {also cGMP} impact and recommends appropriate corrective action where necessary.

  Complete training activities and maintains records, equipment, and basic lab supplies, in accordance with {Current} Good Manufacturing Practices {part of GxP} requirements.

  Participate in laboratory investigations as required.

  Prepare Quality Performance Review.

  Adhere to safe work practices, such as wearing appropriate personal protective equipment including lab coat, safety glasses, and gloves.

  Perform equipment verification and calibration in accordance to procedures.

  Maintain area and equipment in clean, safe, functional order.

  Primary responsibility is to perform environmental sampling in aseptic/ classified processing area.

  This will include setting up sampling materials and data summaries in a computerized database, incubating samples, interpreting, and documenting results.

  Recognizes atypical data and informs supervision of relevant problems.

  Enters, reviews, and approves data in computerized database.

  Will second-check the work of others.

  Transports samples and supplies between the laboratory and production environments.

  Applies technical knowledge of microbiological principles, theories, concepts and Pfizer processes and industry practices/standards to their daily work.

  Is able to work both independently and as part of a team.

  May perform assays on purchased materials, investigative samples, and in-process samples in a laboratory service operation so that the unit and organizational objectives are met.

  Performs equipment & laboratory maintenance.

  Orders and maintains laboratory supplies.

  Operates within established HR policies and basic colleague relations guidelines.

  Contributes to the completion of specific team objectives and assigned project milestones.

  Qualifications

  Must-Have

  High school diploma (or equivalent) plus 2 years of relevant experience; in a laboratory, QA role, or manufacturing environment, or customer focused/ customer service role.

  Good oral, written and interpersonal communication skills within a diverse team setting are required.

  Basic math skills and computer skills such as data entry, along with a high level of attention to detail are required.

  The successful candidate will possess a demonstrated ability to organize time independently, be able to perform several tasks concurrently (ability to multi-task), and be able to meet objectives in a flexible, team-oriented environment.

  Preferred candidate will have previous laboratory experience, including a basic understanding of microbiology and aseptic technique, and/or previous experience in an aseptic/ classified manufacturing environment, and/ or previous experience in a manufacturing, or customer service/ customer focused role.

  Nice-to-Have

  Bachelor's Degree in biological sciences plus 6-12 months of experience.

  Quality Control experience in a pharmaceutical industry.

  Experience in a GMP environment.

  PHYSICAL/MENTAL REQUIREMENTS

  Must be capable of maintaining aseptic gowning qualification in a production environment.

  Must be capable of manual manipulations with fine dexterity.

  Must be capable of walking for extended periods, bending, reaching and lifting (less than 35 lbs.) during routine job activities.

  Extended time working at a computer terminal is also required.

  NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

  This is a Third Shift position (10:00PM - 06:30AM).

  Weekend, Holiday, and Overtime hours will be required in order to meet business and/or customer needs.

  Work Location Assignment:On Premise colleagues work in a Pfizer site because it's needed to get their job done. They may have flexibility to work remotely from time to time, but they are primarily on-site.

  Other Job Details

  Last Date to Apply for Job: March 1st, 2024.The salary for this position ranges from $18.74 to $31.23 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company's policies. 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 applies only to the United States - Michigan - Kalamazoo location.

  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.

  Quality Assurance and Control

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