Pfizer Posted August 11, 2026

Global Materials Management Technician Tech Ops 2

Groton, United States Full time
Manufacturing & CMC

Pfizer is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Use Your Power for Purpose

Our dedicated manufacturing logistics and supply team ensures that customers and patients receive the essential medicines they require precisely when they need them. By embracing challenges, envisioning new possibilities, and taking decisive action, you will contribute to delivering medicines to the world with greater speed and efficiency. Your role is crucial in making sure that the supply chain operates smoothly, overcoming obstacles, and continuously innovating to meet the demands of healthcare.

What You Will Achieve

The Global Material Management (GMM) Technician position is responsible for supporting all activities within the Groton Pharmaceutical Sciences Drug Product Supply Global Material Management Group.

Seeking a material handler to support Groton GMM’s, GMP space, and associated daily activities. As a member of the GMM team the candidate will be required to learn a wide variety of support activities and functions while supporting development and clinical materials.  This role will be required to follow GMP standards, and for assuring compliance with Pfizer Standard Operating Procedures (SOPs), policies along with all applicable worldwide regulations and guidelines (e.g. FDA, DEA, TSA, MHRA).

How You Will Achieve It

Receive, sample, dispense, ship, manage and maintain all material types (e.g., API’s, Excipients, Raw Materials, Drug Substance, Controlled Substance and Hazardous Materials) to support development and clinical activities.

Strict adherence to quality, GMP, safety and environmental standards is required.

Responsible for identifying, reporting and supporting the resolution of quality concerns.

Becoming proficient working within multiple approved electronic inventory systems.

Performing electronic and physical inventory transactions for all materials.

Perform GMP warehouse infrastructure duties to include; warehouse management, cycle counts, stock rotation, transferring, picking, cleaning, destruction/waste management, segregation of materials, etc.

Subdividing and sampling of all material types, to include hazardous materials.

Follow and understand applicable SOPs/procedures in relation to activities being complete.

Demonstrates sound understanding and advanced knowledge of practices/concepts of GMM and a working knowledge of principles, practices, concepts and operations within other partner disciplines.

Must be adaptable and maintain flexibility in completing daily tasks in a dynamic work environment.

Proven ability to multitask, manage time and workload.  Ability to escalate issues immediately.

Maintain excellent customer service and assure on time delivery.

Display and influence appropriate behaviors and adhere to Pfizer standards and values.

Effective collaboration with partner lines and customers bases.

Participating on teams as required (i.e. safety team, process improvement teams, procedure teams, project teams).

Must be responsible and dependable.

Identify and support continuous improvement initiatives throughout GMM.

Operate forklift or other powered or manual material handling equipment to unload, move and load materials through the facility.

Ability to work in and adapt within an AI environment

Qualifications

Must-Have

High School with minimum 2+ years Pharma experience and/or Bachelor’s degree with 1-2 years of related experience.

Must be responsible/dependable and can manage own time independently

Experience and or knowledge of a cGMP environment

Experience working in a regulated work environment

Language Skills: Effective written and oral communication skills

Electronic Skills: Experience with computers to include: databases, email, software, navigation of shared drives, search engines, word processing, spreadsheets

Excellent interpersonal and team building skills, to include good behaviors

Ability to obtain the following certifications: Power Jack certification, Fork Lift, Raymond Lift, DOT/IATA regulations

Must have a valid driver’s license

Nice-to-Have

Experience working within the Pharma Industry, GMP materials management

Advanced electronic and computer skills including: Excel, Word, Microsoft dynamics, Visio, SharePoint

Experience with powered pallet movers and powered industrial vehicles, i.e. fork lifts, swing lifts, platform lifts, etc

Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity

PHYSICAL/MENTAL REQUIREMENTS

Ability to lift to 50 pounds

Ability to complete repetitive physical activity

Ability to work with and around power industrial vehicles

Ability to drive multiple vehicles, including Pfizer trucks

Ability to physically move materials (i.e. drums, boxes, crates, modules)

Must be able to stand for long periods of time

Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently

Must be able to gown up as required, to include specific PPE (i.e. respirators, full gear, safety glasses, daily uniform, etc.)

Must be able to perform in a fast-paced dynamic work place

Must be able to work outside of normal scheduled business hours as necessary including opportunities of overtime

Must be able to perform mathematical calculations and data analysis

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Position will require 40 hours per week

Overtime is based on business needs

Must be available to work during current business hours of 6:30 am -4:30 pm

Business hours/shifts may vary dependent on business needs

Work Location Assignment: On Premise


The salary for this position ranges from $26.86 to $44.77 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 - Connecticut - Groton location.



 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   disabilityrecruitment@pfizer.com . 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 .


Logistics & Supply Chain Mgmt


Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Groton, United States
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 1527 comparable Manufacturing & CMC roles across 125 biopharma companies.

1527Comparable roles tracked
1435Currently active
125Companies hiring similar roles
44Countries represented

Salary context

456 of 1527 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $540,400 (median $140,000)

Where these roles are based

Top locations among the 1527 comparable roles

United States781
India104
Germany74
Singapore67
France64
Ireland54

+ 38 more countries

Seniority mix

705 of 1527 peers have a known seniority level

Senior251
Manager165
Principal79
Associate68
Director64
Associate Director44
Senior Director21
Intern/Fellow/Postdoc8
Executive/VP5

Therapeutic area mix

7 of 1527 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease6
Oncology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Alexion New Haven, Connecticut, United States of America
Same function Same country
40%similar
AstraZeneca Cambridge, Massachusetts, United States of America Director
Same function Same country
40%similar
Alexion New Haven, Connecticut, United States of America
Same function Same country
40%similar
40%similar
Lilly Boston, Massachusetts, United States of America Associate
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Scientist II, LC Development, Biologics Analytical Development
Alexion · New Haven, Connecticut, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
40%
Director, Global Regulatory Affairs – Chemistry, Manufacturing and Controls (CMC), Platform Innovation – Synthetic Peptides and Oligonucleotides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Senior/Principal Scientist, Bioprocess Purification Development
Lilly · Indianapolis, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
40%
Senior Principal Scientist - Bioanalytical Research
Lilly · Louisville, Colorado, United States of America · Principal
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.