1+ months

Technical Associate, Inventory Management

Pfizer
Andover, MA 01810
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**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**



The Technical Associate, Inventory Management position is responsible for supporting activities within the Andover Clinical Manufacturing Facility's (ACMF) Warehouse and Inventory Storage locations. This includes materials receipt, movement, transactions and outbound shipments. This role will also interact with ACMF Operations and Quality Assurance to ensure GMP campaign success and compliance within the Inventory Management space.



**How You Will Achieve It**



+ Complete GMP/quality inspections on incoming materials, to include but not limited to Raw Materials, Processing Aides / Consumables, Drug Substance, and Hazardous Materials.

+ Receive, sample, dispense, ship, manage and maintain all material types to support development, clinical, and commercial activities.

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

+ Performing electronic and physical inventory transactions for all materials (i.e. picking, stock checks, consumption, discarding)

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

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

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

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

+ Identify, implement and support continuous improvement initiatives throughout IM.



**Qualifications**



**Must-Have**



+ HS diploma, Associates Degree with minimum 0-3 years of experience in a biotechnology manufacturing or laboratory environment.

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

+ Must have a valid driver's license



**Nice-to-Have**



+ Bachelor's Degree in relevant field (Life Sciences, Engineering or Business preferred) with 0-2 years' experience.

+ Experience working within the Pharma Industry and/or GMP materials management preferred

+ Experience with GMP Enterprise Systems preferred: Microsoft Dynamics, SAP, LIMS, Document Management Systems, Axis360

+ 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.



**PHYSICAL/MENTAL REQUIREMENTS**



+ Ability to lift up to 50 pounds

+ Ability to complete repetitive physical activity

+ Ability to work with and around power industrial vehicles

+ 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, plant uniform, etc.)

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



**NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS**



+ Position will require 40 hours per week

+ Must be available to work during business hours of 7:00 am -4:30 pm (estimated)

+ Overtime is based on business needs

+ Hours may vary dependent on business needs



**Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.**



**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.



Manufacturing
Posted: 2022-05-16 Expires: 2022-07-18
Sponsored by:
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Technical Associate, Inventory Management

Pfizer
Andover, MA 01810

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