Logistics Specialist (Contractor)

Posted 4 Hours Ago
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Hillsboro, OR
Entry level
Healthtech • Biotech
The Role
The Logistics Specialist manages product logistics in a compliant environment, including the receipt, storage, shipping, and data entry of GMP raw materials and finished goods. Responsibilities include inventory management, maintaining compliance with procedures, and utilizing computer systems for accurate data processing. The role also involves assisting with equipment checks, organizing materials, and overseeing contract staff activities.
Summary Generated by Built In

Logistics Specialists in the Hillsboro Distribution Center are responsible for the execution of product logistics in a cGMP environment. This includes the receipt, storage, and issuance of GMP raw materials used in production and marketed product distribution to our customers. Other responsibilities include shipping and receiving of GMP Materials and Finished Goods, International Shipping, and performing data entry into various business systems and databases ensuring department compliance with policies and procedures.
Responsible for performing duties in the Warehouse and Distribution function including; GMP receipt, quarantine, sampling, shipping to include raw materials, tanks and bulk drug substance, non-GMP receiving/delivery. Functions can include one or all of the following: Materials Operations and Logistics, Receipt, Store and Control, Transfer and Issue Raw Materials within cGMP guidelines. Package and ship bulk, semi-finished and finished products (both Domestic and International, Truckload and Air Freight). Manage raw material inventory, transfer materials to Mfg. Computer system/ERP knowledge (SAP). Verifies quantity and conformance of materials; prepares records of materials shipped and boxes, and prepare materials for shipment. May develop reports, prepare metrics and/or analyze data. May support site change controls and discrepancy management.

Pay Rate - $24-$26
Shift: 4X10, 6:00 am to 5:00 pm (Monday - Thursday OR Tuesday – Friday)

Contract duration: 6/30/2025
Job Responsibilities
Accurately pick and pack marketed product against shipping order.
Using manual labor, pallet jacks, and forklifts, move product and both GMP and non-GMP supplies to and from storage locations and delivery trucks
Perform all work activities in a safe and compliant manner according to all Genentech policy, procedure and training and maintaining a clean work environment.
Perform physical counts of product and materials.
Perform functionality / safety checks of equipment (i.e. forklifts, etc.)
Access various business systems and input data with a high level of accuracy (i.e. SAP, MS Office, etc.)
Record creation, collection and storage per corporate retention schedules
Perform department related project activity that may include investigating, analyzing, formulating possible solutions, documenting processes, and communicating results
Ability to use automated and paper based documentation systems.
Adhering to batch instructions and standard operating procedures.
Maintaining and accurately completely batch documentation;
Manage inventory of equipment parts and consumable materials in support of process development, maintenance, manufacturing, quality control and other related areas utilizing industry wide standard inventory control practices.
Perform parts staging for PM and other planned activities.
Maintain Kanbans for various customers.
Assist mechanics, technicians, and other customers with identifying parts and materials if needed.
Perform routine clerical duties including data entry, answering telephones and assisting over‐the counter customers.
Organize and maintain accurate database master data.
Oversee the work of contract staff as directed by the supervisor and report status and issues to
the supervisor in a timely manner.
All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA).
Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt.

Education and Experience Requirements
Bachelor’s Degree; Associate Degree and 2 years experience; or HS and 4 years experience
Minimum 4-year experience in warehouse or GMP regulated environment
Experience in a GMP environment is a plus.
Familiarity with ERP/MRP systems.
APICS training / experience a plus.
Ability to meet visual requirements.
Valid driver’s license and good driving record.
Forklift experience a plus


Skills
Inventory management or Bio / Pharma industry experience in logistics.
Ability to follow detailed verbal and written instruction.
Good Mathematical skills
Ability to repeatedly lift up to 50lbs
Proficiency with PC desktop applications and business operations software system
Ability to work in a highly cooperative team environment
Flexibility in duty assignment and ability to work over-time, holidays and weekends as required and different shifts
Strong organizational, communication and interpersonal skills
Work Environment/Physical Demands/Safety Considerations
Schedule could include a non-rotating 4-day (10 hour shift), one weekend day, evening or night hours, or full off-shift hours.
Expected to be on feet for 8 to 10 hours a day.
May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility.
Lift up to 40lbs may be required.
Environment may require gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn.
Exposure to level 1 chemicals.
Operate a forklift, electric pallet truck and other material handling equipment
Job descriptions are not intended, and should not be construed, to be all-inclusive lists of all responsibilities, skills, efforts, or working conditions associated with a job. While this description is intended to be an accurate reflection of the job requirements, management reserves the right to modify, add, or remove duties and to assign other duties as necessary.
Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.

 

Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.

Top Skills

SAP
The Company
HQ: South San Francisco, CA
20,069 Employees
On-site Workplace
Year Founded: 1976

What We Do

Considered the founder of the industry, Genentech, now a member of the Roche Group, has been delivering on the promise of biotechnology for more than 40 years.

Genentech is a biotechnology company dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis.

We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal.

Making a difference in the lives of millions starts when you make a change in yours.

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