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The Stockroom MRO Analyst performs routine warehouse functions including material handling, receiving, kitting, and cycle counting within a manufacturing environment. They are responsible for maintaining inventory accuracy, managing vendor support, and ensuring all operations comply with safety and GMP standards.
Requirements
Candidates must have a high school diploma or G.E.D. and at least 5 years of experience in a regulated manufacturing or distribution environment. Proficiency in ERP systems, Microsoft Office, and the ability to operate heavy machinery like forklifts are required.
Full job description
Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
This individual will be doing a variety of routine warehouse functions in a typical stockroom environment and external storage areas with little to no supervision where some judgement is required. Responsibilities include but are not limited to material handling, receiving, kitting, stocking, preparing parts to be sent for repair, cycle counting, transportation on site, and die management vendor support.
As needed, performs supply chain responsibilities of contacting suppliers for pricing and part availability.
Creates purchase requisitions in ERP system.
Performs function in focused areas (multiple stockrooms, both inside production and outside) as trained and assigned where some tasks are well defined and others are loosely defined and will require some judgement and interpretation. Proficiently sit down forklift and pallet jack operate.
Role Responsibilities
Demonstrates commitment to the success of the department goals, supports the efforts of individuals, and teamwork in all aspects of job responsibilities. Contributes to team problem solving efforts.
Performs all department operations proficiently and has comprehensive knowledge of job duties to act as SME for training purposes.
Responsible for stockroom support to meet customer needs.
Responsible for issuing out parts to plant personnel as requested.
Maintains inventories of stockroom parts necessary to support plant engineering, laboratory and production.
Responsible for reporting stockroom KPI reports.
Responsible for following SOP and providing feedback when SOP needs to be revised. Always uses safe working methods/procedures to avoid personal injury, injury to co-workers, or damage to company property.
Observes all corporate and Northridge plant safety rules, SOPs and procedures.
Reports unsafe working conditions or equipment operation to supervisor immediately.
Ability to read, write legibly, understand, and communicate verbally in English.
Operates sit down forklift, pallet jack and electric cart. At a Certified level of proficiency, the employee conducts the more difficult assignments, provides input on work procedures, and guides the work of others. May be assigned to represent the department on committees such as safety or continuous improvement. Maintains assigned areas in a clean, neat, and orderly fashion. Makes suggestions and contributes to stockroom related process improvements.
Performs other duties, as assigned.
Utilizes handheld barcode scanners to read barcodes and record transactions in ERP system. General mastery of receiving, stocking, and issue out processes of stockroom. Ability to identify, troubleshoot and correct any inventory and/or documentation discrepancies. Physically move goods from receiving locations to stockroom
Label goods with description and stockroom location.
Put away goods and do corresponding ERP transactions. Count and verify quantities physically in stock and verify ERP system.
Issue out in ERP system from manual records and log sheets. Count and verify quantities physically in stock and verify ERP system.
Administer new inventory requests.
Put away returns physically in stockroom and do ERP system transaction.
Replenish other stocking locations within production.
Manage small equipment components that require repair, package for shipment.
Pick up recycled batteries from various locations within the plant.
Forklift and pallet jack driver for material movement
Required Skills & Experience
High school diploma/G.E.D. level of education
5+ years’ experience working in a GMP or other regulated manufacturing or distribution work environment.
Intermediate to advanced level of computer skills including Microsoft office, Excel and ERP.
Good communication skills
Good math skills
Preferred Skills & Experience
AA Degree, BS/BA Degree.
Advanced knowledge of material flow, GMP guidelines, accuracy and cycle counting.
Significant prior use of ERP System and barcode scanning equipment.
Related job experience in shipping, receiving, warehouse, transportation, picking, kitting, staging and cycle counting.
The expected compensation range for this position represents a good faith estimate. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, & Vision, Health Savings Accounts, Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and 401k Benefits, etc.).
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!
Kindeva is a purpose-fueled, people-centric CDMO dedicated to advancing your project, your ambitions, and our industry. With a legacy of innovation and deep expertise in complex drug development, we serve as a trusted partner to pharmaceutical companies worldwide.
For us, fast-tracking healthier tomorrows starts with industry-leading finished-dose expertise. From early-stage formulation to full-scale commercial production, we optimize every step to help bring life-changing therapies to patients faster.
Built on a rich heritage of regulatory diligence and blockbuster devices, our expertise sharpens, optimizes, and maximizes your project—combining best-in-class facilities with specialist capabilities in injectable, inhalation, and dermal delivery, to ensure exceptional-by-design solutions throughout.
Strategically minded and dedicated to your lasting legacy, we provide value beyond manufacturing, turning your long-term possibilities into achievable milestones.
Because every patient deserves tomorrow.
For more information about how we can transform tomorrows together, please visit www.kindevadd.com.
Offices: 11200 Hudson Rd, Woodbury, Minnesota 55129, US · St. Paul, Minnesota 55144, US · Loughbourgh, Leicestershire LE11 5RB, GB · Northridge, CA 91324, US
InhalationMicroneedlesContract Development Manufacturing OrganizationMDIPulmonaryNasalDermalInjectablesand CDMOManufacturing
Kindeva is a purpose-fueled, people-centric CDMO dedicated to advancing your project, your ambitions, and our industry. With a legacy of innovation and deep expertise in complex drug development, we serve as a trusted partner to pharmaceutical companies worldwide.
For us, fast-tracking healthier tomorrows starts with industry-leading finished-dose expertise. From early-stage formulation to full-scale commercial production, we optimize every step to help bring life-changing therapies to patients faster.
Built on a rich heritage of regulatory diligence and blockbuster devices, our expertise sharpens, optimizes, and maximizes your project—combining best-in-class facilities with specialist capabilities in injectable, inhalation, and dermal delivery, to ensure exceptional-by-design solutions throughout.
Strategically minded and dedicated to your lasting legacy, we provide value beyond manufacturing, turning your long-term possibilities into achievable milestones.
Because every patient deserves tomorrow.
For more information about how we can transform tomorrows together, please visit www.kindevadd.com.
Offices: 11200 Hudson Rd, Woodbury, Minnesota 55129, US · St. Paul, Minnesota 55144, US · Loughbourgh, Leicestershire LE11 5RB, GB · Northridge, CA 91324, US
InhalationMicroneedlesContract Development Manufacturing OrganizationMDIPulmonaryNasalDermalInjectablesand CDMOManufacturing