Production Associate II

posted:
Location
Madison, Wisconsin
Industry
Science & Research
Job Type
Full-Time
Salary
$0 per hour + none
Ref. Number
S_13837
Contact
Burton,Loraine, Spherion
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Job Description

Our biotechnology client has an excellent opportunity for a direct hire role as a Production Associate!

The Production Associate II will lead or assist in a variety of Production functions which include label printing, bulk reagent production and dispensing, and kitting of finished goods. The position will work within defined protocols and procedures, and may develop and document new procedures for Production. This role is expected to follow procedures with periodic direct supervision.

Responsibilities:
Essential Duties and Responsibilities include but are not limited to the following:
Participate in or lead simple and complex buffer preparation, Automated Fill / Cap / Label, label printing, and kitting of finished goods.
Participate in Capture Bead manufacture.
Mentor and develop junior level Production associates via operator training/certification programs, acting as a certified trainer.
Assist in developing, transferring, scaling and validating manufacturing processes, in accordance with company procedures, cGMPs, FDA, and ISO 13485 guidelines.
Assist or lead process improvement efforts, through the Change Request / Change Order process, or via other means.
Generate Nonconforming Material Reports, Change Orders, Change Requests, Out of Specifications, Investigations, and Corrective Actions including any deliverables associated with these items.
Manage inventory via KANBAN system for raw materials, intermediates, disposables and spare parts related to the Production areas.

Occasional Duties and Responsibilities
Assist with continuous improvement projects and support other areas needs dependent on demand.
Perform other related duties as assigned by management.

Working hours: 8-5, M-F

Skills:
Qualifications:
Strong communication skills and ability to coordinate work with other teams.
Ability to follow written procedures with minimal direction.
Strong documentation skills and attention to detail necessary in a GMP environment.
Demonstrates a basic theoretical understanding of the work tasks assigned.
MS Word and Excel aptitude


Preferred Qualifications
Experience in a biotech manufacturing environment, preferably in a GMP and/or ISO 13485 environment.


Education and Experience
Bachelors or Associates degree in Life Sciences, or related field or the equivalent combination of education and experience.
1-3 years experience in a relevant manufacturing setting. Experience in a GMP environment preferred.
Experience in using basic software applications including Microsoft Office.

Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.

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