What are the responsibilities and job description for the MCS Manufacturing Associates, Visual Inspection - multiple needed Job at Randsta position at Randstad Life Sciences?
Job Description
Job Description
Immediate opportunity for four (4) MCS Manufacturing Manufacturing Associates to perform visual inspection at one of the world's leading biotechnology companies located in Thousand Oaks, CA.
Position Overview : This MCS Manufacturing Associate position will be focused on manual visual inspection. If candidate excels in inspection there may be opportunities to expand training to analytical testing. This role is supporting the Drug Product Supply, Manufacturing team. Apply today!
Schedule / Shift : 1st shift, 5 / 6am-3pm; should be flexible.
The current shift structure is 6am-3pm. Some training does require a start time of 5am.
Possibility to move to graves / swing shift but job seekers should be flexible.
Position type : 3 months contract (through June 2025); extension possible
Essential Duties and Responsibilities :
Under minimal supervision, performs manufacturing according to Standard Operating Procedure
Understand process parameters and can identify process anomalies
Operate critical processing equipment
Assist in ensuring operations are completed per manufacturing schedule
Resource related to processing operations on the mfg. floor
Responsible for identifying and communicating problems during operations
Review, revise, and audit documents
Ability to perform computer operations (MES, EBR, MAXIMO, LIMS and SAP Knowledge)
Recognizes and escalates problems
Able to establish working relationships with others outside area of expertise
Ability and willingness to support flexible shift structure in support of operations (may include weekend)
Ability to understand, apply, and evaluate basic chemistry, biology, and physical principals as appropriate for the position
Organizational skills and an ability to perform assignments with a high degree of attention to detail
Written and oral communication skills.
GMP knowledge with ability to interpret and apply applicable regulations
Ability to understand analytical methods for manufacturing / laboratory area
Qualifications :
High school / GED 2 years work experience OR Associate’s (AA / AS) and 6 months work experience OR Bachelor's (BA / BS)
Experience with manual visual inspection of drug product, analytical testing lab, or in a GMP regulated environment.
Experience with PAS X Werum software for electronic batch records with some understanding of editing and validation
Knowledgeable of manual visual inspection or strong understanding of related disciplinary areas in bioprocessing (Drug Product operations)
Demonstrated ability to work in a team and professional environment.
Company Description
A great company doing groundbreaking and important work with a great reputation in the industry!
Company Description
A great company doing groundbreaking and important work with a great reputation in the industry!
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