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Job Requirements of Quality Assurance Associate:
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Employment Type:
Contractor
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Location:
Fremont, CA (Onsite)
Do you meet the requirements for this job?
Quality Assurance Associate
Careers Integrated Resources Inc
Fremont, CA (Onsite)
Contractor
Duration:0-12 month(s)
Description/Comment:
Conducts routine and non-routine analysis, including but not limited to biochemical and chemical analysis, of raw materials, in-process items and finished product according to established operating procedures. Compiles data for documentation of test procedures that may include stability program testing and formulation studies. Calibrates and maintains lab and analytical equipment. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. May develop testing and analysis methods and procedures in accordance with established guidelines. This position requires knowledge that is acquired through experience, specialized education or training. The role has clearly defined procedures and tasks as well as defined guidelines to aid in decision making. The job requires a basic understanding of work routines and procedures in own discipline. The technical procedures for this level are well defined. The job works within well-defined procedures that may involve a variety of work routines. This job typically requires a minimum of 2 or more years experience.
Additional Job Details:
Hiring Manager notes: Local candidates only, Hybrid role. 2+ years experience. Exp with medical device or pharma companies, highly preferred. QA or regulatory affairs, highly preferred. Day to Day Managing compliance. Interview Process: Panel interview.
Description/Comment:
Conducts routine and non-routine analysis, including but not limited to biochemical and chemical analysis, of raw materials, in-process items and finished product according to established operating procedures. Compiles data for documentation of test procedures that may include stability program testing and formulation studies. Calibrates and maintains lab and analytical equipment. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. May develop testing and analysis methods and procedures in accordance with established guidelines. This position requires knowledge that is acquired through experience, specialized education or training. The role has clearly defined procedures and tasks as well as defined guidelines to aid in decision making. The job requires a basic understanding of work routines and procedures in own discipline. The technical procedures for this level are well defined. The job works within well-defined procedures that may involve a variety of work routines. This job typically requires a minimum of 2 or more years experience.
Additional Job Details:
Hiring Manager notes: Local candidates only, Hybrid role. 2+ years experience. Exp with medical device or pharma companies, highly preferred. QA or regulatory affairs, highly preferred. Day to Day Managing compliance. Interview Process: Panel interview.
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