Job Requirements
Barceloneta
Public Trust Polygraph Unspecified
Career Level not specified
Salary not specified
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Job Description
Title: MQA Technician I
Location: Barceloneta, PR
Duration: 06+ months
Payrate: $12/hr to $13.09/hr
Purpose
Describe the primary goals, objectives or functions or outputs of this position.
The primary purpose of this position is to ensure the quality of the pharmaceutical product (Drug Product) and the manufacturing process. Also, to make sure raw materials and commodities used are of the expected quality. Receive, sample and test materials as per specifications. Perform in-process testing in the manufacturing/packaging areas.
Responsibilities
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
• Perform samplings and testing in manufacturing, packaging or IQA. Deliver samples to the laboratory as required.
• Perform the necessary documentation and transactions in the systems (SAP, POMs, LIMS) according with the procedures.
• Perform Line Clearance or verification. Also, perform cleanings as established in the local procedures.
• Perform daily checks to instruments and equipment.
• Handling file and Stability Samples.
• Place Material on Hold Status.
• Handling and delivery of printed materials to the packaging areas.
• Responsible for performing tasks assigned based on identified business area needs.
• Provide assistance to operations in accordance with environmental management, occupational health and safety (EHS) systems and promote continuous improvement. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.
Qualifications
List required and preferred qualifications (up to 10). Include education, skills and experience.
• Associate Degree in Science or related field
• Computer skills proficiency including word processing, spreadsheets, instrumentation related and Client network systems.
• Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired.
• Verbal and written communication skills in English and Spanish. Excellent interpersonal skills. Basic math skills.
Top 3-5 Skills / Requirements
• Fully bilingual English & Spanish
• GMP and documentation acknowledge
• Available to learn and work
Nice to Have
• POMS
• SAP
• Sample Management acknowledge
Work Environment
In what type of environment would this individual be working (i.e.: Team; Individual; type of office, etc.) ?
Team work
Mostly In areas of manufacturing and packaging and sampling
Schedule Expectations
Daily Work Schedule Expectations: 3rd shift / Training will be on 1st and 2nd shift for 2-3 months after that will move to 3rd shift - Candidates must be available to work any shift/weekend based in business needs
Is overtime offered or required? Yes, Is required
Additional Details
Is the new hire going to be working with Toxins? NO
How many rounds of interviews? 1 round
Location: Barceloneta, PR
Duration: 06+ months
Payrate: $12/hr to $13.09/hr
Purpose
Describe the primary goals, objectives or functions or outputs of this position.
The primary purpose of this position is to ensure the quality of the pharmaceutical product (Drug Product) and the manufacturing process. Also, to make sure raw materials and commodities used are of the expected quality. Receive, sample and test materials as per specifications. Perform in-process testing in the manufacturing/packaging areas.
Responsibilities
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
• Perform samplings and testing in manufacturing, packaging or IQA. Deliver samples to the laboratory as required.
• Perform the necessary documentation and transactions in the systems (SAP, POMs, LIMS) according with the procedures.
• Perform Line Clearance or verification. Also, perform cleanings as established in the local procedures.
• Perform daily checks to instruments and equipment.
• Handling file and Stability Samples.
• Place Material on Hold Status.
• Handling and delivery of printed materials to the packaging areas.
• Responsible for performing tasks assigned based on identified business area needs.
• Provide assistance to operations in accordance with environmental management, occupational health and safety (EHS) systems and promote continuous improvement. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.
Qualifications
List required and preferred qualifications (up to 10). Include education, skills and experience.
• Associate Degree in Science or related field
• Computer skills proficiency including word processing, spreadsheets, instrumentation related and Client network systems.
• Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired.
• Verbal and written communication skills in English and Spanish. Excellent interpersonal skills. Basic math skills.
Top 3-5 Skills / Requirements
• Fully bilingual English & Spanish
• GMP and documentation acknowledge
• Available to learn and work
Nice to Have
• POMS
• SAP
• Sample Management acknowledge
Work Environment
In what type of environment would this individual be working (i.e.: Team; Individual; type of office, etc.) ?
Team work
Mostly In areas of manufacturing and packaging and sampling
Schedule Expectations
Daily Work Schedule Expectations: 3rd shift / Training will be on 1st and 2nd shift for 2-3 months after that will move to 3rd shift - Candidates must be available to work any shift/weekend based in business needs
Is overtime offered or required? Yes, Is required
Additional Details
Is the new hire going to be working with Toxins? NO
How many rounds of interviews? 1 round
group id: artech