QA Specialist I

Please Contact To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Anshul Bawankar at email address   can be reached on #

630-576-1940

.
 
We have Contract Role QA Specialist I for our client at Scarborough, Maine. Please let me know if you or any of your friends would be interested in this position.
 
Position Details :  
QA Specialist I - Scarborough, Maine
Location                         : Scarborough, Maine
Project Duration          : 12 Months of contract
Pay Rate                         : $30/hr on W2
 
Description:
The position of Quality Assurance Specialist I is within our Infectious Disease Business
Unit located at Scarborough, Maine. In this role you will, under basic direction and supervision,
provide support for product quality assurance, process improvements and all quality system
programs at the Scarborough Site.
 
RESPONSIBILITIES:

• Review production batch records (DHRs) for accuracy and completeness in order to approve intermediate products for use in production.
• Review finished goods batch records.
• Report all deviations in these records and assure they have been addressed and resolved prior to issuing approval.
• Conduct spot-checks inspections/audits of production operations
• Write Standard Operating Procedures (SOPs) as necessary
• Assist in testing of complaint samples and stability samples and report results out of acceptance limits Initiate Quality Incidents (QI)
• Provide backup to other Quality Specialists
• May organize the long-term stability program and be responsible for administering the sample retention program
• May administer or support the site’s current electronic Document Control System (eDCS)
• May administer or support the site’s current electronic Quality Incident and CAPA tracking system.

 
BASIC QUALIFICATIONS | EDUCATION:

• Bachelor's Degree in Chemistry, Biology, Life Science, or other related technical field in a scientific or technical area or the equivalent combination of education and experience.
• 1+ years in Quality Assurance role or similar support for manufacturing.

 
PREFERRED QUALIFICATIONS:

• Prior experience in a Quality Assurance role or similar support role in the medical device industry

 
COMPETENCIES:

• Knowledge of spreadsheet software and word processing software
• Ability to follow procedures and accurately document results
• Ability to understand the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
• Ability to write routine reports and correspondence
• Ability to apply mathematical concepts such as fractions, percentages, ratios, and proportions to practical situations

 
 
To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Anshul Bawankar at email address   can be reached on #

630-576-1940

.
 
About generis tek: generis tek is a boutique it/professional staffing based in Chicago land. We offer both contingent labor & permanent placement services to several fortune 500 clients nationwide. Our philosophy is based on delivering long-term value and build lasting relationships with our clients, consultants and employees. Our fundamental success lies in understanding our clients’ specific needs and working very closely with our consultants to create a right fit for both sides. We aspire to be our client has most trusted business partner.