Senior QA Associate

Main Tasks and Responsibilities 

• Provide QA floor support and oversight to the production of registration batches for clinical and commercial product materials to ensure that product is manufactured in accordance with specifications, customer’s market authorizations and GMP requirements.  Conducts floor audits and periodic checks of in process documentation and logbooks for compliance during second shift.
• Provide guidance to manufacturing and laboratory personnel to proactively ensure GMP compliance.
• Ensures timely initiation of deviations when quality issues are identified. 
• Perform room and equipment releases and line clearance activities in support of on-time manufacturing.
• Review and release raw materials and components for dispensing to be used in manufacturing.
• Review and approval of the executed cleaning validation/verification reports.   
• Review and issue product labels for use in manufacturing.  
• Participate in investigations related to deviations, out-of-specifications or atypical results, and customer complaints.  Identify and implement corrective and preventive actions that mitigate potential for issue recurrence.    
• Communicate quality-related information and data to key stakeholders within and outside of QA.   
• Engage on manufacturing meetings and assure appropriate assignments of quality activities.
• Perform other duties as assigned, and may need to adjust the timing based on the manufacturing schedule.

Physical Demands

• While performing the duties of this job, the employee is frequently required to stand and walk
• The employee is occasionally required to sit, reach with hands and arms, climb or balance, stoop, kneel, crouch or crawl.
• The employee must occasionally lift and/or move up to 10 pounds.
• Specific vision abilities required by this job include close vision, color vision and ability to adjust focus.
• Must be able to qualify for respiratory protective equipment use.

The Candidate

• Associate degree in a scientific field, or equivalent experience
• Minimum three (3) years’ related experience in QA or QC in life sciences
• Good understanding of CGMP requirements
• Good organization and time management skills
• Effective written and oral communication skills
• Good interpersonal skills with a special focus on customer satisfaction

Application Requirements

When applying for a position with Quotient Sciences to be able to work in our organisation you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined. 

Our Commitment to Diversity, Equity and Inclusion 

Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organisation. As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today. 
 

Specifically we will not discriminate on the basis of race, colour, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws. 
 

This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.