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Job Title: QA Associate
Job Description
Perform QA duties in support of pharmaceutical production. Allocate materials to batches for manufacturing. Assign raw materials to batch records. Verify material use at end of production runs. Review batch records to assure only released ingredients, components, and labeling are used in production. Assure compliance with applicable SOPs. Assure compliance of manufacturing with Batch Record Instructions and requirements. Perform other QA/Doc Control duties as a support to the QA Operations team including label making, printing records, document revisions, issuing records. Cross-train as a QA Inspector to include raw material sampling, log book reviews, line clearances. Participate in weekly QA walkarounds to ensure cleanliness of facility, identify compliance risks, etc.
Hard Skills
This is a Contract-to-Hire position with a duration of 9 Month(s).
Work Site
This is a fully on-site position in Saint Louis, Missouri.
Work Environment
Hours are flexible day shift (start time 7 or 8:00am – 8 hours from there). May have to cover a night shift schedule once or twice a year. Primarily working at a computer but will be needed for weekly walkthroughs of the facility and backing up inspectors, which could be 50/50 desk or floor related responsibilities. Work within an office environment in the operations building. Environments can be dusty due to powdered products or animal feed-based products.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
Job Description
Perform QA duties in support of pharmaceutical production. Allocate materials to batches for manufacturing. Assign raw materials to batch records. Verify material use at end of production runs. Review batch records to assure only released ingredients, components, and labeling are used in production. Assure compliance with applicable SOPs. Assure compliance of manufacturing with Batch Record Instructions and requirements. Perform other QA/Doc Control duties as a support to the QA Operations team including label making, printing records, document revisions, issuing records. Cross-train as a QA Inspector to include raw material sampling, log book reviews, line clearances. Participate in weekly QA walkarounds to ensure cleanliness of facility, identify compliance risks, etc.
Hard Skills
- 1-3 years of QA experience within the pharmaceutical industry
- Basic computer skills
- Excel (basic knowledge: download information, not creating formulas or graphs)
- Team player
- Ability to take constructive criticism
- Ability to take instruction
- Ability to get along with others
- Ability to handle stress and shift priorities quickly
This is a Contract-to-Hire position with a duration of 9 Month(s).
Work Site
This is a fully on-site position in Saint Louis, Missouri.
Work Environment
Hours are flexible day shift (start time 7 or 8:00am – 8 hours from there). May have to cover a night shift schedule once or twice a year. Primarily working at a computer but will be needed for weekly walkthroughs of the facility and backing up inspectors, which could be 50/50 desk or floor related responsibilities. Work within an office environment in the operations building. Environments can be dusty due to powdered products or animal feed-based products.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
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