QA Supervisor - cGMP - food, pharma - Middlesex County, CT
Murphy Search Group
Our client is a leader in their niche product in the U.S.
They develop and manufacture over-the-counter medications, nutritional
supplements, prescriptions, beverages and other
consumer products on a contract basis. They continually expand their product
base and currently have several new and interesting products in the R&D
phase right now.
This Quality professional is responsible for ensuring that
the Quality Assurance auditing in our client’s two (2) CT facilities operates
effectively and efficiently while remaining fully integrated with company
business objectives. Responsibilities include performing necessary inspection
and testing required for product release, supporting the manufacturing
operation, providing timely information and
communicating with both internal and external customers.
Successful candidate will present a high level of
integrity and ethics, strong commitment to quality and a proven track record
in quality assurance within GMP environment.
the daily activities of the QA Associates;
providing direction of responsibilities and guidance for completing
tasks as well as providing any necessary training.
packaging audit, ensuring final product meets packaging specifications
and is within the allowed accepted quality limits (AQL); inspect all
incoming packaging components, ensuring specifications are met by
performing appropriate tests following determined component
investigations as directed and collect information to assess root causes
when product or processes are not meeting specifications.
in the conduct of internal audits of cGMP to ensure compliance to cGMP
and internal procedures and policies.
collaboration with other key personnel, review Quality SOPs and manufacturing
records on a periodic basis and revise or create new documents
finished/completed batch production documents for procedural or
mathematical errors and approve for release of product.
identified manufacturing deficiencies to key personnel (Machine
Operator, Technical Director, Production Supervisor…etc.).
packaging specifications; review and approve
Bill of Materials (BOM).
all work in accordance with established Safety, cGMP and company procedures; support company mission and values.
years experience in Quality Assurance in the
pharmaceutical manufacturing industry.
current knowledge of cGMP regulations and industry standards.
3 years Supervisory experience
- Strong team player,
demonstrated team attitude and behaviors.
organizational skills; ability to delegate.
writing skills, Strong attention to detail, Strong problem-solving and