Quality Assurance Manager
Full Time
Conway, SC
$80,000 - $90,000 a year
Posted Today
Job description
Carolinas Staffing is seeking to hire a Quality Assurance Manager for Direct Hire in Bristol, PA!!!
About the role:
You will manage, plan, organize, direct, and evaluate all activities and QA staff to ensure that Quality support is present on the production floor and documentation is reviewed and issued are resolved promptly and providing Quality oversight over production ensuring compliance with site and corporate standards. You will support to improve safety, customer satisfaction, employee development, continuous improvement, and financial performance consistent with Plant goals. You will make important decisions in ensuring the deviations are investigated, alerts resolved, complaints examined, and product dispositioned promptly. You will report to the Vice President, Quality Assurance.
How you will contribute:
About the role:
You will manage, plan, organize, direct, and evaluate all activities and QA staff to ensure that Quality support is present on the production floor and documentation is reviewed and issued are resolved promptly and providing Quality oversight over production ensuring compliance with site and corporate standards. You will support to improve safety, customer satisfaction, employee development, continuous improvement, and financial performance consistent with Plant goals. You will make important decisions in ensuring the deviations are investigated, alerts resolved, complaints examined, and product dispositioned promptly. You will report to the Vice President, Quality Assurance.
How you will contribute:
- Will provide strong leadership, project and people management skills, and ability to make critical decisions.
- Willing to learn new aspects of the business.
- Hire and retain great talent, develop, and provide challenging work for team members; support the career development of their employees. Manage people performance, maintain performance records, and development.
- Assure a safe and non-discriminatory working environment for employees.
- Ensure compliance with manufacturing, specifications, and company policies. Ensure the departmental SOPs are current and staff trained on activities being performed
- Manages the supplier quality program to ensure cGMP compliance over vendors that provide materials/services for the site
- Ensures GMP compliance of quality systems/tools used at the site including a quality manual, policies, procedures, and work instruction documentation that make up the hierarchy of the Document Control system
- Maintains metrics program with measurables that achieve continuous improvements of processes and procedures
- Prepare the department for both internal and external authorities during audits ensuring facility is always audit ready
- Provide necessary floor support to the production teams and help in resolving compliance concerns.
- Responsible for change control activities/documentation in QMS. Required to perform review of submission documents.
- Ensure deviations and non-conformances are initiated, investigated, and closed.
- Support approval of manufacturing documents (SOP's/WI, Forms)
- Participate / lead teams which impact production, increase efficiency, solve problems, create cost savings, improve quality, and provide new product support.
- Manage relationship with Third Party Testing Labs, Vendors of Equipment and Calibration, suppliers
- Any other duties as assigned
Education and Background:
- Bachelor’s Degree in science preferred or combination of education and working knowledge
- 5 + Years’ experience in pharmaceutical, packaging, or similar regulated industry
- 2+ years direct/indirect supervisory experience and/or leading a team or process
- Working knowledge of cGMPs, ISO standards and production processes.
- Ability to work autonomously applying strong problem-solving skills
- Strong communication skills are needed to manage support personnel.
- Can navigate through CERM (ERP) and QISS (QMS)
- Must be able to lift, push, pull and carry up to 35 lbs.
- In general, you will do a combination of sedentary work and walking around observing conditions in the facility
- 5% Travel.
To Apply: Please send your resume or call
Ryan at
910-754-5393 for any
questions concerning this position.
Job Type: Full-time.
Salary: $80,000.00 - $90,000.00 per year.
Schedule: Monday - Friday 8:30 am to 5:00 pm.
Schedule: Monday - Friday 8:30 am to 5:00 pm.
Benefits:
- 401(k).
- Dental insurance.
- Health insurance.
- Vision insurance.
Schedule:
- Day shift.
- Monday to Friday.
Ability to commute/relocate:
- Bristol, PA: Reliably commute or planning to relocate before starting work (Required).
Experience:
- Quality assurance: 2 years (Required).
Work Location: In person.
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