Are you a Quality Engineer who is looking to join one of the top companies within the Manufacturing Industry? Are you looking to further your career and grow? Do you have GMP experience preferably in Pharma? If you answered yes to those three questions, then apply today! Acara Solutions is seeking highly qualified candidates to work Onsite with our client in Paris, KY. Interested? Here's what you'd do:
- Under general supervision, develop, modify, apply, and maintain quality evaluation and control systems/protocols.
- Devise and implement methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
- Design and analyse inspection and testing processes, mechanisms, and equipment.
- Conduct quality assurance tests and perform statistical analysis to assess the level of control and manage product quality risks.
- Responsible for Quality System maintenance.
- Performs root cause analysis and implementation of corrective action for process-related issues.
- Identifies statistical methods relevant to the manufacturing process.
- Responsible for continual improvement activities to enhance the Quality System.
- Develops and performs training to build quality awareness throughout the company.
- Collaborates with Manufacturing, Research and Development and Engineering to ensure
- the transfer of newly developed products that are in accordance with approved data and analysis.
- Conducts audits, including closing out audit findings, creating audit finding reports and works with multi-functional teams to determine proper corrective and preventive actions.
- Assists in the creation and maintaining quality documentation.
- Implements and maintains Statistical Process Control (SPC) for products and identifies potential process improvements.
- Conduct Active Pharmaceutical Ingredient product review.
- Evaluate the impact of process improvement efforts and manufacturing deviation on process validation and product design.
- Demonstrates good communication and project management skills.
- Collaborate with team members to support company goals.
- Develop experiments by applying full and fractional factorial techniques.
- Assist in validation processes, including TM validation, manufacturing process validation, cleaning validation.
Here's what you'll get:
- Pay rate: $37.40/Hour
- Hours: 5/40
- Length: Temp
Sound like a good fit? APPLY TODAY
Email resume to: kruzickia@acarasolutions.com About Acara Solutions Acara is a premier provider of recruiting and workforce solutions, and we help companies compete for talent. With a legacy of needs in various industries worldwide, we partner with clients, listen to them, and customize visionary talent solutions that drive desired business outcomes. We leverage decades of experience to deliver contingent staffing, direct placement, executive search, and workforce services worldwide.
Required Skills / Qualifications:
- Bachelor of Science Degree in Chemistry or Chemical Engineering or Material Science
- Minimum 3 years of GMP experience, preferably in Pharma
- Minimum 3 years of experience in ISO 9000/ AS9100.
- Minimum 3 years of experience with LEAN and Six Sigma methodologies.
- Minimum 3 years of experience with the Design of Experiments (DOE) and the ability to lead the implementation of improvements.
- Minimum 3 years of experience working with Microsoft Excel and Word.
- Minimum 3 years of experience in statistical process and quality control principles.
Preferred Skills / Qualifications:
- Minimum 3 years of experience in a quality engineering role in chemical, rubber, or plastic industries
- ASQ Certified Quality Engineer
- Experience with Minitab or other statistical software
- Skilled in metrology tools.
- Ability to work optimally in a team environment.
- Ability to identify problems and communicate solutions in a constructive and positive manner.
- Attention to detail; excellent organisational and record-keeping skills..
Additional Information:
- Upon offer of employment, the individual will be subject to a background check and a drug screen.
- In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.
Aleron companies (Acara Solutions, Aleron Shared Resources, Broadleaf Results, Lume Strategies, TalentRise, Viaduct) are Equal Employment Opportunity and Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender identity, sexual orientation, national origin, genetic information, sex, age, disability, veteran status, or any other legally protected basis. The Aleron companies welcome and encourage applications from diverse candidates, including people with disabilities. Accommodations are available upon request for applicants taking part in all aspects of the selection process.
Applicants for this position must be legally authorized to work in the United States. This position does not meet the employment requirements for individuals with F-1 OPT STEM work authorization status.
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