• Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
• We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Responsibilities:

• Proactively investigating, identifying, and implementing best-in-class quality engineering practices.
• Providing focused quality engineering support and assuming responsibility for timely and effective coordination and execution of assigned development project activities.
• Establishing effective corrective action plans and leading in implementing quality assurance plans, process controls, and CAPA systems designed to meet or exceed internal and external requirements.
• Acting as an effective leader or team member in supporting quality disciplines, decisions, and practices.
• Applying sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
• Reviewing and approving product and process qualifications, validations, and other change control-related documentation.
• Developing product/process assurance plans, which include all required elements, and identifying and implementing effective process control systems to support the development, qualification, and ongoing manufacturing of products.
• Generating internal quality documentation such as quality plans, standard operating procedures, and inspection procedures.
• Participating in product review boards, identifying non-conformance trends, and developing technical investigation plans, including investigating and analyzing customer/internal complaints.
• Performing analytical measurements and experiments to qualify or resolve product and process issues.
• Developing and implementing strategic quality plans, master validation plans, validation protocols, inspection plans, and quality/regulatory compliance operating procedures to meet FDA and ISO requirements.
• Tracking quality trends and initiating action items to resolve issues while managing assigned corrective actions.
• Monitoring field quality and analyzing field returns to determine root causes.
• Providing training and support for quality system processes and quality engineering practices.

Requirements:

• A bachelor's degree (minimum) in engineering, life sciences, or a related field.
• 3 to 10 years of progressively responsible experience in medical device quality assurance.
• One to two years of auditing experience is preferred.
• Certification as a CQA, CQE, or CQM and membership with ASQ are highly desirable.
• Advanced computer skills to efficiently utilize quality systems and tools.
• Strong writing, mathematical, and statistical skills for data-driven decision-making.
• Adept at managing multiple projects and meeting deadlines with precision.
• Proficient in verbal and written communication to effectively convey complex information.

All your information will be kept confidential according to EEO guidelines.