Contracts Specialist jobs at State of Connecticut

Requirements Required Qualifications & Experience: Bachelor's degree in life sciences, engineering, or related discipline 2+ years of quality experience in pharmaceutical, medical device, or other related industries. Familiarity with regulatory requirements for a 503B Compounding Outsourcing Facility, or applicable experience in sterile pharmaceutical, medical device, or biotech manufacturing and a thorough knowledge and understanding of cGMP. Desired Knowledge, Skills, and Abilities: Proficient in Microsoft Office Suite (Word, Excel, Outlook, and PowerPoint) Strong written and verbal communication skills. Detail oriented and strong organization skills with the ability to provide strategic and improvement recommendations/solutions. Some exposure to regulatory agency inspections (e.g., FDA, notified bodies, etc.). Proven ability to work cross-functionally to achieve business outcomes. Ability spend time in a warehouse environment to quarantine raw materials. Ability to travel (~15%) required to perform external audits. Ability to multitask efficiently and identify roadblocks prior to project milestones. Strong communication skills driving organizational engagement. Ability to be flexible in a fast-paced environment. Ability to work independently with minimal supervision and collaboratively with cross functional teams. SCA Pharma is an equal opportunity employer (Minorities/Females/Disabled/Veterans). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state, or local law.