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Company Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them.
At Viral Vector Services (VVS) a division of Company we deliver, from process development through commercial supply, we offer the expertise and resources necessary to help clients deliver innovative gene therapies. Placed in the forefront of our leading and cutting edge Cell and Gene Therapy business enabling clients to cure genetic, rare, and otherwise untreatable diseases.
How will you make an impact?
The Manufacturing Compliance Specialist reports into the Viral Vector Services group at Company and is based in the Cambridge, MA office. The Specialist I in this role will be part of a cohesive team responsible for Deviations and CAPAs for all phases of manufacturing. The Specialist I uses expert knowledge of cGMP regulations and project management to ensure manufacturing readiness. The incumbent will also support investigations and improvement initiatives within the manufacturing operations. Works independently with minimal supervision and direction. Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion.
What will you do?
Support manufacturing corrective and preventative actions
Support manufacturing internal and external observations
Lead manufacturing investigations if needed
Support daily huddle meetings if needed
Practices and promotes safe work habits and adheres to safety procedures and guidelines
Utilizes manufacturing process knowledge and investigational skills to identify and resolve manufacturing issues and drive continuous improvement in process operations
Support and develop consistent manufacturing/quality standards and/or process for Deviations, and CAPAs in new Quality System
Conducts complex document revisions and/or document management including batch production records and manufacturing procedures
Performs training with staff for Deviations and CAPAs as needed
Supports cross-functional continuous improvement teams, with Engineering, Validation, Quality Assurance, Quality Control, Facilities, and Manufacturing Science and Technology
Supports cross-functional company goals for Site Metrics
Builds cross-functional relationships and enhances
Works cooperatively with others to meet group and organizational goals
Participates in initiatives to support, innovation and continuous improvement activities and improved compliance with quality procedures, policies and regulations.
Participate in client and planning meetings as requested
How will you get here?
Bachelor's preferred with 0-3 years experience in pharmaceuticals manufacturing and/or quality
Will consider HS/GED or Associate’s degree with 3- 5 years of related industry experience
Knowledge, Skills, Abilities
Ability to function in a fast paced, dynamic environment with multiple priorities simultaneously
Strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in a diverse community
Ability to make decisions and work with minimal to moderate supervision
Able to provide effective written or verbal communication to peers, senior associates, and area management within their operational groups
Strong planning, organization and multitasking skills
Solid understanding of root cause analysis tools
Strong Leadership skills
Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Company Scientific, Unity Lab Services and Patheon. For more information, please visit Company website.
is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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