Life Sciences jobs

• Fishers
• $170,000-195,000
• Posted about 11 hours ago

n//a

• Boston
• 0
• Posted 9 days ago

Director, Cell Culture Process Development Location: Waltham, MA Our client a company focused on developing innovative treatments for chronic dermatological diseases. Their mission is to improve patients' lives by achieving high rates of disease clearance with minimal dosing. They have secured si...

• Lexington
• $170,000 - $205,00
• Posted 10 days ago

Associate Director, Regulatory Affairs CMC Job Summary: The Associate Director, Regulatory Affairs CMC will develop and execute global regulatory CMC strategies to support drug development programs across all phases of the product lifecycle, from IND/IMPD through NDA/MAA submissions and post-appr...

• Gaithersburg
• Commensurate with experience
• Posted 10 days ago

Position Overview: This role is a critical position within the organization, focused on executing the company’s short-term production goals and objectives. The Manager of Production Manufacturing is responsible for overseeing departmental activities across all aspects of the tissue manufacturing ...

• Gaithersburg
• Commensurate with experience
• Posted 10 days ago

Manager, Quality Assurance and Quality Control Position Overview: This role is a key position within the organization, contributing to setting short- and medium-term goals related to quality assurance. The Manager of Quality Assurance & Quality Control is responsible for overseeing and maintainin...

• Cranbury
• 265000
• Posted 11 days ago

Senior Director, Clinical Quality Assurance Join our team dedicated to curing rare diseases! We value our team members' growth and well-being as much as our scientific progress. We seek collaborative, hands-on individuals passionate about making a difference for patients. This is an opportunity t...

• South San Francisco
• $190,000 - $215,000
• Posted 11 days ago

POSITION SUMMARY Reporting to the Sr. Dir., Clinical Outsourcing, this position will be responsible as required for supervising staff in the Clinical Outsourcing group. This position will work with internal teams (e.g. Clinical Development, Clinical Science, Legal, Finance and Procurement Departm...

• Watertown
• $35 to $37 an hour
• Posted 16 days ago

Title: Manufacturing Technician Status: 12-contract Location: Onsite Monday through Friday in Lexington, MA 1st shift from 8 am to 5 pm and 2nd shift from 3:30 pm to 11 pm EST Compensation: $35-$37 per hour DOE   Position Summary: The Manufacturing Technician is responsible for manufacturing oral...

• Watertown
• $80 to $90 an hour
• Posted 16 days ago

Title: Facilities Engineer Status: 12 month contract Location: onsite Monday through Friday in Lexington, MA   This Facilities Engineer will be responsible for providing onsite support of the equipment and facilities at the Lexington location.   Responsibilities:   Manages building systems to ens...

• Boston
• 200,000-225,000 a year
• Posted 25 days ago

Job Title: Director Regulatory Affairs Strategy      Location:  Remote OR Menlo Park, CA OR Waltham, MA Position Overview: The Director Regulatory Affairs Strategy provides global regulatory oversight and project leadership of assigned development products and reports to the Vice President Regula...

• San Francisco
• $290,000 - $350,000
• Posted 26 days ago

Reporting to the Senior Vice President of Global Regulatory Affairs and Quality Assurance, this position will serve as an in-house champion on GxP compliance as well as establish, maintain, and ensure effectiveness of quality programs and documentation to assure compliance in a GxP international ...

• San Francisco
• $250,000 - $300,000
• Posted 26 days ago

ESSENTIAL DUTIES AND RESPONSIBILITIES Support the preparation and implementation of regulatory strategies, for new drug Lead Clinical Quality oversight, including creation and revision of SOPs and training programs for GCP compliance Ensure involvement of Quality from early phases of development ...

• San Francisco
• $255,000 - $300,000
• Posted 26 days ago

POSITION SUMMARY Guide the overall CMC regulatory strategy globally and manage the required resources to meet an aggressive regulatory submission schedule, ensuring the effective fulfillment of company goals and objectives.  This will be an individual contributor role reporting to Sr. VP, Regulat...

• San Francisco
• $90,000 - $120,000
• Posted 26 days ago

POSITION SUMMARY The Sr. CTA acts as a central contact for the designated clinical study team and in this key support role supports the team in the planning, implementation, and completion of clinical studies both outsourced or in-house, through interaction with investigative sites, vendors, and ...

• San Francisco
• $110,000 - $120,000
• Posted 26 days ago

POSITION SUMMARY The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. This position works closely with a cross-functiona...

• San Francisco
• $160,000 - $190,000
• Posted 29 days ago

Sr. Clinical Trial Manager San Francisco, California POSITION SUMMARY Seeking a highly motivated Senior Clinical Trial Manager (Sr. CTM) to be a part of our Clinical Operations team. This is a unique opportunity to join a growing company committed to converting biologics and peptides into life-ch...

• Stamford
• $200,000 - 240,000
• Posted about 1 month ago

The Regulatory Affairs Labeling Director will serve as an expert resource for regulatory labeling and will lead the successful development and implementation of labeling for the company.  Location – Remote: Essential Duties And Responsibilities   Create and maintain labeling content for marketed ...

• Lakewood
• 90,000
• Posted about 2 months ago

Job Title: Validation Engineer II Location: Onsite in Lakewood, NJ Monday through Friday Compensation: $89,000-$92,000 DOE   Overview: The Validation Engineer II is responsible for duties associated with qualifying manufacturing and packaging equipment and Pharmaceutical utilities, including: HVA...

• San Diego
• $167,000.00-$241,925.00
• Posted 3 months ago

Responsible for contributing to the strategy and execution of regulatory CMC plans for emerging gene therapy portfolio. Will require relocation to Southern California with primarily onsite working policy. Your Role Responsible for the regulatory CMC strategy and execution for assigned commercial ...

• Lakewood
• 125,000
• Posted 3 months ago

Job Title: Validation Supervisor Location: Lakewood, NJ Status: Full time direct hire Compensation: $115,000 to $130,000 depending on experience Please note, this position is not able to provide visa transfer, or sponsorship. Overview: This position is responsible for equipment, critical utilitie...