Location: Boston,MA, USA
About Pacira
Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results.
Why work with us?
Rarely do you have an opportunity to do work that really matters. What drives us is our mission. What makes us successful are our people. At Pacira, you are part of an inclusive culture that fosters collaboration, growth, and innovative thinking - a place where you can make an impact and help change the standard of care in non-opioid pain management. Be part of our movement, let's pursue excellence together.
Summary:
The purpose of this position is to provide gene therapy expertise, management of analytical development efforts, and general contribution to the gene therapy program.
Essential Duties & Responsibilities:
The following statements are intended to describe the general nature and level of work being performed by an individual assigned to this job. Other duties may be assigned.
* Manage the external development, qualification, and validation of analytical release and characterization methods for the helper dependent adenoviral gene therapy program.
* Manage multiple stability and/or comparability programs and critically evaluate the experimental results.
* Work closely with other departments for manufacturing efforts including internal and external collaborative organizations.
* Contribute to documents for regulatory submissions and/or review.
* Represent CMC at project team meetings as needed.
* Provide cross-training and guidance from within CMC to ensure a high functioning program.
* Maintain high level of technical knowledge in areas of responsibility.
* Apply the knowledge, skills and experience obtained to increase efficiency in solving new problems.
Supervisory Responsibilities:
This position may have supervisory responsibility.
Education and Experience:
* The position requires a PhD in biology, chemistry, or a related field with at least 8 years of experience in development or a related role. Alternatively, candidates with an MS in a relevant field can be considered if they have a minimum of 12 years of experience in a similar role.
* Strong preference for experience within the CGT field
Knowledge, Skills, and Abilities:
* Extensive knowledge of the analytical techniques and trends within adenoviral CGT, particularly molecular and cellular biology
* Thorough understanding of the principals upon which CMC analytical and process development methodology is based
* Extensive knowledge of GMP, regulatory requirements, guidelines and standard CGT practices
* Ability to develop experimental plans for characterization and optimization of existing processes
* Strong organizational skills (e.g. daily tasks, documentation, archived information)
* Strong interpersonal skills (e.g. working with other teams and organizations to achieve shared goals)
* Proficient in the use of computers and widely used workplace applications (e.g. Microsoft Office, Outlook, graphing software, etc.)
* Hands-on approach with a strategic and operational focus; capable decision maker in the execution of responsibilities with a high degree of flexibility to adapt to company and industry changes
* Collaborative leader able to operate effectively and with a strong sense of urgency in a fast-paced environment
* Organized problem solving and troubleshooting skills (e.g. rational progression of investigation)
* Comfortable challenging the status quo and bringing forward innovative solutions to make better possible
* Proficient at creating and communicating a clear vision among team members effectively aligning resources and activities to achieve functional area and/or organizational goals
* Excellent documentation skills (e.g. notebook, reports)
* Outstanding communicator: direct, effective, clear, concise, well organized and appropriate. (e.g. able to participate in scientific discussions and written interactions)
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
This may be a remote position with some visitations of laboratory settings.
Benefits:
* Medical, Prescription, Dental, Vision Coverage
* Flexible Spending Account & Health Savings Account with Company match
* Employee Assistance Program
* Mental Health Resources
* Disability Coverage
* Life insurance
* Critical Illness and Accident Insurance
* Legal and Identity Theft Protection
* Pet Insurance
* Fertility and Maternity Assistance
* 401(k) with company match
* Flexible Time Off (FTO) and 11 paid holidays
* Paid Parental Leave