ABOUT US

Bioserv, a company of Sorrento Therapeutics Inc. is a fast growing, clinical stage, antibody-centric, biopharmaceutical company developing new therapies to turn malignant cancers into manageable and possibly curable diseases. Sorrento's multimodal multipronged approach to fighting cancer is made possible by its' extensive immuno-oncology platforms, including key assets such as fully human antibodies ("G-MAB™ library"), clinical stage immuno-cellular therapies ("CAR-T"), intracellular targeting antibodies ("iTAbs"), antibody-drug conjugates ("ADC"), and clinical stage oncolytic virus ("Sephrevir®").

We attract smart people who play well with others. We're small enough for your ideas to make a big impact, and large enough to offer you opportunities to grow professionally at any stage of your career.

If you’re a quick learner, enjoy working in the biotech industry, and share our mission of providing ground-breaking impact to medicine, each other, and our patients, Sorrento Therapeutics is the place for you!

Sorrento Therapeutics, Inc. is a federal government contractor and, in compliance with its obligations under current federal regulations and guidance from the Safer Federal Workforce Task Force, Sorrento requires all employees, including newly hired employees, to present proof of vaccination against COVID-19, unless the employee is legally entitled to an accommodation. For further information, please refer to the Safer Federal Workforce Task Force’s 2021 Guidance for Federal Contractors and Subcontractors (Updated November 10, 2021), available at:

https://www.saferfederalworkforce.gov/contractors/.

WHAT WE ARE LOOKING FOR:

Sorrento Therapeutics (“Sorrento”) is seeking an experienced Manufacturing Associate I/ II to join our team.

Target Salary Range ($64,480-$75,000)

WHAT YOU’LL DO:

The Manufacturing Associate I/ II is responsible for performing moderately complex and diverse procedures and analysis, exercises judgement and initiative associated with the manufacturing process. Champion and mentor others in safety, process improvement and compliance. This role is responsible for the manufacture of products in compliance with current Good Manufacturing Practice (cGMP), regulatory entities, and industry best practices in support of the organization’s goals and objectives. Project coordinate and run processes associated with the manufacture of product per customer specifications.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Lead and execute activities required for the cGMP manufacturing processes.
• Support the maintenance of cGMP-controlled environments.
• Lead efforts in staging materials and equipment for manufacturing activities.
• Lead and execute the implementation of corrective and preventative actions in response to manufacturing deviations.
• Assist and support training of junior staff. Create a culture of safety, support training objectives, compliance and collaboration while implementing process improvements where applicable.
• Perform and role model good documentation practices that meet cGMP guidelines.
• Create, update, and process documentation related to manufacturing jobs.
• Provide support to cross-functional teams to meet production or timeline demands
• Perform environmental monitoring, identify discrepancies, and complete associated documents.
• Responsible for supporting essential supply inventory and equipment.
• Perform aseptic filtration, filling and crimping of product.
• Coordinate the scheduling of product, space, and equipment with management.
• Author batch records, SOPs, and material specifications.
• Performs other duties as assigned.

EDUCATION AND QUALIFICATIONS:

• Bachelor’s degree in Life Sciences, chemistry, or related discipline; or 3 years’ experience in biotechnology, pharmaceutical or related industry; or equivalent combination of relevant education and experience.
• Strong knowledge of QA/QC compliance, deviation management, training, and cGMP compliance.
• Experience with both paper and electronic documentation systems.
• Strong computer skills for all aspects of the manufacturing environment including Outlook, Word, Excel, and web-based programs.
• Strong knowledge and understanding of cGMP.
• Strong attention to detail.
• Ability to work on problems of complex scope, conduct analysis of situations or data, exercise judgement, initiative, and independence.
• Strong written and verbal communication skills.
• Strong organizational skills to prioritize tasks.
• Ability to work on a team and independently

YOUR REWARD:

Support scientists who are on the leading edge of immunotherapies for the treatment of cancer.

Earn a competitive salary that allows you to focus your attention on your passion.

A comprehensive benefits package including: medical, dental, vision, life and disability insurance, matching 401k, 10 paid holidays, and three-weeks’ PTO, plus stock options.

If this sounds like the right career to fit your personality and interests, please apply, we’re looking forward to meeting you!

Principals only. Recruiters, please don't contact this job poster.

Sorrento Therapeutics, Inc. is an Equal Opportunity Employer

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c)