Halozyme Therapeutics, Inc

Senior Engineer II, Manufacturing Science and Technology

Halozyme Therapeutics, Inc$116K — $162K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • B.S. Degree in Engineering/Sciences required; advanced degree is a plus.
  • 8 years of experience in a cGMP/cGCP environment, preferably in biologics or cell & gene therapy.
  • 5 years of experience supporting process technology transfers and new site startups.
  • 5 years of experience with aseptic bulk formulation and filling for mABs and other therapies.
  • Proven ability to inspire change within a diverse, matrixed environment.

Responsibilities

  • Execute technology transfers and provide routine manufacturing support for aseptic processes.
  • Develop technology transfer plans and campaign summary reports.
  • Lead process and manufacturing risk assessments with mitigation plans.
  • Review engineering drawings, P&IDs, and validation strategies.
  • Align internal and external production plans with clinical demands.

Benefits

  • Comprehensive benefits package including Employee Stock Purchase Program and 401(k) matching.
  • Opportunities for career growth through learning and development programs.
  • Collaborative team environment focused on innovation and impact.
Full Job Description
Senior Engineer II, Manufacturing Science and Technology, and you'll be part of a culture that welcomes diversity, thinks differently to solve problems, works collaboratively as one team, and delivers meaningful innovations that impact people's lives.

How you will make an impact

Halozyme Hypercon is seeking a talented, enthusiastic, and experienced Senior Engineer II, Manufacturing Science and Technology to execute technology transfer and continuous process improvements for our patented and proprietary HyperconTM formulation process. This role reports to the Sr. Director, Manufacturing Science & Technology and will support the company with multiple technology transfers and routine manufacturing process support at global CDMOs and business partner manufacturing sites. This role operates will manage stakeholders cross-functionally both internally and externally. The work for this role is highly matrixed with the complexity of working on several technology transfer programs in parallel as the company executes the 5-year manufacturing strategy for projected growth. The role will serve as an interface between Program Management, Analytical & Process Development, Quality, Supply Chain, Engineering, and Manufacturing for internal, partner, and CDMO stakeholders. The role will participate in cross-functional teams to successfully accomplish goals and objectives, while continuously improving manufacturing supply and process performance. Global travel up to 25% of time may be required during start-up of new manufacturing sites to support technology transfer and batch manufacturing. Lean six sigma methodologies will be leveraged to create, implement, measure, and report on key performance indicators (KPIs) for manufacturing performance. The individual should thrive in a fast-paced and dynamic environment and be a key player in the company's growth. The individual will join a growing, multidisciplinary team of scientists/engineers and industry professionals.

In this role, you'll have the opportunity to:
  • Perform all duties according to the company's core values, policies, and applicable regulations.
  • As a member of the MS&T Team, be a change leader to develop and implement innovative approaches to meet the challenges of the rapidly growing business.
  • Responsible for technology transfer execution and routine manufacturing support for bulk aseptic formulation and filling processes from Phase I clinical through commercialization.
  • Create technology transfer plans, campaign summary reports, process change documentation to support change controls, and CMC support documentation.
  • Lead and own process and manufacturing risk assessments with mitigation action plans.
  • Review engineering drawings, P&IDs, automation control modules, batch records, process control and validation strategies.
  • Partner closely with stakeholders to ensure internal & external production plans and capacity are aligned with clinical demand needs.
  • Support manufacturing network during regulatory site inspections.
  • Partner with PM and IT functions to implement new technologies for data analysis and process monitoring


Requirements

To succeed in this role, you'll need:
  • B.S. Degree in Engineering/Sciences is required; Advanced M.S./PhD degree in Engineering is a plus consideration.
  • Minimum of 8 years of experience working in a cGMP/cGCP environment is required, preferably working in biologics or cell & gene therapy within the biopharmaceutical industry. Preferred experience should be a combination of work experience in Manufacturing, MS&T, Technical Operations, and/or Development.
  • Minimum of 5 years supporting process technology transfers and new manufacturing site start up is strongly preferred.
  • Minimum of 5 years of experience with aseptic bulk formulation and filling processes for monoclonal antibodies (mABs), antibody-drug conjugates (ADCs), antibody oligonucleotide conjugates (AOCs), vaccines, and/or cell & gene therapies.
  • Having both bulk drug substance and aseptic drug product experiences is a plus consideration.
  • Shown ability to inspire change and build new processes within a diverse and matrix organizational environment is required.
  • Advanced manufacturing and technical acumen with ability to influence and direct stakeholder decision-making at senior levels is required.
  • Excellent verbal and written communication skills.
  • Strong organizational and customer service-oriented skills.
  • Ability to work independently and as part of a team.
  • Proficient computer skills.

In return, we offer you:
  • Full and comprehensive benefit program, including an Employee Stock Purchase Program and 401(k) matching.
  • Opportunities to grow in a culture that prioritizes learning, development and progression through in-house programs and tuition reimbursement.
  • A collaborative, innovative team that works as one to amplify your impact-on your career, the work you do and patients' lives.

The most likely base pay range for this position is $116,000-$162,750 per year. Several factors, such as experience, tenure, skills, and particular business needs, will determine an individual's exact level of compensation. Base salary is only one element of employee compensation at Halozyme. Total compensation could include bonuses, sales incentives, and equity awards.

#LI-Onsite

Salary Description

$116,000-$162,750

About Halozyme Therapeutics, Inc

Halozyme Therapeutics, Inc. is a biotechnology company focused on developing and commercializing novel oncology therapies that target the tumor microenvironment. The company's proprietary enzyme rHuPH20 is used to facilitate the delivery of injected drugs and fluids, potentially reducing the treatment burden of other drugs and improving patient convenience and compliance. Halozyme's lead investigational drug candidate, PEGPH20, is a PEGylated recombinant human hyaluronidase under clinical development for the treatment of pancreatic cancer and other solid tumors. The company was founded in 1998 and is headquartered in San Diego, California.
Learn more about Halozyme Therapeutics, Inc
Size
145 employees
Market Cap
$7.7 billion
Industry
Net Income
$129 million
Founded
1998
5 Year Trend
+24.8%
Revenue
$267.5 million
NASDAQ

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