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Director Synthetic Genomics Jobs (NOW HIRING)

Earli

Senior Scientist, Bio AI

Redwood City, CA · On-site

$112K - $153K/yr

... design cancer-specific synthetic promoters and contribute to Earli's clinical pipeline ... genomic/bioinformatic data using state-of-the-art GenAI models • Deep, direct expertise ...

LGC Group

Technician, Manufacturing

Petaluma, CA · On-site

$42.31/hr

Processes include: synthesis, cleavage and deprotection, purification, desalting, and ... Maintain batch records, logs, and other production records as directed per company procedures and ...

LGC Group

Technician, Manufacturing

Petaluma, CA · On-site

$42.31/hr

Processes include: synthesis, cleavage and deprotection, purification, desalting, and ... Maintain batch records, logs, and other production records as directed per company procedures and ...

LGC Group

Technician, Manufacturing

Petaluma, CA

Processes include: synthesis, cleavage and deprotection, purification, desalting, and ... Maintain batch records, logs, and other production records as directed per company procedures and ...

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Director Synthetic Genomics information

What does a director of synthetic genomics do?

A Director of Synthetic Genomics leads research and development initiatives that involve designing, constructing, and modifying genetic material for specific purposes, such as biotechnology, healthcare, or agriculture. They oversee teams of scientists and engineers, manage project timelines and budgets, and ensure compliance with regulatory guidelines. Their role also involves collaborating with external partners, staying updated on scientific advancements, and translating breakthroughs into practical applications or products. The Director is instrumental in shaping the strategic vision for synthetic genomics within their organization.

What are the key skills and qualifications needed to thrive as a director of synthetic genomics?

A Director of Synthetic Genomics typically requires an advanced degree (PhD or equivalent) in genetics, molecular biology, or a related field, along with extensive experience in genomics research and leadership. Expertise with DNA synthesis platforms, next-generation sequencing (NGS) technologies, bioinformatics tools, and regulatory compliance is essential. Strong leadership, strategic thinking, and communication skills are vital for managing multidisciplinary teams and fostering innovation. These skills ensure effective oversight of complex genomic projects, drive scientific advancements, and maintain competitive positioning in the field.

What are some common challenges faced by a director of synthetic genomics when leading multidisciplinary teams?

A Director of Synthetic Genomics often manages teams comprising molecular biologists, bioinformaticians, and engineers, which can present communication and coordination challenges due to differing technical backgrounds. Aligning project goals and timelines while fostering collaboration between research and development functions requires strong leadership and strategic planning. Additionally, staying current with rapid technological advances and regulatory requirements is essential, as these can impact project direction and resource allocation. Effective directors proactively encourage cross-functional knowledge sharing and maintain clear communication channels to ensure project success.
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Infographic showing various Director Synthetic Genomics job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 83% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Director, Formulation and Process Development

AstraZeneca

New Haven, CT • On-site

Full-time

Re-posted 26 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

Are you ready to lead science and engineering that turn breakthrough molecules into reliable, patient-centered injectable medicines? Want to shape how complex biologics, peptides, and genomic medicines are formulated, manufactured, and delivered worldwide?
The Director, Formulation and Process Development, will set the strategy and steer execution for injectable drug products across multiple modalities and presentations, from preclinical through successful licensure. Your work will drive how life-changing therapies reach people with serious and rare conditions, ensuring products are robust, manufacturable, and ready for global scale-up. You will lead a high-performing team, build strong technical networks inside and outside the company, and guide technology transfers that accelerate time to patients.
This role sits at the intersection of science, engineering, and delivery! Partner closely with colleagues in product development, clinical supply, operations, quality, and regulatory to design phase-appropriate solutions, integrate devices and combination products, and shape the technology roadmap that underpins our injectable portfolio.
Accountabilities:
  • End-to-End Injectable Development: Lead formulation and process development for liquid and lyophilized injectables in vials, prefilled syringes, and cartridges, advancing programs from preclinical to commercial licensure.
  • Portfolio Strategy and Integration: Define drug product strategies across biologics, peptides, nucleic acids, and gene delivery modalities, including integration with combination products and delivery devices.
  • Modality and Presentation Expansion:
  • Enable high-concentration proteins and other meaningful modalities, optimizing stability, manufacturability, and patient usability across multiple formats.
  • Technology Transfer and Engineering Solutions:
  • Drive phase-appropriate tech transfer with fit-for-purpose engineering solutions for equipment, processes, and scale, collaborating with internal teams and external partners.
  • Technology Roadmap and Investment:
  • Lead the injectable drug product technology roadmap; evaluate and prioritize critical investments that unlock capability, quality, and speed.
  • Talent Development and Matrix Leadership:
  • Mentor and develop scientists and engineers at multiple levels; build and lead matrixed teams that deliver reliably at pace.
  • Cross-Functional Partnership:
  • Work with development, operations, regulatory, and commercial partners to craft product and supply strategies that connect patient needs to technical and business outcomes.
  • Regulatory Leadership:
  • Serve as authority for regulatory filings and interactions; ensure the technical integrity of drug product sections and inspection readiness.
  • Phase-Appropriate Delivery and Budget Stewardship:
  • Ensure plans, resources, and budgets are aligned to program phase and risk; own delivery and resolve issues to keep achievements on track.

Essential Skills/Experience:
  • BS or equivalent in Bio/Chemical Engineering, Pharmaceutical Sciences, Biochemistry, or related field with meaningful experience
  • 8 years of experience in leading a group of drug product development scientists or engineers with end-to-end drug product development experience (spanning formulation, process development, quality attribute assessment, tech transfer and manufacturing support) for mAbs, fusion proteins, injectable peptides/synthetics programs.
  • 5 years of experience leading a team of scientists and engineers at different levels (directly or in a matrix team) and ensuring their career growth.
  • Proficient in current approaches for formulation and drug product process development, manufacturing processes and equipment, regulatory expectations and applying these to developing efficient approaches to ensure product licensure.
  • Knowledge of high concentration protein formulation development, aseptic processes, vial, prefilled syringe, cartridge presentations, liquid and lyophilization dosage forms is meaningful.
  • Knowledge of current regulatory guidelines and cGMP requirements is necessary

Desirable Skills/Experience:
  • Experience with drug-device combination products and human factors considerations for injectables.
  • Expertise in lyophilization cycle development, scale-up, and aseptic fill-finish operations.
  • Demonstrated application of QbD, PAT, and advanced analytics to define and control critical quality attributes.
  • Leadership of global CMC teams and authorship of BLA/MAA drug product sections.
  • Proven success leading CDMOs/CMOs and complex external partnerships.
  • Background in rare or specialty disease programs and accelerated development pathways.

When we put unexpected teams in the same room, we spark ambitious thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our outstanding and ambitious world.
Why AstraZeneca:
Harness the energy of a fast-paced biotech environment with the reach and investment of a global organization. We bring unexpected teams together to solve hard problems in injectable drug product science-advancing groundbreaking modalities, modernizing aseptic manufacturing, and shaping drug-device combinations that make treatment simpler for patients. We value patience alongside ambition, backing bold ideas with real resources, tailored development, and leaders who empower you to ask sharp questions, take smart risks, and translate data into decisive action that changes lives.
If you are ready to define the technology, teams, and standards that deliver reliable injectables to patients faster, step forward and start the conversation today!
Date Posted
17-Jul-2026
Closing Date
30-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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