Associate Director, Technical Operations - Small Molecule Drug Substance

We have an exciting opportunity for an Associate Director, Technical Operations - Drug Substance at our Elkton Site in Virginia, USA.

At our company, we aspire to be the premier research-intensive biopharmaceutical company, using the power of leading-edge science to save and improve lives around the world. We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals.

Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence.

At our site, you'll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best work. We are building deep small molecule expertise in the U.S., and we want team members who are excited to grow their skills, help improve how we operate, and contribute to a site positioned for future growth.

The successful candidate will provide technical leadership and operational support for the startup, technology transfer, validation, and ongoing commercial manufacture of active pharmaceutical ingredients (APIs).

This role is responsible for leading technical activities across assigned processes and projects , supporting the capital project and facility startup phase through to commercialization and lifecycle management . The Associate Director will ensure safe, compliant, and reliable process performance , while driving continuous improvement and technical excellence.

- Recognized subject matter expert in Drug Substance process support, and commercial manufacturing

- Provide technical oversight and hands-on leadership for API manufacturing processes, including:

- Support the Capital Project Team , contributing to design, commissioning, qualification, and startup readiness

- Lead process scale-up, technology transfer, and validation (pre-PPQ, PPQ) activities for assigned processes

- Drive improvements in process performance, yield, robustness, and impurity control

- Analyze technical data and support decision-making for process performance and improvements

- Identify and escalate risks, proposing practical, science-based solutions

- Lead and execute technology transfer activities for assigned processes across internal sites and external partners

- Support development and execution of tech transfer plans aligned with project timelines

- Ensure accurate process documentation, knowledge transfer, and batch record readiness

- Support process validation and continued process verification

- Partner with Manufacturing to ensure safe, efficient, and reliable plant performance

- Lead and support deviation investigations, OOS, and CAPA , applying structured root cause analysis

- Monitor process performance and cycle times , identifying improvement opportunities

- Drive continuous improvement initiatives for yield, cycle time, and cost

- Ensure assigned processes operate in compliance with cGMP and regulatory expectations

- Contribute to regulatory submissions and responses , including data generation and technical input

- Ensure data integrity and adherence to quality and safety standards

- Maintain compliance from startup through commercial operations

- Collaborate with Engineering, Capital Projects, R&D, Quality, Supply Chain, and Manufacturing

- Act as a technical representative for assigned processes within cross-functional teams

- Support technology transfer and process improvements across the network

- Participate in interactions with external partners and CMOs as required

- Lead and develop a team of technical specialists and engineers

- Provide coaching, technical guidance, and performance feedback

- Support resource planning and execution of departmental priorities

- Contribute to budget tracking and departmental administration

- Support recruitment, onboarding, and capability development initiatives

- Degree (BSc/BEng/Masters) or higher in Chemistry, Chemical Engineering, or related discipline

- Electronic batch records and process systems (e.g., DeltaV)

- Strong analytical, problem-solving, and communication skills

- Ability to work effectively across cross-functional teams and multiple priorities

We keep the patient at the heart of everything we do and strive to deliver solutions for some of the world's most challenging healthcare needs. We believe breakthrough innovation happens when experienced leaders empower talented teams in an inclusive environment .

- Support delivery of new Drug Substance manufacturing capability

- Drive operational and technical excellence in API production

- Develop your leadership capability in a high-impact environment

Required Skills: Adaptability, Adaptability, Automation Systems, Batch Processing, Biopharmaceutical Industry, Business Management, Capital Project Management, Change Management, Chemical Engineering, Clinical Manufacturing, Commercialization, Data Analysis, Data Integrity, Decision Making, Drug Product Manufacturing, Interpersonal Relationships, Knowledge Transfer, Lean Manufacturing, Manufacturing Scale-Up, Operational Excellence, Process Documentation, Process Optimization, Regulatory Compliance, Root Cause Analysis (RCA), Strategic Thinking {+ 2 more}

Job Posting End Date: 08/15/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.