Job Description:As the Sr. Specialist, External Manufacturing reports into the Senior Manager, External Manufacturing you will be responsible for supporting external manufacturing projects. This individual will facilitate scheduling meetings, follow up on project tasks, and track progress against key project milestones and KPI's. This position is located onsite in Hamilton, Ontario, Canada.
Note: This is a 5 day/week on-site position.
Key Responsibilities:- Collaborating with Contract Development Manufacturing Organizations (CDMOs), the internal manufacturing site, and Clinical Supply Chain team to ensure drug supply is delivered on time.
- Working with internal stakeholders to plan new material introduction activities within the master manufacturing schedule and providing regular updates on ongoing activities and project statuses.
- Support cross-functional planning and execution of tech transfer, scale-up, process characterization, and validation (PPQ/PV). Ensure equipment/facility readiness, comparability, and robust control strategies.
- Partner with QA to ensure GMP compliance, inspection readiness, data integrity, and robust deviation/CAPA and change control. Support internal and external audits and regulatory inspections. Assisting in outlining and drafting Standard Operating Procedures (SOPs) and Work Instructions for departmental activities.
- Support with financial management of invoice approval for payment.
- Performing other duties as required by the business.
Qualifications:- Minimum BSc in chemistry, engineering, or health sciences.
- 3+ years of experience in manufacturing, supply chain management, or project management within the pharmaceutical or radiopharmaceutical industry.
- Strong organizational skills with a proven ability to manage multiple tasks and meet deadlines.
- Excellent communication and interpersonal skills to work collaboratively with internal and external stakeholders.
- Knowledge of GMP regulations and clinical drug supply processes is a strong asset.
- Detail-oriented with a proactive approach to problem-solving.
- Ability to work effectively in a fast-paced, multidisciplinary team environment.
- Willingness to take on new tasks and responsibilities as required.
Preferred Qualifications:- MSc. In chemistry, engineering, or health sciences
- Experience with CDMOs and familiarity with external manufacturing processes
- Ability to communicate effectively in Mandarin
Annual base salary for this position ranges from 99,552.80 to 130,663.05.
AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The range provided in this posting represents an offer pay range used in a majority of situations. The base pay offered will vary depending on multiple individualized factors, including the candidate's skills and experience, job-related knowledge, and other specific business and organizational needs. In some cases, offers outside the range may also be considered to address unique circumstances.
In addition, our permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role). Benefits offered for permanent roles include a competitive Flex Benefits & Retirement Savings Program, 4 weeks' paid vacation, and annual Personal Days. Fixed Term Contract/Temporary positions (excluding students) are offered a Contract Benefits Program.
We are using AI as part of the recruitment process.
This advertisement relates to a current vacancy.
