Chemical Engineer at AstraZeneca - Remote Job Position
Job Description
Company Overview
AstraZeneca is a global, science‑driven biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines. With a commitment to innovative research and a culture that values collaboration, AstraZeneca delivers life‑changing therapies to patients worldwide. The company operates across multiple therapeutic areas, including oncology, cardiovascular, renal and metabolism, and respiratory diseases, and is recognised for its rigorous quality standards and dedication to scientific excellence.
Position Summary
The Chemical Engineer will join AstraZeneca’s Remote Quality Engineering team, supporting the development and implementation of robust quality control and assurance processes for pharmaceutical manufacturing. This role is responsible for ensuring compliance with industry standards such as ISO, conducting statistical analyses, and driving continuous improvement through root‑cause investigations. The successful candidate will act as a technical liaison between production, quality, and regulatory functions, applying strong problem‑solving skills to maintain the highest level of product integrity.
Key Responsibilities
- Develop, validate, and maintain quality control procedures for chemical manufacturing processes.
- Implement and monitor quality assurance standards, including ISO 9001 and GMP requirements.
- Perform statistical analysis of process data to identify trends, variances, and opportunities for optimisation.
- Conduct routine inspections and audits of production lines, documenting findings and corrective actions.
- Lead root‑cause investigations for quality deviations, preparing detailed reports and recommendations.
- Collaborate with production teams to communicate quality expectations, resolve issues, and support process improvements.
- Prepare and maintain comprehensive documentation of quality incidents, investigations, and corrective actions.
- Provide technical guidance and training to cross‑functional teams on inspection techniques and quality best practices.
- Support regulatory submissions by ensuring all quality data meets compliance requirements.
- Continuously evaluate and enhance existing quality systems to align with evolving industry standards.
Required Qualifications
- 4 to 13 years of professional experience in chemical engineering within a regulated manufacturing environment.
- Demonstrated expertise in quality control processes and quality assurance standards (e.g., ISO, GMP).
- Proficiency in statistical analysis tools (e.g., Minitab, JMP, or similar) for data‑driven decision making.
- Strong knowledge of inspection techniques and documentation of quality issues.
- Experience conducting root‑cause analysis and implementing corrective actions.
- Excellent communication skills with the ability to interact effectively with production, quality, and regulatory teams.
- Proven problem‑solving abilities and meticulous attention to detail.
- Technical knowledge of chemical processes, equipment, and safety protocols.
Required Education
Post‑graduate degree in Chemical Engineering, Pharmaceutical Engineering, or a closely related scientific discipline.
Desired Skills
- Familiarity with advanced process analytical technology (PAT) and process control systems.
- Experience with continuous improvement methodologies such as Six Sigma or Lean.
- Knowledge of regulatory frameworks beyond ISO, such as FDA 21 CFR Part 210/211.
- Ability to develop and deliver training programs on quality and safety topics.
- Proficiency in data visualisation software (e.g., Tableau, Power BI).
Compensation & Benefits
The position offers a competitive salary range of $63,000 to $80,000 annually, commensurate with experience and qualifications. AstraZeneca provides a comprehensive benefits package that includes health, dental and vision insurance, retirement savings plans, paid time off, professional development opportunities, and access to employee wellness programs.
How to Apply
Interested candidates should submit their updated resume and a cover letter outlining relevant experience through the AstraZeneca Careers portal. Please ensure that your application highlights how your background aligns with the responsibilities and qualifications listed above. Applications will be reviewed on a rolling basis, and qualified candidates will be contacted for further assessment.
Required Skills
- Quality control processes Quality assurance standards (e.g.
- ISO) Statistical analysis Inspection techniques Documenting quality issues Root cause analysis Communication with production teams Problem-solving Attention to detail Technical knowledge
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